Apoptosis
Apoptosis inhibitors are compounds that prevent or delay the process of programmed cell death, known as apoptosis. These inhibitors are vital in studying cell survival mechanisms and are used to investigate diseases where apoptosis is dysregulated, such as cancer, neurodegenerative disorders, and autoimmune diseases. By modulating apoptosis, these inhibitors can help in the development of therapies aimed at controlling cell death. At CymitQuimica, we provide a comprehensive selection of high-quality apoptosis inhibitors to support your research in cell biology, oncology, and related fields.
Subcategories of "Apoptosis"
- ASK(6 products)
- BCL(11 products)
- Caspase(125 products)
- FOXO1(3 products)
- IAP(66 products)
- Mdm2(12 products)
- PD-1/PD-L1(125 products)
- PDK(9 products)
- PERK(25 products)
- Serine/threonin kinase(15 products)
- Survivin(13 products)
- TNF(92 products)
- c-RET(51 products)
- p53(62 products)
Show 6 more subcategories
Found 5593 products of "Apoptosis"
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PD-1/PD-L1-IN-28
CAS:<p>PD-1/PD-L1-IN-28, an inhibitor of the PD-1/PD-L1 signaling pathway (IC 50 = 0.744 µM), demonstrates promising research potential in tumor immunity.</p>Formula:C24H24N4O2Color and Shape:SolidMolecular weight:400.47HDACs/mTOR Inhibitor 1
CAS:<p>HDACs/mTOR Inhibitor 1 is a dual HDACs and mammalian target of Rapamycin (mTOR) target inhibitor for treating hematologic malignancies (IC50s: 0.19 nM, 1.8 nM,</p>Formula:C28H38N8O5Color and Shape:SolidMolecular weight:566.65Ro 31-7837
CAS:<p>Ro 31-7837 is an opener of potassium channel.</p>Formula:C17H16N2O2Color and Shape:SolidMolecular weight:280.32EAPB 02303
CAS:<p>EAPB 02303, a microtubule inhibitor, induces mitotic arrest, spindle impairment, apoptosis, and has antitumor effects, enhancing Paclitaxel.</p>Formula:C17H14N4O2Color and Shape:SolidMolecular weight:306.32ARN5187 trihydrochloride
CAS:<p>ARN5187 trihydrochloride: a REV-ERBβ inhibitor that blocks transcription, autophagy, and induces apoptosis with lysosomal cytotoxicity.</p>Formula:C24H35Cl3FN3OColor and Shape:SolidMolecular weight:506.912ACA-28
CAS:<p>ACA-28 is an ERK MAPK signalling modulator that induces apoptosis in melanoma cells by overexpressing ERK.</p>Formula:C17H16O6Purity:98.73%Color and Shape:SolidMolecular weight:316.31LWG-301
<p>LWG-301, a GLS1 allosteric inhibitor, IC50 7 nM, impedes glutamine metabolism and prompts apoptosis; shows antitumor effects.</p>Formula:C28H38N8O3SColor and Shape:SolidMolecular weight:566.72SB 706504
CAS:<p>SB 706504 is an effective p38 MAPK inhibitor that suppresses inflammatory gene expression in macrophages and inhibits TNFα production in COPD.</p>Formula:C24H19F3N8OPurity:98.686%Color and Shape:SolidMolecular weight:492.46A 410099.1
CAS:<p>A 410099.1 is a BIRC (baculoviral IAP repeat-containing protein) inhibitor with EC50 values of 4.6, 9.2, 15.6, 19.9, and 93.9 nM for BIRC2/3/4/7/8.</p>Formula:C27H41ClN4O3Purity:99.30%Color and Shape:SolidMolecular weight:505.1JS-K
CAS:<p>JS-K is a Nitric oxide donor. It has antiproliferative activity.</p>Formula:C13H16N6O8Color and Shape:SolidMolecular weight:384.3Obatoclax
