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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S65487 sulfate
CAS:<p>S65487 (VOB560) sulfate, a potent and selective Bcl-2 inhibitor, demonstrates activity against BCL-2 mutations, including G101V and D103Y.</p>Fórmula:C41H43ClN6O8SForma y color:SolidPeso molecular:815.34Thalidomide-O-amido-C3-NH2
CAS:<p>Thalidomide-derived cereblon ligand linked to a PROTAC technology linker, Thalidomide-O-amido-C3-NH2, is a synthetic E3 ligase ligand-linker.</p>Fórmula:C18H20N4O6Forma y color:SolidPeso molecular:388.37Thalidomide-O-amido-C4-N3
CAS:<p>Thalidomide-O-amido-C4-N3 (Cereblon Ligand-Linker Conjugates 4) is an E3 ligase ligand-linker conjugate incorporating the Thalidomide-based cereblon ligand and</p>Fórmula:C19H20N6O6Pureza:97.01%Forma y color:SolidPeso molecular:428.4Cytostatin (sodium salt)
CAS:<p>Cytostatin: natural antitumor, inhibits cell adhesion, blocks melanoma, induces apoptosis, targets PP2A selectively, IC50s: 1.3-3.1 µg/ml & 29 nM.</p>Fórmula:C21H33NaO7PForma y color:SolidPeso molecular:451.452HDAC6 degrader-5
<p>HDAC6degrader-5 (Compound 6) exhibits inhibitory and degradative activity against HDAC6, with an IC50 of 4.95 nM and a DC50 of 0.96 nM. It suppresses the release of TNF-α, IL-1β, and IL-6, and prevents apoptosis in liver cells. Additionally, HDAC6degrader-5 demonstrates anti-inflammatory properties in a mouse model of APAP-induced liver injury.</p>Fórmula:C21H22N4O3Forma y color:SolidPeso molecular:378.424Mcl-1 inhibitor 16
<p>Mcl-1 Inhibitor 16 (Compound 9), a platinum-based mitochondrial-targeting agent, inhibits Mcl-1 and induces Bax/Bak-dependent apoptosis in cancer cells.</p>Fórmula:C25H29Cl2N3PtForma y color:SolidPeso molecular:637.51Zalypsis
CAS:<p>Zalypsis, a transcription factor inhibitor, is used potentially for the treatment of lymphoma, and cervical carcinoma.</p>Fórmula:C37H38F3N3O8Forma y color:SolidPeso molecular:709.71Tubulin/MMP-IN-3
<p>Tubulin/MMP-IN-3 (Compound 15j) is a dual inhibitor of tubulin polymerization and MMP, effectively inhibiting MMP-2 and MMP-9 with IC50 values of 21.13 μM and 19.24 μM, respectively. It disrupts the NF-κB signaling pathway, leading to mitochondrial dysfunction and mitochondrial-dependent apoptosis. Tubulin/MMP-IN-3 shows antiproliferative activity in various cancer cells by causing cell cycle arrest at the G2/M phase and demonstrates antitumor effects in mouse models.</p>Fórmula:C38H41N2O12PForma y color:SolidPeso molecular:748.712HG-7-85-01
CAS:<p>HG-7-85-01 is a novel ATP-competitive and type II tyrosine kinase inhibitor targeting both wild-type and watchman mutant BCR-ABL, PDGFRα, Kit, and Src kinases.</p>Fórmula:C31H31F3N6O2SPureza:98.08%Forma y color:SolidPeso molecular:608.68GPLGIAGQ
CAS:GPLGIAGQ, a MMP2-cleavable polypeptide, is used as a stimulus-sensitive linker in both liposomal and micellar nanocarriers for MMP2-triggered tumor targeting.Fórmula:C31H53N9O10Pureza:98%Forma y color:SolidPeso molecular:711.81Trimebutine
CAS:<p>Trimebutine (Mebutin) is a spasmolytic agent that regulates intestinal and colonic motility and relieves abdominal pain with antimuscarinic and weak mu-opioid</p>Fórmula:C22H29NO5Pureza:98.13% - 99.49%Forma y color:SolidPeso molecular:387.47Anticancer agent 102
CAS:<p>Anticancer Agent 102, a tetracaine derivative, exhibits anti-cancer activity by inducing apoptosis [1].</p>Fórmula:C20H19F6N3OForma y color:SolidPeso molecular:431.37Taltirelin acetate
