
Apoptosi
Sottocategorie di "Apoptosi"
- ASK(9 prodotti)
- BCL(1 prodotti)
- Caspasi(154 prodotti)
- FOXO1(2 prodotti)
- IAP(67 prodotti)
- Mdm2(12 prodotti)
- PD-1/PD-L1(109 prodotti)
- PDK(9 prodotti)
- PERK(26 prodotti)
- Chinasi di serina/treonina(18 prodotti)
- Survivin(14 prodotti)
- TNF(64 prodotti)
- c-RET(61 prodotti)
- p53(63 prodotti)
Trovati 6100 prodotti di "Apoptosi"
2',5'-Dimethoxyacetophenone
CAS:Prodotto controllatoFormula:C10H12O3Colore e forma:NeatPeso molecolare:180.2Aurintricarboxylic Acids (Technical Grade)
CAS:Prodotto controllatoApplications Aurintricarboxylic Acid is a cell-permeable apoptosis inhibitor.
Formula:C22H14O9Colore e forma:NeatPeso molecolare:422.34Monosialoganglioside GM3 Sodium Salt
CAS:Prodotto controllatoApplications Monosialoganglioside GM3 can have anti-tumor effects by regulating cell apoptosis, angiogenesis. Monosialoganglioside GM3 can also regulate peripheral insulin receptor signaling and increases in GM3 in adipose tissue of obese humans may contribute to insulin resistance.
References Zhu, Y., et al.: Zhongliu Fangzhi Yanjiu, 42, 450 (2015); Herzer, S., et al.: Diabetes, 64, 3363 (2015); Wentworth, J., et al.: ?Int. J. Obes., 40, 706 (2016)Formula:C59H107N2NaO21Colore e forma:NeatPeso molecolare:1203.474-[4-[[2-(4-Chlorophenyl)-5,5-dimethyl-1-cyclohexen-1-yl]methyl]-1-piperazinyl]benzoic Acid
CAS:Prodotto controllatoApplications Intermediate in the production of cell death regulators and apoptosis promoters.
References Park, C., et al.: J. Med. Chem., 51, 6902 (2008),Formula:C26H31ClN2O2Colore e forma:NeatPeso molecolare:438.99PHA 767491 Dihydrochloride Salt
CAS:Prodotto controllatoStability Hygroscopic
Applications A potent and selective ATP-competitive dual inhibitor cdc7/cdk9. It blocks DNA synthesis and affects the phosphorylation of the replicative DNA helicase at Cdc7-dependent phosphorylation sites. Inhibits cell proliferation in a variety of human cell lines and induces apoptosis in a p53-independent manner in vivo. Also inhibits mitogen-activated protein kinase-activated protein kinase-2 (MK-2).
References Anderson, D.R. et al.: J. Med. Chem., 50, 2647 (2007); Montagnoli, A. et al.: Nature Chem. Biol., 4, 357 (2008); Charych, D.H. et al.: J Cell. Biochem., 104, 1075 (2008); Jackson, P.K. et al.: Nature Chem. Biol., 4, 331 (2008);Formula:C12H11N3O·2ClHColore e forma:Light Yellow PowderPeso molecolare:286.16(R)-Irofulven
CAS:Prodotto controllatoApplications Semi-synrhetic antitumor agent derived from Illudin S. Inhibits DNA synthesis and induces apoptosis in tumor cells. Antineoplastic.
References Woynarowski, J.M., et al.: Biochem. Pharmacol., 54, 1181 (1997), Alexandre, J., et al.: Clin. Cancer Res., 10, 3377 (2004), Senzer, N., et al.: Am. J. Clin. Oncol., 28, 36 (2005),Formula:C15H18O3Colore e forma:NeatPeso molecolare:246.31N-(Ethoxycarbonylmethyl)piperazine
CAS:Prodotto controllatoApplications N-(Ethoxycarbonylmethyl)piperazine is used in the preparation of aralkylpiperazine- and aryl-substituted hydrazines, particularly benzylpiperazineacetyl hydrazones of hydroxyaryl aldehydes, as selective inducers of apoptosis and activators of procaspases for use as anticancer agents.
