Apoptose
Os inibidores da apoptose são compostos que previnem ou retardam o processo de morte celular programada, conhecido como apoptose. Esses inibidores são vitais no estudo dos mecanismos de sobrevivência celular e são usados para investigar doenças onde a apoptose é desregulada, como câncer, distúrbios neurodegenerativos e doenças autoimunes. Ao modular a apoptose, esses inibidores podem ajudar no desenvolvimento de terapias destinadas a controlar a morte celular. Na CymitQuimica, oferecemos uma ampla seleção de inibidores da apoptose de alta qualidade para apoiar sua pesquisa em biologia celular, oncologia e áreas relacionadas.
Subcategorias de "Apoptose"
- ASK(6 produtos)
- BCL(11 produtos)
- Caspase(125 produtos)
- FOXO1(3 produtos)
- IAP(66 produtos)
- Mdm2(12 produtos)
- PD-1/PD-L1(125 produtos)
- PDK(9 produtos)
- PERK(25 produtos)
- Serina/treonina quinase(15 produtos)
- Survivina(13 produtos)
- TNF(92 produtos)
- c-RET(51 produtos)
- p53(62 produtos)
Exibir 6 mais subcategorias
Foram encontrados 5593 produtos de "Apoptose"
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VK-28
CAS:<p>VK-28 is a brain permeable iron chelator with neuroprotection. VK-28 inhibits basal as well as iron-induced mitochondrial lipid peroxidation.</p>Fórmula:C16H21N3O2Pureza:99.87%Cor e Forma:SolidPeso molecular:287.36BU 224 hydrochloride
CAS:<p>BU 224 hydrochloride is a selective imidazoline I(2) binding site ligand and has antinociceptive and antidepressant-like activities.</p>Fórmula:C12H12ClN3Pureza:99.51%Cor e Forma:SolidPeso molecular:233.7CST626
CAS:<p>CST626 is a PROTAC degrader that targets XIAP, cIAP1, and cIAP2.</p>Fórmula:C61H82N8O9SPureza:95.87%Cor e Forma:SolidPeso molecular:1103.42HX009
<p>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).</p>Cor e Forma:Odour LiquidBax inhibitor peptide, negative control
CAS:<p>The compound is a negative control peptide for the Bax inhibitor peptides V5 and P5.</p>Fórmula:C28H52N6O6SPureza:98%Cor e Forma:SolidPeso molecular:600.81Thalidomide-NH-C10-COOH
<p>Compound 6b is a synthetic Thalidomide-VHL E3 ligase-linker for PROTACs.</p>Fórmula:C24H31N3O6Pureza:98%Cor e Forma:SolidPeso molecular:457.52PPIA-IN-1
<p>PPIA-IN-1 (Compound 20b) is an inhibitor of peptidyl-prolyl isomerase A (PPIA) with a KD of 0.52 μM. It demonstrates antiproliferative activity across various cancer cell lines, including an IC50 of 0.69 μM in HCT116 cells, induces cell cycle arrest at the G0/G1 phase, and exhibits antimetastatic effects in HCT116 cells. PPIA-IN-1 elevates ROS levels, causing DNA damage, ER stress, and mitochondrial dysfunction, and induces apoptosis in HCT116 cells via the MAPK pathway. Additionally, PPIA-IN-1 shows antitumor activity in a CT26 xenograft mouse model.</p>Fórmula:C23H21Cl2FN4O7Cor e Forma:SolidPeso molecular:555.34Mangafodipir trisodium
CAS:<p>Mangafodipir trisodium can enhance contrast in magnetic resonance imaging (MRI) of the liver, is a contrast agent delivered intravenously.</p>Fórmula:C22H27MnN4Na3O14P2Pureza:98%Cor e Forma:SolidPeso molecular:757.32Tauro-β-muricholic acid
CAS:<p>Tauro-β-muricholic acid (TβMCA), a trihydroxylated bile acid, acts as a competitive and reversible FXR antagonist (IC 50 = 40 μM) and exhibits antiapoptotic</p>Fórmula:C26H45NO7SPureza:98%Cor e Forma:SolidPeso molecular:515.78-Bromo-cAMP
CAS:<p>8-Bromo-cAMP is a cell-permeable cAMP analogue and activator of CAMP-dependent protein kinase A that induces cell death and reduces proliferation.</p>Fórmula:C10H11BrN5O6PPureza:97.30%Cor e Forma:SolidPeso molecular:408.1Thevetiaflavone
CAS:<p>Thevetiaflavone, a natural flavonoid from W. indica, blocks LDH leakage, boosting cell survival.</p>Fórmula:C16H12O5Pureza:98%Cor e Forma:SolidPeso molecular:284.26BCL6-IN-6
CAS:<p>BCL6-IN-6 is an inhibitor of Bcl-6 and can be used in studies about diffuse large B-cell lymphoma.</p>Fórmula:C27H31FN6O2SPureza:98.90%Cor e Forma:SolidPeso molecular:522.64S65487 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:C41H43ClN6O8SCor e Forma:SolidPeso molecular:815.34EGFR/BRAFV600E-IN-4
<p>EGFR/BRAFV600E-IN-4 (Compound 10f) is a dual inhibitor of EGFR and BRAFV600E, with IC50 values of 61 nM and 43 nM, respectively. It halts the cell cycle, induces apoptosis in both early and late stages, and inhibits cancer cell growth in vitro, showing broad-spectrum anticancer activity.</p>Fórmula:C22H16N4OSCor e Forma:SolidPeso molecular:384.45Diphenhydramine hydrochloride