CAS:<p>Taltirelin acetate (TA-0910 acetate) is a superagonist at thyrotropin-releasing hormone receptor (TRH-R)(IC50 of 910 nM and EC50 of 36 nM for stimulating an</p>Fórmula:C19H27N7O7Pureza:99.21%Forma y color:SolidPeso molecular:465.46HDAC3-IN-6
<p>HDAC3-IN-6 (Compound SC26) is a selective HDAC3 inhibitor with an IC50 of 53 nM. It induces PD-L1 expression in a dose-dependent manner and leads to significant apoptosis and reactive oxygen species (ROS) production. HDAC3-IN-6 exhibits strong antitumor efficacy against colorectal cancer.</p>Fórmula:C23H23N5O3Forma y color:SolidPeso molecular:417.46Z-VDVA-(DL-Asp)-FMK
CAS:<p>Z-VDVA-(DL-Asp)-FMK is a derivative compound of Z-VDVAD-FMK specifically designed as an inhibitor targeting caspase-2.</p>Fórmula:C32H46FN5O11Forma y color:SolidPeso molecular:695.742Thalidomide-O-amido-C6-NH2
CAS:<p>Thalidomide-O-amido-C6-NH2 is a synthetic E3 ligase used for PROTAC creation, containing cereblon ligand and linker.</p>Fórmula:C21H26N4O6Forma y color:SolidPeso molecular:430.45YX-02-030
CAS:<p>YX-02-030M is a PROTACMDM2 degrader. It inhibits the binding of MDM2 to p53 and VHL to HIF1α, with IC50 values of 63 nM and 1.35 μM, respectively. YX-02-030M binds to MDM2 and recruits the VHL E3 ubiquitin ligase to initiate MDM2 degradation, effectively killing p53 mutant or deficient triple-negative breast cancer (TNBC) cells.</p>Fórmula:C66H85Cl2N9O10SPeso molecular:1267.41Sandalore
CAS:<p>Sandalore boosts hair growth, reduces cell death, and raises IGF-1, acting on olfactory receptor OR2AT4.</p>Fórmula:C14H26OPureza:97.96%Forma y color:Light Yellow Viscous LiquidPeso molecular:210.36PROTAC RIPK degrader-6
CAS:<p>PROTAC RIPK degrader-6 (example 1) is a PROTAC designed for the targeted degradation of RIP Kinase, featuring a RIP2 kinase inhibitor connected through a linker</p>Fórmula:C43H48N6O11S2Forma y color:SolidPeso molecular:889.01Rosamultic acid
<p>Rosamultic acid is a useful organic compound for research related to life sciences and the catalog number is T125342.</p>Fórmula:C30H46O5Forma y color:SolidPeso molecular:486.693Thevetiaflavone
CAS:<p>Thevetiaflavone, a natural flavonoid from W. indica, blocks LDH leakage, boosting cell survival.</p>Fórmula:C16H12O5Pureza:98%Forma y color:SolidPeso molecular:284.26Hematein
CAS:<p>Hematein blocks Akt/PKB, Wnt signaling, promotes apoptosis in lung cancer, is a dye from hematoxylin, and inhibits casein kinase II (IC50: 0.74 μM).</p>Fórmula:C16H12O6Pureza:98%Forma y color:Dark Brown Crystalline PowderPeso molecular:300.26Curcumin 5-8
CAS:<p>CUR5-8: potent, oral CUR analog, reduces lipid droplets, boosts autophagy, hinders apoptosis, enhances insulin sensitivity.</p>Fórmula:C20H21NO4Forma y color:SolidPeso molecular:339.39H-20
CAS:<p>H-20 is a PD-1 agonist that reduces the required dosage of morphine for analgesia. It can be used in studies related to chronic pain.</p>Fórmula:C44H64N10O15Forma y color:SolidPeso molecular:973.037Solanidine
CAS:<p>Solanidine is a cholestane alkaloid isolated from potato species with antitumor effects. Solanidine inhibits proliferation.</p>Fórmula:C27H43NOPureza:96.83%Forma y color:SolidPeso molecular:397.64PROTAC EGFR degrader 7
<p>Compound 13b, a potent EGFR degrader, inhibits and induces apoptosis in NSCLC cells with a DC50 of 13.2 nM.</p>Fórmula:C46H48N10O6Forma y color:SolidPeso molecular:836.94Bak BH3