CAS:<p>Obatoclax (GX15-070), a pan-BCL-2 inhibitor (Ki 220 nM) induces autophagy, degrades cyclin D1, and has anti-cancer/antiparasitic properties.</p>Formula:C20H19N3OPurity:99.44%Color and Shape:SolidMolecular weight:317.38NMK-TD-100
CAS:<p>NMK-TD-100: Microtubule disruptor, anti-proliferative, blocks mitosis, causes apoptosis in HeLa; IC50=17.5µM for tubulin polymerization.</p>Formula:C19H17N3O3SPurity:98%Color and Shape:SolidMolecular weight:367.42Metaproterenol
CAS:<p>Metaproterenol also has anti-inflammatory activity. Metaproterenol is a direct-acting sympathomimetic and a β2-adrenergic receptor (β2AR) agonist (IC50: 68 nM).</p>Formula:C11H17NO3Purity:98%Color and Shape:SolidMolecular weight:211.26KY1022
CAS:<p>KY1022 is a ras destabilizer. KY1022 targets the Wnt/ß-catenin pathway and inhibits development of metastatic colorectal cancer.</p>Formula:C17H19N3OSColor and Shape:SolidMolecular weight:313.42PS121912
CAS:<p>PS121912 is a potent and selective inhibitor of VDR-coactivator.</p>Formula:C24H21F3N2OPurity:98%Color and Shape:SolidMolecular weight:410.43MBM-17
CAS:<p>MBM-17 is a potent inhibitor of NIMA-related kinase 2 (Nek2,IC50 of 3 nM).</p>Formula:C28H28N6O2Purity:98%Color and Shape:SolidMolecular weight:480.56DPQZ
CAS:<p>DPQZ is an anti-tubulin compound acting by inducing cell apoptosis in human oral cancer cells through Ras/Raf inhibition and MAP kinases activation.</p>Formula:C20H17N3OPurity:98%Color and Shape:SolidMolecular weight:315.37SKLB70326
CAS:<p>SKLB70326 is a cell-cycle progression inhibitor that acts by inducing G0/G1 phase arrest and apoptosis in human hepatic carcinoma cells.</p>Formula:C15H13N3O2SPurity:98%Color and Shape:SolidMolecular weight:299.35NSC-741909
CAS:<p>NSC-741909 is an anticancer agent that acts by suppressing the growth of several cell lines.</p>Formula:C16H14ClNOPurity:98%Color and Shape:SolidMolecular weight:271.74ATB-337
CAS:<p>S-Diclofenac, an NSAID with H2S-releasing moiety, protects gastric mucosa while inhibiting prostaglandins.</p>Formula:C23H15Cl2NO2S3Color and Shape:SolidMolecular weight:504.47KF24345
CAS:<p>KF24345 is an inhibitor of adenosine uptake.</p>Formula:C31H38N6O5Color and Shape:SolidMolecular weight:574.67HI5
CAS:<p>HI5: potent tubulin/IDO inhibitor, IC50 70 nM (HeLa), blocks kynurenine, G2/M arrest, spurs T cell activity, & triggers apoptosis.</p>Formula:C42H43N5O8Color and Shape:SolidMolecular weight:745.82MpsBAY2a
CAS:<p>carcinoma cell proliferation.</p>Formula:C29H28N6OPurity:98%Color and Shape:SolidMolecular weight:476.57Anticancer agent 32
CAS:<p>Compound 2g, an anticancer agent, disrupts cell cycle and induces apoptosis for cancer research.</p>Formula:C24H21F2N5OColor and Shape:SolidMolecular weight:433.45Nevanimibe
CAS:<p>Nevanimibe is an orally active and selective inhibitor of acyl-coenzyme A:cholesterol O-acyltransferase 1 (ACAT1) (EC50 of 9 nM).</p>Formula:C27H39N3OPurity:98%Color and Shape:SolidMolecular weight:421.62NU-8165
CAS:<p>NU-8165 is an MDM2-p53 protein-protein interaction inhibitor.</p>Formula:C24H22ClNO3Purity:98%Color and Shape:SolidMolecular weight:407.89PARP1-IN-10