CAS:<p>DPH: antihistamine for cough, nausea, itching, allergy, Parkinson's, sleep aid, cold remedy.</p>Fórmula:C17H22ClNOPureza:99.84%Cor e Forma:Taste Ph (5% Aqueous Solution) 4-6 (Ntp 1992)Peso molecular:291.82Cytostatin (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:C21H33NaO7PCor e Forma:SolidPeso molecular:451.452MYC-RIBOTAC
<p>MYC-RIBOTAC, a ribonuclease-targeting chimera (RIBOTAC) specific to the MYC internal ribosome entry site (IRES), comprises an MYC mRNA-binding element tethered</p>Fórmula:C55H58N10O11SPureza:98%Cor e Forma:SolidPeso molecular:1067.17TAPI 0
CAS:<p>ADAM-17 (TACE) and MMP inhibitor; attenuates TNF-α processing. Acts in concert with GM6001 to inhibit Chlamydia trachomatis growth.</p>Fórmula:C24H32N4O5Pureza:98%Cor e Forma:SolidPeso molecular:456.54Zalypsis
CAS:<p>Zalypsis, a transcription factor inhibitor, is used potentially for the treatment of lymphoma, and cervical carcinoma.</p>Fórmula:C37H38F3N3O8Cor e Forma: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:C38H41N2O12PCor e Forma:SolidPeso molecular:748.712HPOB
CAS:<p>HPOB is an effective and specific HDAC6 inhibitor (IC50: 56 nM), >30-fold selectivity over other HDACs.</p>Fórmula:C17H18N2O4Pureza:99.91%Cor e Forma:SolidPeso molecular:314.34Glutathione arsenoxide hydrochloride
<p>Glutathione arsenoxide hydrochloride: anti-cancer, inhibits tumour metabolism, targets ANT, promotes apoptosis, marks cell proteins.</p>Fórmula:C18H26AsClN4O9SPureza:99.74%Cor e Forma:SoildPeso molecular:584.86Anticancer agent 102
CAS:<p>Anticancer Agent 102, a tetracaine derivative, exhibits anti-cancer activity by inducing apoptosis [1].</p>Fórmula:C20H19F6N3OCor e Forma:SolidPeso molecular:431.37BOC-D-FMK
CAS:<p>Boc-D-FMK is an irreversible, cell-permeable, and broad-spectrum caspase inhibitor and inhibits apoptosis stimulated by TNF-α (IC50: 39 μM).</p>Fórmula:C11H18FNO5Pureza:97.02%Cor e Forma:SolidPeso molecular:263.26HDAC3-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:C23H23N5O3Cor e Forma: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:C32H46FN5O11Cor e Forma: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:C21H26N4O6Cor e Forma:SolidPeso molecular:430.45PROTAC 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:C43H48N6O11S2Cor e Forma: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:C30H46O5Cor e Forma:SolidPeso molecular:486.693PROTAC Bcl-xL degrader-3
CAS:<p>PROTAC Bcl-xL degrader-3 is a potent ROTAC Bcl-xL degrader.</p>Fórmula:C82H105ClF3N11O11S4Cor e Forma:SolidPeso molecular:1641.49MD-222
CAS:<p>MD-222: a first-in-class, highly potent PROTAC that degrades MDM2, activates p53, and exhibits anticancer properties.</p>Fórmula:C48H47Cl2FN6O6Cor e Forma:SolidPeso molecular:893.84Curcumin 5-8
CAS:<p>CUR5-8: potent, oral CUR analog, reduces lipid droplets, boosts autophagy, hinders apoptosis, enhances insulin sensitivity.</p>Fórmula:C20H21NO4Cor e Forma:SolidPeso molecular:339.39LH1307
CAS:<p>LH1307 blocks PD-1/PD-L1 interaction, IC50 = 3 nM (HTRF assay), activates Jurkat cells, EC50s: 79 nM (U2OS), 763 nM (CHO).</p>Fórmula:C54H58N8O6Cor e Forma:SolidPeso molecular:915.108FF2039
<p>FF2039 (compound 1j) is a PROTAC degrader specifically targeting HDAC1, HDAC6, and various subtypes of class I, IIa, and IIb HDACs. It induces cell cycle arrest and apoptosis, showing significant antiproliferative activity against both hematological and solid tumor cell lines. The IC50 values for FF2039 against HDAC1, HDAC2, HDAC4, and HDAC6 are 1.03, 2.15, 12.4, and 0.053 μM, respectively. FF2039 exhibits antiproliferative effects on solid tumors such as MM.1S, MDA-MB-231, and U-87MG, with EC50 values of 2.8, 28, and 30 μM, respectively.</p>Fórmula:C43H56Cl3N5O6Cor e Forma:SolidPeso molecular:845.29UBX1325
CAS:<p>UBX1325, a potent Bcl-xL inhibitor, induces cell death in aging cells, useful for age-related eye disease research.</p>Fórmula:C53H59ClF3N6O10PS3Cor e Forma:SolidPeso molecular:1159.69Z-DQMD-FMK
CAS:<p>Caspase-3 inhibitor. Inhibits MG 132-induced small cell lung cancer cell death in vitro.</p>Fórmula:C29H40FN5O11SPureza:98%Cor e Forma:SolidPeso molecular:685.72PROTAC 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:C46H48N10O6Cor e Forma:SolidPeso molecular:836.948-Aminoadenosine
CAS:<p>8-Aminoadenosine reduces ATP, blocks mRNA synthesis, and Akt/mTOR signaling, triggering autophagy and apoptosis independently of p53, with antitumor effects.</p>Fórmula:C10H14N6O4Cor e Forma:SolidPeso molecular:282.26Chloranil
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%Cor e Forma:SolidPeso molecular:245.88Antiproliferative agent-25