<p>Flu-BakBH3 peptide, derived from Bak's BH3 domain, binds tightly to a crucial pocket of Bcl-XL, essential for its anti-death role.</p>Fórmula:C72H125N25O24Pureza:98%Forma y color:SolidPeso molecular:1724.9Antiproliferative agent-25
<p>Antiproliferative Agent-25 (Compound 3s4) is a selective PRMT5 inhibitor displaying an IC50 of 0.11 μM.</p>Fórmula:C20H21BrN2O2Pureza:98%Forma y color:SolidPeso molecular:401.3Linsidomine
CAS:<p>Lincydomine relaxes smooth muscles, treats unstable angina, and opens human and guinea pig respiratory tracts.</p>Fórmula:C6H10N4O2Forma y color:Solid Off-WhitePeso molecular:170.17Thalidomide-NH-C8-NH2
CAS:<p>Thalidomide-NH-C8-NH2 is a synthetic E3 ligase ligand-linker for PROTAC, combining cereblon ligand and a specific linker.</p>Fórmula:C21H28N4O4Forma y color:SolidPeso molecular:400.479Anti-inflammatory agent 42
CAS:<p>Anti-inflammatory agent 42 has anti-inflammatory activity and inhibits the expression of TNF-α and IL-6 in LPS-stimulated macrophages.</p>Fórmula:C20H12N2OSPureza:98.13%Forma y color:SolidPeso molecular:328.39Oxybenzone-d3
<p>Oxybenzone-d3 (Benzophenone 3-d3) is a deuterium-labeled form of Oxybenzone. Commonly used as a UV filter in tanning and skin protection products, Oxybenzone (Benzophenone 3) acts as an endocrine-disrupting chemical (EDC) that can cross both the placental and blood-brain barriers. It impairs autophagy, alters epigenetic states, and disrupts retinoid X receptor signaling in apoptotic neuronal cells.</p>Fórmula:C14H9D3O3Forma y color:SolidPeso molecular:231.26EGFR/HER2/DHFR-IN-3
<p>EGFR/HER2/DHFR-IN-3 (compound 4c) serves as an efficacious dual inhibitor specifically targeting EGFR/HER2, exhibiting IC50 values of 0.138 μM for EGFR and 0.</p>Pureza:98%Forma y color:Odour SolidAspochalasin D
CAS:<p>Aspochalasin D, isolated from A. microcysticus, shows antibacterial properties and cytotoxicity affecting Ba/F3-V12 cells, with IC50s of 0.49 and 1.9 μg/ml.</p>Fórmula:C24H35NO4Forma y color:SolidPeso molecular:401.54ABBV-167
CAS:<p>ABBV-167 is a phosphate prodrug of the BCL-2 inhibitor venetoclax.</p>Fórmula:C46H53ClN7O11PSForma y color:SolidPeso molecular:978.45Cyanoacetamide
CAS:<p>Cyanoacetamide has inhibitory activity against the myeloid leukaemia cell differentiation protein Mcl-1</p>Fórmula:C3H4N2OPureza:97.04%Forma y color:Needles From Alcohol White To Light Cream Crystalline PowderPeso molecular:84.08PROTAC GPX4 degrader-4
CAS:<p>PROTACGPX4 degrader-4 is a GPX4 PROTAC degrader with a DC50 of 5.32 nM. It inhibits the activity of cancer cell lines RT4, T24, and J82 with IC50 values of 0.09, 2.97, and 7.58 μM, respectively. This compound elevates lipid ROS levels and induces ferroptosis in T24 and RT4 cells. In T24 tumor-bearing BALB/c nude mouse models, PROTACGPX4 degrader-4 demonstrates antitumor activity. It is applicable to bladder cancer research.</p>Fórmula:C43H58N2O13Forma y color:SolidPeso molecular:810.93PAA5
<p>PAA5, a polynuclear Au(I) cluster, triggers ferroptosis and has anticancer effects by increasing pH2AX over time.</p>Fórmula:C14H8Au5B2F8N2Forma y color:SolidPeso molecular:1348.66TNF-α (46-65), human
CAS:Human TNF alpha (46-65) peptide.Fórmula:C110H172N24O30Pureza:98%Forma y color:SolidPeso molecular:2310.69Dapirolizumab
<p>Dapirolizumab is an anti-CD40 monoclonal antibody used in research on systemic lupus erythematosus (SLE) and other autoimmune diseases.</p>Pureza:>95%Forma y color:LiquidPeso molecular:145.5 kDaFerroptosis-IN-16
