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 5592 produtos de "Apoptose"
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SC-236
CAS:<p>SC-236 (Sc 236) is an orally active and selective inhibitor of COX-2 (IC50 of 0.005 μM and 17.8 μM for COX-2 and COX-1, respectively).</p>Fórmula:C16H11ClF3N3O2SPureza:99.74%Cor e Forma:SolidPeso molecular:401.79SNS-032
CAS:<p>SNS-032 (BMS-387032) is a selective inhibitor of CDK2 and is 10- and 20-fold selective over CDK1/CDK4. SNS-032 is sensitive to CDK7/9, and no effect on CDK6.</p>Fórmula:C17H24N4O2S2Pureza:98.27% - 99.91%Cor e Forma:SolidPeso molecular:380.53Fulvestrant
CAS:<p>Fulvestrant (ZM 182780) is an estrogen receptor (ER) antagonist (IC50=9.4 nM) and an agonist of GPR30.</p>Fórmula:C32H47F5O3SPureza:99.1% - >99.99%Cor e Forma:White PowderPeso molecular:606.77Resatorvid
CAS:<p>Resatorvid (TAK-242) inhibits TLR4, with IC50s for IL-6, TNF-R, NO at 1.3, 1.9, 1.8 nM respectively.</p>Fórmula:C15H17ClFNO4SPureza:99.31% - >99.99%Cor e Forma:SolidPeso molecular:361.82Quercetin
CAS:<p>Quercetin (Sophoretin) is a natural flavonoid and is an agonist of SIRT1.</p>Fórmula:C15H10O7Pureza:96.29% - 98.05%Cor e Forma:Sensitive To Exposure To Air And Light Insoluble In Water Alcoholic Solutions Taste Very Bitter (Ntp 1992)Peso molecular:302.24NPS-1034
CAS:<p>NPS-1034 is a dual Met/Axl inhibitor with IC50 of 48 nM and 10.3 nM, respectively.</p>Fórmula:C31H23F2N5O3Pureza:98.48%Cor e Forma:SolidPeso molecular:551.54YK-4-279
CAS:<p>YK 4-279, an inhibitor of RNA Helicase A (RHA), binds to the oncogenic transciption factor EWS-FLI1.</p>Fórmula:C17H13Cl2NO4Pureza:99.80% - ≥95%Cor e Forma:SolidPeso molecular:366.2SecinH3
CAS:<p>SecinH3 is selective cytohesin inhibitor.</p>Fórmula:C24H20N4O4SPureza:97.49% - 99.37%Cor e Forma:SolidPeso molecular:460.51EB-3D
CAS:<p>EB-3D is a potent and selective choline kinase alpha 1 (ChoKα1) inhibitor(IC50 : 1 μM).with anti-cancer activity.</p>Fórmula:C30H36Br2N4O2Pureza:99.48%Cor e Forma:SolidPeso molecular:644.4Pogostone
CAS:<p>Pogostone: anti-bacterial/fungal, blocks T-cells, modulates cytokines, protects against gastric ulcers, boosts antioxidants/PGE2/NP-SH.</p>Fórmula:C12H16O4Pureza:98.46% - 99.03%Cor e Forma:SolidPeso molecular:224.25NVP-CGM097
CAS:<p>NVP-CGM097 (CGM097) is an effective and specific MDM2 inhibitor (IC50: 1.7 nM for hMDM2).</p>Fórmula:C38H47ClN4O4Pureza:98.77%Cor e Forma:SolidPeso molecular:659.26NVP-TNKS656
CAS:<p>NVP-TNKS656 (TNKS656) is a highly potent, selective, and orally active TNKS2 inhibitor.</p>Fórmula:C27H34N4O5Pureza:99.59%Cor e Forma:SolidPeso molecular:494.58Linifanib
CAS:<p>Linifanib (AL-39324) (ABT-869) is a novel, potent ATP-competitive VEGFR/PDGFR inhibitor for KDR (IC50: 4 nM), CSF-1R (IC50: 3 nM), Flt-1/3 (IC50: 3/4 nM) and</p>Fórmula:C21H18FN5OPureza:98% - 98.24%Cor e Forma:SolidPeso molecular:375.4Amifostine thiol dihydrochloride
CAS:<p>Amifostine (WR 1065) activates p53 via JNK and shields tissues from cancer drug toxicity.</p>Fórmula:C5H16Cl2N2SPureza:>99.99%Cor e Forma:SolidPeso molecular:207.165Coniferaldehyde
