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 5592 products of "Apoptosis"
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
HDAC1/6-IN-1
CAS:<p>HDAC1/6-IN-1, a dual HDAC1 (89 nM) and HDAC6 (13 nM) inhibitor, blocks cancer cell cycle, triggers apoptosis, and halts metastasis.</p>Formula:C32H45N7O4Color and Shape:SolidMolecular weight:591.74CZS-241
<p>CZS-241: Oral PLK4 inhibitor (IC50=2.6 nM), less potent TRKA blocker (IC50=2.74 μM), triggers apoptosis and S/G2 arrest, anti-leukemia, safe for normal cells.</p>Formula:C26H24ClF2N9OColor and Shape:SolidMolecular weight:551.98AP23464
CAS:<p>AP23464 inhibits Src/Abl kinases, effective on imatinib-resistant CML cells (IC50=14nM), blocks cell cycle, induces apoptosis, not against T315I mutant.</p>Formula:C26H30N5O2PColor and Shape:SolidMolecular weight:475.52Antitumor agent-57
CAS:<p>Antitumor agent-57 (Compound 3o) is a potent NQO1-directed antitumor compound.</p>Formula:C20H15NO5Color and Shape:SolidMolecular weight:349.34CMC2.24
CAS:<p>CMC2.24 inhibits Ras and ERK1/2, fights pancreatic tumors in mice, blocks MMPs (IC50: 2-69 µM), and reduces osteoarthritis by stabilizing cartilage.</p>Formula:C26H21NO5Color and Shape:SolidMolecular weight:427.45Bcl-2/Mcl-1-IN-3
CAS:<p>Bcl-2/Mcl-1-IN-3 is a Bcl-2/Mcl-1 inhibitor that acts on Mcl-1 (Ki: 0.14 μM) and Bcl-2 (Ki: 0.23 μM) and can be used in cancer research.</p>Formula:C27H26ClNO4Color and Shape:SolidMolecular weight:463.95GGTI-2154
CAS:<p>GGTI-2154 is a potent, selective geranylgeranyltransferase I (GGTase I) inhibitor, boasting an IC50 of 21 nM and demonstrating over 200-fold selectivity against</p>Formula:C24H28N4O3Color and Shape:SolidMolecular weight:420.5Mcl1-IN-3
CAS:<p>Mcl1-IN-3 is an Mcl1 inhibitor. It has an IC50 and Ki of 0.67 and 0.13 μM, respectively.</p>Formula:C27H22ClN3O4Purity:98%Color and Shape:SolidMolecular weight:487.93Anticancer agent 72
CAS:<p>Compound 8c inhibits K+ channel and induces apoptosis, showing promise as an anticancer agent.</p>Formula:C20H19N7O2Color and Shape:SolidMolecular weight:389.41DMH2
CAS:<p>DMH2 is an antagonist of bone morphogenetic protein (BMP) type I receptor. It acts by decreasing growth and inducing cell death of lung cancer cell lines.</p>Formula:C27H25N5O2Purity:98%Color and Shape:SolidMolecular weight:451.52ZT55
CAS:<p>ZT55: Oral JAK2 inhibitor, IC50: 0.031 μM, hinders JAK2 V617F HEL cell growth, induces apoptosis, arrests cell cycle, effective in mice HEL tumor studies.</p>Formula:C17H16N2O3Color and Shape:SolidMolecular weight:296.32Quinidine polygalacturonate
CAS:<p>Quinidine polygalacturonate: oral cytochrome P450db inhibitor, K+ channel blocker (IC50 19.9 μM), induces apoptosis, anti-arrhythmic, aids malaria research.</p>Formula:C26H34N2O9Color and Shape:SolidMolecular weight:518.22643MMP2-IN-1
CAS:<p>MMP2-IN-1, an MMP2 inhibitor (IC50 = 6.8μM), halts growth and induces apoptosis in some cancers.</p>Formula:C15H13NO5SColor and Shape:SolidMolecular weight:319.33SAHA-OH