References Nakagawara, A., et al.: Cancer Res., 57, 4578 (1997), Denault, J., et al.: J. Biol. Chem., 278, 34042 (2003), Traven, A., et al.: Cancer Cell, 5, 107 (2004), Becattini, B., et al.: Chem. Biol., 11, 389 (2004),Formula:C8H16N2O2Colore e forma:NeatPeso molecolare:172.22L-Cystathionine
CAS:L-Cystathionine: nonprotein amino acid; important for sulfur amino acid metabolism; used in cardiovascular research.
Formula:C7H14N2O4SPurezza:96.43% - >99.99%Colore e forma:SolidPeso molecolare:222.26Camptothecin
CAS:Camptothecin (CPT) belongs to the alkaloid group of natural products and is a specific DNA topoisomerase I (Topo I) inhibitor (IC50=679 nM) with specificity.Formula:C20H16N2O4Purezza:99.52% - 99.88%Colore e forma:Solid PowderPeso molecolare:348.35SU11274
CAS:SU11274 (Met Kinase Inhibitor)(IC50=10 nM) is a specific Met inhibitor. It shows no significant effects on PGDFRβ, EGFR or Tie2.Formula:C28H30ClN5O4SPurezza:98.62% - 99.53%Colore e forma:Orange PowderPeso molecolare:568.09Ref: TM-T6154
1mg44,00€2mg56,00€5mg92,00€10mg142,00€25mg268,00€50mg442,00€100mg652,00€1mL*10mM (DMSO)142,00€Dibenz[a,h]anthracene
CAS:Dibenz[a,h]anthracene (CCRIS 208) has induced DNA damage and gene mutations in bacteria and gene mutations and transformation in several types of mammalian cell
Formula:C22H14Purezza:99.97%Colore e forma:Colorless Plates Or Leaflets /Recrystallized/ From Acetic Acid Physical Description White Crystals Or Pale Yellow Solid Sublimes (Ntp 1992)Peso molecolare:278.35Flurochloridone
CAS:Flurochloridone (R 40244) is a selective herbicide. Flurochloridone induces apoptosis and is regulated by mitochondrial dysfunction and oxidative stresses.Formula:C12H10Cl2F3NOPurezza:99.86%Colore e forma:SolidPeso molecolare:312.12Cot inhibitor-2
CAS:Cot inhibitor-2: Potent, selective Tpl2/MAP3K8 blocker. IC50: 1.6 nM; hampers LPS-induced TNF-α, IC50: 0.3 μM. Orally active.Formula:C26H25Cl2FN8Purezza:99.85%Colore e forma:SolidPeso molecolare:539.43Ref: TM-T10866
1mg69,00€5mg149,00€10mg230,00€25mg485,00€50mg713,00€100mg1.018,00€200mg1.369,00€1mL*10mM (DMSO)172,00€NPB
CAS:NPB (Alpha-NPB) is a potent BAD phosphorylation inhibitor(at Ser99,IC50 of 0.41 μM.)Formula:C29H31Cl2N3O2Purezza:99.93%Colore e forma:SolidPeso molecolare:524.48Ref: TM-T12249
1mg52,00€5mg105,00€10mg170,00€25mg279,00€50mg386,00€100mg510,00€200mg700,00€1mL*10mM (DMSO)117,00€SAR405838
CAS:MI-773 (SAR405838 (MI 773)) is an orally available MDM2 antagonist with Ki of 0.88 nM. Phase 1.Formula:C29H34Cl2FN3O3Purezza:98.63%Colore e forma:SolidPeso molecolare:562.5Ref: TM-T6585
1mg50,00€2mg86,00€5mg126,00€10mg202,00€25mg396,00€50mg585,00€100mg833,00€500mg1.684,00€Riviciclib hydrochloride