CAS:<p>Coniferaldehyde (Ferulaldehyde) is a member of the class of cinnamaldehydes. Coniferaldehyde has a role as an antifungal agent and a plant metabolite.</p>Fórmula:C10H10O3Pureza:96.35% - 99.96%Cor e Forma:SolidPeso molecular:178.18LDC000067
CAS:<p>LDC000067 (LDC067) is a highly specific and selective CDK9 inhibitor with an IC50 value of 44±10 nM.</p>Fórmula:C18H18N4O3SPureza:98.08% - 99.07%Cor e Forma:SolidPeso molecular:370.43DC661
CAS:<p>DC661 is a palmitoyl-protein thioesterase 1 (PPT1) inhibitor that acts as an anti-lysosomal agent by inhibiting autophagy, demonstrating anti-cancer activity.</p>Fórmula:C31H39Cl2N5Pureza:99.07%Cor e Forma:SolidPeso molecular:552.58Cobimetinib
CAS:<p>Cobimetinib (GDC-0973) is a MEK1 inhibitor with selective and oral activity. Cobimetinib exhibits antitumor activity. Cost-effective and quality-assured.</p>Fórmula:C21H21F3IN3O2Pureza:98% - 99.61%Cor e Forma:SolidPeso molecular:531.31GW 5074
CAS:<p>GW 5074 (Raf1 Kinase Inhibitor I)(IC50=9 nM) is an effective and specific c-Raf inhibitor.</p>Fórmula:C15H8Br2INO2Pureza:99.32%Cor e Forma:SolidPeso molecular:520.94K858 (Racemic)
CAS:<p>K858 Racemic (K858) is a selective mitotic kinesin Eg5 inhibitor which acts in an ATP-noncompetitive manner.</p>Fórmula:C13H15N3O2SPureza:>99.99%Cor e Forma:SolidPeso molecular:277.34ELR510444
CAS:<p>ELR510444 (LR510444) is a novel microtubule disruptor; inhibits MDA-MB-231 cell proliferation with IC50 of 30.9 nM.</p>Fórmula:C19H16N2O2S2Pureza:97.67% - 98.69%Cor e Forma:SolidPeso molecular:368.47YH239-EE
CAS:<p>YH239-EE, the ethyl ester of YH239, is a potent p53-MDM2 antagonist and an apoptosis inducer.</p>Fórmula:C25H27Cl2N3O4Pureza:99.61%Cor e Forma:SolidPeso molecular:504.41Tolcapone
CAS:<p>Tolcapone (Ro 40-7592) is a catechol-O-methyltransferase inhibitor used in the therapy of Parkinson disease as adjunctive therapy in combination with levodopa</p>Fórmula:C14H11NO5Pureza:98.93% - 99.68%Cor e Forma:SolidPeso molecular:273.24TAK-243
CAS:<p>TAK-243 (MLN7243) is a selective inhibitor of the ubiquitin-activating enzyme UAE (IC50=1 nM).</p>Fórmula:C19H20F3N5O5S2Pureza:98.09% - 98.93%Cor e Forma:SolidPeso molecular:519.52Didymin
CAS:<p>Didymin, an antioxidant, may treat neuroblastoma and neurodegeneration by blocking N-Myc and boosting RKIP.</p>Fórmula:C28H34O14Pureza:99.12% - 99.87%Cor e Forma:Faintly Beige PowderPeso molecular:594.56SCR7 pyrazine
CAS:<p>SCR7 pyrazine (SCR7) enhances CRISPR-Cas9-mediated homology-directed repair (HDR) efficiency in vitro up to 19-fold. Inhibits nonhomologous end-joining (NHEJ).</p>Fórmula:C18H12N4OSPureza:98.72% - 99.85%Cor e Forma:SolidPeso molecular:332.38GSK2256098
CAS:<p>GSK2256098 (GTPL7939) is a small molecule FAK kinase inhibitor.</p>Fórmula:C20H23ClN6O2Pureza:99.46% - 99.74%Cor e Forma:SolidPeso molecular:414.893,6-Dihydroxyflavone
CAS:<p>3,6-Dihydroxyflavone suppresses the epithelial-mesenchymal transition in breast cancer cells by inhibiting the Notch signaling pathway.</p>Fórmula:C15H10O4Pureza:99.92%Cor e Forma:SolidPeso molecular:254.24PP1