<p>Antiproliferative Agent-25 (Compound 3s4) is a selective PRMT5 inhibitor displaying an IC50 of 0.11 μM.</p>Fórmula:C20H21BrN2O2Pureza:98%Cor e Forma:SolidPeso molecular:401.3PB28
CAS:<p>PB28: A potent σ2 agonist (Ki 0.68 nM), σ1 antagonist (Ki 0.38 nM), with anti-tumor properties and inhibits SARS-CoV-2 interactions.</p>Fórmula:C24H38N2OCor e Forma:SolidPeso molecular:370.581DC-Y13-27
<p>Dc-y13-27, a derivative of DC-Y13, is a potent YTHDF2 inhibitor (KD: 37.9 μM).</p>Fórmula:C14H10N2O2SPureza:99.75%Cor e Forma:SoildPeso molecular:270.31Linsidomine
CAS:<p>Lincydomine relaxes smooth muscles, treats unstable angina, and opens human and guinea pig respiratory tracts.</p>Fórmula:C6H10N4O2Cor e Forma: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:C21H28N4O4Cor e Forma:SolidPeso molecular:400.479AVJ16
CAS:<p>AVJ16 as a member of the insulin growth factor 2 mRNA-binding protein family, binds to the mRNA of certain genes to regulate protein translation.</p>Fórmula:C28H27N3O4Pureza:98.87% - 99.72%Cor e Forma:SolidPeso molecular:469.53Anti-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%Cor e Forma:SolidPeso molecular:328.39RBN013209
CAS:<p>RBN013209 is a potent CD38 inhibitor. RBN013209 is useful in the treatment of cancer.</p>Fórmula:C19H24N6O3Pureza:99.84%Cor e Forma:SoildPeso molecular:384.43Syringolin A
CAS:<p>Syringolin A is a useful organic compound for research related to life sciences. The catalog number is T125354 and the CAS number is 212115-96-3.</p>Fórmula:C24H39N5O6Cor e Forma:SolidPeso molecular:493.605BLU-222
CAS:<p>BLU-222 is a potent, selective and orally active CDK2 inhibitor. BLU-222 shows robust antitumor activity.</p>Fórmula:C15H17F2N7O2Pureza:99.17% - 99.92%Cor e Forma:SoildPeso molecular:365.34PARP1-IN-17
<p>PARP1-IN-17 is an inhibitor that targets PARP-1 (IC50=19.24 nM ) with a slightly reduced affinity for PARP-2 (IC50=32.58 nM ) and induces apoptosis.</p>Pureza:98%Cor e Forma:Odour SolidKRAS inhibitor-40
CAS:<p>KRAS inhibitor-40 (Compound 41) is an inhibitor of KRAS, disrupting the KRAS G12C-BRAF complex and suppressing the phosphorylation of the downstream ERK signaling pathway. This compound also inhibits the proliferation of tumor cells with various KRAS mutations, exhibiting antitumor activity.</p>Fórmula:C53H66ClF4N9O8SCor e Forma:SolidPeso molecular:1100.66S-Adenosyl-L-methionine iodide
CAS:<p>S-(5'-Adenosyl)-L-methionine iodide, also known as S-Adenosyl-L-methionine iodide, is a vital methyl donor present in all living organisms [1].</p>Fórmula:C15H23IN6O5SCor e Forma:SolidPeso molecular:526.355α-dihydro Levonorgestrel
CAS:<p>5α-dihydro Levonorgestrel is a metabolite of the synthetic progestin levonorgestrel .</p>Fórmula:C21H30O2Cor e Forma:SolidPeso molecular:314.469FKBP12 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%Cor e Forma:SolidPeso molecular:1426.69Thalidomide-O-amido-C4-NH2
CAS:<p>Thalidomide-O-amido-C4-NH2 is a thalidomide cereblon ligand-linker used for PROTAC synthesis as an E3 ligase.</p>Fórmula:C19H22N4O6Pureza:98%Cor e Forma:SolidPeso molecular:402.4Mycophenolic acid-d3
CAS:<p>Mycophenolic acid-d3 is a derivative that lowers GTP, affects RNA polymerase II transcription, changes polyadenylation, and counters cordyceps.</p>Fórmula:C17H20O6Pureza:98%Cor e Forma:SolidPeso molecular:323.361,4-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%Cor e Forma:SolidPeso molecular:150.2(Rac)-Apremilast D5
CAS:<p>(Rac)-Apremilast D5 is a deuterium-labeled version of the enantiomer (R)-Apremilast, also known as (R)-CC-10004, which itself is one specific form of Apremilast</p>Fórmula:C22H24N2O7SPureza:98%Cor e Forma:SolidPeso molecular:465.53Alantolactone
CAS:Fórmula:C15H20O2Pureza:>95.0%(GC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:232.325-(N,N-Hexamethylene)-amiloride
CAS:<p>5-(N,N-Hexamethylene)-amiloride (5-HMA) is an amiloride derivative that inhibits TRPA1-mediated calcium signaling (IC50: 35 μM). It functions as an inhibitor of the Na+/H+ exchanger (NHE) with Ki values ranging from 0.013 to 2.4 μM for various NHE isoforms. Additionally, 5-HMA blocks ASIC3 channels by 51% at 20 μM.</p>Fórmula:C12H18ClN7OPureza:85.48%Cor e Forma:SolidPeso molecular:311.774-(Dimethylamino)-N-[7-(hydroxyamino)-7-oxoheptyl]benzamide
CAS:Fórmula:C16H25N3O3Pureza:>97.0%(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:307.39Belinostat
CAS:Fórmula:C15H14N2O4SPureza:>98.0%(HPLC)Cor e Forma:White to Light yellow to Light orange powder to crystalPeso molecular:318.35Forodesine hydrochloride
CAS:<p>Forodesine hydrochloride blocks lymphocyte growth and induces leukemia cell death by inhibiting PNP, effective across species.</p>Fórmula:C11H15ClN4O4Cor e Forma:SolidPeso molecular:302.71Rapamycin-d3