CAS:<p>PARP1-IN-10 (12c) is a potent, non-toxic PARP1 inhibitor with a 50.62 nM IC50, enhancing TMZ effects and causing G2/M arrest and apoptosis.</p>Formula:C20H23N3O5Color and Shape:SolidMolecular weight:385.41SLMP53-2
CAS:<p>SLMP53-2 is a mutant p53 reactivator that restores the wild-type-like conformation and DNA-binding ability of mutp53-Y220C through enhanced interaction with</p>Formula:C26H22N2O2Color and Shape:SolidMolecular weight:394.47GW837016X
CAS:<p>GW837016X, also known as NEU-391, is a potent inhibitor of protozoan parasite proliferation.</p>Formula:C25H20ClFN4OSColor and Shape:SolidMolecular weight:478.97MDK-4204
CAS:<p>MDK-4204, an anticancer agent, shows significant anti-cancer activity with IC50 values of 8.8 µM and 9.5 µM in PC-3 and DU-145 cells, respectively.</p>Formula:C31H29FN4OPurity:98%Color and Shape:SolidMolecular weight:492.59RC-33 HCl
CAS:<p>RC-33 HCl is a selective and metabolically stable σ1 receptor agonist potentiating NGF-induced neurite outgrowth.</p>Formula:C21H28ClNPurity:98%Color and Shape:SolidMolecular weight:329.91SMBA2
CAS:<p>SMBA2 is a Bax activator. It acts by specifically targeting the binding pocket at S184.</p>Formula:C8H16N4Purity:98%Color and Shape:SolidMolecular weight:168.24Epirubicin
CAS:<p>Epirubicin, a doxorubicin derivative, is an antineoplastic, inhibits topoisomerase, DNA/RNA synthesis, and Foxp3, reducing T cell activity.</p>Formula:C27H29NO11Color and Shape:SolidMolecular weight:543.52Perillic acid
CAS:<p>Perillic acid, a perillyl alcohol metabolite, induces lung cancer cell arrest, apoptosis, and has anti-HSV-1 and immune-modulating effects.</p>Formula:C10H14O2Color and Shape:SolidMolecular weight:166.22D44
CAS:<p>D44 is a Plasmodium FKBPs inhibitor.</p>Formula:C16H16N4OSColor and Shape:SolidMolecular weight:312.39Anti-inflammatory agent 47
CAS:<p>Flo8, an anti-inflammatory and antioxidant agent, effectively suppresses the release of reactive oxygen species (ROS) and nitric oxide (NO) while inhibiting</p>Formula:C25H18N2O3Purity:98%Color and Shape:SolidMolecular weight:394.42PHA-680626
CAS:<p>PHA-680626 is a PLK inhibitor, effective on resistant leukemia cells, with IC50: Plk1 (0.53 μM), Plk2 (0.07 μM), Plk3 (1.61 μM).</p>Formula:C23H26N6O2SColor and Shape:SolidMolecular weight:450.56Zonisamide sodium
CAS:<p>Zonisamide sodium is a 1,2 benzisoxazole derivative. It is the first agent of this chemical class to be developed as an antiepileptic drug.</p>Formula:C8H8N2NaO3SPurity:98%Color and Shape:Off-White SolidMolecular weight:235.22LG308
CAS:<p>LG308, a synthetic compound, has anti-tumor properties, inducing apoptosis and mitotic arrest, thereby suppressing prostate cancer growth.</p>Formula:C19H17FN2OColor and Shape:SolidMolecular weight:308.35BTK-IN-24
CAS:<p>BTK-IN-24 is a Bruton's tyrosine kinase (BTK) inhibitor with potential anticancer activity, and it can be used in the study of myeloproliferative disorders.</p>Formula:C26H19F4N5O2Purity:99.61%Color and Shape:SolidMolecular weight:509.46GSK962