<p>Ferroptosis-IN-16 (Compound 13l) acts as a specific inhibitor of ferroptosis, demonstrating EC50 values of 0.7 nM in ES-2 cells and 0.9 nM in LX-2 cells. It effectively alleviates acute liver injury induced by Acetaminophen in mouse models and shows excellent metabolic stability in mouse liver microsomes.</p>Fórmula:C26H23N5OForma y color:SolidPeso molecular:421.492-Chloronaphthalene
CAS:<p>2-Chloronaphthalene is an organochlorine chemical compound and is a chlorinated derivative of naphthalene. The compound is an isomer for 1-chloronaphthalene.</p>Fórmula:C10H7ClPureza:98%Forma y color:SolidPeso molecular:162.62GPLGIAGQ acetate
<p>GPLGIAGQ acetate: MMP2-cleavable peptide; stimulus-sensitive linker for MMP2-targeted liposomal/micellar carriers in photodynamic therapy.</p>Fórmula:C33H57N9O12Pureza:97.85%Forma y color:SolidPeso molecular:771.864-N-Nonyloxyphenol
CAS:<p>4-N-Nonyloxyphenol, kaolinite nanotube photosensitizer, degrades phenolic pesticides, and disrupts endocrine.</p>Fórmula:C15H24O2Pureza:99.94%Forma y color:SoildPeso molecular:236.35Oenothein B
CAS:<p>Oenothein B inhibits PAR-glycohydrolase with antioxidant, anti-inflammatory, antifungal, anti-HCV, and antitumor effects.</p>Fórmula:C68H48O44Pureza:99.30%Forma y color:SolidPeso molecular:1569.08MNK8
CAS:MNK8 is a potent STAT3 inhibitor, impairs DNA binding, and inhibits liver cancer cell growth.Fórmula:C15H12N2O2Pureza:99.74%Forma y color:SolidPeso molecular:252.27PD0166285 dihydrochloride
CAS:<p>PD-166285 is an effective and broadly active inhibitor of protein tyrosine kinase.</p>Fórmula:C26H29Cl4N5O2Forma y color:SolidPeso molecular:585.35Diethylnorspermine HCl
CAS:Diethylnorspermine HCl (N1,N11-Diethylnorspermine tetrahydrochloride) potently induces SSAT (spermidine/spermine N1-acetyltransferase) mRNA and effectivelyFórmula:C13H36Cl4N4Pureza:99.79% - 99.86%Forma y color:SolidPeso molecular:390.26Mcl1-IN-12
CAS:<p>Mcl1-IN-12 has anti-tumor activity.It is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.29 and 3.1 μM, respectively.</p>Fórmula:C45H46N4O6S2Pureza:98%Forma y color:SolidPeso molecular:803Thalidomide 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:279.293PPA-904 FA
<p>PPA-904 FA is a cationic photosensitizer with antimicrobial activity that can be used to study chronic leg ulcers and diabetic foot ulcers.</p>Fórmula:C29H43N3O2SPureza:98%Forma y color:SolidPeso molecular:497.74JAK/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:570.7HX009
HX009 is a bispecific antibody that targets PD1 and CD47, though its binding to CD47 is attenuated. HX009 functions by blocking PD1/CD47 and can be utilized in research related to non-Hodgkin lymphoma (NHL).Forma y color:Odour Liquidβ-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:1810.69d-(KLAKLAK)2, Proapoptotic Peptide
CAS:<p>d-(KLAKLAK)2 is an antimicrobial and antitumor peptide, notable within the group of antimicrobial peptides, and exhibits strong anticancer properties. It kills bacteria by disrupting their cell membranes, causing leakage of cell contents. Additionally, d-(KLAKLAK)2 inhibits tumor cell proliferation by inducing apoptosis through mitochondrial swelling and membrane damage.</p>Fórmula:C72H139N21O14Forma y color:SolidPeso molecular:1523.01YTHDF2-IN-1
