Apoptosis
Los inhibidores de la apoptosis son compuestos que previenen o retrasan el proceso de muerte celular programada, conocido como apoptosis. Estos inhibidores son vitales para estudiar los mecanismos de supervivencia celular y se utilizan para investigar enfermedades donde la apoptosis está desregulada, como el cáncer, los trastornos neurodegenerativos y las enfermedades autoinmunes. Al modular la apoptosis, estos inhibidores pueden ayudar en el desarrollo de terapias dirigidas a controlar la muerte celular. En CymitQuimica, ofrecemos una amplia selección de inhibidores de la apoptosis de alta calidad para apoyar su investigación en biología celular, oncología y campos relacionados.
Subcategorías de "Apoptosis"
- ASK(6 productos)
- BCL(11 productos)
- Caspasa(127 productos)
- FOXO1(3 productos)
- IAP(65 productos)
- Mdm2(12 productos)
- PD-1 / PD-L1(126 productos)
- PDK(9 productos)
- PERK(24 productos)
- Serina / treonina quinasa(15 productos)
- Survivin(13 productos)
- TNF(91 productos)
- c-RET(51 productos)
- p53(62 productos)
Mostrar 6 subcategorías más
Se han encontrado 5622 productos de "Apoptosis"
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BM-962
CAS:<p>BM-962 (Compound 31) is a potent small-molecule inhibitor with an IC50 value of 4 nM (Ki=0.8 nM) for Bcl-2 and an IC50 of 3.9 nM (Ki<1 nM) for Bcl-xL. It inhibits H1417 and H146 cell lines with IC50 values of 9 and 13 nM, respectively, and shows potential for use in cancer research.</p>Fórmula:C53H58ClF3N6O7S3Forma y color:SolidPeso molecular:1079.71Bfl-1-IN-5
<p>Bfl-1-IN-5 (Compound (R,R,S)-26) is a selective inhibitor of Bfl-1, demonstrating an IC50 of 0.022 μM. This compound enhances the activity of caspase-3/7, with an EC50 of 0.37 μM, and also inhibits the viability of SU-DHL-1 cells, showing an EC50 of 1.3 μM.</p>Fórmula:C24H24F3N3O2Forma y color:SolidPeso molecular:443.46RET ligand-3
<p>RETligand-3 is the ligand for PROTAC QZ2135, which targets RET.</p>Fórmula:C38H42N10O3Forma y color:SolidPeso molecular:686.81HDAC-IN-77
HDAC-IN-77 (HL-5s), an HDAC inhibitor, has the capability to induce ferroptosis and suppress the Nrf2/HO-1 signaling pathway. This compound is utilized in cancer research.Fórmula:C22H26N4O2SForma y color:SolidPeso molecular:410.533MB-PP1
CAS:<p>3MB-PP1 is a bulky purine analog and a Polo-like kinase 1 (Plk1) inhibitor.</p>Fórmula:C17H21N5Pureza:99.96%Forma y color:White SolidPeso molecular:295.38DAPK-IN-2
CAS:<p>DAPK-IN-2: DAPK inhibitor with anticancer potential. Used in cerebral infarction and ischemia research.</p>Fórmula:C17H14N2O4Pureza:98.26%Forma y color:SolidPeso molecular:310.3SL-01
CAS:<p>SL-01, an oral gemcitabine derivative, potently induces apoptosis to hinder breast cancer more effectively than gemcitabine.</p>Fórmula:C18H18ClNO3Pureza:98%Forma y color:White PowderPeso molecular:331.79Sorafenib-d4
CAS:<p>Sorafenib D4 is deuterium-labeled Sorafenib, a multi-kinase inhibitor (Raf-1, B-Raf, VEGFR-3) with IC50s: 6, 20, 22 nM.</p>Fórmula:C21H16ClF3N4O3Pureza:98%Forma y color:SolidPeso molecular:468.85Thalidomide 4'-oxyacetamide-alkyl-C2-amine HCl
CAS:<p>Thalidomide 4'-oxyacetamide-alkyl-C2-amine HCl is an E3 ligase ligand-linker conjugate containing the E3 ubiquitin ligase cereblon (CRBN) and linker.</p>Fórmula:C17H19ClN4O6Pureza:99.78%Forma y color:SolidPeso molecular:410.81Apoptosis inducer 33
<p>Apoptosisinducer 33 (compound H2) is a hydrazone derivative. It exhibits antioxidant and antimicrobial properties, capable of inhibiting the growth of Staphylococcus aureus, Escherichia coli, and Candida albicans. Additionally, Apoptosisinducer 33 can suppress tumor cell proliferation and induce apoptosis (apoptosis), making it useful for tumor research.</p>Fórmula:C16H13N3O2Forma y color:SolidPeso molecular:279.293icFSP1
CAS:<p>icFSP1 is a mitochondria-associated apoptosis-inducing factor regulator with antitumor activity for the study and treatment of tumor diseases.</p>Fórmula:C26H25N3O5Pureza:99.87% - 99.93%Forma y color:SoildPeso molecular:459.49Z-DQMD-FMK
CAS:<p>Caspase-3 inhibitor. Inhibits MG 132-induced small cell lung cancer cell death in vitro.</p>Fórmula:C29H40FN5O11SPureza:98%Forma y color:SolidPeso molecular:685.72JAK/HDAC-IN-2
<p>JAK/HDAC-IN-2, a potent 2-amino-4-phenylaminopyrimidine dual-target inhibitor, effectively suppresses JAK1/2 and HDAC3/6 at nanomolar concentrations.</p>Fórmula:C28H38N6O5SPureza:98%Forma y color:SolidPeso molecular:570.7CIGB-300 acetate
<p>CIGB-300 acetate (P15-Tat acetate) is a peptide that acts as an inhibitor of casein kinase 2 (CK2). It exhibits anticancer properties by disrupting the phosphorylation activity of CK2. CIGB-300 acetate induces apoptosis in various tumor cell lines and is applicable for cancer research.</p>Forma y color:Odour SolidA947
CAS:<p>A947 is a potent and selective SMARCA2 PROTAC that induces the degradation of SMARCA2, with significant antitumor activity in SMARCA4-mutant NSCLC cells.</p>Fórmula:C61H76N12O7SPureza:98.84%Forma y color:SolidPeso molecular:1121.4Antitumor agent-96
<p>"Antitumor agent-96 (Compound D34) is a potent MRE11 inhibitor that down-regulates the homologous recombination (HR) pathway by binding to and suppressing the</p>Fórmula:C27H32N2O2Pureza:98%Forma y color:SolidPeso molecular:416.56WAY-118959-A
CAS:<p>WAY-118959-A is a potential microtubule acetylation inhibitor.</p>Fórmula:C16H14N4OS2Pureza:99.92%Forma y color:SolidPeso molecular:342.44ROS inducer 4
<p>Compound TE3, also known as ROS inducer 4, serves as a mitochondrial inhibitor. This compound induces a variety of mitochondria-related physiological alterations in tumors, including mitochondrial fragmentation, intense generation and accumulation of ROS, reduced mitochondrial membrane potential, and lower ATP content. Additionally, it activates ROS-mediated apoptotic signaling within mitochondria.</p>Fórmula:C49H62BrO4PForma y color:SolidPeso molecular:825.89Thalidomide-Piperazine-Piperidine
