Apoptosis
Los inhibidores de la apoptosis son compuestos que previenen o retrasan el proceso de muerte celular programada, conocido como apoptosis. Estos inhibidores son vitales para estudiar los mecanismos de supervivencia celular y se utilizan para investigar enfermedades donde la apoptosis está desregulada, como el cáncer, los trastornos neurodegenerativos y las enfermedades autoinmunes. Al modular la apoptosis, estos inhibidores pueden ayudar en el desarrollo de terapias dirigidas a controlar la muerte celular. En CymitQuimica, ofrecemos una amplia selección de inhibidores de la apoptosis de alta calidad para apoyar su investigación en biología celular, oncología y campos relacionados.
Subcategorías de "Apoptosis"
- ASK(6 productos)
- BCL(11 productos)
- Caspasa(127 productos)
- FOXO1(3 productos)
- IAP(66 productos)
- Mdm2(12 productos)
- PD-1 / PD-L1(126 productos)
- PDK(9 productos)
- PERK(23 productos)
- Serina / treonina quinasa(15 productos)
- Survivin(13 productos)
- TNF(91 productos)
- c-RET(51 productos)
- p53(62 productos)
Mostrar 6 subcategorías más
Se han encontrado 5618 productos de "Apoptosis"
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Nafamostat
CAS:<p>Nafamostat is a synthetic serine protease inhibitor and an anticoagulant used in haemodialysis. It induces apoptosis, inhibiting SARS-CoV-2 and COVID-19.</p>Fórmula:C19H17N5O2Pureza:98%Forma y color:SolidPeso molecular:347.37Cis-5-Norbornene-exo-2,3-dicarboxylic Anhydride
CAS:<p>Cis-5-Norbornene-exo-2,3-dicarboxylic Anhydride: sensitizing, induces HepG2/SK-Hep1 apoptosis, inhibits PP2A. IC50: HepG2=62μM, SK-Hep1=151μM.</p>Fórmula:C9H8O3Pureza:99.32%Forma y color:SolidPeso molecular:164.16Barbadin
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%Forma y color:SolidPeso molecular:333.41PB28 dihydrochloride
CAS:ZD-6888 Hydrochloride (ZD-6888 HCl) is an angiotensin II antagonist that mediates AII receptor blockade and induces AII-mediated inhibition of renin release.Fórmula:C24H40Cl2N2OPureza:99.97%Forma y color:SolidPeso molecular:443.49Alisol B 23-Acetate
CAS:Fórmula:C32H50O5Pureza:>98.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:514.75Pevonedistat hydrochloride
CAS:Pevonedistat(MLN4924) hydrochloride is a NEDD8-activating enzyme inhibitor that induces apoptosis and can be used in the study of acute myeloid leukemias.Fórmula:C21H26ClN5O4SPureza:98.44% - 99.19%Forma y color:SolidPeso molecular:479.98N-deacetylated BMS-202
CAS:N-deacetylated BMS-202 is an inhibitor of PD-1/PD-L1 interaction with potential anticancer activity for cancer research.Fórmula:C23H27N3O2Pureza:98.13% - 98.13%Forma y color:SolidPeso molecular:377.48MCL-1/BCL-2-IN-2
CAS:<p>MCL-1/BCL-2-IN-2 is a selective Mcl-1 and Bcl-2 inhibitor with potential antitumor activity for tumor research.</p>Fórmula:C20H15BrN2O2SPureza:98.03%Forma y color:SolidPeso molecular:427.31Melflufen hydrochloride
CAS:<p>Melflufen HCl: prodrug of Melphalan, has antitumor and antiangiogenic effects, causes DNA damage in MM cells.</p>Fórmula:C24H31Cl3FN3O3Forma y color:SolidPeso molecular:534.88AK-778-XXMU