CAS:Riviciclib hydrochloride (P276-00) is a novel CDK1, CDK4 and CDK9 inhibitor with IC50 of 79 nM, 63 nM and 20 nM, respectively. Phase 2/3.Formula:C21H20ClNO5·HClPurezza:99.51%Colore e forma:SolidPeso molecolare:438.3Metaproterenol
CAS:Metaproterenol also has anti-inflammatory activity. Metaproterenol is a direct-acting sympathomimetic and a β2-adrenergic receptor (β2AR) agonist (IC50: 68 nM).Formula:C11H17NO3Purezza:98%Colore e forma:SolidPeso molecolare:211.26PI3K-IN-34
CAS:PI3K-IN-34 targets PI3K-α/β/δ (IC50: 11.73/6.09/11.18 μM); potential leukemia research tool.Formula:C23H22N6O3Colore e forma:SolidPeso molecolare:430.46hGGPPS-IN-1
CAS:HGGPPS-IN-1: analog of C2-ThP-BPs, inhibits hGGPPS, triggers apoptosis in MM cells, shows anti-myeloma effects in vivo.Formula:C13H13N3O6P2SColore e forma:SolidPeso molecolare:401.27EC359
CAS:EC359 is a Leukemia Inhibitory Factor Receptor (LIFR) inhibitor with anticancer activity for the study of leukemia and endometrial cancer.Formula:C36H38F2O2Purezza:98.11% - 98.11%Colore e forma:SolidPeso molecolare:540.68Simmiparib
CAS:Simmiparib (SMOCL-9112) is a PARP1 and PARP2 inhibitor that promotes apoptosis.Simmiparib is used to study Parkinson's disease and melanoma.
Formula:C23H18F4N6O2Purezza:99.05% - 99.51%Colore e forma:SolidPeso molecolare:486.42IW-927
CAS:IW-927 is a potent and selective TNFα/TNFRc1 interaction antagonist.Formula:C22H23N3O3S2Colore e forma:SolidPeso molecolare:441.57Prinomastat hydrochloride
CAS:Prinomastat HCl, an oral MMP (1, 3, 9) inhibitor, IC50s: 79, 6.3, 5.0 nM, shows antitumor activity.
Formula:C18H22ClN3O5S2Purezza:98%Colore e forma:SolidPeso molecolare:459.97CCCI-01
CAS:CCCI-01: Centrosome cluster inhibitor with anticancer properties, induces apoptosis, aids in non-cross-resistant drug research.Formula:C11H9N3O4Purezza:99.97%Colore e forma:SolidPeso molecolare:247.21Mps1-IN-5
CAS:Mps1-IN-5: oral Mps1 inhibitor with 29 nM IC50, induces apoptosis, G2/M arrest, and has anti-tumor properties.Formula:C24H25N9Colore e forma:SolidPeso molecolare:439.52GK563
CAS:GK563, an iPLA2 inhibitor (IC50=1nM), is 22,000x more potent vs. cPLA2 and may reduce β-cell death in type 1 diabetes.Formula:C16H22O2Colore e forma:SolidPeso molecolare:246.34hnRNPK-IN-1
CAS:hnRNPK-IN-1 binds hnRNPK tightly (Kd 4.6-2.6 μM), disrupting c-myc transcription and inducing apoptosis in Hela cells.Formula:C23H21N3O5Colore e forma:SolidPeso molecolare:419.43Thioxodihydroquinazolinone-19
CAS:Thioxodihydroquinazolinone-19 triggers apoptosis in A2780cis ovarian cancer cells and enhances cisplatin efficacy.Formula:C16H14N2OSPurezza:98%Colore e forma:SolidPeso molecolare:282.36NSC 146109 hydrochloride
CAS:NSC 146109 hydrochloride is an activator of p53 targeting MDMX. NSC 146109 hydrochloride can be used for studies on breast cancer.Formula:C17H17ClN2SPurezza:99.28%Colore e forma:SolidPeso molecolare:316.85cRIPGBM