YTHDF2-IN-1 (Compound CK-75) is an inhibitor of YT521-B homology domain family 2 (YTHDF2) with a dissociation constant (Kd) of 26.2 μM, and it effectively blocks the interaction between YTHDF2 and m6A RNA. It suppresses colony formation in JAR cells and exhibits antiproliferative activity in various cancer cell lines, with an IC50 in the micromolar range. Additionally, YTHDF2-IN-1 induces apoptosis in K562 cells and causes cell cycle arrest at the G0/G1 phase.Fórmula:C21H14N2O4Forma y color:SolidPeso molecular:358.35PROTAC 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:1329.6PERK-IN-4
CAS:<p>PERK-IN-4 is a potent and selective PERK inhibitor with an IC50 value of 0.3 nM.PERK-IN-4 can be used in the study of cancer and neurological disorders.</p>Fórmula:C24H19F4N5OPureza:98.07% - 98.95%Forma y color:SolidPeso molecular:469.43RMC-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:1012.26Pimagedine
CAS:<p>Pimagedine is a prototype therapeutic agent for the prevention of formation of advanced glycation endproducts.</p>Fórmula:CH6N4Forma y color:SolidPeso molecular:74.09PROTAC KDM4 degrader-1
<p>PROTACKDM4 degrader-1 (Compound 11) is a proteolysis-targeting chimera (PROTAC) degrader specifically designed for KDM4. It effectively degrades KDM4A-C while sparing KDM4D. In esophageal cancer cells, PROTACKDM4 degrader-1 demonstrates strong antiproliferative activity, inducing apoptosis and cell cycle arrest, and inhibits lysine demethylation of histone H3.</p>Forma y color:Odour Solid4-(Dimethylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]benzamide
CAS:Fórmula:C16H25N3O3Pureza:>97.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:307.399-Nitrocamptothecin
CAS:Fórmula:C20H15N3O6Pureza:>98.0%(HPLC)Forma y color:White to Yellow powder to crystalPeso molecular:393.36Forodesine hydrochloride
CAS:Forodesine hydrochloride blocks lymphocyte growth and induces leukemia cell death by inhibiting PNP, effective across species.Fórmula:C11H15ClN4O4Forma y color:SolidPeso molecular:302.71FKBP12 PROTAC RC32
CAS:<p>FKBP12 PROTAC RC32 is a PROTAC-like degrader targeting FKBP12. It can degrade FKBP12 in organs after intraperitoneal administration.</p>Fórmula:C75H107N7O20Pureza:98.57% - 99.57%Forma y color:SolidPeso molecular:1426.69Saquinavir mesylate
CAS:Saquinavir mesylate (Ro 31-8959/003) is an Inhibitor of HIV Proteaseused in antiretroviral therapyFórmula:C39H54N6O8SPureza:99.19%Forma y color:White Or Pale Yellow PowderPeso molecular:766.9Curcumin-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:374.422Atractylenolide III
CAS:Fórmula:C15H20O3Pureza:>98.0%(T)(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:248.32AZD-5991
CAS:<p>AZD-5991, an antitumor compound, is a highly selective, potent and direct MCL-1 inhibitor, rapid apoptosis by Bak-dependent mitochondrial apoptotic pathway.</p>Fórmula:C35H34ClN5O3S2Pureza:98.08% - 98.95%Forma y color:SolidPeso molecular:672.26BCL6-IN-5
CAS:<p>BCL6-IN-5 is a highly effective inhibitor of BCL6. It exhibits a pIC50 value of 5.82.</p>Fórmula:C17H19Cl2N5O2Forma y color:SolidPeso molecular:396.27Mepazine 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:346.92Methoxyacetic 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:90.08ODN 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:6364.1Methylisothiazolinone hydrochloride
CAS:<p>Methylisothiazolinone is a powerful synthetic biocide and preservative.</p>Fórmula:C4H6ClNOSForma y color:SolidPeso molecular:151.62PI3Kα-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:383.4Phenoxyethanol (Standard)
