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Products from BOC Sciences:

1 - 50 of 10000+ CBP p300 IN 1 from BOC Sciences

  • CBP-93872 is a G2 checkpoint inhibitor. CBP-93872 specifically abrogates the DNA double-stranded...
    Cat# 67427-51-4, Inquire Ask
  • Ee-CBP is a hevein-type antimicrobial peptide from bark of the spindle tree (Euonymus europaeus L.).
    Cat# BAT-012324, Inquire Ask
  • I-CBP112 has been found to be a CBP/p300 bromodomain inhibitor and could reduce the...
    Cat# 1640282-31-0, Inquire Ask
  • PD-1-IN-1 is an inhibitor of programmed cell dealth-1 (PD-1).
    Cat# 1673534-76-3, Inquire Ask
  • PKC-IN-1 has been found to be a PKCβII inhibitor that probably has biological activity in...
    Cat# 1046787-18-1, Inquire Ask
  • ILK-IN-1, a ILK inhibitor, has been found to restrain the tumor cell growth through regulating...
    Cat# B2693-474480, 10 mg/unit USD $488 Ask
  • Prenyl-IN-1 is a protein prenylation inhibitor, especially a geranylgeranyltransferase (GGT) or...
    Cat# 360561-53-1, Inquire Ask
  • PTP1B-IN-1 is a potent protein tyrosine phosphatase-1B (PTP1B) inhibitor.
    Cat# 612530-44-6, Inquire Ask
  • PGD2-IN-1 is an antagonist of DP (IC50= 0.3 nM).
    Cat# 885066-67-1, Inquire Ask
  • GPR120-IN-1, a cell-permeable azaspiroundecanyl acetic acid compound, is an orally available,...
    Cat# 1599477-75-4, Inquire Ask
  • A potent inhibitor of ROCK2 (IC50= 1.2 nM)
    Cat# 934387-35-6, Inquire Ask
  • HSP70-IN-1 is a heat shock protein (HSP) inhibitor that interferes with the formation of...
    Cat# 1268273-90-0, Inquire Ask
  • mAChR-IN-1 is a potent muscarinic cholinergic receptor(mAChR) antagonist with IC50 of 17 nM.
    Cat# 119391-56-9, Inquire Ask
  • A potent and selective inhibitor of E-selectin (IC50= 7 nM) and ICAM-1 (IC50= 5 nM)
    Cat# 251994-14-6, Inquire Ask
  • Mcl1-IN-1 is a potent Mcl-1-selective inhibitor with IC50 of 2.4 uM, relative to the related...
    Cat# 713492-66-1, Inquire Ask
  • Selective inhibitors of mammalian target of rapamycin (mTOR) kinase based upon saturated...
    Cat# 1207358-59-5, Inquire Ask
  • BoNT-IN-1 is a potent inhibitor of Botulinum neurotoxin A light chain (IC50 = 0.9 uM).
    Cat# 694443-03-3, Inquire Ask
  • CSF1R-IN-1 is a CSF1R inhibitor with IC50 of 0.5 nM.
    Cat# 2095849-04-8, Inquire Ask
  • CARM1-IN-1 is a potent and specific CARM1(Coactivator-associated arginine methyltransferase 1)...
    Cat# 1020399-49-8, Inquire Ask
  • DCLK1-IN-1 is a selective DCLK1 inhibitor and a powerful tool to dissect DCLK1 biological...
    Cat# 2222635-15-4, Inquire Ask
  • Kif15-IN-1 is a potent Kif15 kinesin inhibitor, which inhibits cellular proliferation in tumor...
    Cat# 672926-32-8, Inquire Ask
  • RSV-IN-1 is a human respiratory syncytical virus (hRSV) inhibitor with IC50 value of 0.11 μM.
    Cat# 861139-16-4, Inquire Ask
  • Among CDKs, CDK9 is a validated pathological target in HIV infection, inflammation and cardiac...
    Cat# 1415559-43-1, Inquire Ask
  • An inhibitor of monoamine oxidase B (MAO B) (IC50= 20 nM)
    Cat# 124991-40-8, Inquire Ask
  • Nampt-IN-1, a pyridyloxyacetyl tetrahydroisoquinoline compound, is a novel inhibitor of...