CAS:cRIPGBM induces apoptosis in GBM CSCs by targeting RIPK2, with an EC50 of 68 nM in GBM-1 cells.Formula:C26H20FN2O2Purezza:98%Colore e forma:SolidPeso molecolare:411.45Anticancer agent 99
CAS:Anticancer agent 99 targets HepG2 cells, IC50 at 35.9 μM, induces apoptosis and hinders cell growth.Formula:C19H20F3N3O2Colore e forma:SolidPeso molecolare:379.38DPBQ
CAS:DPBQ (ZINC1620467) is a p53 activator.Formula:C24H14N2O2Purezza:98.08%Colore e forma:SolidPeso molecolare:362.38Ref: TM-T11092
1mg100,00€2mg149,00€5mg245,00€10mg354,00€25mg532,00€50mg735,00€100mg982,00€500mgPrezzo su richiestaCaspase-3/7 activator 2
Caspase-3/7 activator 2 triggers apoptosis with tumor selectivity and anti-proliferative properties.Formula:C32H34N2O7Colore e forma:SolidPeso molecolare:558.62PI3Kα-IN-6
CAS:PI3Kα-IN-6 (Compound 5b) is a PI3Kα inhibitor that exhibits anticancer effects without toxicity to normal cells.Formula:C16H15IN2OSColore e forma:SolidPeso molecolare:410.27MRS 2693 trisodium salt
CAS:MRS 2693 trisodium salt is a P2Y6 agonist.Formula:C9H22IN5O12P2Purezza:98%Colore e forma:SolidPeso molecolare:581.15Luxeptinib
CAS:Luxeptinib (CG-806) is an oral, non-covalent pan-FLT3/BTK inhibitor for acute myeloid leukemia.Formula:C25H17F4N5O2Colore e forma:SolidPeso molecolare:495.43CB-64D
CAS:CB-64D is a sigma2R selective agonist which releases calcium in human neuroblastoma cells and produces cell death in tumor cell lines.Formula:C22H23NO2Colore e forma:SolidPeso molecolare:333.42EGFR/HER2/TS-IN-1
CAS:EGFR/HER2/TS-IN-1 inhibits EGFR (0.203 μM), HER2 (0.088 μM), TS (0.168 μM), and induces apoptosis in MCF7 cells.Formula:C24H15N5O4S2Colore e forma:SolidPeso molecolare:501.54Bcl-2/Mcl-1-IN-1
CAS:Bcl-2/Mcl-1-IN-1 is an inhibitor of Bcl-2 (Ki: 4.53 μM) and Mcl-1 (Ki: 1.19 μM).Bcl-2/Mcl-1-IN-1 can be used in cancer research.Formula:C28H23NO3Colore e forma:SolidPeso molecolare:421.49(Z)-4EGI-1
CAS:(Z)-4EGI-1, a Z-isomer, inhibits eIF4E/eIF4G; binds eIF4E (IC50=43.5 μM, Kd=8.74 μM); anticancer properties.Formula:C18H12Cl2N4O4SColore e forma:SolidPeso molecolare:451.28CDK6/PIM1-IN-1
CAS:CDK6/PIM1-IN-1: A dual inhibitor for CDK6 (39 nM IC50) & PIM1 (88 nM), also targets CDK4 (3.6 nM IC50), halts AML cell growth, and induces apoptosis.Formula:C25H28FN9Colore e forma:SolidPeso molecolare:473.55TPB15
CAS:TPB15, an oral Hh inhibitor, blocks Smo activity, arrests cell cycle, induces apoptosis, and shows potent antitumor effects with low toxicity.Formula:C18H9Cl4N5OColore e forma:SolidPeso molecolare:453.11Z-LEVD-FMK
CAS:Z-LEVD-FMK is a caspase-4 inhibitor with anti-cancer activity, capable of eliminating LPS-induced GCLC protein degradation.Formula:C31H45FN4O10Colore e forma:SolidPeso molecolare:652.71Tubulin/MMP-IN-2