CAS:<p>SAHA-OH selectively inhibits HDAC6 (IC50 = 23 nM) with 10-47x preference over HDACs 1, 2, 3, 8, and reduces inflammation and macrophage apoptosis.</p>Formula:C15H22N2O4Purity:98%Color and Shape:SolidMolecular weight:294.35Aurora 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-29
CAS:<p>PD-1/PD-L1-IN-29 (S4-1) is a potent inhibitor of the PD-1/PD-L1 interaction, with an IC50 value of 6.1 nM.</p>Formula:C26H24N2O6Color and Shape:SolidMolecular weight:460.48MPT0B214
CAS:<p>MPT0B214, a potent microtubule inhibitor, disrupts tubulin polymerization and kills various cancer cells, including drug-resistant types.</p>Formula:C20H20N2O5Color and Shape:SolidMolecular weight:368.38VEGFR-2-IN-23
CAS:<p>VEGFR-2-IN-23 (11b) is a potent VEGFR-2 inhibitor with an IC50 of 0.34 nM, exhibits antitumor effects, and causes G1 cell cycle arrest.</p>Formula:C22H15N5O2Color and Shape:SolidMolecular weight:381.39LG308
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:308.35PHA-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:450.56Anti-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:394.42GW837016X
CAS:<p>GW837016X, also known as NEU-391, is a potent inhibitor of protozoan parasite proliferation.</p>Formula:C25H20ClFN4OSColor and Shape:SolidMolecular weight:478.97HDAC-IN-51
<p>HDAC-IN-51 is an HDAC inhibitor.</p>Formula:C27H24N4O2Purity:97.19%Color and Shape:SolidMolecular weight:436.51MX107
CAS:<p>MX107 is a survivin inhibitor which induces degradation of XIAP and/or cIAP1, and suppresses genotoxic NF-kappaB activation.</p>Formula:C24H28N2O2Color and Shape:SolidMolecular weight:376.49PD-1/PD-L1-IN-20
CAS:<p>PD-1/PD-L1-IN-20 is a small molecule inhibitor of PD-1/PD-L1 protein-protein interaction.</p>Formula:C30H26BrClN2O3Color and Shape:SolidMolecular weight:577.9Undecylprodigiosin
CAS:<p>Undecylprodigiosin is a classical cytotoxic immunosuppressant, suppressing immune functions. It also inhibits DNA synthesis.</p>Formula:C25H35N3OColor and Shape:SolidMolecular weight:393.56FAK-IN-5
CAS:<p>FAK-IN-5 is a FAK signaling inhibitor that induces apoptosis and autophagy.</p>Formula:C29H29ClF3N3O4Color and Shape:SolidMolecular weight:576.01VEGFR-2-IN-22
CAS:<p>VEGFR-2-IN-22 blocks VEGFR-2/beta-tubulin, IC50=19.82 nM, induces apoptosis.</p>Formula:C26H24ClFN4O6Color and Shape:SolidMolecular weight:542.94EGFR/BRAFV600E-IN-1
CAS:<p>EGFR/BRAFV600E-IN-1 inhibits EGFR (0.08 μM) & BRAFV600E (0.15 μM), affects A-549, MCF-7, Panc-1 & HT-29 (IC50: 0.79-1.3 μM).</p>Formula:C24H24ClN3O3Color and Shape:SolidMolecular weight:437.92MDM2/XIAP-IN-3
CAS:<p>MDM2/XIAP-IN-3 (compound 3e), a dual inhibitor of MDM2/XIAP, diminishes MDM2 and XIAP protein levels while augmenting p53 expression, consequently suppressing</p>Formula:C29H30N2O5SColor and Shape:SolidMolecular weight:518.62DNA topoisomerase II inhibitor 1
CAS:<p>Potent DNA topoisomerase II blocker; arrests cell cycle, induces apoptosis, anti-growth effects.</p>Formula:C28H24N4O3SColor and Shape:SolidMolecular weight:496.58CS1
CAS:<p>CS1: potent topoisomerase II alpha inhibitor, broad-spectrum antitumor, low toxicity, anti-resistance, induces DNA damage, G2/M arrest, apoptosis.</p>Formula:C16H12O3Color and Shape:SolidMolecular weight:252.26HDAC-IN-42