CAS:<p>Thalidomide-based E3 ligase ligand linked to a PROTAC piperazine-piperidine chain.</p>Fórmula:C22H27N5O4Forma y color:SolidPeso molecular:425.4894-Epianhydrotetracycline hydrochloride
CAS:<p>EATC, a tetracycline byproduct, combats Pseudomonas to E. coli with MIC50s of 0.75-16 mg/L.</p>Fórmula:C22H23ClN2O7Forma y color:SolidPeso molecular:462.88TAT-BH4 (Bcl-xL)
<p>TAT-BH4 (Bcl-xL), primarily localized at the mitochondria, inhibits apoptotic cell death.</p>Fórmula:C159H268N58O45Pureza:98%Forma y color:SolidPeso molecular:3712.19Malformin A
CAS:Malformin A, from A. niger, is a plant growth regulator and has anti-TMV and cancer cell cytotoxic properties. Intraperitoneal LD50 in mice is 3.1 mg/kg.Fórmula:C23H39N5O5S2Forma y color:SolidPeso molecular:529.72MDM2/4-p53-IN-2
<p>MDM2/4-p53-IN-2 (2q) is a dual MDM2/MDM4 inhibitor, p53 activator; IC50: 70.7 nM(MDM2), 81.4 nM(MDM4); tumor suppressor.</p>Fórmula:C25H17Cl3FN3O3Forma y color:SolidPeso molecular:532.78Ch282-5
CAS:<p>Ch282-5, an orally active inhibitor targeting the Bcl-2 protein, promotes mitochondria-dependent apoptosis (Apoptosis) by disrupting mitophagy and the mTOR pathway. It demonstrates antiproliferative effects on colorectal cancer cells, effective both in vitro and in vivo, while also inhibiting metastasis. Further, Ch282-5 augments Oxaliplatin-induced autophagy (Autophagy) by downregulating Mcl-1 protein and raising platelet count, which helps mitigate the adverse effects of Navitoclax.</p>Fórmula:C34H34N2Na2O14S2Forma y color:SolidPeso molecular:804.75eIF4A3-IN-5
CAS:<p>eIF4A3-IN-5 potently inhibits eIF4AI/II, promising for cancer research.</p>Fórmula:C26H22N2O7Forma y color:SolidPeso molecular:474.469Pyridinium bisretinoid A2E
CAS:<p>Pyridinium bisretinoid A2E (A2E) is a fluorescent molecule isolated from the lipofuscin of retinal pigment epithelium, a weak photosensitizer.</p>Fórmula:C42H58NOPureza:98.19%Forma y color:SolidPeso molecular:592.92β-Glucuronide-dPBD-PEG5-NH2 TFA
CAS:<p>β-Glucuronide-dPBD-PEG5-NH2 TFA is a β-glucuronide-linked pyrrolobenzodiazepine dimer employed in the synthesis of the antibody-drug conjugate (ADC) cIRCR201-</p>Fórmula:C80H102F3N7O37Forma y color:SolidPeso molecular:1810.69Hellebrin
CAS:<p>Cytotoxic and antiproliferative effects of Hellebrin on breast and lung cancer cells.</p>Fórmula:C36H52O15Forma y color:SolidPeso molecular:724.79Dehydroaltenusin
CAS:<p>Dehydroaltenusin is a selective eukaryotic DNA polymerase α inhibitor and a type of antibiotic produced by a fungus (IC50: 0.68 μM).</p>Fórmula:C15H12O6Pureza:98%Forma y color:SolidPeso molecular:288.255Chloranil
CAS:<p>Chloranil (tetrachloro-p-benzoquinone) induces inflammation and neurological dysfunction and can be used to model inflammation in mice.</p>Fórmula:C6Cl4O2Pureza:99.38%Forma y color:SolidPeso molecular:245.88Giloralimab
CAS:<p>Giloralimab (ABBV-927) is a antibody targeting CD40 with anticancer activity for the study of triple-negative breast cancer and non-small cell lung cancer.</p>Pureza:95.6% (SDS-PAGE); 95.1% (SEC-HPLC) - 95.6% (SDS-PAGE); 95.1% (SEC-HPLC)Forma y color:LiquidTAT-BH4 (Bcl-xL) (TFA)
<p>"TAT-BH4 (Bcl-xL) TFA, primarily localized at the mitochondria, inhibits apoptotic cell death.</p>Fórmula:C159H268N58O45·xC2HF3O2Pureza:98%Forma y color:SolidPeso molecular:3712.19 (free acid)Antitumor agent-113
<p>Antitumor Agent-113 exhibits cytotoxicity in A549 cells, with an IC50 of 46.60 μM, and induces apoptosis, making it applicable for research in non-small cell</p>Fórmula:C21H22ClN5O2SPureza:98%Forma y color:SolidPeso molecular:443.95PARP1-IN-15
<p>PARP1-IN-15 (Compound 6) is a PARP1 inhibitor that also inhibits tankyrase (TNKS) and promotes DNA double-strand breaks, leading to tumor cell apoptosis.</p>Fórmula:C16H12N2O2Pureza:98%Forma y color:SolidPeso molecular:264.28FPR1 antagonist 2
<p>Compound 25b, an FPR1 antagonist, exhibits potent inhibition of the formyl peptide receptor 1 with an IC50 of 70 nM.</p>Fórmula:C25H25F3O5Forma y color:SolidPeso molecular:462.462,2'-Dihydroxy chalcone
CAS:<p>2,2'-Dihydroxy chalcone inhibits β-glucuronidase (IC50=1.6 μM) and lysozyme (IC50=1.4 μM), and fights E. coli, S. fowleri, S. albicans, S. aureus.</p>Fórmula:C15H12O3Pureza:99.7%Forma y color:SolidPeso molecular:240.25PROTAC GPX4 degrader-1
CAS:PROTAC GPX4 Degrader-1 (DC-2) is a PROTAC-based compound that efficiently degrades GPX4, demonstrating a degradation concentration (DC 50) of 0.03 μM in HT1080Fórmula:C50H57ClN10O10Forma y color:SolidPeso molecular:993.5Ferroptosis-IN-13
<p>Ferroptosis-IN-13 (compound NY-26) is an inhibitor of ferroptosis. It effectively suppresses RSL3-induced ferroptosis in 786-O cells, with an EC50 value of 62 nM.</p>Fórmula:C32H30F2N4O3Forma y color:SolidPeso molecular:556.602A-1248767
CAS:<p>A-1248767, a derivative of A-1210477, is an MCL-1 inhibitor (IC50=23.9 nM; Ki=0.41 nM) known for its anticancer properties. It binds to MCL-1 with high affinity, induces an increase in MCL-1 protein levels inside cells, and promotes apoptosis in tumor cells.</p>Fórmula:C47H55N7O6Forma y color:SolidPeso molecular:813.98MG-C-30
CAS:<p>MG-C-30 is an orally active CD27 agonist with an EC50 of 0.84 μM. It activates co-stimulatory signaling in NK cells and T cells, thereby enhancing the immune response. In the EG7-OVA mouse model, MG-C-30 demonstrates antitumor activity.</p>Fórmula:C24H26N4O3SForma y color:SolidPeso molecular:450.55HDAC6-IN-22