CAS:<p>Rapamycin-d3 is the deuterium labeled Rapamycin. Rapamycin is a potent and specific inhibitor of mTOR(IC50 of 0.1 nM in HEK293 cells).</p>Fórmula:C51H79NO13Pureza:98%Cor e Forma:SolidPeso molecular:917.19EIF2α 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%Cor e Forma:SolidPeso molecular:446.39SC144 hydrochloride
CAS:<p>SC144 hydrochloride: oral gp130 inhibitor, blocks Stat3 and gene expression, triggers apoptosis in ovarian cancer cells.</p>Fórmula:C16H12ClFN6OCor e Forma:SolidPeso molecular:358.76Parthenolide
CAS:Fórmula:C15H20O3Pureza:>97.0%(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:248.32Acyclovir-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:C8H7D4N5O3Cor e Forma:SolidPeso molecular:229.23Thalidomide-5-CH2-NH2 hydrochloride
CAS:<p>Thalidomide-5-CH2-NH2 (HCl) recruits CRBN protein, used to create PROTACs via a linker.</p>Fórmula:C14H14ClN3O4Cor e Forma:SolidPeso molecular:323.73Mepazine 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%Cor e Forma:SolidPeso molecular:346.926-Formylpterin
CAS:<p>6-Formylpterin (Pterin-6-aldehyde) is an inhibitor of Xanthine Oxidase, which induces ROS generation and apoptosis in HL-60 cells.</p>Fórmula:C7H5N5O2Pureza:98%Cor e Forma:SolidPeso molecular:191.15ABT-751
CAS:Fórmula:C18H17N3O4SPureza:>98.0%(HPLC)Cor e Forma:White to Yellow to Orange powder to crystalPeso molecular:371.41Sunitinib-d10
CAS:<p>Sunitinib D10, a deuterium-enriched version, inhibits VEGFR2 and PDGFRβ tyrosine kinases (IC50: 80 nM/2 nM).</p>Fórmula:C22H27FN4O2Pureza:98%Cor e Forma:SolidPeso molecular:408.54(-)-Gallocatechin Gallate
CAS:Fórmula:C22H18O11Pureza:>95.0%(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:458.382-Thiocytidine
CAS:<p>2-Thiocytidine is a purine nucleoside analog that targets malignant tumors of the inert lymphatic system and has a broad spectrum of antitumor activity.2-</p>Fórmula:C9H13N3O4SPureza:98.59%Cor e Forma:SolidPeso molecular:259.28Mardepodect hydrochloride
CAS:<p>Mardepodect hydrochloride (Mardepodect HCl) is a PDE10A inhibitor.Mardepodect hydrochloride upregulates genes encoding specific growth factors.</p>Fórmula:C25H21ClN4OPureza:95.1%Cor e Forma:SolidPeso molecular:428.91Thalidomide-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%Cor e Forma:SolidPeso molecular:487.43Necrostatin 2
CAS:<p>Necrostatin 2 is a RIPK1 inhibitor that can be used to study inner ear disorders such as sudden deafness, dizziness and tinnitus.</p>Fórmula:C13H12ClN3O2Pureza:99.92% - 99.92%Cor e Forma:SolidPeso molecular:277.71Thalidomide-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:C19H22N4O7Cor e Forma:SolidPeso molecular:418.4Ancitabine
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%Cor e Forma:SolidPeso molecular:225.2Tegaserod
CAS:<p>Tegaserod is a 5-HT4R agonist and 5-HT2B receptor antagonist with antitumor activity used in the treatment of irritable bowel syndrome (IBS).</p>Fórmula:C16H23N5OPureza:99.20% - 99.89%Cor e Forma:SolidPeso molecular:301.39NCX 4040
CAS:<p>COX-2 expression inhibitor</p>Fórmula:C16H13NO7Pureza:98%Cor e Forma:SolidPeso molecular:331.28Acyclovir 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:C8H12ClN5O3Cor e Forma:SolidPeso molecular:261.67Thalidomide-O-amido-PEG3-C2-NH2 hydrochloride
CAS:<p>Thalidomide-based E3 ligase linker for PROTACs with a PEG3 chain and hydrochloride salt.</p>Fórmula:C23H31ClN4O9Pureza:98%Cor e Forma:SolidPeso molecular:542.97Condurango 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:C53H78O17Cor e Forma:SolidPeso molecular:987.18PI-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%Cor e Forma:SolidPeso molecular:384.82OTS193320
CAS:<p>OTS193320, an imidazo[1,2-a]pyridine, inhibits SUV39H2, reduces H3K9me3, and induces apoptosis in breast cancer; enhances DOX effects.</p>Fórmula:C28H30ClN5O4Cor e Forma:SolidPeso molecular:536.02Meisoindigo
CAS:Fórmula:C17H12N2O2Pureza:>98.0%(HPLC)Cor e Forma:Orange to Brown to Dark red powder to crystalPeso molecular:276.30Bax inhibitor peptide V5
CAS:<p>Bax inhibitor peptide V5 (BIP-V5) is a Bax-mediated apoptosis inhibitor with anticancer activity.</p>Fórmula:C27H50N6O6SCor e Forma:SolidPeso molecular:586.79AZD5582
CAS:AZD5582 is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. It induces apoptosis.Fórmula:C58H78N8O8Pureza:98.75%Cor e Forma:SolidPeso molecular:1015.29Diphenyl disulfide
CAS:<p>Diphenyl disulfide fights breast cancer by inducing cell death and stopping growth.</p>Fórmula:C12H10S2Pureza:99.95%Cor e Forma:White To Light Yellow CrystalPeso molecular:218.34MRT00033659