CAS:<p>HDAC-IN-42, a potent HDAC inhibitor: IC50 - 0.19μM (HDAC1), 4.98μM (HDAC6); halts cancer cell growth, triggers apoptosis & G2/M arrest.</p>Formula:C20H15NO7Color and Shape:SolidMolecular weight:381.34Tubulin polymerization-IN-14
CAS:<p>Tubulin-IN-14 (20a) inhibits polymerization (IC50=3.15μM), has anti-cancer and anti-vascular effects, inducing cell death.</p>Formula:C15H15ClN2O2Color and Shape:SolidMolecular weight:290.74KRC-108
CAS:<p>KRC-108 is a potent kinase inhibitor targeting Ron, Flt3, TrkA, and c-Met with strong anti-proliferative effects on various cancer cells.</p>Formula:C20H20N6OColor and Shape:SolidMolecular weight:360.41(S)-Elobixibat
CAS:<p>(S)-Elobixibat is the S-isomer of Elobixibat. It is an orally active inhibitor of Apical Sodium-Dependent Bile (IBAT) and can reduce LDL cholesterol, increase serum GLP-1, and promote colonic motility. This compound shows potential for treating metabolic syndrome and can be studied for constipation, dyslipidemia, non-alcoholic hepatitis, and liver tumors.</p>Formula:C36H45N3O7S2Color and Shape:SolidMolecular weight:695.89Mcl-1 inhibitor 10
CAS:<p>Mcl-1 inhibitor10 (compound 43) is a relatively potent MCL-1 inhibitor with an IC50 of 0.67 μM. It interacts with a specific binding site on the MCL-1 protein, disrupting its pro-survival signals and inducing apoptosis in cancer cells. This compound is useful for research on MCL-1-dependent cancers.</p>Formula:C21H15F3O4Color and Shape:SolidMolecular weight:388.34PARP1-IN-31
CAS:<p>PARP1-IN-31 (compound 11f) is a PARP1 inhibitor with an IC₅₀ of 97 nM. It induces apoptosis and inhibits proliferation in lung cancer cell lines (e.g., A549).</p>Formula:C22H15ClFN3O2Purity:98.99%Color and Shape:SolidMolecular weight:407.83ATAD2-IN-1
CAS:<p>ATAD2-IN-1 (compound 19f) serves as a potent ATAD2 inhibitor (IC 50: 0.27 μM), capable of inducing apoptosis. Additionally, it suppresses c-Myc activation and impedes the migration of BT-549 cells [1].</p>Formula:C22H26N6O5Color and Shape:SolidMolecular weight:454.48α-NETA
CAS:<p>α-NETA is a ChA inhibitor and an ALDH1A1 and CMKLR1 antagonist with anticancer activity and inhibits cholinesterase and acetylcholinesterase (AChE).</p>Formula:C16H20INOPurity:99.54%Color and Shape:SolidMolecular weight:369.24BMH-9
CAS:<p>BMH-9 is an RNA polymerase I inhibitor that acts by causing nucleolar stress and showing potent anticancer activity across many tumor types.</p>Formula:C19H27N3O2Color and Shape:SolidMolecular weight:329.44L 741742 (free base)
CAS:<p>L 741742 is an effective and highly selective antagonist of the D4 dopamine receptor (Ki: 1700, 770, and 3.5 nM at cloned human D2, D3, and D4 receptors).</p>Formula:C23H25ClN2OPurity:98%Color and Shape:SolidMolecular weight:380.91ALC67
CAS:<p>ALC67, a novel 3-propionyl thiazolidine-4-carboxylic acid ethyl ester, activates caspase-9, showing potent anticancer properties.</p>Formula:C15H15NO3SPurity:98%Color and Shape:SolidMolecular weight:289.35Dabuzalgron HCl