<p>HDAC6-IN-22 (compound 30), an HDAC6 inhibitor, exhibits an IC50 of 4.63 nM and demonstrates antiproliferative effects against multiple myeloma both in vitro and</p>Fórmula:C24H24N4O2Pureza:98%Forma y color:SolidPeso molecular:400.47Enniatin complex
CAS:<p>Enniatin complex: fungal cyclohexadepsipeptides inhibit enzymes, induce cancer cell apoptosis, and have ionophoric, antibiotic, and hypolipidemic effects.</p>Pureza:98%Forma y color:SolidPROTAC Bcl-xL degrader-2
<p>PROTAC Bcl-xL degrader-2, based on von Hippel-Lindau ligand, is a potent degrader of Bcl-xL (a Bcl-2 family member), demonstrating an IC 50 of 0.6 nM.</p>Fórmula:C68H80N8O14S3Forma y color:SolidPeso molecular:1329.6sEH inhibitor-19
<p>sEH inhibitor-19 (Compound (R)-14i) is an orally active soluble epoxide hydrolase (sEH) inhibitor with an IC50 of 1.2 nM. This compound suppresses the expression of TNF-α and IL-6 and exhibits anti-inflammatory effects in mouse models of acute pancreatitis and Carrageenan-induced edema.</p>Fórmula:C28H28F3N3O4Forma y color:SolidPeso molecular:527.535RMC-6291
CAS:<p>RMC-6291: Oral, covalent KRAS G12C inhibitor, blocks signaling, forms tri-complex with CypA, suppresses RAS activity in tumors.</p>Fórmula:C55H78FN9O8Pureza:98.73%Forma y color:SolidPeso molecular:1012.26Waltonitone
CAS:<p>Waltonitone is a natural ursane-type pentacyclic triterpene isolated from Gentian waltonii Burkill.</p>Fórmula:C30H48O2Pureza:98%Forma y color:SolidPeso molecular:440.7Didocosahexaenoin
CAS:<p>Didocosahexaenoin, omega-3 diglyceride, disrupts mitochondria, induces ROS, apoptosis, and is cytotoxic to prostate cancer cells.</p>Fórmula:C25H40O5Forma y color:SolidPeso molecular:420.58Pimagedine
CAS:<p>Pimagedine is a prototype therapeutic agent for the prevention of formation of advanced glycation endproducts.</p>Fórmula:CH6N4Forma y color:SolidPeso molecular:74.09GPX4-IN-5
CAS:GPX4-IN-5 is a GPX4 inhibitor with antitumor activity.GPX4-IN-5 induces iron death and may be used for the treatment of triple negative breast cancer.Fórmula:C18H17ClFNO5Pureza:99.58%Forma y color:SoildPeso molecular:381.78Ac-VDVAD-CHO TFA
<p>Ac-VDVAD-CHO (TFA) is a caspase-2/3 inhibitor with IC50 values of 46 nM and 15 nM, respectively.</p>Forma y color:Odour SolidRET-IN-28
CAS:RET-IN-28 (Compound 16) is an inhibitor of RET (a transmembrane receptor tyrosine kinase). It specifically inhibits the activity of a mutant RET enzyme (RET-V804M) and is utilized in cancer research.Fórmula:C26H29N9Forma y color:SolidPeso molecular:467.57Human membrane-bound PD-L1 polypeptide
CAS:<p>Human membrane-bound PD-L1 polypeptide serves as an antigen for inducing the production of PD-L1 antibodies [1].</p>Fórmula:C85H140N26O36SPureza:98%Forma y color:SolidPeso molecular:2134.24Enterodiol
Enterodiol is a natural product that can be used as a reference standard.Fórmula:C18H22O4Forma y color:SolidPeso molecular:302.37Thailanstatin D
CAS:<p>Thailanstatin D blocks AR-V7 splicing, disrupts U2AF65/SAP155 binding, and induces apoptosis in CRPC xenografts.</p>Fórmula:C28H41NO8Forma y color:SolidPeso molecular:519.635Z-VEID-FMK
CAS:<p>Z-VEID-FMK is a selective caspase-6 peptide inhibitor that irreversibly covalently binds to the enzyme, thereby inhibiting apoptosis and DNA breakage.</p>Fórmula:C31H45FN4O10Pureza:98%Forma y color:SolidPeso molecular:652.71EGFR/VEGFR2-IN-1
<p>EGFR/VEGFR2-IN-1 (Compound 10e) serves as an inhibitor for VEGFR-2 and EGFR, with respective IC50 values of 0.26 and 0.14 μM. It inhibits microtubule protein polymerization with an IC50 of 40.9 μM and induces cell apoptosis (Apoptosis). EGFR/VEGFR2-IN-1 is applicable in research related to anti-leukemia and anti-lymphoma treatments.</p>Forma y color:Odour SolidValproic acid sodium salt
CAS:Sodium valproate is an anti-epileptic, boosting brain GABA levels and possibly affecting potassium channels for membrane stability.Fórmula:C8H15NaO2Pureza:98% - 99.78%Forma y color:White PowderPeso molecular:166.22,2-Dimethyl-2,3-dihydrobenzofuran-7-ol
CAS:<p>2,2-Dimethyl-2,3-dihydrobenzofuran-7-ol inhibits the proliferation of the THP-1 cell line and anti-infective Leishmania and Toxoplasma gondii RH.</p>Fórmula:C10H12O2Pureza:99.07%Forma y color:SolidPeso molecular:164.20CS4
<p>CS4 is a selective HDAC inhibitor, with IC50 values for HDAC1, HDAC6, HDAC8, HDAC4, and HDAC11 reported as 38 nM, 12 nM, 5.8 μM, 19 μM, and 61 μM, respectively. It enhances the acetylation of α-tubulin and histone 3 (histone 3). Additionally, CS4 activates PPARγ and blocks glycolysis (glycolysis). It induces cell cycle arrest at the G2 phase and triggers apoptosis (apoptosis), exhibiting anticancer effects both in vitro and in vivo.</p>Forma y color:Odour SolidYN14-H
<p>YN14-H is a PROTAC degrader that targets KRASG12C. It effectively inhibits the growth of NCI-H358 and MIA PaCa-2 cells, with IC50 values of 0.042 μM and 0.021 μM, respectively, and DC50 values of 28.9 nM and 18.1 nM. YN14-H significantly induces apoptosis and suppresses cell migration. It demonstrates favorable pharmacokinetics and excellent in vivo antitumor activity.</p>Forma y color:Odour SolidAlbanol B
CAS:<p>Albanol B, from mulberries, combats Alzheimer's, bacteria, and oxidation, hinders cancer growth, and triggers cell arrest and apoptosis.</p>Fórmula:C34H22O8Forma y color:SolidPeso molecular:558.53dTAG-47
CAS:dTAG-47 targets FKBP12 F36V for protein degradation, useful in basal-like breast cancer research.Fórmula:C59H73N5O14Forma y color:SolidPeso molecular:1076.2413-Methyltetradecanoic acid
CAS:<p>LeDSF3 controls HSAF production in Lysobacter, has antifungal properties, and acts as an anti-tumor by inhibiting p-AKT and activating caspase-3.</p>Fórmula:C15H30O2Forma y color:SolidPeso molecular:242.4Rottlerin
CAS:Fórmula:C30H28O8Pureza:>95.0%(HPLC)(qNMR)Forma y color:Light yellow to Brown powder to crystalPeso molecular:516.55Fenvalerate