CAS:<p>AK-778-XXMU is an ID2 antagonist with a KD value of 129 nM.AK-778-XXMU has potential antitumor and anticancer activity and can be used for the study of gliomas.</p>Fórmula:C22H17ClN2O3Pureza:>99.99%Forma y color:SolidPeso molecular:392.835Cl-amidine TFA
CAS:Cl-amidine TFA: oral PAD inhibitor, induces cancer cell apoptosis, IC50s: PAD1 - 0.8μM, PAD3 - 6.2μM, PAD4 - 5.9μM.Fórmula:C16H20ClF3N4O4Forma y color:SolidPeso molecular:424.84-PQBH
CAS:4-PQBH is a potent Nur77-binding agent with antitumour activity.4-PQBH is used in the study of hepatocellular carcinoma.Fórmula:C22H17N5OPureza:99.08%Forma y color:SolidPeso molecular:367.4Degarelix
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%Forma y color:SolidPeso molecular:1632.26AZT triphosphate
CAS:<p>AZT triphosphate is a Nucleoside Triphosphate.</p>Fórmula:C10H16N5O13P3Forma y color:SolidPeso molecular:507.18Palmatine hydroxide
CAS:<p>Palmatine hydroxide: oral IDO-1 inhibitor (IC50: 3-157μM), targets WNV protease, has anti-cancer/viral and neuroprotective properties.</p>Fórmula:C21H23NO5Forma y color:SolidPeso molecular:369.41Isoalantolactone
CAS:Fórmula:C15H20O2Pureza:>98.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:232.32FPA-124
CAS:<p>FPA-124 is a cell-permeable copper complex that acts as a selective Akt (protein kinase B) inhibitor to induce apoptosis in a variety of cancer cell lines.</p>Fórmula:C11H9Cl2CuN3O2SPureza:95.04%Forma y color:SolidPeso molecular:381.73CuATSM
CAS:<p>Cu/Zn-SOD1 enzyme scavenges radicals; mutations cause ALS. Cu-ATSM, crossing blood-brain barrier, targets hypoxic tissue, may aid ALS mice.</p>Fórmula:C8H14CuN6S2Forma y color:SolidPeso molecular:321.92Thalidomide-piperazine-Boc
CAS:<p>Thalidomide-piperazine-Boc is an intermediate utilized for synthesizing BCL6 PROTAC, which targets B-cell lymphoma 6 protein.</p>Fórmula:C22H26N4O6Forma y color:SolidPeso molecular:442.46Bax inhibitor peptide V5
CAS:<p>Bax inhibitor peptide V5 (BIP-V5) is a Bax-mediated apoptosis inhibitor with anticancer activity.</p>Fórmula:C27H50N6O6SForma y color: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%Forma y color:SolidPeso molecular:1015.29Thalidomide-5,6-F
CAS:<p>Thalidomide-5,6-F, a cereblon ligand for CRBN protein recruitment, forms PROTACs for targeted protein degradation.</p>Fórmula:C13H8F2N2O4Forma y color:SolidPeso molecular:294.21MRT00033659
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:C15H14N4OForma y color:SolidPeso molecular:266.3Thalidomide-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%Forma y color:SolidPeso molecular:487.43Phenoxyethanol (Standard)
CAS:Phenoxyethanol (Standard) is the standard substance of Phenoxyethanol, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Phenoxyethanol (NSC-1864) is germicidal. It often used together with quaternary ammonium compounds.Fórmula:C8H10O2Peso molecular:138.16Venetoclax-d8
CAS:Venetoclax-d8 (ABT-199-d8) is a deuterated form of Venetoclax, a potent, selective, and orally active Bcl-2 inhibitor that induces autophagy and apoptosis.Fórmula:C45H42D8ClN7O7SForma y color:SolidPeso molecular:876.49Acyclovir sodium