CAS:<p>GSK962 is a GSK963 inactive enantiomer. It can be used to confirm the on-target effects.</p>Formula:C14H18N2OPurity:99.75%Color and Shape:SolidMolecular weight:230.31Ferroptosis inducer-1
CAS:<p>Ferroptosis inducer-1 is a Ferroptosis inducer with antitumor potential .</p>Formula:C25H21ClN2O5Color and Shape:SolidMolecular weight:464.9MYRA-A
CAS:<p>MYRA-A is an inducer of apoptosis in a Myc-dependent manner that acts by inhibiting Myc-driven transformation and disrupting MYC-Max interaction.</p>Formula:C19H20N2O4Purity:98%Color and Shape:SolidMolecular weight:340.37EGFR-IN-88
CAS:<p>EGFR-IN-88 (Compound 4i), an EGFR inhibitor with an IC50 of 87 nM, exhibits cytotoxic effects on A549 cells at an IC50 of 3.902 μM and can induce cell apoptosis</p>Formula:C22H18Cl2N4O2SPurity:98%Color and Shape:SolidMolecular weight:473.37Pim-1 kinase inhibitor 1
CAS:<p>Pim-1 kinase inhibitor 1, IC50 0.11 μM, combats various cancers by inducing apoptosis.</p>Formula:C19H13N3O3Color and Shape:SolidMolecular weight:331.32NHI-2
CAS:<p>NHI-2 is an LDHA inhibitor (IC50 14.7 µM) that blocks glycolysis, induces apoptosis and cell cycle arrest, and suppresses tumor growth in melanoma models.</p>Formula:C17H12F3NO3Purity:99.981%Color and Shape:SolidMolecular weight:335.28MG-262
CAS:<p>MG-262 is a reversible proteasome inhibitor with multiple biological activities [1] [2] [3].</p>Formula:C25H42BN3O6Color and Shape:SolidMolecular weight:491.43M199
CAS:<p>M199, a novel inhibitor of TLR3/9 activation, induces secretion of IL-6, IL-8 and TNFalpha in human PBMCs.</p>Formula:C17H17N3OPurity:98%Color and Shape:SolidMolecular weight:279.34CDK8/19-IN-1
CAS:<p>CDK8/19-IN-1 is a selective and oral bioavailable CDK8/19 dual inhibitor (IC50s: 0.46 nM, 0.99 nM, and 270 nM for CDK8, CDK19, and CDK9).</p>Formula:C19H18N4O4S2Purity:98%Color and Shape:SolidMolecular weight:430.5DC-5163
CAS:<p>DC-5163 inhibits GAPDH (IC50: 176.3 nM, Kd: 3.192 μM), targets cancer cell growth and glycolysis.</p>Formula:C18H20ClN3OSPurity:98%Color and Shape:SolidMolecular weight:361.89E64FC26
CAS:<p>E64FC26 is a PDI family pan-inhibitor with antitumor activity that inhibits PDIA1 and PDIA6 and can be used to study multiple myeloma and pancreatic cancer.</p>Formula:C19H23F3O2Purity:98.1% - 98.1%Color and Shape:SolidMolecular weight:340.38AMPK activator 11
CAS:<p>AMPK Activator 11 is a nanomolar potent inhibitor of cell proliferation in various colorectal carcinomas (CRCs), acting through the selective activation of AMP-</p>Formula:C25H20N4O2Purity:98%Color and Shape:SolidMolecular weight:408.45DJ001
CAS:<p>DJ001: specific PTPσ inhibitor, non-competitive, IC50=1.43 μM, aids hematopoietic stem cell regeneration.</p>Formula:C15H12N2O3Purity:99.54%Color and Shape:SolidMolecular weight:268.27YLT205
CAS:<p>YLT205 is an inducer of apoptosis in human colorectal cells that acts by inhibiting tumor growth.</p>Formula:C16H12BrClN4O2S2Purity:98%Color and Shape:SolidMolecular weight:471.78(E)-[6]-Dehydroparadol
CAS:<p>(E)-[6]-Dehydroparadol ((6)-Dehydroparadol), an oxidative metabolite of [6]-Shogaol, is a potent Nrf2 activator.</p>Formula:C17H24O3Purity:99.85%Color and Shape:SolidMolecular weight:276.37MR2938