CAS:Fenvalerate (Evercide 2362) is a protein phosphatase 2B (calcineurin) inhibitor, a synthetic pyrethroid insecticide, that inhibits PP2B-Aα.Fórmula:C25H22ClNO3Pureza:99.62%Peso molecular:419.90Mepazine hydrochloride
CAS:<p>Mepazine hydrochloride (Pecazine hydrochloride) is a MALT1 inhibitor with anticancer and antitumor activity, inhibiting RANK-induced osteoclastogenesis.</p>Fórmula:C19H23ClN2SPureza:99.76%Forma y color:SolidPeso molecular:346.92PR-924
CAS:PR-924 is a selective inhibitor of tripeptide epoxyketone immunoproteasome subunit LMP-7 (IC50: 22 nM).Fórmula:C37H38N4O5Pureza:98%Forma y color:SolidPeso molecular:618.72Ulipristal Acetate
CAS:Fórmula:C30H37NO4Pureza:>98.0%(T)(HPLC)Forma y color:White to Yellow to Green powder to crystalPeso molecular:475.63PND-1186 hydrochloride
CAS:<p>PND-1186 hydrochloride (VS-4718 hydrochloride) is a highly specific, reversible and potent inhibitor of FAK (IC50: 1.5 nM), which can selectively induce</p>Fórmula:C25H27ClF3N5O3Forma y color:SolidPeso molecular:537.97MRT00033659
CAS:<p>MRT00033659 inhibits CK1 (IC50=0.9 μM), CHK1 (IC50=0.23 μM), activates p53, and destabilizes E2F-1; it's a pyrazolo-pyridine.</p>Fórmula:C15H14N4OForma y color:SolidPeso molecular:266.3(±)-Shikonin
CAS:Fórmula:C16H16O5Pureza:>98.0%(HPLC)Forma y color:Orange to Brown powder to crystalPeso molecular:288.30Parthenolide
CAS:Fórmula:C15H20O3Pureza:>97.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:248.32Zardaverine
CAS:<p>Zardaverine (BY 290) is a PDE3/4 inhibitor with anti-hepatocarcinogenic activity and is used in the study of acute renal failure and chronic airflow obstruction</p>Fórmula:C12H10F2N2O3Pureza:99.11%Forma y color:SolidPeso molecular:268.22Methopterin
CAS:<p>Methopterin shows the activation and bone resorption function of murine osteoclasts.</p>Fórmula:C20H21N7O6Pureza:98%Forma y color:SolidPeso molecular:455.43LG100268
CAS:<p>LG100268 is a selective, and oral RXR agonist，inducing transcriptional activation in adipocytes; inhibits keratin 17 increases PD-L1 expression.</p>Fórmula:C24H29NO2Pureza:99.83%Forma y color:SolidPeso molecular:363.49Dynole 34-2
CAS:<p>Dynole 34-2 is a non-competitive inhibitor of dynamin1 and dynamin2 GTPases that inhibits receptor-mediated endocytosis and synaptic vesicle endocytosis.</p>Fórmula:C25H36N4OPureza:99.61%Forma y color:SolidPeso molecular:408.58Batabulin sodium
CAS:<p>Batabulin sodium, an antitumor compound, disrupts microtubules, alters cell shape, halts cell cycle, and induces apoptosis.</p>Fórmula:C13H6F6NNaO3SForma y color:SolidPeso molecular:393.24Cyclamic acid sodium
CAS:<p>Sodium cyclamate is a carbonic anhydrase inhibitor, artificial sweetener, with anticonvulsant properties, and used in cancer research.</p>Fórmula:C6H12NNaO3SPureza:99.84%Forma y color:SolidPeso molecular:201.22Thalidomide-O-C6-NH2 TFA
CAS:<p>Thalidomide-O-C6-NH2 TFA is a synthesized E3 ligase ligand-linker conjugate used in the PROTAC dTAG-13, a degrader of FKBP12F36V and BET[1].</p>Fórmula:C21H24F3N3O7Pureza:98%Forma y color:SolidPeso molecular:487.43Cl-amidine TFA
CAS:Cl-amidine TFA: oral PAD inhibitor, induces cancer cell apoptosis, IC50s: PAD1 - 0.8μM, PAD3 - 6.2μM, PAD4 - 5.9μM.Fórmula:C16H20ClF3N4O4Forma y color:SolidPeso molecular:424.8Tetrac
CAS:<p>Tetrac (Tetraiodothyroacetic acid) is a derivative of L-thyroxine (T4), a thyroxine integrin receptor antagonist.Tetrac induces antiproliferation by blocking</p>Fórmula:C14H8I4O4Pureza:99.04%Forma y color:SolidPeso molecular:747.83(E/Z)-E64FC26
CAS:<p>(E/Z)-E64FC26 is a protein disulfide isomerase (PDI) family inhibitor with affinity for PDIA1, PDIA3, PDIA4, TXNDC5, and PDIA6.</p>Fórmula:C19H23F3O2Pureza:98.23%Forma y color:SolidPeso molecular:340.38ODN 1826
CAS:<p>ODN 1826 is a TLR9 agonist and immunostimulant, which has antitumor effects and promotes cell apoptosis.</p>Pureza:90% - 90%Forma y color:SolidPeso molecular:6364.1Acyclovir-d4
CAS:<p>Acyclovir-d4 is a deuterated compound of Acyclovir. Acyclovir has a CAS number of 59277-89-3. Acyclovir is a synthetic analog of the purine nucleoside, guanosine, with potent antiviral activity against herpes simplex viruses type 1 and 2, varicella-zoster virus and other viruses of the herpesvirus family.</p>Fórmula:C8H7D4N5O3Forma y color:SolidPeso molecular:229.23Thalidomide-piperazine-Boc
CAS:<p>Thalidomide-piperazine-Boc is an intermediate utilized for synthesizing BCL6 PROTAC, which targets B-cell lymphoma 6 protein.</p>Fórmula:C22H26N4O6Forma y color:SolidPeso molecular:442.46Apremilast-d5
CAS:Apremilast D5 (CC-10004 D5) is a deuterium-labeled Apremilast.Fórmula:C22H24N2O7SForma y color:SolidPeso molecular:465.53Pancratistatin
CAS:<p>Pancratistatin, an isoquinoline from Hymenocallis littoralis, triggers apoptosis in melanoma and is studied for neuroblastoma, leukemia, and breast cancer.</p>Fórmula:C14H15NO8Forma y color:SolidPeso molecular:325.27Iodoacetyl-LC-Biotin
CAS:<p>Iodoacetyl-LC-Biotin (Iaa-Biotin) is a sulfhydryl-responsive probe that forms irreversible thioether bonds at alkaline pH, label protein cysteines.</p>Fórmula:C18H31IN4O3SPureza:97.47%Forma y color:SolidPeso molecular:510.43Bleximenib oxalate
CAS:<p>Bleximenib oxalate (Menin-MLL inhibitor 24 oxalate) is a menin-MLL inhibitor that blocks the binding of the menin-KMT2A complex to chromatin at gene promoters.</p>Fórmula:C34H52FN7O7Pureza:98%Forma y color:SolidPeso molecular:689.82Metronidazole-d4
CAS:<p>Metronidazole-d4 is a deuterium labeled compound isotopic tracing.Metronidazole is an antibiotic and antiprotozoal oral and BBB penetration anaerobic bacteria.</p>Fórmula:C6H9N3O3Forma y color:SolidPeso molecular:175.18PT-262