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:C15H14N4OCor e Forma:SolidPeso molecular:266.3KRA-533
CAS:<p>KRA-533 is an effective KRAS agonist that targets the GTP/GDP binding pocket within the KRAS protein, inhibiting GTP cleavage.</p>Fórmula:C13H16BrNO3Pureza:98.11%Cor e Forma:SolidPeso molecular:314.18SC-560
CAS:Fórmula:C17H12ClF3N2OPureza:>98.0%(HPLC)Cor e Forma:White to Light yellow to Light orange powder to crystalPeso molecular:352.74Apremilast-d5
CAS:<p>Apremilast D5 (CC-10004 D5) is a deuterium-labeled Apremilast.</p>Fórmula:C22H24N2O7SCor e Forma:SolidPeso molecular:465.53Fosfenopril
CAS:<p>Fosfenopril is an ACE inhibitor reducing LPS-induced inflammation via TLR4/NF-κB suppression, used in cardiovascular and anti-inflammatory molecular studies.</p>Fórmula:C23H34NO5PCor e Forma:SolidPeso molecular:435.49Br-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%Cor e Forma:SolidPeso molecular:356.22PERK-IN-2
CAS:<p>PERK-IN-2 is a potent inhibitor of PERK(IC50 of 0.2 nM).</p>Fórmula:C23H18F3N5OPureza:98%Cor e Forma:SolidPeso molecular:437.42Pyridoclax
CAS:<p>Pyridoclax is an inhibitor of potential Mcl-1.</p>Fórmula:C29H22N4Pureza:98%Cor e Forma:SolidPeso molecular:426.519-Nitrocamptothecin
CAS:Fórmula:C20H15N3O6Pureza:>98.0%(HPLC)Cor e Forma:White to Yellow powder to crystalPeso molecular:393.36PRIMA-1MET
CAS:Fórmula:C10H17NO3Pureza:>95.0%(GC)(qNMR)Cor e Forma:White to Light yellow powder to crystalPeso molecular:199.25PI3Kα-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%Cor e Forma:SolidPeso molecular:383.4Vandetanib
CAS:Fórmula:C22H24BrFN4O2Pureza:>98.0%(T)(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:475.36Pancratistatin
CAS:<p>Pancratistatin, an isoquinoline from Hymenocallis littoralis, triggers apoptosis in melanoma and is studied for neuroblastoma, leukemia, and breast cancer.</p>Fórmula:C14H15NO8Cor e Forma:SolidPeso molecular:325.27KT-474
CAS:<p>KT-474 (KYM-001) is a PROTAC degrader targeting IRAK4 with antitumor activity for the study of autoimmune diseases.</p>Fórmula:C44H49F2N11O6Pureza:98.50% - 99.57%Cor e Forma:SolidPeso molecular:865.93Prinaberel
CAS:<p>Prinaberel (ERB-041) is an effective and selective ERβ agonist and >200-fold selective for ERβ.</p>Fórmula:C15H10FNO3Pureza:97.1%Cor e Forma:SolidPeso molecular:271.24KS100
CAS:<p>KS100 inhibits ALDH1A1, ALDH2, ALDH3A1, boosts ROS, triggers apoptosis, and has anti-cancer properties.</p>Fórmula:C17H14Br3N3O2SPureza:97.05%Cor e Forma:SolidPeso molecular:564.09Amoscanate
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:C13H9N3O2SCor e Forma:SolidPeso molecular:271.29Melflufen hydrochloride
CAS:<p>Melflufen HCl: prodrug of Melphalan, has antitumor and antiangiogenic effects, causes DNA damage in MM cells.</p>Fórmula:C24H31Cl3FN3O3Cor e Forma:SolidPeso molecular:534.88Vitamin E succinate
CAS:<p>Vitamin E succinate (D-alpha-Tocopherol Succinate) is an antioxidant tocopherol with antitumor activity that induces apoptosis.</p>Fórmula:C33H54O5Pureza:99.24%Cor e Forma:SolidPeso molecular:530.78CLZ-8
CAS:<p>CLZ-8 (Mcl1-IN-8) is a Mcl-1-PUMA inhibitor with radioprotective activity and inhibits radiation-induced overexpression of PUMA.</p>Fórmula:C22H23N3O2SPureza:99.85%Cor e Forma:SolidPeso molecular:393.5Sonrotoclax
CAS:<p>Sonrotoclax is a potent, orally active inhibitor of Bcl2, demonstrating effective cell-killing activity against a range of lymphoma and leukemia cell lines [1].</p>Fórmula:C49H59N7O7SPureza:97.33% - 99.47%Cor e Forma:SolidPeso molecular:890.10Momelotinib 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%Cor e Forma:SolidPeso molecular:610.62TZ9
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%Cor e Forma:SolidPeso molecular:366.33Everolimus-d4
CAS:<p>Everolimus-d4 is a deuterated compound of Everolimus.</p>Fórmula:C53H83NO14Cor e Forma:SolidPeso molecular:962.264Traumatic Acid
CAS:<p>Traumatic Acid aids wound healing in plants by stimulating cell division to create a callus.</p>Fórmula:C12H20O4Pureza:99.64%Cor e Forma:SolidPeso molecular:228.28Melatonin-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%Cor e Forma:SolidPeso molecular:236.3Celosin K
CAS:<p>Celosin K (compound 8), isolated from Semen Celosiae seeds, effectively inhibits t-BHP-induced neuronal injury.</p>Fórmula:C47H74O19Pureza:98%Cor e Forma:SolidPeso molecular:943.08MM-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:C31H47F3N8O7Cor e Forma:SolidPeso molecular:700.75SU11652