CAS:<p>Acyclovir sodium is an antimetabolite. Acyclovir sodium inhibits HSV-specified DNA polymerases and prevents further viral DNA synthesis.</p>Fórmula:C8H10N5NaO3Pureza:99.59% - 99.89%Forma y color:SolidPeso molecular:247.192,6-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%Forma y color:Yellowish-Beige PowderPeso molecular:152.153-Phenoxybenzoic acid
CAS:3-Phenoxybenzoic acid is a natural product for research related to life sciences. The catalog number is T35359 and the CAS number is 3739-38-6.Fórmula:C13H10O3Forma y color:SolidPeso molecular:214.22Fmoc-D-Cha-OH
CAS:<p>Fmoc-D-Cha-OH (FDCO) is an apoptotic DNase γ inhibitor that inhibits the release of HMGB1.</p>Fórmula:C24H27NO4Pureza:98.62%Forma y color:SolidPeso molecular:393.48Apremilast-d5
CAS:Apremilast D5 (CC-10004 D5) is a deuterium-labeled Apremilast.Fórmula:C22H24N2O7SForma y color:SolidPeso molecular:465.53Methylstat
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%Forma y color:SolidPeso molecular:505.56Fluorizoline
CAS:<p>Fluorizoline is a PHB-binding compound with anticancer and antiproliferative activity and induces apoptosis.</p>Fórmula:C15H8Cl2F3NSPureza:98.22% - 99.52%Forma y color:SolidPeso molecular:362.20(S)-Oxiracetam
CAS:<p>(S)-Oxiracetam is a positive allosteric the AMPA receptorsmodulator.</p>Fórmula:C6H10N2O3Forma y color:SolidPeso molecular:158.16p,p'-DDD
CAS:<p>TDE is an organochlorine insecticide with slightly irritating to the skin.</p>Fórmula:C14H10Cl4Forma y color:Colourless To Off-White CrystalsPeso molecular:320.03Forodesine
CAS:<p>Forodesine inhibits lymphocyte growth and induces apoptosis in leukemic cells; oral purine nucleoside phosphorylase blocker; IC50: 0.48-1.57 nM.</p>Fórmula:C11H14N4O4Pureza:98.75% - 99.88%Forma y color:SolidPeso molecular:266.25Macitentan-d4
CAS:<p>Macitentan-d4 (ACT-064992 D4) is a C13-labeled inhibitor of the peptides ETA and ETB used to study diseases mediated by endothelin receptor mediation.</p>Fórmula:C19H20Br2N6O4SPureza:96.51%Forma y color:SolidPeso molecular:592.3Tubastatin A TFA
CAS:<p>Tubastatin A is a potent HDAC6 inhibitor with IC50 of 15 nM.</p>Fórmula:C22H22F3N3O4Pureza:98%Forma y color:SolidPeso molecular:449.42Pitavastatin D4
CAS:Pitavastatin D4 is deuterium labeled Pitavastatin. Pitavastatin is a potent inhibitor of HMG-CoA reductase.Fórmula:C25H24FNO4Pureza:98%Forma y color:SolidPeso molecular:425.49PRIMA-1MET
CAS:Fórmula:C10H17NO3Pureza:>95.0%(GC)(qNMR)Forma y color:White to Light yellow powder to crystalPeso molecular:199.2513-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:C15H30O2Forma y color:SolidPeso molecular:242.43,4,5-Trihydroxycinnamic acid decyl ester
CAS:<p>3,4,5-Trihydroxycinnamic acid decyl ester is an anti-obesity agent that inhibits lipid absorption and pancreatic lipase (EC50 ≈ 0.9μM).</p>Fórmula:C19H28O5Pureza:98.28%Forma y color:SolidPeso molecular:336.42Celosin K
CAS:<p>Celosin K (compound 8), isolated from Semen Celosiae seeds, effectively inhibits t-BHP-induced neuronal injury.</p>Fórmula:C47H74O19Pureza:98%Forma y color:SolidPeso molecular:943.08Tegaserod
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%Forma y color:SolidPeso molecular:301.39Thalidomide-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:C19H22N4O7Forma y color:SolidPeso molecular:418.4Cobimetinib hemifumarate