CAS:PT-262: ROCK inhibitor, causes cytoskeleton change, halts lung cancer cell migration.Fórmula:C14H13ClN2O2Pureza:98%Forma y color:SolidPeso molecular:276.72GGTI-2418
CAS:GGTI-2418 is a GGTase I inhibitor with potential antitumor activity and inhibits the growth of human breast tumors.Fórmula:C23H31N5O4Pureza:99.18%Forma y color:SolidPeso molecular:441.52YZ129
CAS:<p>YZ129, an HSP90-calcineurin-NFAT inhibitor with 820 nM IC50, halts GBM growth, arrests G2/M phase, and induces apoptosis.</p>Fórmula:C19H12N2O2Forma y color:SolidPeso molecular:300.31Macitentan-d4
CAS:<p>Macitentan-d4 (ACT-064992 D4) is a C13-labeled inhibitor of the peptides ETA and ETB used to study diseases mediated by endothelin receptor mediation.</p>Fórmula:C19H20Br2N6O4SPureza:96.51%Forma y color:SolidPeso molecular:592.34-Benzoyl-L-phenylalanine
CAS:4-Benzoyl-L-phenylalanine is an L-phenylalanine derivative and optically active amino acid.Fórmula:C16H15NO3Pureza:98.01%Forma y color:SolidPeso molecular:269.30Diphenyl disulfide
CAS:<p>Diphenyl disulfide fights breast cancer by inducing cell death and stopping growth.</p>Fórmula:C12H10S2Pureza:99.95%Forma y color:White To Light Yellow CrystalPeso molecular:218.34Capsazepine
CAS:Fórmula:C19H21ClN2O2SPureza:>98.0%(HPLC)(qNMR)Forma y color:White to Light yellow powder to crystalPeso molecular:376.90(-)-Gallocatechin Gallate
CAS:Fórmula:C22H18O11Pureza:>95.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:458.38J22352
CAS:J22352, a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC50 value of 4.7 nM, enhances anticancer effects inFórmula:C24H21N3O4Forma y color:SolidPeso molecular:415.44Necrostatin 2 S enantiomer
CAS:<p>Necrostatin 2 S enantiomer is the S enantiomer of Necrostatin 2</p>Fórmula:C13H12ClN3O2Pureza:98%Forma y color:SolidPeso molecular:277.71Tubastatin A TFA
CAS:<p>Tubastatin A is a potent HDAC6 inhibitor with IC50 of 15 nM.</p>Fórmula:C22H22F3N3O4Pureza:98%Forma y color:SolidPeso molecular:449.42Thalidomide-O-amido-PEG-C2-NH2
CAS:<p>Thalidomide-based cereblon ligand linked to PEG-C2-NH2 for use in PROTAC E3 ligase conjugates.</p>Fórmula:C19H22N4O7Forma y color:SolidPeso molecular:418.4Casein Kinase inhibitor A86
CAS:<p>Casein Kinase inhibitor A86 is a highly effective and orally bioavailable inhibitor of casein kinase 1α (CK1α) and also inhibits CDK7 (TFIIH) and CDK9 (P-TEFb). It induces apoptosis in leukemia cells, exhibiting substantial anti-leukemic effects.</p>Fórmula:C18H25FN6Forma y color:SolidPeso molecular:344.438Tegaserod
CAS:Tegaserod is a 5-HT4R agonist and 5-HT2B receptor antagonist with antitumor activity used in the treatment of irritable bowel syndrome (IBS).Fórmula:C16H23N5OPureza:99.20% - 99.89%Forma y color:SolidPeso molecular:301.39Cis-5-Norbornene-exo-2,3-dicarboxylic Anhydride
CAS:<p>Cis-5-Norbornene-exo-2,3-dicarboxylic Anhydride: sensitizing, induces HepG2/SK-Hep1 apoptosis, inhibits PP2A. IC50: HepG2=62μM, SK-Hep1=151μM.</p>Fórmula:C9H8O3Pureza:99.32%Forma y color:SolidPeso molecular:164.16Curcumin-d6
CAS:<p>Curcumin D6 (difluoroformylmethane D6) is deuterium-labeled curcumin (Turmeric yellow). Curcumin (Turmeric yellow) is a natural phenolic compound with various pharmacological effects, including anti-inflammatory, antioxidant, anti-proliferative and anti-a</p>Fórmula:C21H20O6Pureza:98%Forma y color:SolidPeso molecular:374.422Acyclovir hydrochloride
CAS:<p>Acyclovir (Aciclovir) hydrochloride is an effective oral antiviral agent with potent anti-herpetic activity. It exhibits IC50 values of 0.85 μM for HSV-1 and 0.86 μM for HSV-2, indicating strong inhibitory effects against these strains. Additionally, Acyclovir hydrochloride induces cell cycle disturbances and apoptosis. This compound also prevents bacterial infections during induction therapy for acute leukemia.</p>Fórmula:C8H12ClN5O3Forma y color:SolidPeso molecular:261.67TZ9
CAS:<p>TZ9 is a Rad6 inhibitor with anticancer activity.TZ9 inhibits Rad6B-induced ubiquitination of histone H2A.TZ9 induces cell cycle arrest and apoptosis.</p>Fórmula:C17H14N6O4Pureza:99.69%Forma y color:SolidPeso molecular:366.33TMI-1
CAS:<p>TMI-1 (WAY-171318), a novel orally active inhibitor of ADAM17 (TACE) and MMP, induces tumor apoptosis in a breast cancer.</p>Fórmula:C17H22N2O5S2Pureza:97.36%Forma y color:SolidPeso molecular:398.5Indirubin-3'-monoxime
CAS:Fórmula:C16H11N3O2Pureza:>98.0%(HPLC)Forma y color:Light yellow to Brown powder to crystalPeso molecular:277.28Isoscabertopin
CAS:<p>Isoscabertopin has anticancer activity.</p>Fórmula:C20H22O6Pureza:98%Forma y color:SolidPeso molecular:358.39Everolimus-d4
CAS:<p>Everolimus-d4 is a deuterated compound of Everolimus.</p>Fórmula:C53H83NO14Forma y color:SolidPeso molecular:962.264Thalidomide-Piperazine 5-fluoride
CAS:<p>Thalidomide-Piperazine 5-fluoride: a cereblon ligand-linked E3 ligase via PROTAC tech.</p>Fórmula:C17H17FN4O4Forma y color:SolidPeso molecular:360.34Momelotinib sulfate
CAS:<p>Momelotinib sulfate is an ATP-competitive JAK1/JAK2 inhibitor (IC50: 11 nM/18 nM). It has 10-fold selectivity versus JAK3.</p>Fórmula:C23H26N6O10S2Pureza:98%Forma y color:SolidPeso molecular:610.62Atractylenolide III
CAS:Fórmula:C15H20O3Pureza:>98.0%(T)(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:248.32Chiisanoside
CAS:<p>Chiisanoside is a useful organic compound for research related to life sciences. The catalog number is T123983 and the CAS number is 89354-01-8.</p>Fórmula:C48H74O19Forma y color:SolidPeso molecular:955.101Licofelone
CAS:Fórmula:C23H22ClNO2Pureza:>95.0%(HPLC)Forma y color:White to Almost white powder to crystalPeso molecular:379.88Tamoxifen-d5
CAS:<p>Tamoxifen-d5 is a deuterium labeled Tamoxifen.</p>Fórmula:C26H29NOPureza:98%Forma y color:SolidPeso molecular:376.55PERK-IN-2