CAS:<p>PP1 (AGL 1872), a specific and effective Src inhibitor, is with IC50 for Lck/Fyn is 5 nM/ 6 nM, respectively.</p>Fórmula:C16H19N5Pureza:99% - 99.88%Cor e Forma:Off-White To Grey SolidPeso molecular:281.36Oroxin B
CAS:<p>Oroxin B (Hypocretin-2) has antioxidant activity.</p>Fórmula:C27H30O15Pureza:98.22% - 99.81%Cor e Forma:SolidPeso molecular:594.52Penicillic acid
CAS:<p>Penicillic acid, a mycotoxin from Aspergillus/Penicillium, blocks Fas ligand apoptosis and is cytotoxic to rat lung macrophages.</p>Fórmula:C8H10O4Pureza:98%Cor e Forma:Needles From Petroleum Ether Slight Yellow PowderPeso molecular:170.16Nystatin
CAS:<p>Nystatin (Fungicidin) is a topical and oral antifungal agent with activity against many species of yeast and candida albicans, which is used largely to treat</p>Fórmula:C47H75NO17Pureza:69.55% - 99.53%Cor e Forma:Yellow SuspensionPeso molecular:926.1Thonningianin A
CAS:<p>Thonningianin A: an anti-cancer compound with antioxidant effects, GST inhibitor, and radical scavenger.</p>Fórmula:C42H34O21Pureza:98.37% - 99.94%Cor e Forma:SolidPeso molecular:874.71Capmatinib
CAS:<p>Capmatinib (INCB28060) is an orally bioavailable inhibitor of the proto-oncogene c-Met (HGFR)with potential antineoplastic activity.</p>Fórmula:C23H17FN6OPureza:99.24%Cor e Forma:SolidPeso molecular:412.42CDDO-Im
CAS:<p>CDDO-Im (TP-235) is an activator of Nrf2 and PPAR (Kis: 232/344 nM for PPARα/PPARγ).</p>Fórmula:C34H43N3O3Pureza:98.3% - 99.61%Cor e Forma:SolidPeso molecular:541.72Betulinic acid
CAS:<p>Betulinic acid, a lupane-type triterpene from white birch bark, has antiretroviral, antimalarial, anti-inflammatory, and anticancer properties.</p>Fórmula:C30H48O3Pureza:99.12% - 99.7%Cor e Forma:White Crystalline PowderPeso molecular:456.7MK-4101
CAS:<p>MK-4101 inhibits Hedgehog pathway, causing apoptosis and reduced proliferation in cancer cells.</p>Fórmula:C24H24F5N5OPureza:98.2% - 99.13%Cor e Forma:SolidPeso molecular:493.47KEA1-97
CAS:<p>Kea1-97 is a selective disruptor of interaction between thioredoxin and caspase-3 (IC50 = 10 μ M).</p>Fórmula:C15H9Cl2FN4Pureza:97.07%Cor e Forma:SolidPeso molecular:335.16Pralatrexate
CAS:<p>Pralatrexate (10-Propargyl-10-deazaaminopterin) is a folate analogue inhibitor of dihydrofolate reductase (DHFR) exhibiting high affinity for reduced folate</p>Fórmula:C23H23N7O5Pureza:94.32% - 99.59%Cor e Forma:SolidPeso molecular:477.47Vistusertib
CAS:<p>Vistusertib (AZD2014) is an orally bioavailable inhibitor of the mammalian target of rapamycin (mTOR) with potential antineoplastic activity.</p>Fórmula:C25H30N6O3Pureza:97.08% - 99.06%Cor e Forma:SolidPeso molecular:462.54C188-9
CAS:<p>C188-9 (TTI-101) is a Stat3 inhibitor with an IC50 of 4-7 μM.</p>Fórmula:C27H21NO5SPureza:98.07% - >99.99%Cor e Forma:SolidPeso molecular:471.52Vatalanib dihydrochloride
CAS:<p>Vatalanib dihydrochloride (PTK787 dihydrochloride)(IC50=37 nM) is an inhibitor of VEGFR2/KDR.</p>Fórmula:C20H15ClN4·2HClPureza:99.16%Cor e Forma:White To Off-White Crystalline PowderPeso molecular:419.73NADPH tetrasodium salt
CAS:<p>NADPH tetrasodium salt is the reduced form of the electron acceptor nicotinamide adenine dinucleotide phosphate, which acts as an electron donor in a variety of</p>Fórmula:C21H26N7Na4O17P3Pureza:97.15% - >99.99%Cor e Forma:SolidPeso molecular:833.35L-BUTHIONINE-(S,R)-SULFOXIMINE