CAS:<p>MR2938: AChE inhibitor (IC50=5.04μM), reduces NO (IC50=3.29μM), blocks MAPK/JNK, NF-κB; for AD research.</p>Formula:C21H24N4O3Color and Shape:SolidMolecular weight:380.44Irbesartan HCl
CAS:<p>Irbesartan: angiotensin II blocker; treats hypertension by inhibiting receptor binding.</p>Formula:C25H29ClN6OPurity:98%Color and Shape:SolidMolecular weight:465AD-2646
CAS:<p>AD-2646 has antidepressant activity and inhibits 2-deoxy-D-glucose (2-DG)-induced gastric acid secretion.</p>Formula:C23H40N2O4Color and Shape:SolidMolecular weight:408.57ABD56
CAS:<p>ABD56 inhibits osteoclast formation and activity in vitro and in vivo.</p>Formula:C17H18O3Color and Shape:SolidMolecular weight:270.32Trehalose 6-behenate
CAS:<p>Trehalose 6-behenate is a Th1/Th17 skewing vaccine adjuvant.</p>Formula:C34H64O12Purity:98%Color and Shape:SolidMolecular weight:664.86EL-102
CAS:<p>EL-102 is a HIF1α inhibitor with anticancer activity that inhibits microtubule protein polymerization and can be used to study prostate cancer.</p>Formula:C19H16N2O3S2Purity:99.34%Color and Shape:SolidMolecular weight:384.47MCL-1/BCL-2-IN-4
CAS:<p>MCL-1/BCL-2-IN-4 is a selective and potent Mcl-1 and Bcl-2 dual inhibitor.</p>Formula:C26H23BrN2O5SPurity:98%Color and Shape:SolidMolecular weight:555.44DCP-LA
CAS:<p>DCP-LA (FR236924), linoleic acid derivatives, selective and direct activation of PKCε.</p>Formula:C20H36O2Purity:98%Color and Shape:SolidMolecular weight:308.5Anti-inflammatory agent 11
CAS:<p>Potent anti-inflammatory compound 16 combats tuberculosis, inhibiting Mtb H37Rv and M299 (MICs: 1.3, 6.9 μM) and reduces NO, TNF-α, IL-1β production.</p>Formula:C14H14N4OSColor and Shape:SolidMolecular weight:286.35Rooperol
CAS:<p>Rooperol: a norlignan with p38α inhibiting, immunomodulatory, antitumor, antibacterial, anticonvulsant, and antioxidant properties.</p>Formula:C17H14O4Purity:98%Color and Shape:SolidMolecular weight:282.29Pentabromophenol
CAS:<p>Pentabromophenol (NSC-5717) suppressed TGF-β response by accelerating the turnover rate of TGF-β receptors.</p>Formula:C6HBr5OPurity:99.83%Color and Shape:Monoclinic Prisms From Acetic Acid; Needles From Alcohol Physical Description Light Brown Powder Insoluble In Water (Ntp 1992)Molecular weight:488.59BTK-IN-9
CAS:<p>BTK-IN-9 reversibly inhibits BTK, disrupts mitochondria, boosts ROS, and triggers apoptosis in Z138 cells, impeding condyloma cell growth.</p>Formula:C25H19N7O4Color and Shape:SolidMolecular weight:481.46T-3256336
CAS:<p>T-3256336 is an oral IAP blocker targeting cIAP-1, cIAP-2, and XIAP.</p>Formula:C31H45F2N5O5Purity:98%Color and Shape:SolidMolecular weight:605.72Antitumor agent-62
CAS:<p>Antitumor agent-62 releases NO, inhibits cancer cell growth, triggers apoptosis, and halts cell cycle at G2/M.</p>Formula:C21H19N3O9SColor and Shape:SolidMolecular weight:489.46PD-1/PD-L1-IN-14
CAS:<p>PD-1/PD-L1-IN-14 (compound 17) is an inhibitor of PD-1/PD-L1 interaction (IC50=27.8 nM).</p>Formula:C24H24N4O2Color and Shape:SolidMolecular weight:400.47Tubulin inhibitor 33