CAS:Tubulin/MMP-IN-2 blocks tubulin polymerization, MMP-2/-3/-9, induces apoptosis, aids cancer research, IC50: 24.95, 31.60, 22.37 µM.Formula:C40H48NO11PColore e forma:SolidPeso molecolare:749.78Antiproliferative agent-19
Antiproliferative agent-19 induces apoptosis and G2/M cell cycle arrest in lung cancer cells.Formula:C26H23NOColore e forma:SolidPeso molecolare:365.47Anticancer agent 47
CAS:Compound 4j: potent anticancer agent; halts cell growth, induces apoptosis and G0/G1 arrest; significant in vivo tumor reduction.Formula:C19H14N2O4SColore e forma:SolidPeso molecolare:366.39Oxythiamine chloride HCl
CAS:Oxythiamine chloride is a thiamine antagonist and anticancer agent that inhibits transketolase, affecting RNA/DNA synthesis and inducing apoptosis.Formula:C12H17Cl2N3O2SColore e forma:SolidPeso molecolare:338.25BRD0476
CAS:BRD0476 prevents pancreatic β-cell death by blocking IFN-γ-induced JAK2 & STAT1 without inhibiting JAK kinase activity.Formula:C35H38N4O8SPurezza:98%Colore e forma:SolidPeso molecolare:674.76Verticillin A
CAS:Verticillin A, an apoptosis inducer, inhibits Leiomyosarcoma and Malignant peripheral nerve sheath tumor growth.Formula:C30H28N6O6S4Purezza:98%Colore e forma:SolidPeso molecolare:696.84SK-7041
CAS:SK-7041 is an effective HDAC inhibitor that acts by preferentially inhibiting class I HDAC1 and HDAC2.Formula:C19H21N3O3Purezza:98%Colore e forma:SolidPeso molecolare:339.39PBENZ-DBRMD
CAS:PBENZ-DBRMD inhibits DIO3, has anti-growth effects, and aids apoptosis, showing promise for cancer research.Formula:C11H5Br2NO4Colore e forma:SolidPeso molecolare:374.97AFG206
CAS:AFG206 is the novel first-generation type II" FLT3 inhibitor."Formula:C20H19N3O2Colore e forma:SolidPeso molecolare:333.38GW-3333
CAS:GW-3333 inhibits matrix metalloproteinases and TNF-Converting Enzyme, showing potential as an antiarthritic therapy.Formula:C22H36N4O4Purezza:98%Colore e forma:SolidPeso molecolare:420.55p-DDAP
CAS:p-DDAP inhibits cell invasion and reduces MMP-9 activity and expression.Formula:C18H31NOPurezza:98%Colore e forma:SolidPeso molecolare:277.44HDAC6-IN-4
CAS:HDAC6-IN-4 (C10), an oral, selective, potent HDAC6 inhibitor with low toxicity, IC50: 23 nM, promotes apoptosis and strong anti-tumor action.Formula:C30H38N2O5Colore e forma:SolidPeso molecolare:506.63VEGFR-2/BRAF-IN-2
VEGFR-2/BRAF-IN-2 inhibits VEGFR-2, BRAF V600E, BRAF WT (IC50: 0.111/0.089/0.071 µM); induces G1 arrest and apoptosis.Formula:C26H21ClF3N5O3S2Colore e forma:SolidPeso molecolare:608.05ZINC69391
CAS:ZINC69391 inhibits Rac1, reduces cancer cell growth and metastasis, and induces apoptosis.Formula:C14H14F3N5Purezza:99.61%Colore e forma:SolidPeso molecolare:309.29Ref: TM-T24833
1mg34,00€5mg78,00€10mg112,00€25mg197,00€50mg275,00€100mg371,00€200mg494,00€1mL*10mM (DMSO)86,00€SAR125844