CAS:<p>L-Buthionine-(S,R)-sulfoximine is a cell-permeable and irreversible inhibitor of γ-glutamylcysteine synthetase that induces oxidative stress by depleting GSH.</p>Fórmula:C8H18N2O3SPureza:97.07% - ≥98%Cor e Forma:White Fine PowderPeso molecular:222.31ML385
CAS:<p>ML385 is an NRF2 inhibitor (IC50=1.9 μM) with novelty and specificity.</p>Fórmula:C29H25N3O4SPureza:98.08% - >99.99%Cor e Forma:SolidPeso molecular:511.59XL019
CAS:<p>XL019 is a potent and selective JAK2 inhibitor with IC50 of 2.2 nM, 100 fold selectivity over JAK1.</p>Fórmula:C25H28N6O2Pureza:99.19%Cor e Forma:SolidPeso molecular:444.53Vandetanib
CAS:<p>Vandetanib (ZD6474) is a potent inhibitor of VEGFR2 (IC50: 40 nM). It also inhibits VEGFR3 and EGFR.</p>Fórmula:C22H24BrFN4O2Pureza:99.7% - >99.99%Cor e Forma:White SolidPeso molecular:475.35Domatinostat
CAS:<p>Domatinostat (4SC202) is a selective class I HDAC inhibitor. Domatinostat also displays inhibitory activity against Lysine specific demethylase 1 (LSD1).</p>Fórmula:C23H21N5O3SPureza:99.57% - 99.74%Cor e Forma:SolidPeso molecular:447.51CP-31398 dihydrochloride
CAS:<p>CP-31398 dihydrochloride is a p53 stabilizer which stabilizes the active conformation of p53 and promotes p53 activity in cancer cell lines.</p>Fórmula:C22H28Cl2N4OPureza:98.23%Cor e Forma:SolidPeso molecular:435.4tubuloside B
CAS:<p>Tubuloside B from Cistanche salsa stems guards SH-SY5Y cells against TNFalpha-induced apoptosis.</p>Fórmula:C31H38O16Pureza:97.59% - 99.72%Cor e Forma:SolidPeso molecular:666.62Suberoyl bis-hydroxamic acid
CAS:<p>SBHA is an HDAC inhibitor, an enzyme key to transcription, cell cycle, and development.</p>Fórmula:C8H16N2O4Pureza:99.88%Cor e Forma:SolidPeso molecular:204.22ABT-737
CAS:<p>ABT-737 is a BH3 mimetic and an inhibitor of Bcl-2, Bcl-xL, and Bcl-w. ABT-737 exhibits antitumor activity and anti-aging activity. Cost-effective and quality-assured.</p>Fórmula:C42H45ClN6O5S2Pureza:98.15% - >99.99%Cor e Forma:SolidPeso molecular:813.43PF-4989216
CAS:<p>PF-4989216 is a potent and selective PI3K inhibitor with IC50 of 2 nM, 142 nM, 65 nM, 1 nM, and 110 nM for p110α, p110β, p110γ, p110δ, and VPS34, respectively.</p>Fórmula:C18H13FN6OSPureza:99.85%Cor e Forma:SolidPeso molecular:380.4C25-140
CAS:<p>C25-140 is a small-molecule inhibitor of TRAF6-Ubc13.</p>Fórmula:C26H31N7OPureza:98.81%Cor e Forma:SolidPeso molecular:457.57Ziyuglycoside II
CAS:<p>1.</p>Fórmula:C35H56O8Pureza:99.52% - ≥95%Cor e Forma:SolidPeso molecular:604.81JX06
CAS:<p>JX06, a potent, selective and covalent PDK inhibitor, inhibits PDK1, PDK2 and PDK3 with IC50 of 49 nM, 101 nM and 313 nM respectively.</p>Fórmula:C10H16N2O2S4Pureza:99.4%Cor e Forma:SolidPeso molecular:324.51WT-161
CAS:<p>WT161 is a potent and selective inhibitor of HDAC6 (IC50:0.40 nM).</p>Fórmula:C27H30N4O3Pureza:95.98% - 98.34%Cor e Forma:SolidPeso molecular:458.55Diosgenin glucoside