CAS:<p>Cobimetinib hemifumarate is a potent and selective MEK1 inhibitor with an IC50 value of 4.2 nM for MEK1.</p>Fórmula:C46H46F6I2N6O8Forma y color:SolidPeso molecular:1178.707PR-924
CAS:PR-924 is a selective inhibitor of tripeptide epoxyketone immunoproteasome subunit LMP-7 (IC50: 22 nM).Fórmula:C37H38N4O5Pureza:98%Forma y color:SolidPeso molecular:618.72Sunitinib-d10
CAS:<p>Sunitinib D10, a deuterium-enriched version, inhibits VEGFR2 and PDGFRβ tyrosine kinases (IC50: 80 nM/2 nM).</p>Fórmula:C22H27FN4O2Pureza:98%Forma y color:SolidPeso molecular:408.54Momelotinib 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%Forma y color:SolidPeso molecular:610.62PERK-IN-2
CAS:<p>PERK-IN-2 is a potent inhibitor of PERK(IC50 of 0.2 nM).</p>Fórmula:C23H18F3N5OPureza:98%Forma y color:SolidPeso molecular:437.42AZD-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%Forma y color:SolidPeso molecular:672.26Triclabendazole (Standard)
CAS:Triclabendazole (Standard) is the standard substance of Triclabendazole, and it is applicable for quantitative analysis, quality control, and related research in biochemical experiments. Triclabendazole (CGA89317) has been used in trials studying Parasitic Disease.Fórmula:C14H9Cl3N2OSPeso molecular:359.66Deferasirox (Fe3+ chelate)
CAS:Deferasirox (Fe3+ chelate) is an iron chelator with anticancer activity and can be used to study iron overload.Fórmula:C21H12FeN3O4Pureza:≥98.0%Forma y color:SolidPeso molecular:426.18SB 203580
CAS:Fórmula:C21H16FN3OSPureza:>98.0%(HPLC)Forma y color:White to Orange to Green powder to crystalPeso molecular:377.446-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%Forma y color:SolidPeso molecular:191.15Busulfan-d8
CAS:<p>Busulfan-d8 (Sulphabutin-d8) is the 2H-labeled Busulfan. Busulfan is an anticancer agent with immunosuppressive and myeloablative chemotherapy activities.</p>Fórmula:C6H6D8O6S2Forma y color:SolidPeso molecular:254.35Methopterin
CAS:<p>Methopterin shows the activation and bone resorption function of murine osteoclasts.</p>Fórmula:C20H21N7O6Pureza:98%Forma y color:SolidPeso molecular:455.43Cyclamic acid sodium
CAS:<p>Sodium cyclamate is a carbonic anhydrase inhibitor, artificial sweetener, with anticonvulsant properties, and used in cancer research.</p>Fórmula:C6H12NNaO3SPureza:99.84%Forma y color:SolidPeso molecular:201.22Saquinavir mesylate
CAS:Saquinavir mesylate (Ro 31-8959/003) is an Inhibitor of HIV Proteaseused in antiretroviral therapyFórmula:C39H54N6O8SPureza:99.19%Forma y color:White Or Pale Yellow PowderPeso molecular:766.9KRA-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%Forma y color:SolidPeso molecular:314.189-Nitrocamptothecin
CAS:Fórmula:C20H15N3O6Pureza:>98.0%(HPLC)Forma y color:White to Yellow powder to crystalPeso molecular:393.36SB 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%Forma y color:SolidPeso molecular:367.8Zardaverine
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%Forma y color:SolidPeso molecular:268.22Vandetanib
CAS:Fórmula:C22H24BrFN4O2Pureza:>98.0%(T)(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:475.36Everolimus-d4
CAS:<p>Everolimus-d4 is a deuterated compound of Everolimus.</p>Fórmula:C53H83NO14Forma y color:SolidPeso molecular:962.264MX1013