CAS:SAR125844, a potent and highly selective inhibitor of the MET receptor tyrosine kinase (RTK), for intravenous administration. (IC50 value of 4.2 nmol/L)Formula:C25H23FN8O2S2Purezza:98.73%Colore e forma:SolidPeso molecolare:550.63Ref: TM-T5467
1mg34,00€5mg74,00€10mg110,00€25mg215,00€50mg344,00€100mg557,00€200mg790,00€1mL*10mM (DMSO)92,00€AZD 1152 (hydrochloride)
CAS:AZD 1152, an oral prodrug, becomes AZD 1152-HQPA in plasma, selectively inhibits Aurora kinase B (IC50=0.36 nM), and blocks tumor growth.Formula:C26H33Cl2FN7O6PColore e forma:SolidPeso molecolare:660.47VU0424465
CAS:VU0424465 is a mGlu5-selective allosteric agonist.Formula:C19H19FN2O2Colore e forma:SolidPeso molecolare:326.36SCAL-266
CAS:SCAL-266, a potent inhibitor of mitochondrial complex I (CI), exhibits an IC50 of 0.83 μM.Formula:C27H28F3N5O2Purezza:98%Colore e forma:SolidPeso molecolare:511.54CAY10747
CAS:CAY10747, a celastrol derivative, inhibits Hsp90-Cdc37 interaction, decreases client proteins, and induces apoptosis in various cancer cells.Formula:C42H48FNO6Colore e forma:SolidPeso molecolare:681.83CDK9-IN-18
CAS:CDK9-IN-18: Potent CDK9 blocker, anticancer, induces apoptosis, low cellular activity.Formula:C27H20N8OColore e forma:SolidPeso molecolare:472.5MI-3
CAS:MI-3 (Menin-MLL Inhibitor) (Menin-MLL Inhibitor) is an effective inhibitor of Menin-MLL interaction (IC50: 648 nM).Formula:C18H25N5S2Purezza:98.66% - 99.61%Colore e forma:SolidPeso molecolare:375.55Esuberaprost Sodium
CAS:Famitinib (SHR1020), an oral drug, inhibits c-kit, VEGFR-2, and PDGFRβ (IC50: 2.3/4.7/6.6 nM) and triggers apoptosis in gastric cancer.Formula:C23H27FN4O2Colore e forma:SolidPeso molecolare:410.48Vin-C01
CAS:Vin-C01, a potent protector of pancreatic β-cells (EC50=0.22μM), aids in type 2 diabetes research by preventing STZ-induced β-cell apoptosis.Formula:C20H24N2OColore e forma:SolidPeso molecolare:308.42Gemcitabine monophosphate
CAS:R306465, a potent HDAC1/8 inhibitor, has broad antitumor effects (IC50: 30-300 nM) on solid and blood cancers.Formula:C9H12F2N3O7PColore e forma:SolidPeso molecolare:343.18IST5-002
CAS:IST5-002: Potent Stat5a/b blocker, IC50 1.5μM/3.5μM, targets prostate cancer & CML.Formula:C17H20N5O7PPurezza:99.36%Colore e forma:SolidPeso molecolare:437.34Epofolate
CAS:Epofolate: folate receptor-targeted antimitotic, delivers epothilone to cancer cells, inhibits mitosis, may halt tumor growth. Check clinical trials.Formula:C67H92N16O22S3Colore e forma:SolidPeso molecolare:1569.74MMP-9-IN-5
CAS:MMP-9-IN-5: MMP-9 and AKT inhibitor (IC50: 4.49 nM and 1.34 nM), induces apoptosis for cancer research.Formula:C27H20IN3O4Colore e forma:SolidPeso molecolare:577.37PK9327
CAS:PK9327 is a small-molecule stabilizer that targets cavity-creating p53 cancer mutations.Formula:C21H22N2SColore e forma:SolidPeso molecolare:334.48PD1-PDL1-IN 1