CAS:<p>Dabuzalgron, an adrenoceptor agonist, is used potentially for the treatment of urinary incontinence.</p>Formula:C12H17Cl2N3O3SPurity:98%Color and Shape:SolidMolecular weight:354.25RC-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:168.24Dimethoate
CAS:<p>Dimethoate (L-395) is a systemic and contact insecticide for control of cattle grubs and certain other insect pests of farm animals.</p>Formula:C5H12NO3PS2Purity:99.74% - 99.91%Color and Shape:White Crystalline SolidMolecular weight:229.26BMS-242
CAS:<p>BMS-242 is an effective inhibitor of PD-1/PD-L1 interaction.</p>Formula:C28H35NO4Purity:98%Color and Shape:SolidMolecular weight:449.58ABD56
CAS:<p>ABD56 inhibits osteoclast formation and activity in vitro and in vivo.</p>Formula:C17H18O3Color and Shape:SolidMolecular weight:270.32MBC-11
CAS:<p>MBC-11: First bone-targeting bisphosphonate-etidronate conjugate with araC, may treat TIBD.</p>Formula:C11H20N3O14P3Purity:>99.99% - >99.99%Color and Shape:SolidMolecular weight:511.21CN128 hydrochloride
CAS:<p>CN128 hydrochloride is an oral, selective hydroxypyridone iron chelator for β-thalassemia research.</p>Formula:C15H18ClNO3Color and Shape:SolidMolecular weight:295.76A-802715
CAS:<p>A-802715 is a novel methylxanthine derivative that decreases the endogenous formation and blood levels of pro-inflammatory substances and increases the</p>Formula:C16H26N4O3Purity:96.29%Color and Shape:SolidMolecular weight:322.4Selicrelumab
CAS:<p>Selicrelumab (RG-7876) is an antibody targeting CD40 with potential anti-tumor activity for the study of pancreatic cancer.</p>Purity:98.7% (SDS-PAGE); 95.2% (SEC-HPLC) - 98.7% (SDS-PAGE); 95.2% (SEC-HPLC)Color and Shape:LiquidZ-LEVD-FMK
CAS:<p>Z-LEVD-FMK is a caspase-4 inhibitor with anti-cancer activity, capable of eliminating LPS-induced GCLC protein degradation.</p>Formula:C31H45FN4O10Color and Shape:SolidMolecular weight:652.71MI-3
CAS:<p>MI-3 (Menin-MLL Inhibitor) (Menin-MLL Inhibitor) is an effective inhibitor of Menin-MLL interaction (IC50: 648 nM).</p>Formula:C18H25N5S2Purity:98.66% - 99.61%Color and Shape:SolidMolecular weight:375.55RSH-7
CAS:<p>RSH-7 is a potent dual inhibitor of BTK and FLT3, with IC50s of 47 and 12 nM, respectively.RSH-7 has antiproliferative and antitumor activities, inducing</p>Formula:C22H25FN8OPurity:98.31%Color and Shape:SolidMolecular weight:436.49Ceranib-2
CAS:<p>Ceranib-2, a ceramidase inhibitor (IC50: 28 μM, SKOV3), reduces sphingosine/S1P and promotes apoptosis, showing anticancer properties.</p>Formula:C25H19NO3Purity:98.49%Color and Shape:SolidMolecular weight:381.42Mcl1-IN-11
CAS:<p>Mcl1-IN-11 (Compound G) is a selective Mcl-1 inhibitor, less potent at Bcl-2, with Kis of 0.06 and 4.2 μM, respectively.</p>Formula:C38H41N3O5S2Purity:98%Color and Shape:SolidMolecular weight:683.88Anisperimus
CAS:<p>Anisperimus (LF 15-0195) is an immunosuppressant that prevents CNS autoimmunity by promoting the development of regulatory CD4 T cells expressing Foxp3.</p>Formula:C18H39N7O3Purity:98.10%Color and Shape:SolidMolecular weight:401.55VII-31
CAS:<p>VII-31 is an activator of the NEDDylation pathway, capable of inducing apoptosis in MCF-7, PC-3, and MGC-803 cells.</p>Formula:C23H25NO5SColor and Shape:SolidMolecular weight:427.51Jolkinolide B