CAS:<p>SU11652 is an effective and competitive receptor tyrosine kinase (RTK) inhibitor, including VEGFR, FGFR, PDGFR, and Kit.</p>Fórmula:C22H27ClN4O2Pureza:99.14%Cor e Forma:SolidPeso molecular:414.93Tetrac
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%Cor e Forma:SolidPeso molecular:747.835-NIdR
CAS:<p>5-NIdR is a Nucleoside Derivative - Indole nucleoside.</p>Fórmula:C13H14N2O5Cor e Forma:SolidPeso molecular:278.26Thalidomide-piperazine-Boc
CAS:<p>Thalidomide-piperazine-Boc is an intermediate utilized for synthesizing BCL6 PROTAC, which targets B-cell lymphoma 6 protein.</p>Fórmula:C22H26N4O6Cor e Forma:SolidPeso molecular:442.46Cobimetinib hemifumarate
CAS:<p>Cobimetinib hemifumarate is a potent and selective MEK1 inhibitor with an IC50 value of 4.2 nM for MEK1.</p>Fórmula:C46H46F6I2N6O8Cor e Forma:SolidPeso molecular:1178.707SB 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%Cor e Forma:SolidPeso molecular:367.8SB 203580
CAS:Fórmula:C21H16FN3OSPureza:>98.0%(HPLC)Cor e Forma:White to Orange to Green powder to crystalPeso molecular:377.44Thalidomide D4
CAS:<p>Thalidomide D4 is a deuterium labeled Thalidomide, has immunomodulatory, anti-inflammatory and anti-angiogenic cancer properties.</p>Fórmula:C13H10N2O4Pureza:98%Cor e Forma:SolidPeso molecular:262.25Pentagamavunon-1
CAS:<p>PGV-1, an oral Curcumin analog, induces apoptosis by inhibiting COX-2, VEGF, and NF-κB activation.</p>Fórmula:C23H24O3Cor e Forma:SolidPeso molecular:348.43Bucladesine calcium
CAS:<p>Bucladesine calcium: PDE inhibitor, boosts cAMP, activates PKA.</p>Fórmula:C36H46CaN10O16P2Cor e Forma:SolidPeso molecular:976.844Chlorhexidine digluconate
CAS:<p>Chlorhexidine digluconate is a disinfectant with antibacterial activity that induces apoptosis and can be used to study bacterial infections.</p>Fórmula:C34H54Cl2N10O14Pureza:98.53%Cor e Forma:Less To Pale Yellow Clear Liquid Colorless To Pale Yellow Clear LiquidPeso molecular:897.76YZ129
CAS:<p>YZ129, an HSP90-calcineurin-NFAT inhibitor with 820 nM IC50, halts GBM growth, arrests G2/M phase, and induces apoptosis.</p>Fórmula:C19H12N2O2Cor e Forma:SolidPeso molecular:300.31Buparlisib Hydrochloride
CAS:<p>Buparlisib Hydrochloride is an inhibitor of pan-class I PI3K (IC50: 52 nM/166 nM/116 nM/262 nM for p110α/p110β/p110δ/p110γ, respectively).</p>Fórmula:C18H22ClF3N6O2Pureza:98.94%Cor e Forma:SolidPeso molecular:446.85Tubastatin A TFA
CAS:<p>Tubastatin A is a potent HDAC6 inhibitor with IC50 of 15 nM.</p>Fórmula:C22H22F3N3O4Pureza:98%Cor e Forma:SolidPeso molecular:449.42Fenobucarb
CAS:<p>Fenobucarb is a broad-spectrum carbamate insecticide and AChE inhibitor. It exhibits neurotoxicity to zebrafish foetal development and induces muscle spasms</p>Fórmula:C12H17NO2Pureza:98.80%Cor e Forma:White CrystalPeso molecular:207.27Hydrolyzed 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%Cor e Forma:SolidPeso molecular:405.62Amifostine thiol
CAS:<p>Amifostine thiol (WR-1065), an active Amifostine metabolite, is a radioprotective cytoprotectant that activates p53 via JNK pathway.</p>Fórmula:C5H14N2SPureza:≥95.0%Cor e Forma:SolidPeso molecular:134.24Isoalantolactone
CAS:Fórmula:C15H20O2Pureza:>98.0%(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:232.32C8-Ceramide
CAS:<p>C8 Ceramide, a cell-permeable analog, is analog to naturally occur ceramides.</p>Fórmula:C26H51NO3Cor e Forma:SolidPeso molecular:425.69Lestaurtinib
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%Cor e Forma:Off-White SolidPeso molecular:439.46Barbadin
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%Cor e Forma:SolidPeso molecular:333.41Necrostatin 2 S enantiomer
CAS:<p>Necrostatin 2 S enantiomer is the S enantiomer of Necrostatin 2</p>Fórmula:C13H12ClN3O2Pureza:98%Cor e Forma:SolidPeso molecular:277.71Fenitrothion
CAS:<p>Fenitrothion (Arbogal) is a insecticide that exhibits reproductive toxicity, inhibits acetylcholinesterase, and is commonly used in agriculture.</p>Fórmula:C9H12NO5PSPureza:95.07%Cor e Forma:Yellow-Brown Liquid Insecticide Against Chewing And Sucking Insects On Rice Orchard Fruits Vegetables Cereals CottonPeso molecular:277.23Etoposide Phosphate
CAS:<p>Etoposide Phosphate is a selective and orally active topoisomerase II inhibitor and anticancer chemotherapy drug that apoptosise, the p53, and G2/M</p>Fórmula:C29H33O16PCor e Forma:SolidPeso molecular:668.54Indirubin-3'-monoxime
CAS:Fórmula:C16H11N3O2Pureza:>98.0%(HPLC)Cor e Forma:Light yellow to Brown powder to crystalPeso molecular:277.282,6-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%Cor e Forma:Yellowish-Beige PowderPeso molecular:152.15Edaravone-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%Cor e Forma:SolidPeso molecular:179.23Methoxyacetic acid