CAS:<p>Tubulin Inhibitor 33 is a dose-dependent inhibitor of tubulin polymerization, exhibiting an IC50 value of 9.05 μM.</p>Formula:C24H22N4O3Color and Shape:SolidMolecular weight:414.46Tubulin/HDAC-IN-1
CAS:<p>Tubulin/HDAC-IN-1 is a dual inhibitor for tubulin & HDAC8, blocking polymerization & targeting HDAC8 (IC50: 150 nM), and induces cancer cell apoptosis.</p>Formula:C21H18N4O3Color and Shape:SolidMolecular weight:374.39SB-218078
CAS:<p>SB-218078 is less potently inhibits Cdc2 (IC50: 250 nM) and PKC (IC50: 1000 nM).</p>Formula:C24H15N3O3Purity:98%Color and Shape:SolidMolecular weight:393.39CYD-2-11
CAS:<p>CYD-2-11 is an effective and selective Bax agonist. It acts by targeting the structural pocket proximal to S184 in the C-terminal region of Bax.</p>Formula:C22H18N2O3Color and Shape:SolidMolecular weight:358.39DX2-201
CAS:<p>DX2-201 is a potent and selective inhibitor of oxidative phosphorylation (OXPHOS) complex I (IC50: 312 nM) and exhibits anticancer activity.</p>Formula:C18H28N2O6S2Color and Shape:SolidMolecular weight:432.55TrxR inhibitor D9
CAS:<p>TrxR-IN-D9 is a novel inhibitor of thioredoxin reductase (TrxR).</p>Formula:C25H20AuOPSColor and Shape:SolidMolecular weight:596.43Antitumor agent-19
CAS:<p>Antitumor agent-19 is a modulator of tumor-associated macrophages with EC50s of 17.18 μM and 18.87 μM in the RAW 264.7 cells and the BMDM cells.</p>Formula:C24H21ClF3N5OPurity:98.95% - 99.38%Color and Shape:SolidMolecular weight:487.9QTX125
CAS:<p>QTX125: potent, selective HDAC6 inhibitor with strong antitumor effects.</p>Formula:C23H19N3O5Color and Shape:SolidMolecular weight:417.41Topoisomerase II inhibitor 7
CAS:<p>Topoisomerase II inhibitor 7 halts cell division and induces apoptosis, targeting topoisomerase II alpha with a 3.19 μM IC50.</p>Formula:C32H28BrN5O5SColor and Shape:SolidMolecular weight:674.56ATX inhibitor 13
CAS:<p>ATX inhibitor 13: orally active, IC50 3.4 nM, halts RAW264.7 cells at G2, curbs growth/migration, prompts apoptosis, suppresses tumors.</p>Formula:C31H35Cl2N5O3Color and Shape:SolidMolecular weight:596.55HDAC-IN-36
CAS:<p>HDAC-IN-36: Oral HDAC6 inhibitor, IC50 = 11.68 nM, promotes apoptosis & autophagy, anti-tumor & anti-metastatic, for breast cancer research.</p>Formula:C29H39N5O5Color and Shape:SolidMolecular weight:537.65CN128 hydrochloride
CAS:<p>CN128 hydrochloride is an oral, selective hydroxypyridone iron chelator for β-thalassemia research.</p>Formula:C15H18ClNO3Color and Shape:SolidMolecular weight:295.76EGFR-IN-59
CAS:<p>EGFR-IN-59: EGFR inhibitor, IC50 = 190 nM, induces apoptosis, cytotoxic to A549 cells (IC50 = 8.62 μM) and WI38 cells (IC50 = 52.6 μM). Use: Various cancers.</p>Formula:C27H23N5O4SColor and Shape:SolidMolecular weight:513.57Aurora kinase-IN-1
<p>Aurora kinase-IN-1: potent aurora kinase inhibitor, alters G1 cycle proteins, induces G1/S arrest and apoptosis, potential chemotherapy lead.</p>Formula:C30H25Br2N3O5Color and Shape:SolidMolecular weight:667.34PD-1/PD-L1-IN 6
CAS:<p>Compound A13 inhibits PD-1/PD-L1, enhances interferon-γ, lacks toxicity, and boosts immune response in co-culture models. IC50=132.8 nM.</p>Formula:C25H26N2O3Color and Shape:SolidMolecular weight:402.49MDM2/XIAP-IN-2