CAS:<p>Jolkinolide B is a bioactive diterpene isolated from the roots of Euphorbia fischeriana Steud.</p>Formula:C20H26O4Purity:99.39% - 99.7%Color and Shape:SolidMolecular weight:330.42TJ08
CAS:<p>TJ08 has anticancer properties and can effectively induce G1/S phase blockade while promoting apoptosis in a variety of cancer cells.</p>Formula:C22H16FN3O4Purity:99.89%Color and Shape:SolidMolecular weight:405.38EP12
CAS:<p>EP12, a c-Myc inhibitor and G4 stabilizer, induces apoptosis and DNA damage in multiple myeloma cells while obstructing P65/P50 nuclear translocation by</p>Formula:C26H22FN3O2Purity:98%Color and Shape:SolidMolecular weight:427.47Anticancer agent 164
CAS:<p>CML-IN-1, also known as compound 7 and compound 4, is a potent anticancer agent that demonstrates a strong induced-apoptosis effect in the human chronic myeloid</p>Formula:C21H23F3N8O2S2Purity:98%Color and Shape:SolidMolecular weight:540.58Anticancer agent 147
CAS:<p>Compound 6j (Anticancer agent 147), a sophoridine derivative and ferroptosis inducer, promotes intracellular accumulation of Fe2+, reactive oxygen species (ROS</p>Formula:C32H40BrN3O2Purity:98%Color and Shape:SolidMolecular weight:578.58Antitumor agent-115
CAS:<p>Antitumor agent-115 (SS-12) is a potent anti-tumor compound, exhibiting an IC50 range of 0.34 μM-24.14 μM against the 4T1 mouse breast cancer cell line.</p>Formula:C19H38ClNO2Purity:98%Color and Shape:SolidMolecular weight:347.96CK2/ERK8-IN-1
CAS:<p>TMCB inhibits CK2 (Ki: 0.25 µM), ERK8 (IC50: 0.50 µM), PIM1, DYRK1A, HIPK2 (Ki: 8.65-15.25 µM), and induces apoptosis.</p>Formula:C11H9Br4N3O2Purity:98.22%Color and Shape:SolidMolecular weight:534.82NSC 146109 hydrochloride
CAS:<p>NSC 146109 hydrochloride is an activator of p53 targeting MDMX. NSC 146109 hydrochloride can be used for studies on breast cancer.</p>Formula:C17H17ClN2SPurity:99.28%Color and Shape:SolidMolecular weight:316.85DNL343
CAS:<p>DNL343 is an eIF2B activator that inhibits stress granule (SG) assembly induced by the C9ORF72 dipeptide repeat.</p>Formula:C20H19ClF3N3O4Purity:99.96%Color and Shape:SolidMolecular weight:457.83Infliximab
CAS:<p>Infliximab is a chimeric monoclonal antibody that inhibits TNF-α. Infliximab can be used to treat Crohn's disease and rheumatoid arthritis. Cost-effective and quality-assured.</p>Purity:98% - 99.70%Color and Shape:LiquidMolecular weight:149 kDaAllethrin
CAS:<p>Allethrin induces oxidative stress, apoptosis and calcium release. Allethrin, a pyrethroid insecticide is a major mosquito repellent agent.</p>Formula:C19H26O3Purity:99.52%Molecular weight:302.41CFM 4
CAS:<p>CFM 4 is a potent small molecule CARP-1/APC-2 antagonist that prevents CARP-1 from binding to APC-2, contributes to G2M cell cycle arrest, and induces apoptosis</p>Formula:C22H16ClN3OSPurity:98.82%Color and Shape:SolidMolecular weight:405.9VU0285655-1
CAS:<p>VU0285655-1, a PLD2 inhibitor, halts PLD2-deficient cell growth and protects against high glucose-induced cell death. Used in diabetic retinopathy research.</p>Formula:C25H27N5O2Purity:99.73%Color and Shape:SolidMolecular weight:429.51Dinoprost