CAS:<p>Methoxyacetic acid is an endogenous metabolite.</p>Fórmula:C3H6O3Cor e Forma:Less Liquid (Ntp 1992) Physical Description Colorless Liquid (Ntp 1992)Peso molecular:90.08Licofelone
CAS:Fórmula:C23H22ClNO2Pureza:>95.0%(HPLC)Cor e Forma:White to Almost white powder to crystalPeso molecular:379.88CuATSP
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%Cor e Forma:SolidPeso molecular:446.05CCW16
CAS:<p>CCW16 is a covalent E3 ubiquitin ligase RNF4 ligand, cysteine reactivity, inducing ferroptosis in AML cells by activating ROS signalling.</p>Fórmula:C22H20ClNO3Pureza:97%Cor e Forma:SolidPeso molecular:381.85Capsazepine
CAS:Fórmula:C19H21ClN2O2SPureza:>98.0%(HPLC)(qNMR)Cor e Forma:White to Light yellow powder to crystalPeso molecular:376.90Wedelolactone
CAS:Fórmula:C16H10O7Pureza:>98.0%(HPLC)Cor e Forma:White to Dark green powder to crystalPeso molecular:314.25Bleximenib 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%Cor e Forma:SolidPeso molecular:689.82VK3-OCH3
CAS:Fórmula:C14H14O3SPureza:>98.0%(HPLC)Cor e Forma:Light yellow to Yellow to Orange powder to crystalPeso molecular:262.32PND-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:C25H27ClF3N5O3Cor e Forma:SolidPeso molecular:537.97(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%Cor e Forma:SolidPeso molecular:340.38Batabulin sodium
CAS:<p>Batabulin sodium, an antitumor compound, disrupts microtubules, alters cell shape, halts cell cycle, and induces apoptosis.</p>Fórmula:C13H6F6NNaO3SCor e Forma:SolidPeso molecular:393.24Dynole 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%Cor e Forma:SolidPeso molecular:408.58Degarelix
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%Cor e Forma:SolidPeso molecular:1632.26SLF
CAS:<p>SLF is a synthetic ligand for FKBP12 and increases Ca2+ efflux and protein synthesis.</p>Fórmula:C30H40N2O6Pureza:99.91%Cor e Forma:SolidPeso molecular:524.65PBOX 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%Cor e Forma:SolidPeso molecular:396.4413-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:C15H30O2Cor e Forma:SolidPeso molecular:242.4Thalidomide-O-amido-PEG4-C2-NH2 hydrochloride
CAS:<p>Thalidomide-O-amido-PEG4-C2-NH2 hydrochloride is a synthesized E3 ligase ligand-linker conjugate incorporating the Thalidomide-based cereblon ligand and a</p>Fórmula:C25H35ClN4O10Pureza:98%Cor e Forma:SolidPeso molecular:587.02Hydroxy-PP-Me
CAS:<p>Hydroxy-PP-Me is a CBR1 inhibitor that inhibits apoptosis induced by serum withdrawal.Hydroxy-PP-Me is used in the study of leukemia.</p>Fórmula:C16H18N4OPureza:99.92%Cor e Forma:SolidPeso molecular:282.34GSK-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%Cor e Forma:SolidPeso molecular:377.49Methylstat
CAS:<p>Methylstat is a methyl ester prodrug of a Jumonji C domain-containing histone demethylase (JMJD) inhibitor that has favorable cell permeability.</p>Fórmula:C28H31N3O6Pureza:98.34% - 98.34%Cor e Forma:SolidPeso molecular:505.56Isoginkgetin
CAS:Fórmula:C32H22O10Pureza:>95.0%(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:566.52Demethoxycurcumin
CAS:Fórmula:C20H18O5Pureza:>98.0%(HPLC)Cor e Forma:Light red to Yellow to Red powder to crystalPeso molecular:338.36Palmatine hydroxide
CAS:<p>Palmatine hydroxide: oral IDO-1 inhibitor (IC50: 3-157μM), targets WNV protease, has anti-cancer/viral and neuroprotective properties.</p>Fórmula:C21H23NO5Cor e Forma:SolidPeso molecular:369.41Propylparaben sodium
CAS:<p>Propylparaben sodium, a plant-based preservative used in cosmetics, pharma, and food, hinders follicle growth and sperm health.</p>Fórmula:C10H12NaO3Cor e Forma:SolidPeso molecular:203.193Ubiquitin Isopeptidase Inhibitor I, G5
CAS:<p>Ubiquitin Isopeptidase Inhibitor I, G5 is a caspase-independent inducer of cell necrosis that induces cell death via the death receptor pathway .</p>Fórmula:C19H14N2O7SPureza:96.56%Cor e Forma:SolidPeso molecular:414.39Lacto-N-neotetraose
CAS:<p>LNnT is a metabolite that reduces IL-8, has anti-inflammatory effects, and aids in wound healing.</p>Fórmula:C26H45NO21Cor e Forma:SolidPeso molecular:707.63MC1742
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%Cor e Forma:SolidPeso molecular:395.48FTI-277
CAS:<p>FTI-277, an FTase inhibitor, blocks H-Ras/K-Ras signaling and HDV infection; mimics Ras CAAX peptide.</p>Fórmula:C22H29N3O3S2Cor e Forma:SolidPeso molecular:447.61Tamoxifen-d5
CAS:<p>Tamoxifen-d5 is a deuterium labeled Tamoxifen.</p>Fórmula:C26H29NOPureza:98%Cor e Forma:SolidPeso molecular:376.55(-)-Apomorphine hydrochloride hydrate