CAS:<p>MX1013, a dipeptide pan-caspase inhibitor, inhibits caspase-1, -3, -6, -7, -8, and -9.</p>Fórmula:C18H23FN2O6Forma y color:SolidPeso molecular:382.39Ubiquitin 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%Forma y color:SolidPeso molecular:414.39Demethoxycurcumin
CAS:Fórmula:C20H18O5Pureza:>98.0%(HPLC)Forma y color:Light red to Yellow to Red powder to crystalPeso molecular:338.36SB 202190
CAS:Fórmula:C20H14FN3OPureza:>95.0%(HPLC)Forma y color:White to Light yellow to Light orange powder to crystalPeso molecular:331.35Tamoxifen-d5
CAS:<p>Tamoxifen-d5 is a deuterium labeled Tamoxifen.</p>Fórmula:C26H29NOPureza:98%Forma y color:SolidPeso molecular:376.55Isoginkgetin
CAS:Fórmula:C32H22O10Pureza:>95.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:566.52PARG-IN-4
CAS:<p>PARG-IN-4 (compound A) is an orally active and cell-membrane permeable PARG inhibitor (EC50=1.9 nM) that inhibits tumour growth in mice with antitumour .</p>Fórmula:C20H25F2N7O2S2Pureza:98.51%Forma y color:SolidPeso molecular:497.59RKI-1447 dihydrochloride
CAS:<p>RKI 1447 dihydrochloride: selective ROCK inhibitor, inhibits colorectal cancer growth, promotes apoptosis (ROCK1 IC50=14.5 nM, ROCK2 IC50=6.2 nM).</p>Fórmula:C16H16Cl2N4O2SForma y color:SolidPeso molecular:399.29CD 437
CAS:Fórmula:C27H26O3Pureza:>93.0%(qNMR)Forma y color:White to Light gray to Light yellow powder to crystalPeso molecular:398.50Thalidomide D4
CAS:<p>Thalidomide D4 is a deuterium labeled Thalidomide, has immunomodulatory, anti-inflammatory and anti-angiogenic cancer properties.</p>Fórmula:C13H10N2O4Pureza:98%Forma y color:SolidPeso molecular:262.25Alantolactone
CAS:Fórmula:C15H20O2Pureza:>95.0%(GC)Forma y color:White to Light yellow powder to crystalPeso molecular:232.32Lacto-N-neotetraose
CAS:<p>LNnT is a metabolite that reduces IL-8, has anti-inflammatory effects, and aids in wound healing.</p>Fórmula:C26H45NO21Forma y color:SolidPeso molecular:707.63Baohuoside I
CAS:Fórmula:C27H30O10Pureza:>95.0%(T)(HPLC)Forma y color:White to Light yellow to Green powder to crystalPeso molecular:514.53SLF
CAS:SLF is a synthetic ligand for FKBP12 and increases Ca2+ efflux and protein synthesis.Fórmula:C30H40N2O6Pureza:99.91%Forma y color:SolidPeso molecular:524.65Givinostat
CAS:<p>Givinostat (ITF-2357) is a non-selective, orally active HDAC inhibitor capable of inhibiting STAT5 phosphorylation which is antitumour and anti-inflammatory .</p>Fórmula:C24H27N3O4Pureza:98.56%Forma y color:SolidPeso molecular:421.5Batabulin sodium
CAS:<p>Batabulin sodium, an antitumor compound, disrupts microtubules, alters cell shape, halts cell cycle, and induces apoptosis.</p>Fórmula:C13H6F6NNaO3SForma y color:SolidPeso molecular:393.24Cystamine
CAS:Cystamine (2,2'-Disulfanediyldiethanamine) is an inhibitor of transglutaminase and inhibits caspase-3 with an IC50 value of 23.6 μM.Fórmula:C4H12N2S2Pureza:99.84%Forma y color:SolidPeso molecular:152.28Fosfenopril
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:C23H34NO5PForma y color:SolidPeso molecular:435.49Methyl pyropheophorbide-a