CAS:<p>PERK-IN-2 is a potent inhibitor of PERK(IC50 of 0.2 nM).</p>Fórmula:C23H18F3N5OPureza:98%Forma y color:SolidPeso molecular:437.42Citrinin
CAS:<p>Citrinin: a mycotoxin with antifungal, antibacterial, potential anticancer, and neuroprotective properties; contaminates food.</p>Fórmula:C13H14O5Pureza:98%Forma y color:Lemon-Yellow Needles From Alc SolidPeso molecular:250.25Ibuprofen-d3
CAS:<p>Ibuprofen D3 is a deuterium labeled Ibuprofen. Ibuprofen is a COX-1 and COX-2 inhibitor (IC50s: 13 μM and 370 μM).</p>Fórmula:C13H18O2Forma y color:SolidPeso molecular:209.3Prinaberel
CAS:<p>Prinaberel (ERB-041) is an effective and selective ERβ agonist and >200-fold selective for ERβ.</p>Fórmula:C15H10FNO3Pureza:97.1%Forma y color:SolidPeso molecular:271.24Octreotide
CAS:Octreotide (SMS 201-995) is a potent inhibitor of growth hormone, glucagon, and insulin.Fórmula:C49H66N10O10S2Pureza:99.3% - 99.64%Forma y color:White PowderPeso molecular:1019.24FTI-277
CAS:<p>FTI-277, an FTase inhibitor, blocks H-Ras/K-Ras signaling and HDV infection; mimics Ras CAAX peptide.</p>Fórmula:C22H29N3O3S2Forma y color:SolidPeso molecular:447.61PI-103 Hydrochloride
CAS:<p>PI-103 Hydrochloride is a dual PI3K/Akt and mTOR inhibitor exhibiting nM-level inhibition of p110α, p110β, p110δ, p110γ, DNA-PK, mTORC1, and mTORC2.</p>Fórmula:C19H17ClN4O3Pureza:97.07%Forma y color:SolidPeso molecular:384.82Sunitinib-d10
CAS:<p>Sunitinib D10, a deuterium-enriched version, inhibits VEGFR2 and PDGFRβ tyrosine kinases (IC50: 80 nM/2 nM).</p>Fórmula:C22H27FN4O2Pureza:98%Forma y color:SolidPeso molecular:408.54Rutin trihydrate
CAS:<p>Rutin trihydrate is a natural flavonoid with antioxidant, anti-inflammatory, anti-diabetic, and anti-cancer benefits, plus heart and brain protection.</p>Fórmula:C27H36O19Forma y color:SolidPeso molecular:664.56RKI-1447 dihydrochloride
CAS:<p>RKI 1447 dihydrochloride: selective ROCK inhibitor, inhibits colorectal cancer growth, promotes apoptosis (ROCK1 IC50=14.5 nM, ROCK2 IC50=6.2 nM).</p>Fórmula:C16H16Cl2N4O2SForma y color:SolidPeso molecular:399.29Z-Ile-Leu-aldehyde
CAS:<p>Z-Ile-Leu-aldehyde is an effective and competitive peptide aldehyde inhibitor of γ-secretase and notch.</p>Fórmula:C20H30N2O4Pureza:98%Forma y color:SolidPeso molecular:362.46MCL-1/BCL-2-IN-2
CAS:<p>MCL-1/BCL-2-IN-2 is a selective Mcl-1 and Bcl-2 inhibitor with potential antitumor activity for tumor research.</p>Fórmula:C20H15BrN2O2SPureza:98.03%Forma y color:SolidPeso molecular:427.31Alantolactone
CAS:Fórmula:C15H20O2Pureza:>95.0%(GC)Forma y color:White to Light yellow powder to crystalPeso molecular:232.32NCX 4040
CAS:<p>COX-2 expression inhibitor</p>Fórmula:C16H13NO7Pureza:98%Forma y color:SolidPeso molecular:331.28Tubulin inhibitor 1
CAS:Tubulin inhibitor 1 blocks tubulin polymerization, with strong anti-tumor effects, induces apoptosis and G2/M mitotic arrest.Fórmula:C21H24N2O4Pureza:98%Forma y color:SolidPeso molecular:368.43Pitavastatin D4
CAS:Pitavastatin D4 is deuterium labeled Pitavastatin. Pitavastatin is a potent inhibitor of HMG-CoA reductase.Fórmula:C25H24FNO4Pureza:98%Forma y color:SolidPeso molecular:425.49Ancitabine
CAS:<p>Ancitabine is an antitumour drug that improves Hailey-Hailey disease-related phenotypes in yeast models. inhibits DNA synthesis, acute leukaemia.</p>Fórmula:C9H11N3O4Pureza:99.91%Forma y color:SolidPeso molecular:225.2FPA-124
CAS:<p>FPA-124 is a cell-permeable copper complex that acts as a selective Akt (protein kinase B) inhibitor to induce apoptosis in a variety of cancer cell lines.</p>Fórmula:C11H9Cl2CuN3O2SPureza:95.04%Forma y color:SolidPeso molecular:381.73SU11652
CAS:<p>SU11652 is an effective and competitive receptor tyrosine kinase (RTK) inhibitor, including VEGFR, FGFR, PDGFR, and Kit.</p>Fórmula:C22H27ClN4O2Pureza:99.14%Forma y color:SolidPeso molecular:414.936-Azuridine
CAS:<p>6-Azauridine is a purine analog with antitumor effects, inhibiting DNA synthesis and inducing apoptosis in lymphatic cancers.</p>Fórmula:C8H11N3O6Pureza:>99.99%Forma y color:SolidPeso molecular:245.194-Thiothymidine
CAS:<p>4-Thiothymidine is a Nucleoside Derivative - Thio-nucleoside, 5-Modified pyrimidine nucleoside.</p>Fórmula:C10H14N2O4SPureza:99.92%Forma y color:SolidPeso molecular:258.291-(2-Deoxy-2-fluoro-β-D-arabinofuranosyl)uracil
CAS:<p>1-(2-Deoxy-2-fluoro-beta-D-arabinofuranosyl)uracil is a Nucleoside, fluoro-modified nucleoside; Arabino-nucleosidde.</p>Fórmula:C9H11FN2O5Pureza:99.16%Forma y color:SolidPeso molecular:246.192'-Deoxy-2'-fluoro-β-D-arabinoguanosine
CAS:<p>2'-Deoxy-2'-fluoro-beta-D-arabinoguanosine is a purine nucleoside analog with a broad spectrum of antitumor activity, targeting malignant tumors of the inert</p>Fórmula:C10H12FN5O4Pureza:99.42%Forma y color:SolidPeso molecular:285.23FMAU
CAS:<p>FMAU (2'-Deoxy-2'-fluoro-5-methyl-beta-D-arabinouridine) is a thymine nucleoside analog with insertional activity on replicating DNA.FMAU can be used to label</p>Fórmula:C10H13FN2O5Pureza:98.6%Forma y color:SolidPeso molecular:260.22VK3-OCH3
CAS:Fórmula:C14H14O3SPureza:>98.0%(HPLC)Forma y color:Light yellow to Yellow to Orange powder to crystalPeso molecular:262.32NU 9056
CAS:<p>NU 9056 is an effective and selective inhibitor of KAT5 histone acetyltransferase with an IC50 of 2 µM.</p>Fórmula:C6H4N2S4Pureza:95.36% - 97.11%Forma y color:SolidPeso molecular:232.37EIF2α activator 2
CAS:<p>EIF2α activator 2 is an activator of eIF2α phosphorylation, anti-proliferative in SRB, K562, and PBMC cells, suitable for cancer research.</p>Fórmula:C21H20F6N2O2Pureza:98.86%Forma y color:SolidPeso molecular:446.39MC1742
CAS:<p>MC1742 inhibits class I/IIb HDACs, blocks sarcoma CSC growth, and reactivates latent HIV. IC50: HDAC1-3/8 (0.02-0.61 μM), HDAC6/10 (7-40 nM).</p>Fórmula:C21H21N3O3SPureza:99.20%Forma y color:SolidPeso molecular:395.48Baohuoside I