CAS:<p>(-)-Apomorphine hydrochloride hydrate is a broad-spectrum dopamine agonist and ferroptosis inhibitor.</p>Fórmula:C17H17NO2HClXH2OCor e Forma:SolidPeso molecular:303.8GSK778
CAS:<p>GSK778 selectively inhibits BD1 bromodomains (BRD2, BRD3, BRD4, BRDT) and impedes cell growth, causing arrest and apoptosis.</p>Fórmula:C30H33N5O3Pureza:98.42%Cor e Forma:SolidPeso molecular:511.61J22352
CAS:<p>J22352, a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor with an IC50 value of 4.7 nM, enhances anticancer effects in</p>Fórmula:C24H21N3O4Cor e Forma:SolidPeso molecular:415.44(R)-CR8 trihydrochloride
CAS:<p>(R)-CR8 trihydrochloride (CR8, (R)-Isomer trihydrochloride) is a CDK1/2/5/7/9 inhibitor with neuroprotective activity that induces apoptosis.</p>Fórmula:C24H32Cl3N7OPureza:99.33%Cor e Forma:SolidPeso molecular:540.92AZD-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%Cor e Forma:SolidPeso molecular:672.26Metronidazole-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:C6H9N3O3Cor e Forma:SolidPeso molecular:175.18Almorexant hydrochloride
CAS:<p>Almorexant hydrochloride (ACT 078573 hydrochloride) is a dual orexin receptor antagonist that induces apoptosis and can be used to study sleep disorders.</p>Fórmula:C29H32ClF3N2O3Pureza:99.85%Cor e Forma:SolidPeso molecular:549.02PDK1-IN-RS2
CAS:PDK1-IN-RS2, a PIFtide mimic, selectively inhibits PDK1, blocking S6K1 activation (Kd: 9 μM).Fórmula:C15H9ClN2O2S3Pureza:98%Cor e Forma:SolidPeso molecular:380.89EPZ020411
CAS:<p>EPZ020411 is a specific and effective inhibitor of PRMT6 (IC50=10 nM).</p>Fórmula:C25H38N4O3Cor e Forma:SolidPeso molecular:442.6Zardaverine
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%Cor e Forma:SolidPeso molecular:268.22Pitavastatin D4
CAS:<p>Pitavastatin D4 is deuterium labeled Pitavastatin. Pitavastatin is a potent inhibitor of HMG-CoA reductase.</p>Fórmula:C25H24FNO4Pureza:98%Cor e Forma:SolidPeso molecular:425.49Ulipristal Acetate
CAS:Fórmula:C30H37NO4Pureza:>98.0%(T)(HPLC)Cor e Forma:White to Yellow to Green powder to crystalPeso molecular:475.63Benzyl selenocyanate
CAS:<p>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.</p>Fórmula:C8H7NSePureza:99.2%Cor e Forma:SolidPeso molecular:196.11MX1013
CAS:<p>MX1013, a dipeptide pan-caspase inhibitor, inhibits caspase-1, -3, -6, -7, -8, and -9.</p>Fórmula:C18H23FN2O6Cor e Forma:SolidPeso molecular:382.39Glucagon-Like Peptide (GLP) II, human
CAS:<p>GLP-2, an intestinal growth factor, may treat various human intestinal diseases.</p>Fórmula:C165H254N44O55SCor e Forma:SolidPeso molecular:3766.2Pevonedistat hydrochloride
CAS:<p>Pevonedistat(MLN4924) hydrochloride is a NEDD8-activating enzyme inhibitor that induces apoptosis and can be used in the study of acute myeloid leukemias.</p>Fórmula:C21H26ClN5O4SPureza:98.44% - 99.19%Cor e Forma:SolidPeso molecular:479.98Alisol B 23-Acetate
CAS:Fórmula:C32H50O5Pureza:>98.0%(HPLC)Cor e Forma:White to Light yellow powder to crystalPeso molecular:514.75Octreotide
CAS:<p>Octreotide (SMS 201-995) is a potent inhibitor of growth hormone, glucagon, and insulin.</p>Fórmula:C49H66N10O10S2Pureza:99.64%Cor e Forma:White PowderPeso molecular:1019.24Cl-amidine TFA
CAS:<p>Cl-amidine TFA: oral PAD inhibitor, induces cancer cell apoptosis, IC50s: PAD1 - 0.8μM, PAD3 - 6.2μM, PAD4 - 5.9μM.</p>Fórmula:C16H20ClF3N4O4Cor e Forma:SolidPeso molecular:424.8Thalidomide-Piperazine 5-fluoride
CAS:<p>Thalidomide-Piperazine 5-fluoride: a cereblon ligand-linked E3 ligase via PROTAC tech.</p>Fórmula:C17H17FN4O4Cor e Forma:SolidPeso molecular:360.34GO-203
CAS:<p>GO-203 is a useful organic compound for research related to life sciences. The catalog number is T35351 and the CAS number is 1222186-26-6.</p>Fórmula:C89H171F3N52O21S2Cor e Forma:SolidPeso molecular:2426.81Tubulin inhibitor 1
CAS:Tubulin inhibitor 1 blocks tubulin polymerization, with strong anti-tumor effects, induces apoptosis and G2/M mitotic arrest.Fórmula:C21H24N2O4Pureza:98%Cor e Forma:SolidPeso molecular:368.434-[Di(1H-indol-3-yl)methyl]phenol
CAS:Fórmula:C23H18N2OPureza:>97.0%(T)(HPLC)Cor e Forma:White to Light orange to Yellow powder to crystalPeso molecular:338.41C-DIM 12
CAS:Fórmula:C23H17ClN2Pureza:>98.0%(HPLC)(qNMR)Cor e Forma:Orange to Amber to Dark red powder to crystalinePeso molecular:356.85Thalidomide-5,6-F
CAS:<p>Thalidomide-5,6-F, a cereblon ligand for CRBN protein recruitment, forms PROTACs for targeted protein degradation.</p>Fórmula:C13H8F2N2O4Cor e Forma:SolidPeso molecular:294.21
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