CAS:<p>MPPa, a PDT photosensitizer derived from chlorophyll a, absorbs at 667/674 nm with no dark cytotoxicity.</p>Fórmula:C34H36N4O3Pureza:98.17%Forma y color:SolidPeso molecular:548.67Methylisothiazolinone hydrochloride
CAS:<p>Methylisothiazolinone is a powerful synthetic biocide and preservative.</p>Fórmula:C4H6ClNOSForma y color:SolidPeso molecular:151.62Hydroxy-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%Forma y color:SolidPeso molecular:282.34Propylparaben sodium
CAS:<p>Propylparaben sodium, a plant-based preservative used in cosmetics, pharma, and food, hinders follicle growth and sperm health.</p>Fórmula:C10H12NaO3Forma y color:SolidPeso molecular:203.193N-3-oxo-dodecanoyl-L-Homoserine lactone
CAS:<p>N-3-oxo-dodecanoyl-L-Homoserine lactone (3-oxo-C12-HSL), a quorum-sensing signaling molecule synthesized by P. aeruginosa and specific B. cepacia complex strains [1][2], facilitates bacterial gene expression modulation in response to cell density escalation and triggers IL-8 production in 16HBE human bronchial epithelial cells [3].</p>Fórmula:C16H27NO4Forma y color:SolidPeso molecular:297.39Fenvalerate
CAS:Fenvalerate (Evercide 2362) is a protein phosphatase 2B (calcineurin) inhibitor, a synthetic pyrethroid insecticide, that inhibits PP2B-Aα.Fórmula:C25H22ClNO3Pureza:99.62%Peso molecular:419.90Tasisulam
CAS:Fórmula:C11H6BrCl2NO3S2Pureza:>95.0%(HPLC)(qNMR)Forma y color:White to Light yellow powder to crystalPeso molecular:415.102'-Aminoacetophenone
CAS:<p>Compound Fr14273 is a natural product for research related to life sciences. The catalog number is Fr14273 and the CAS number is 551-93-9.</p>Fórmula:C8H9NOPureza:99.88%Forma y color:Pale Yellow Solid Solid CrystallinePeso molecular:135.17OTS193320
CAS:<p>OTS193320, an imidazo[1,2-a]pyridine, inhibits SUV39H2, reduces H3K9me3, and induces apoptosis in breast cancer; enhances DOX effects.</p>Fórmula:C28H30ClN5O4Forma y color:SolidPeso molecular:536.02CLZ-8
CAS:CLZ-8 (Mcl1-IN-8) is a Mcl-1-PUMA inhibitor with radioprotective activity and inhibits radiation-induced overexpression of PUMA.Fórmula:C22H23N3O2SPureza:99.85%Forma y color:SolidPeso molecular:393.5Isoscabertopin
CAS:<p>Isoscabertopin has anticancer activity.</p>Fórmula:C20H22O6Pureza:98%Forma y color:SolidPeso molecular:358.39BCL6-IN-5
CAS:<p>BCL6-IN-5 is a highly effective inhibitor of BCL6. It exhibits a pIC50 value of 5.82.</p>Fórmula:C17H19Cl2N5O2Forma y color:SolidPeso molecular:396.27Rottlerin
CAS:Fórmula:C30H28O8Pureza:>95.0%(HPLC)(qNMR)Forma y color:Light yellow to Brown powder to crystalPeso molecular:516.55Ibuprofen-d3
CAS:<p>Ibuprofen D3 is a deuterium labeled Ibuprofen. Ibuprofen is a COX-1 and COX-2 inhibitor (IC50s: 13 μM and 370 μM).</p>Fórmula:C13H18O2Forma y color:SolidPeso molecular:209.3Nutlin-3
CAS:Fórmula:C30H30Cl2N4O4Pureza:>95.0%(HPLC)Forma y color:White to Light yellow powder to crystalPeso molecular:581.49Octreotide
CAS:Octreotide (SMS 201-995) is a potent inhibitor of growth hormone, glucagon, and insulin.Fórmula:C49H66N10O10S2Pureza:99.3% - 99.64%Forma y color:White PowderPeso molecular:1019.24ML-291
CAS:<p>ML291 triggers UPR, causing apoptosis in solid cancers by activating PERK/eIF2a/CHOP pathway and reducing leukemia cells.</p>Fórmula:C16H16ClN3O6SForma y color:SolidPeso molecular:413.83