CAS:<p>Diosgenin glucoside (Trillin) and other synthetic glycosides with similar activities may be of use in the management of hypercholesterolemia and atherosclerosis</p>Fórmula:C33H52O8Pureza:97.17% - 99.44%Cor e Forma:SolidPeso molecular:576.76MK-2206 dihydrochloride
CAS:<p>MK-2206 dihydrochloride (MK-2206 2HCl) is a variant Akt inhibitor that inhibits Akt1, Akt2, and Akt3 (IC50=8/12/65 nM) with orally active, highly potent and</p>Fórmula:C25H23Cl2N5OPureza:99.228% - 99.94%Cor e Forma:SolidPeso molecular:480.394,5-Dicaffeoylquinic acid
CAS:<p>1.</p>Fórmula:C25H24O12Pureza:98.86% - ≥95%Cor e Forma:SolidPeso molecular:516.45Tauroursodeoxycholate dihydrate
CAS:<p>Tauroursodeoxycholate (TUDCA ,Taurolite) dihydrate is a bile acid that reduces Caspase-3, Caspase-12, ERK, reducing endoplasmic reticulum stress mediated death.</p>Fórmula:C26H49NO8SPureza:99.82%Cor e Forma:SolidPeso molecular:535.73Geranyl acetate
CAS:<p>Geranyl acetate is a monoterpene that has been found in C. sativa with diverse biological activities.</p>Fórmula:C12H20O2Pureza:98% - 99.36%Cor e Forma:Physical Description Clear Colorless Liquid With An Odor Of Lavender (Ntp 1992)Peso molecular:196.29Tubastatin A
CAS:<p>Tubastatin A: Selective HDAC6 inhibitor, IC50 of 15 nM, 1000x less effective on other isozymes except HDAC8.</p>Fórmula:C20H21N3O2Pureza:97.22% - 99.51%Cor e Forma:SolidPeso molecular:335.4Isosilybin A
CAS:<p>Isosilybin A is a partial PPARγ agonist, it significantly induced ABCA1 protein expression, it inhibited both monophenolase (IC50=1.7-7.6μM) and diphenolase (</p>Fórmula:C25H22O10Pureza:98.79%Cor e Forma:SolidPeso molecular:482.44Alisertib
CAS:<p>Alisertib (MLN 8237) is a specific Aurora A inhibitor (IC50: 1.2 nM). The selectivity of Alisertib(MLN 8237) is >200-fold higher for Aurora A than Aurora B.</p>Fórmula:C27H20ClFN4O4Pureza:98.31% - >99.99%Cor e Forma:SolidPeso molecular:518.92Pexidartinib
CAS:<p>Pexidartinib (PLX-3397) is a capsule formulation containing a small-molecule receptor tyrosine kinase (RTK) inhibitor of KIT, CSF1R and FLT3 with potential</p>Fórmula:C20H15ClF3N5Pureza:98.34% - 99.45%Cor e Forma:SolidPeso molecular:417.81Linalool
CAS:<p>Linalool, in essential oils, offers antinociceptive, antimicrobial, and anti-inflammatory effects, protects the liver, and boosts plant defense.</p>Fórmula:C10H18OPureza:98.22%Cor e Forma:Colorless Liquid Drypowder Liquid Othersolid LiquidPeso molecular:154.25CIL56
CAS:<p>CIL56 (CA3) is a small molecule that induces cellular ferroptosis through the production of iron-dependent reactive oxygen species (ROS).</p>Fórmula:C23H27N3O5S2Pureza:99.46% - 99.91%Cor e Forma:SolidPeso molecular:489.61TPEN
CAS:<p>TPEN (TPEDA) is a specific cell-permeable heavy metal chelator.</p>Fórmula:C26H28N6Pureza:98% - 99.72%Cor e Forma:White Crystalline PowderPeso molecular:424.54Nutlin-3b
CAS:<p>Nutlin-3b, a less potent (+)-enantiomer of Nutlin-3, inhibits p53/MDM2 at IC50: 13.6 μM, 150x weaker than Nutlin-3a.</p>Fórmula:C30H30Cl2N4O4Pureza:98.83%Cor e Forma:SolidPeso molecular:581.49SRS16-86
CAS:<p>SRS16-86 is a novel third-generation ferrostatin, is an inhibitor of ferroptosis.</p>Fórmula:C26H32N4O2Pureza:97.73%Cor e Forma:SolidPeso molecular:432.56Rasagiline Mesylate