CAS:PD1-PDL1-IN 1 is a potent inhibitor of programmed cell death 1 (PD-1),and used as immune modulator.Formula:C14H23N7O6Purezza:98%Colore e forma:SolidPeso molecolare:385.38S116836
CAS:S116836 is a tyrosine kinase inhibitor.Formula:C27H21F3N6OPurezza:98%Colore e forma:SolidPeso molecolare:502.49Tubulin inhibitor 30
CAS:Tubulin Inhibitor 30, exhibiting an IC50 value of 0.52 μM, functions as an inhibitor of tubulin assembly. Additionally, it can induce ferroptosis.Formula:C22H19N3O5Colore e forma:SolidPeso molecolare:405.4Lexibulin dihydrochloride
CAS:Lexibulin 2HCl inhibits tubulin polymerization (IC50: 10-100 nM) and shows potent anti-cancer cytotoxicity and vascular disruption in vitro/vivo.Formula:C24H32Cl2N6O2Purezza:98%Colore e forma:SolidPeso molecolare:507.46PSB 0474
CAS:P2Y6 receptor agonistFormula:C17H20N2O13P2Purezza:98%Colore e forma:SolidPeso molecolare:522.29VEGFR-2-IN-28
CAS:VEGFR-2-IN-28 is a potent inhibitor of VEGFR-2 (IC50: 0.83 μM). VEGFR-2-IN-28 induces apoptosis and exhibits antitumor effects.Formula:C26H17N7O7Colore e forma:SolidPeso molecolare:539.46RDR03871
CAS:RDR03871 is an MDM2 inhibitor.
Formula:C18H16ClF3N6Purezza:97.78%Colore e forma:SolidPeso molecolare:408.81CAY10443
CAS:CAY10443 activates apoptosis by binding to apoptosome components, with an EC50 of 5 μM for caspase-3, aiding antitumor drug development.Formula:C17H15Cl2NO2Colore e forma:SolidPeso molecolare:336.21VS 8
CAS:VS 8: potent oral VEGFR-2 inhibitor, anti-angiogenic, induces cancer cell apoptosis & migration, acts on CSCs.Formula:C26H20F3N3O3Colore e forma:SolidPeso molecolare:479.45YL-939
YL-939 is a potent inhibitor of ferroptosis, targeting the PHB2/ferritin/iron axis to impede this form of cell death.Formula:C25H26N6OColore e forma:SolidPeso molecolare:426.51MEK-IN-5
CAS:MEK-IN-5: strong MEK inhibitor and NO donor, reduces pMEK/pERK dose/time-dependently, triggers apoptosis in MDA-MB-231 cells.Formula:C29H27FN4O10S2Colore e forma:SolidPeso molecolare:674.67Cyclamidomycin
CAS:Cyclamidomycin is an antibiotic. It also functions as an inhibitor of nucleoside diphosphokinase of Escherichia coli.Formula:C7H10N2OColore e forma:SolidPeso molecolare:138.17ABI-231 HCl
CAS:ABI-231: Oral tubulin inhibitor, IC50=5.2 nM for melanoma/prostate cancer, in clinical trials for prostate cancer, effective in vivo.Formula:C21H20ClN3O4Colore e forma:SolidPeso molecolare:413.85Anticancer agent 63
CAS:Compound 3h fights various cancers; most effective on MCF-7 (IC50 3.4 μM). Triggers apoptosis; alters Bcl-2, IL-2, Caspase-3 levels, has antioxidant effects.Formula:C17H24F3NOSeColore e forma:SolidPeso molecolare:394.33Caspase-3/7 activator 3
Caspase-3/7 activator 3 triggers apoptosis with tumor selectivity and anti-proliferative effects.Formula:C24H27NO5Colore e forma:SolidPeso molecolare:409.47YLT-11