CAS:<p>MDM2/XIAP-IN-2 is a dual inhibitor targeting murine double minute 2 (MDM2) and X-linked inhibitor of apoptosis protein (XIAP).</p>Formula:C29H32N2O4SColor and Shape:SolidMolecular weight:504.64IZTZ-1
CAS:<p>IZTZ-1: c-MYC G4 stabilizer, reduces expression, blocks cell cycle, induces apoptosis, inhibits B16 melanoma growth.</p>Formula:C32H35N7SColor and Shape:SolidMolecular weight:549.73(S)-PERK-IN-5
CAS:<p>(S)-PERK-IN-5 is the S-enantiomer of PERK-IN-5. (S)-PERK-IN-5 is a PERK inhibitor (IC50: 0.101-0.250 μM).</p>Formula:C25H26F2N4O3Color and Shape:SolidMolecular weight:468.5QM31
CAS:<p>QM31 is a selective Apaf-1 inhibitor(inbitita formation of the apoptosome with IC50 of 7.9μM).</p>Formula:C39H38Cl4N4O4Purity:98%Color and Shape:SolidMolecular weight:768.56ORY-1001 free base
CAS:<p>ORY-1001: potent KDM1A inhibitor (IC50 <20nM), selective, affects THP-1 cell gene regulation and apoptosis, hinders MV(4;11) cell growth (EC50 <1nM).</p>Formula:C15H22N2Purity:98%Color and Shape:SolidMolecular weight:230.35Se-Methylselenocysteine hydrochloride
CAS:<p>Se-Methylselenocysteine hydrochloride, a precursor to Methylselenol, exhibits significant cancer chemopreventive and antioxidant activities.</p>Formula:C4H10ClNO2SePurity:98%Color and Shape:SolidMolecular weight:218.54p53 Activator 5
CAS:<p>Potent p53 Activator 5, SC150 <0.05 mM, restores mutant p53 DNA binding, exhibits anti-tumor properties.</p>Formula:C29H32F6N4OColor and Shape:SolidMolecular weight:566.58PhiKan 083 hydrochloride
CAS:<p>PhiKan 083 HCl: carbazole, binds Y220C (Kd 167 μM), affinity in Ln229 (Kd 150 μM).</p>Formula:C16H19ClN2Purity:98%Color and Shape:SolidMolecular weight:274.79CAY10506
CAS:<p>CAY10506, a hybrid lipoic acid-TZD, activates PPARγ to control glucose and lipid levels with an EC50 of 10 μM.</p>Formula:C20H26N2O4S3Color and Shape:SolidMolecular weight:454.63Tubulin polymerization-IN-24
CAS:<p>HMBA (Tubulin-IN-24) inhibits tubulin assembly, boosts GTP hydrolysis, induces apoptosis, and arrests G2/M phase in MCF-7 cells.</p>Formula:C22H16O3Color and Shape:SolidMolecular weight:328.36Erbstatin
CAS:<p>Erbstatin is a tyrosine-protein kinase inhibitor. When combined with foroxymithine, it has antineoplastic activity against L-1210 leukemia.</p>Formula:C9H9NO3Color and Shape:SolidMolecular weight:179.17Atopaxar
CAS:<p>Atopaxar (E5555), a reversible PAR-1 thrombin receptor antagonist, interferes with platelet signaling.</p>Formula:C29H38FN3O5Purity:97.07% - 98.07%Color and Shape:SolidMolecular weight:527.63BI-0282
CAS:<p>BI-0282 (Compound 1) is a potent inhibitor of the MDM2-p53 interaction.</p>Formula:C30H23Cl2FN4O4Color and Shape:SolidMolecular weight:593.43BPTQ
CAS:<p>BPTQ: DNA intercalator, halts cancer cell growth by blocking S/G2/M phases.</p>Formula:C17H16N4SPurity:98%Color and Shape:SolidMolecular weight:308.4PI3K/Akt/mTOR-IN-3
CAS:<p>PI3K/Akt/mTOR-IN-3 is a powerful inhibitor, halting MCF-7, HeLa, and HepG2 cell migration and triggering S phase arrest and apoptosis.</p>Formula:C34H51NO2Color and Shape:SolidMolecular weight:505.77
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