CAS:Fórmula:C27H30O10Pureza:>95.0%(T)(HPLC)Forma y color:White to Light yellow to Green powder to crystalPeso molecular:514.53Lacto-N-neotetraose
CAS:<p>LNnT is a metabolite that reduces IL-8, has anti-inflammatory effects, and aids in wound healing.</p>Fórmula:C26H45NO21Forma y color:SolidPeso molecular:707.63Thalidomide D4
CAS:<p>Thalidomide D4 is a deuterium labeled Thalidomide, has immunomodulatory, anti-inflammatory and anti-angiogenic cancer properties.</p>Fórmula:C13H10N2O4Pureza:98%Forma y color:SolidPeso molecular:262.25Bz 423
CAS:<p>Bz 423 is a potent immunomodulator that induces apoptosis by activating Bax and Bak to induce mitochondrial outer membrane permeabilization and cytochrome c</p>Fórmula:C27H21ClN2O2Pureza:98.93%Forma y color:SolidPeso molecular:440.92SB 202190 hydrochloride
CAS:<p>SB 202190 hydrochloride is a p38 MAPK inhibitor that inhibits p38α and p38β2 with selective, cell-permeable, and antitumor ,differentiation to cardiomyocytes.</p>Fórmula:C20H15ClFN3OPureza:99.99%Forma y color:SolidPeso molecular:367.8Traumatic Acid
CAS:<p>Traumatic Acid aids wound healing in plants by stimulating cell division to create a callus.</p>Fórmula:C12H20O4Pureza:99.64%Forma y color:SolidPeso molecular:228.28Methoxyacetic acid
CAS:<p>Methoxyacetic acid is an endogenous metabolite.</p>Fórmula:C3H6O3Forma y color:Less Liquid (Ntp 1992) Physical Description Colorless Liquid (Ntp 1992)Peso molecular:90.08PRDX1-IN-1
CAS:<p>PRDX1-IN-1 is a and PRDX1 inhibitor with potential anti-inflammatory and anti-cancer activity for the study of breast and esophageal cancer.</p>Fórmula:C46H55N3O4Pureza:98.04%Forma y color:SolidPeso molecular:713.95Belinostat
CAS:Fórmula:C15H14N2O4SPureza:>98.0%(HPLC)Forma y color:White to Light yellow to Light orange powder to crystalPeso molecular:318.35CuATSP
CAS:<p>CuATSP is a potent free radical trapping antioxidant (RTA) and ferroptosis inhibitor inhibit lipid peroxidation, for (ALS) and Parkinson's disease.</p>Fórmula:C18H18CuN6S2Pureza:97.09%Forma y color:SolidPeso molecular:446.05Olanzapine D3
CAS:<p>Olanzapine D3 is the deuterium labeled Olanzapine.</p>Fórmula:C17H20N4SPureza:98%Forma y color:SolidPeso molecular:315.45Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride
CAS:Thalidomide-based E3 ligase linker for PROTACs with a PEG3 chain and hydrochloride salt.Fórmula:C23H31ClN4O9Pureza:98%Forma y color:SolidPeso molecular:542.97PETCM
CAS:PETCM is a caspase-3 activator and acts as an cytochrome c (cyto c)-dependent manner.Fórmula:C8H8Cl3NOPureza:98%Forma y color:SolidPeso molecular:240.51GSK778
CAS:GSK778 selectively inhibits BD1 bromodomains (BRD2, BRD3, BRD4, BRDT) and impedes cell growth, causing arrest and apoptosis.Fórmula:C30H33N5O3Pureza:98.42%Forma y color:SolidPeso molecular:511.61Pyridoclax
CAS:<p>Pyridoclax is an inhibitor of potential Mcl-1.</p>Fórmula:C29H22N4Pureza:98%Forma y color:SolidPeso molecular:426.519-Nitrocamptothecin
CAS:Fórmula:C20H15N3O6Pureza:>98.0%(HPLC)Forma y color:White to Yellow powder to crystalPeso molecular:393.36Bax inhibitor peptide V5
CAS:<p>Bax inhibitor peptide V5 (BIP-V5) is a Bax-mediated apoptosis inhibitor with anticancer activity.</p>Fórmula:C27H50N6O6SForma y color:SolidPeso molecular:586.79Edaravone-d5
CAS:<p>Edaravone, a potent free radical scavenger, prevents MMP-9-induced brain bleeds in rats and has a deuterium variant, Edaravone D5.</p>Fórmula:C10H10N2OPureza:98%Forma y color:SolidPeso molecular:179.23PI3Kα-IN-9
CAS:<p>PI3Kα-IN-9 is an inhibitor of PI3Kα and PI3Kα with antiproliferative activity, inhibits PI3Kα, PI3Kγ, PI3Kδ, and PI3Kβ, induces apoptosis.</p>Fórmula:C18H21N7O3Pureza:98.29%Forma y color:SolidPeso molecular:383.4Embelin
CAS:Fórmula:C17H26O4Pureza:>95.0%(T)(HPLC)Forma y color:Light yellow to Yellow to Orange powder to crystalPeso molecular:294.39Barbadin
CAS:<p>Barbadin is an inhibitor of β-arrestin/β2-adaptin interaction.Barbadin enhances the effects of lorcaserin on weight loss and can be used to study obesity.</p>Fórmula:C19H15N3OSPureza:98.93% - 99.10%Forma y color:SolidPeso molecular:333.41Isovalerylcarnitine
CAS:Isovalerylcarnitine (3-methylbutyrylcarnitine) is a selective effective calpain activator that can promote cell apoptosis and is related to isovaleric acidemia.Fórmula:C12H23NO4Pureza:98.24%Forma y color:SolidPeso molecular:245.32Lestaurtinib
CAS:<p>Lestaurtinib (CEP 701) is a FLT3 inhibitor that inhibits the phosphorylation of RPTKs and can be used to study leukemia.</p>Fórmula:C26H21N3O4Pureza:99.17%Forma y color:Off-White SolidPeso molecular:439.46Propylparaben sodium
CAS:<p>Propylparaben sodium, a plant-based preservative used in cosmetics, pharma, and food, hinders follicle growth and sperm health.</p>Fórmula:C10H12NaO3Forma y color:SolidPeso molecular:203.193Hydrolyzed Fumonisin B1
CAS:<p>Hydrolyzed Fumonisin B1 is the backbone and the main hydrolysis product of the mycotoxin fumonisin B1 (FB1), can weakly inhibit ceramide synthase.</p>Fórmula:C22H47NO5Pureza:98%Forma y color:SolidPeso molecular:405.62SB 203580
CAS:Fórmula:C21H16FN3OSPureza:>98.0%(HPLC)Forma y color:White to Orange to Green powder to crystalPeso molecular:377.44PB28 dihydrochloride
CAS:ZD-6888 Hydrochloride (ZD-6888 HCl) is an angiotensin II antagonist that mediates AII receptor blockade and induces AII-mediated inhibition of renin release.Fórmula:C24H40Cl2N2OPureza:99.97%Forma y color:SolidPeso molecular:443.494-PQBH
CAS:4-PQBH is a potent Nur77-binding agent with antitumour activity.4-PQBH is used in the study of hepatocellular carcinoma.Fórmula:C22H17N5OPureza:99.08%Forma y color:SolidPeso molecular:367.4Ezatiostat