CAS:Phenoxyethanol (Standard) is the standard substance of Phenoxyethanol, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Phenoxyethanol (NSC-1864) is germicidal. It often used together with quaternary ammonium compounds.Fórmula:C8H10O2Peso molecular:138.16Almorexant hydrochloride
CAS:Almorexant hydrochloride (ACT 078573 hydrochloride) is a dual orexin receptor antagonist that induces apoptosis and can be used to study sleep disorders.Fórmula:C29H32ClF3N2O3Pureza:99.85%Forma y color:SolidPeso molecular:549.02Thalidomide-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:542.97CuATSP
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:446.05SU11652
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:414.93Capsazepine
CAS:Fórmula:C19H21ClN2O2SPureza:>98.0%(HPLC)(qNMR)Forma y color:White to Light yellow powder to crystalPeso molecular:376.90NCX 4040
CAS:<p>COX-2 expression inhibitor</p>Fórmula:C16H13NO7Pureza:98%Forma y color:SolidPeso molecular:331.28Forodesine
CAS:<p>Forodesine inhibits lymphocyte growth and induces apoptosis in leukemic cells; oral purine nucleoside phosphorylase blocker; IC50: 0.48-1.57 nM.</p>Fórmula:C11H14N4O4Pureza:98.75% - 99.88%Forma y color:SolidPeso molecular:266.25Tetrac
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:747.83Batabulin 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:393.24Condurango glycoside A
CAS:<p>Condurango glycoside A activates p53, induces ROS generation, up-regulates p53 expression, and triggers apoptosis as well as premature senescence associated</p>Fórmula:C53H78O17Forma y color:SolidPeso molecular:987.18Benzyl selenocyanate
CAS:Benzyl selenocyanate is a chemopreventive agent that effectively inhibits chemically induced tumors at both initiation and postinitiation stages in animal models. It acts as a potent inhibitor of DNA (cytosine-5)-methyltransferase (Mtase) with an IC50 of 8.4 μM.Fórmula:C8H7NSePureza:99.2%Forma y color:SolidPeso molecular:196.11Bax 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:586.79Cis-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:164.16MM-401 TFA
CAS:<p>MM-401 (TFA), an MLL1 H3K4 methylation inhibitor (IC50 = 0.32 µM), blocks MLL1-WDR5, causing cell cycle arrest and apoptosis, for MLL leukemia studies.</p>Fórmula:C31H47F3N8O7Forma y color:SolidPeso molecular:700.75(S)-Oxiracetam
CAS:<p>(S)-Oxiracetam is a positive allosteric the AMPA receptorsmodulator.</p>Fórmula:C6H10N2O3Forma y color:SolidPeso molecular:158.16PDK1-IN-RS2
CAS:PDK1-IN-RS2, a PIFtide mimic, selectively inhibits PDK1, blocking S6K1 activation (Kd: 9 μM).Fórmula:C15H9ClN2O2S3Pureza:98%Forma y color:SolidPeso molecular:380.895-NIdR
CAS:<p>5-NIdR is a Nucleoside Derivative - Indole nucleoside.</p>Fórmula:C13H14N2O5Forma y color:SolidPeso molecular:278.26EPZ020411
CAS:EPZ020411 is a specific and effective inhibitor of PRMT6 (IC50=10 nM).Fórmula:C25H38N4O3Forma y color:SolidPeso molecular:442.6Venetoclax-d8
CAS:Venetoclax-d8 (ABT-199-d8) is a deuterated form of Venetoclax, a potent, selective, and orally active Bcl-2 inhibitor that induces autophagy and apoptosis.Fórmula:C45H42D8ClN7O7SForma y color:SolidPeso molecular:876.49RKI-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:399.29Nutlin-3
CAS:Fórmula:C30H30Cl2N4O4Pureza:>95.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:581.49Br-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:356.22PND-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:537.97
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