CAS:<p>Dinoprost (Prostaglandin F2a) is a naturally occurring prostaglandin. It is used in medicine to induce labor and as an abortifacient.</p>Formula:C20H34O5Purity:97.94% - 98.04%Color and Shape:White To Off-White Crystalline SolidMolecular weight:354.48TNF-α-IN-1
CAS:<p>TNF-α-IN-1 is a TNF-α inhibitor.</p>Formula:C16H14ClN3O5Purity:98.82%Color and Shape:SolidMolecular weight:363.75MI-1061
CAS:<p>MI-1061 is a orally bioavailable inhibitor of MDM2 (MDM2-p53 interaction) (IC50=4.4 nM).</p>Formula:C30H26Cl2FN3O4Color and Shape:SolidMolecular weight:582.45Bax activator-1
CAS:<p>Bax activator-1 (compound 106) is a Bax activator. It induces Bax-dependent tumor cell apoptosis[1].</p>Formula:C29H36N4O3Color and Shape:SolidMolecular weight:488.62NVS-CECR2-1
CAS:<p>NVS-CECR2-1 is a CECR2 inhibitor with anti-tumor activity that inhibits chromatin binding of the CECR2 BRD.</p>Formula:C27H37N5O2SPurity:98.68%Color and Shape:SolidMolecular weight:495.68MI-389
CAS:<p>MI-389 is a PROTAC degrader that induces the degradation of receptor tyrosine kinases (RTKs), useful for leukemia research.</p>Formula:C35H35FN6O6Purity:98.12%Color and Shape:SolidMolecular weight:654.69BIM-46174
CAS:<p>BIM-46174 has anticancer activity, inhibits the growth of a large number of human cancer cell lines, and induces caspase-3-dependent cancer cell apoptosis.</p>Formula:C22H30N4OSColor and Shape:SolidMolecular weight:398.57(R)-STU104
CAS:<p>(R)-STU104 is a TAK1-MKK3 protein-protein interaction (PPI) inhibitor. (R)-STU104 is a candidate compound for the treatment of ulcerative colitis.</p>Formula:C18H18O4Purity:98.91% - 99.42%Color and Shape:SolidMolecular weight:298.33STAT3-IN-11
CAS:<p>STAT3-IN-11 is a STAT3 inhibitor.STAT3-IN-11 promotes apoptosis in cancer cells and is a candidate compound for the treatment of cancer.</p>Formula:C20H17NO4Purity:98.3%Color and Shape:SolidMolecular weight:335.35L6H21
CAS:<p>L6H21 is an MD-2 inhibitor that can be used to study cognitive impairment and brain damage.</p>Formula:C18H18O4Purity:99.26%Color and Shape:SolidMolecular weight:298.33SMBA1
CAS:<p>SMBA1 is a Bax agonist with antitumor activity that can induce cell cycle arrest and apoptosis in malignant glioma cells.</p>Formula:C20H13NO3Purity:99.2%Color and Shape:SolidMolecular weight:315.32Targapremir-210
CAS:<p>Targapremir-210 (TGP-210) is a miRNA-210 (miRNA-210) inhibitor that inhibits pre-miR-210 processing and induces apoptosis in breast cancer cells.</p>Formula:C32H36N10O2Purity:98%Color and Shape:SolidMolecular weight:592.69EC359
CAS:<p>EC359 is a Leukemia Inhibitory Factor Receptor (LIFR) inhibitor with anticancer activity for the study of leukemia and endometrial cancer.</p>Formula:C36H38F2O2Purity:98.11% - 98.11%Color and Shape:SolidMolecular weight:540.68Simmiparib
CAS:<p>Simmiparib (SMOCL-9112) is a PARP1 and PARP2 inhibitor that promotes apoptosis.Simmiparib is used to study Parkinson's disease and melanoma.</p>Formula:C23H18F4N6O2Purity:99.05% - 99.51%Color and Shape:SolidMolecular weight:486.42CCCI-01