CAS:<p>Rasagiline Mesylate (AGN1135) is a novel MAO-B inhibitor, which can treat idiopathic Parkinson's disease.</p>Fórmula:C13H17NO3SPureza:99.33%Cor e Forma:White PowderPeso molecular:267.342,5-dimethyl Celecoxib
CAS:<p>2,5-dimethyl Celecoxib, a derivative targeting mPGES-1, inhibits PGE2 synthesis in inflammation.</p>Fórmula:C18H16F3N3O2SPureza:99.85%Cor e Forma:SolidPeso molecular:395.4Mitoxantrone
CAS:<p>Mitoxantrone: anthracenedione antibiotic, disrupts DNA/RNA replication, binds to topoisomerase II, less cardiotoxic than doxorubicin.</p>Fórmula:C22H28N4O6Pureza:96.29% - 98.74%Cor e Forma:Blue PowderPeso molecular:444.48dl-Maackiain
CAS:<p>1. dl-Maackiain (Demethylpterocarpin) induces apoptosis and growth suppression 2. MAK1 is the second functional gene cloned from Maackiain detoxification.</p>Fórmula:C16H12O5Pureza:97.36% - 99.89%Cor e Forma:SolidPeso molecular:284.26AT7519 Hydrochloride
CAS:<p>AT7519 Hydrochloride (AT7519 HCl) is a multi-CDK inhibitor for CDK1, 2, 4, 6 and 9.</p>Fórmula:C16H18Cl3N5O2Pureza:99.66% - 99.9%Cor e Forma:SolidPeso molecular:418.71Juglanin
CAS:<p>Juglanin is a JNK activator. Juglanin with inflammation and anti-tumor activities. It can induce apoptosis and autophagy on human breast cancer cells.</p>Fórmula:C20H18O10Pureza:98.8% - 99.33%Cor e Forma:SolidPeso molecular:418.35G-749
CAS:<p>G-749, a new-type FLT3 inhibitor, exhibits effective and sustained inhibition of the FLT3 wild type and mutants.</p>Fórmula:C25H25BrN6O2Pureza:98.32% - 99.60%Cor e Forma:SolidPeso molecular:521.41Aurintricarboxylic acid
CAS:<p>Aurintricarboxylic acid (NSC-4056) blocks nucleases and topoisomerases, stopping nucleic acid binding.</p>Fórmula:C22H14O9Pureza:97.1%Cor e Forma:Deep Red Coarse Crystalline PowderPeso molecular:422.34Obacunone
CAS:<p>Obacunone: cytotoxic to prostate cells, anti-S. Typhimurium, may inhibit breast cancer and aromatase, trigger apoptosis.</p>Fórmula:C26H30O7Pureza:98% - ≥95%Cor e Forma:White PowderPeso molecular:454.51PhiKan 083
CAS:<p>PhiKan 083 is a carbazole derivative</p>Fórmula:C16H18N2Pureza:98.37%Cor e Forma:SolidPeso molecular:238.33Hirsutine
CAS:<p>Hirsutine induces apoptosis and is a potent Dengue virus inhibitor exhibiting low cytotoxicity.Hirsutine has anticancer, cardioprotective, anti-hypertensive and</p>Fórmula:C22H28N2O3Pureza:99.36% - 99.98%Cor e Forma:SolidPeso molecular:368.47Oxibendazole
CAS:<p>Oxibendazole: a benzimidazole antiparasitic for horses and pets against various worms.</p>Fórmula:C12H15N3O3Pureza:99.3% - 99.88%Cor e Forma:Crystalline SolidPeso molecular:249.27(Rac)-Antineoplaston A10
CAS:<p>Antineoplaston A10 is the first identified human antineoplaston, naturally occurring with anti-proliferative properties.</p>Fórmula:C13H14N2O3Pureza:98.41%Cor e Forma:SolidPeso molecular:246.26A-1210477
CAS:<p>A-1210477 is an effective and specific MCL-1 and Bcl-2 inhibitor (Ki/IC50: 0.454/26.2 nM).</p>Fórmula:C46H55N7O7SPureza:99.17% - 99.37%Cor e Forma:SolidPeso molecular:850.04Echinocystic acid
CAS:<p>EA, a natural triterpene, is found in herbs; it has anti-inflammatory and antioxidant properties.</p>Fórmula:C30H48O4Pureza:98% - 99.57%Cor e Forma:SolidPeso molecular:472.7Pseudolaric Acid B