YLT-11: Oral PLK4 inhibitor, Kd 5.2 nM; less effective on PLK1/2/3; inhibits cancer cell growth and induces G2/M arrest and apoptosis.Formula:C24H24N6OColore e forma:SolidPeso molecolare:412.49RO27-3225 TFA
CAS:RO27-3225, a MC4R agonist (EC50=1nM), may treat obesity and brain damage, also acts on MC1R, and helps in hemorrhagic shock.Formula:C41H53F3N12O8Colore e forma:SolidPeso molecolare:898.9462CAY10789
CAS:CAY10789: potent CysLT1R antagonist (IC50 2.8 µM), GPBAR1 agonist (EC50 3 µM), reduces U937 cell adhesion, TNF-α, stable with promising pharmacokinetics.Formula:C17H15NO2Colore e forma:SolidPeso molecolare:265.31DB2313 HCl
CAS:DB2313: first-in-class, potent inhibitor of PU.1, disrupts gene interactions, down-regulates PU.1 targets.Formula:C42H45Cl4FN8O2Colore e forma:SolidPeso molecolare:854.67(R)-eIF4A3-IN-2
CAS:(R)-eIF4A3-IN-2, a weaker eIF4A3-IN-2 isomer, inhibits eIF4A3 selectively with 110 nM IC50.Formula:C25H19Br2ClN4O2Colore e forma:SolidPeso molecolare:602.71RGB-286147
CAS:RGB-286147 is a potent, selective, ATP-competitive Cdks inhibitor.Formula:C23H22Cl2N4O3Purezza:98%Colore e forma:SolidPeso molecolare:473.35p-MPPF dihydrochloride
CAS:p-MPPF dihydrochloride is a 5-HT antagonist that can be used to study neurological diseases.Formula:C25H29Cl2FN4O2Purezza:99.55%Colore e forma:SolidPeso molecolare:507.43CHS-828 nicotinate
CAS:CHS-828, or GMX-1778, is a potent NAMPT inhibitor with anticancer properties, active against tumors and enhanced by certain drugs.Formula:C25H27ClN6O3Colore e forma:SolidPeso molecolare:494.97Autophagy-IN-2
CAS:Autophagy-IN-2 (7h) blocks autophagic flux, triggers cancer cell death, aids in triple-negative breast cancer study.Formula:C17H19N5OColore e forma:SolidPeso molecolare:309.37SPRC
CAS:"SPRC, a synthetic antioxidant, boosts H2S production, activates STAT3, and guards against doxorubicin heart damage."Formula:C6H9NO2SPurezza:98%Colore e forma:SolidPeso molecolare:159.21Nanatinostat TFA
CAS:Nanatinostat (Tractinostat, CHR-3996, VRx-3996) is a second-gen oral HDAC inhibitor with potential cancer treatment properties.Formula:C22H20F4N6O4Colore e forma:SolidPeso molecolare:508.43EGFR-IN-52
CAS:EGFR-IN-52, a potent EGFR inhibitor, has IC50s: 0.358 μM (wild-type), 86.02 μM (L858R-TK), 432.67 μM (T790M-TK); induces cancer cell apoptosis.Formula:C19H18N4O3SColore e forma:SolidPeso molecolare:382.44Benpyrine
CAS:Benpyrine, an oral TNF-α inhibitor (KD 82.1 μM, IC50 0.109 μM), may help in inflammatory/autoimmune studies.Formula:C16H16N6OColore e forma:SolidPeso molecolare:308.34OXPHOS-IN-1
CAS:OXPHOS-IN-1 inhibits oxidative phosphorylation; halts MIA PaCa-2 (IC50: 2.34 μM) and BxPC-3 cells growth (IC50: 13.82 μM).Formula:C19H29N3O6S2Colore e forma:SolidPeso molecolare:459.58