CAS:<p>CCCI-01: Centrosome cluster inhibitor with anticancer properties, induces apoptosis, aids in non-cross-resistant drug research.</p>Formula:C11H9N3O4Purity:>99.99%Color and Shape:SolidMolecular weight:247.21VU 0364739 hydrochloride
CAS:<p>VU 0364739 hydrochloride (VU 0364739 HCl) is a phospholipase D2 (PLD2) inhibitor that induces apoptosis and can be used in cancer research.</p>Formula:C26H28ClFN4O2Purity:99.36%Color and Shape:SolidMolecular weight:482.98PARP-2-IN-3
CAS:<p>PARP-2-IN-3 is used in the study of breast cancer as a PARP-2 inhibitor with antitumor activity that induces apoptosis (apoptosis) and necrosis in cancer cells.</p>Formula:C20H20ClN3O3Purity:99.33%Color and Shape:SolidMolecular weight:385.84KS106
CAS:<p>KS106 inhibits ALDH (1A1: 334 nM, 2: 2137 nM, 3A1: 360 nM), has anti-cancer properties, raises ROS, and promotes aldehyde build-up.</p>Formula:C18H15BrF3N3O2SPurity:99.31%Color and Shape:SolidMolecular weight:474.3Necrostatin-7
CAS:<p>Necrostatin-7 (Necrostatin 7) is a necrotic apoptosis inhibitor with cardioprotective effects that inhibits RANK-NFATc1 signaling.</p>Formula:C16H10FN5OS2Purity:98.71%Color and Shape:SolidMolecular weight:371.41SD-36
CAS:<p>SD-36: Potent, selective PROTAC STAT3 degrader, Kd ~50 nM, effective on mutants, IC50=10 nM, strong anti-tumor effects, enables mouse tumor regression.</p>Formula:C59H62F2N9O12PPurity:98% - >99.99%Color and Shape:SoildMolecular weight:1158.15Declopramide
CAS:<p>Declopramide (OXI-104) is a chemosensitizer with antitumor activity that can be used to study colorectal cancer and inflammatory bowel disease.</p>Formula:C13H20ClN3OPurity:98.53%Color and Shape:SolidMolecular weight:269.77Casein Kinase inhibitor A51
CAS:<p>Casein Kinase inhibitor A51 is a CK1α inhibitor with anticancer activity used in the study of breast and prostate cancer.</p>Formula:C18H25ClN6Purity:99.88%Color and Shape:SolidMolecular weight:360.88Bisindolylmaleimide VIII
CAS:<p>Bisindolylmaleimide VIII (Ro-31-7549) is a selective and highly potent protein kinase C (PKC) inhibitor.</p>Formula:C24H22N4O2Purity:97% - 98.01%Color and Shape:SolidMolecular weight:398.46Perphenazine dihydrochloride
CAS:<p>Perphenazine dihydrochloride: Oral dopamine, histamine-1 antagonist; targets D2, D3, 5-HT2A, Alpha-1A; may treat psychiatric disorders, cancer.</p>Formula:C21H28Cl3N3OSPurity:99.67%Color and Shape:SolidMolecular weight:476.89Exisulind
CAS:<p>Exisulind (CP248) triggers apoptosis via PKG activation, shows antitumor effects, and inhibits growth in various rodent cancer models.</p>Formula:C20H17FO4SPurity:97.94%Color and Shape:SolidMolecular weight:372.41Cipepofol
CAS:<p>HSK3486 is similar to propofol and is a general anesthetic, which may have therapeutic potential in insomnia, migraine, anxiety, analgesia, and other aspects.</p>Formula:C14H20OPurity:99.77%Color and Shape:SolidMolecular weight:204.31Ro 90-7501
CAS:<p>Ro 90-7501, an amyloid β42 (Aβ42) protofibril and TPR-dependent PP5 inhibitor, is a novel cervical cancer cell radiosensitizer that inhibits HCMV.</p>Formula:C20H16N6Purity:97.21% - 99.72%Color and Shape:SolidMolecular weight:340.38