CAS:<p>Pseudolaric acid B, a natural diterpenoid compound, is isolated from Pseudolarix kaempferi.</p>Fórmula:C23H28O8Pureza:98.91% - 99.84%Cor e Forma:SolidPeso molecular:432.46CCI-007
CAS:<p>CCI 007 is a selective inhibitor of MLL-r, CALM-AF10 and SET-NUP214 leukemia with IC50 of 3.5 uM against MLL-r leukemia cell line PER-485</p>Fórmula:C15H16N2O5SPureza:97.61%Cor e Forma:SolidPeso molecular:336.36Loganin
CAS:<p>Loganin inhibits Cox-1, suppresses TNF-α, and has antioxidant and anti-melanogenic properties.</p>Fórmula:C17H26O10Pureza:99.01% - >99.99%Cor e Forma:White PowderPeso molecular:390.38SHR0302
CAS:<p>SHR0302 (ARQ252) is a JAK inhibitor that binds JAK1 with stronger affinity than others (Selectivity for JAK1 is more than 10 times for JAK2, 77 times for JAK3,</p>Fórmula:C18H22N8O2SPureza:99.11%Cor e Forma:SolidPeso molecular:414.48NVP-HSP990
CAS:<p>NVP-HSP990 (HSP990) is an effective and specific HSP90α/β inhibitor (IC50: 0.6 /0.8 nM).</p>Fórmula:C20H18FN5O2Pureza:98.03% - 99.32%Cor e Forma:SolidPeso molecular:379.39Ethyl 3,4-dihydroxybenzoate
CAS:<p>Ethyl 3,4-dihydroxybenzoate (EDHB): a prolyl hydroxylase inhibitor attenuates acute hypobaric hypoxia mediated vascular leakage in brain.</p>Fórmula:C9H10O4Pureza:99.88%Cor e Forma:White Crystal Or PowderPeso molecular:182.17Levistolide A
CAS:<p>1. Levistolide A (Diligustilide) inhibits liver fibrosis and angiogenesis.</p>Fórmula:C24H28O4Pureza:98.93% - 99.22%Cor e Forma:SolidPeso molecular:380.48PF-3758309 hydrochloride
CAS:<p>PF-3758309 hydrochloride (PF-03758309 hydrochloride) , is a PAK4 inhibitor, is also a n orally bioavailable small-molecule inhibitor of p21-activated kinase 4 (</p>Fórmula:C25H31ClN8OSPureza:98.83% - >99.99%Cor e Forma:SolidPeso molecular:527.08Cabozantinib S-malate
CAS:<p>Cabozantinib S-malate (XL184) is the salt form of cabozantinib, an orally bioavailable, small molecule RTK inhibitor with potential antineoplastic activity.</p>Fórmula:C32H30FN3O10Pureza:98% - >99.99%Cor e Forma:SolidPeso molecular:635.59Liproxstatin-1
CAS:<p>Liproxstatin-1 is a potent and selective inhibitor of iron death (IC50=22 nM).</p>Fórmula:C19H21ClN4Pureza:97.11% - 99.44%Cor e Forma:SolidPeso molecular:340.85PP121
CAS:<p>PP-121 inhibits PDGFR, Hck, mTOR, VEGFR2, Src, Abl, and DNA-PK with IC50 values ranging from 2 to 60 nM.</p>Fórmula:C17H17N7Pureza:98.45% - 99.67%Cor e Forma:SolidPeso molecular:319.36SZL P1-41
CAS:<p>SZL P1-41 inhibits Skp2, blocks complex formation, and halts ubiquitination, promoting cell senescence, reducing glycolysis, and exhibiting antitumor effects.</p>Fórmula:C24H24N2O3SPureza:99.60% - 99.87%Cor e Forma:SolidPeso molecular:420.52MK-8745
CAS:<p>MK-8745 is a potent and selective Aurora A inhibitor.</p>Fórmula:C20H19ClFN5OSPureza:99.09% - 99.79%Cor e Forma:SolidPeso molecular:431.91Garcinol
CAS:<p>Garcinol: inhibits HATs/PCAF (IC50=7/5 μM), anti-inflammatory, anti-cancer, anti-cholinesterase (AChE IC50=0.66 μM, BChE IC50=7.39 μM).</p>Fórmula:C38H50O6Pureza:98.59%Cor e Forma:SolidPeso molecular:602.8