CAS:<p>Ezatiostat (TER199(free base)) is a tripeptide analog of glutathione that can selectively inhibit GSTP1-1 catalytic activity.</p>Fórmula:C27H35N3O6SPureza:97.95%Forma y color:SolidPeso molecular:529.652,6-Dihydroxyacetophenone
CAS:<p>Compound Fr16683 is a natural product for research related to life sciences. The catalog number is Fr16683 and the CAS number is 699-83-2.</p>Fórmula:C8H8O3Pureza:99.62% - 99.75%Forma y color:Yellowish-Beige PowderPeso molecular:152.151,4-Dideoxy-1,4-epithio-D-ribitol
CAS:<p>1,4-Dideoxy-1,4-epithio-D-ribitol is a purine nucleoside analog that targets malignant tumors of the inert lymphatic system and possesses a broad spectrum of</p>Fórmula:C5H10O3SPureza:99.76%Forma y color:SolidPeso molecular:150.2Palmatine hydroxide
CAS:<p>Palmatine hydroxide: oral IDO-1 inhibitor (IC50: 3-157μM), targets WNV protease, has anti-cancer/viral and neuroprotective properties.</p>Fórmula:C21H23NO5Forma y color:SolidPeso molecular:369.41OTS193320
CAS:<p>OTS193320, an imidazo[1,2-a]pyridine, inhibits SUV39H2, reduces H3K9me3, and induces apoptosis in breast cancer; enhances DOX effects.</p>Fórmula:C28H30ClN5O4Forma y color:SolidPeso molecular:536.022'-Aminoacetophenone
CAS:<p>Compound Fr14273 is a natural product for research related to life sciences. The catalog number is Fr14273 and the CAS number is 551-93-9.</p>Fórmula:C8H9NOPureza:99.88%Forma y color:Pale Yellow Solid Solid CrystallinePeso molecular:135.17PBOX 6
CAS:<p>PBOX 6 is a pyrrolo-1,5-benzoxazepine (PBOX) compound with anticancer and antitumor activity that inhibits the growth of breast cancer cells.</p>Fórmula:C25H20N2O3Pureza:98.18% - 98.71%Forma y color:SolidPeso molecular:396.44Melatonin-d4
CAS:<p>Melatonin D5, a deuterium-labeled version of melatonin, is a hormone produced by the pineal gland, known for its role as a selective ATF-6 inhibitor that promotes apoptosis in human hepatoma cells via COX-2 downregulation. Additionally, it activates melatonin receptors and exhibits antioxidative and anti-inflammatory properties.</p>Fórmula:C13H16N2O2Pureza:98%Forma y color:SolidPeso molecular:236.3Thalidomide-piperazine hydrochloride
CAS:<p>Thalidomide-piperazine HCl may aid leprosy, multiple myeloma research, and developmental biology studies.</p>Fórmula:C17H19ClN4O4Forma y color:SolidPeso molecular:378.81M47
CAS:<p>M47 is a selective CRY1 (Cryptochrome 1) degradator that enhances nuclear degradation of CRY1, thereby extending the lifespan of p53 knockout mice.</p>Fórmula:C28H22ClNO4Forma y color:SolidPeso molecular:471.93Br-DAPI
CAS:<p>IST5-002 (N6-Benzyladenosine-5'-phosphate) is a Stat5a/b inhibitor with anticancer activity and is used in cancer research.</p>Fórmula:C16H14BrN5Pureza:100%Forma y color:SolidPeso molecular:356.22Givinostat
CAS:<p>Givinostat (ITF-2357) is a non-selective, orally active HDAC inhibitor capable of inhibiting STAT5 phosphorylation which is antitumour and anti-inflammatory .</p>Fórmula:C24H27N3O4Pureza:98.56%Forma y color:SolidPeso molecular:421.5(Rac)-Hesperetin
CAS:(Rac)-Hesperetin, a racemic flavanone, inhibits human UGT activity and triggers apoptosis via p38 MAPK activation.Fórmula:C16H14O6Forma y color:SolidPeso molecular:302.28Amoscanate
CAS:<p>Amoscanate is an antiparasitic agent. It is highly effective in animals against the four major species of schistosomes which infect humans.</p>Fórmula:C13H9N3O2SForma y color:SolidPeso molecular:271.29KS100
CAS:<p>KS100 inhibits ALDH1A1, ALDH2, ALDH3A1, boosts ROS, triggers apoptosis, and has anti-cancer properties.</p>Fórmula:C17H14Br3N3O2SPureza:97.05%Forma y color:SolidPeso molecular:564.09KT-474
CAS:KT-474 (KYM-001) is a PROTAC degrader targeting IRAK4 with antitumor activity for the study of autoimmune diseases.Fórmula:C44H49F2N11O6Pureza:98.50% - 99.57%Forma y color:SolidPeso molecular:865.93Glucagon-Like Peptide (GLP) II, human
CAS:GLP-2, an intestinal growth factor, may treat various human intestinal diseases.Fórmula:C165H254N44O55SForma y color:SolidPeso molecular:3766.2CLZ-8
CAS:CLZ-8 (Mcl1-IN-8) is a Mcl-1-PUMA inhibitor with radioprotective activity and inhibits radiation-induced overexpression of PUMA.Fórmula:C22H23N3O2SPureza:99.85%Forma y color:SolidPeso molecular:393.5N-deacetylated BMS-202
CAS:N-deacetylated BMS-202 is an inhibitor of PD-1/PD-L1 interaction with potential anticancer activity for cancer research.Fórmula:C23H27N3O2Pureza:98.13% - 98.13%Forma y color:SolidPeso molecular:377.48SLF
CAS:SLF is a synthetic ligand for FKBP12 and increases Ca2+ efflux and protein synthesis.Fórmula:C30H40N2O6Pureza:99.91%Forma y color:SolidPeso molecular:524.65C-DIM 12
CAS:Fórmula:C23H17ClN2Pureza:>98.0%(HPLC)(qNMR)Forma y color:Orange to Amber to Dark red powder to crystalinePeso molecular:356.854-[Di(1H-indol-3-yl)methyl]phenol
CAS:Fórmula:C23H18N2OPureza:>97.0%(T)(HPLC)Forma y color:White to Light orange to Yellow powder to crystalPeso molecular:338.41Degarelix
CAS:<p>Degarelix is a peptide and selective GnRH (human gonadotropin-releasing hormone) receptor antagonist prostate cancer by lowering testosterone levels.</p>Fórmula:C82H103ClN18O16Pureza:99.34%Forma y color:SolidPeso molecular:1632.26Vitamin E succinate
CAS:Vitamin E succinate (D-alpha-Tocopherol Succinate) is an antioxidant tocopherol with antitumor activity that induces apoptosis.Fórmula:C33H54O5Pureza:99.24%Forma y color:SolidPeso molecular:530.78GSK-843
CAS:<p>GSK-843 (GSK'843) is a RIP3 inhibitor with analgesic activity, inhibits RIP3 expression, and can be used as an adjunctive treatment for inflammation.</p>Fórmula:C19H15N5S2Pureza:99.18%Forma y color:SolidPeso molecular:377.49(S)-Oxiracetam
CAS:<p>(S)-Oxiracetam is a positive allosteric the AMPA receptorsmodulator.</p>Fórmula:C6H10N2O3Forma y color:SolidPeso molecular:158.16
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