    Cat# 1698878-14-6, Inquire Ask
  • Chitinase-IN-1 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50...
    Cat# 1579991-61-9, Inquire Ask
  • FLT3-IN-1, a Flt3 inhibitor, has been found to have week activity against T lymphoma Jurkat...
    Cat# 1370256-78-2, Inquire Ask
  • BET-IN-1, an oxazole derivative, can be used as a bromodomain inhibitor
    Cat# 1422554-34-4, Inquire Ask
  • DDX3-IN-1 is a DEAD-box polypeptide 3 (DDX3) inhibitor for HCV and HIV, respectively.
    Cat# 1919828-83-3, Inquire Ask
  • MK2-IN-1, a selective MAPKA-PK2 inhibitor, could probably influence the formation of...
    Cat# 1314118-92-7, Inquire Ask
  • SK1-IN-1 is a potent sphingosine kinase 1 (SPHK1) inhibitor (IC50= 58 nM).
    Cat# 1218816-71-7, Inquire Ask
  • hVEGF-IN-1 inhibits human VEGF-A translation and has antitumor activity. Tumor bearing mice...
    Cat# B0084-267747, 2 mg/unit USD $239 Ask
  • STK16-IN-1, a pyrrolonaphthyridinone compound, only potently inhibited STK16 (relative activity...
    Cat# B0084-007329, 300 mg/unit USD $629 Ask
  • Telomerase-IN-1 is a Telomerase inhibitor (IC50= 0.19 μM).
    Cat# 666859-49-0, Inquire Ask
  • Mirk-IN-1, a pyrido[2,3-d]pyrimidine derivative, has been found to be a DYRK1A/B inhibitor and...
    Cat# 1386979-55-0, Inquire Ask
  • LRRK2-IN-1 is a benzodiazepine based derivative and is known as a selective inhibitor of the...
    Cat# 1234480-84-2, Inquire Ask
  • KHK-IN-1, a pyrimidinopyrimidine derivative, is a ketohexokinase inhibitor that could have...
    Cat# 1303469-70-6, Inquire Ask
  • BMX-IN-1 selectively and irreversibly inhibits BMX (IC50=8nM) that is significant for...
    Cat# 1431525-23-3, Inquire Ask
  • FAS-IN-1, a diazaspiro derivative, has been found to be a fatty acid synthase inhibitor that...
    Cat# 1375105-96-6, Inquire Ask
  • USP7-IN-1 is a novel selective and reversible inhibitor of USP7 with IC50 of 33 uM; less or no...
    Cat# 1381291-36-6, Inquire Ask
  • CXCR2-IN-1 is a CXCR2 antagonists (pIC50= 9.3) with favorable central nervous system penetration...
    Cat# 1873376-49-8, Inquire Ask
  • DUBs-IN-1 is a potent deubiquitinase enzyme inhibitor for USP7/USP8.
    Cat# 924296-18-4, Inquire Ask
  • A novel small-molecule-like BRCA1 inhibitor (IC50= 0.53 μM) (Ki= 0.71 μM)
    Cat# 1622262-74-1, Inquire Ask
  • An IDO inhibitor with IC50 of 59 nM, shows activity in Hela cell (IC50=12 nM).
    Cat# 914638-30-5, Inquire Ask
  • Mps1-IN-1 is a highly potent and selectibe Mpsl inhibitor with IC50 of 367 nM; >1000-fold...
    Cat# 1125593-20-5, Inquire Ask
  • A novel histone lysine demethylase 4D (KDM4D) inhibitor (IC50= 0.41±0.03 μM)
    Cat# 2098902-68-0, Inquire Ask
  • IKKε-IN-1 is a potent IKKε inhibitor; inhibit the in-situ ΙKΚ ε-mediated phosphorylation of IRF3...
    Cat# 1292310-49-6, Inquire Ask
  • An orally active inhibitor of monoacylglycerol acyltransferase (MGAT2) (IC50= 7.8 for human, and...
    Cat# 1800025-30-2, Inquire Ask
  • MD2-IN-1 is an inhibitor of myeloid differentiation protein 2 (MD2) with a KD of 189 μM for...
    Cat# 111797-22-9, Inquire Ask
  • KDM5A-IN-1, a pyrrolidine amide compound, is an inhibitor histone demethylases.
    Cat# 1905481-36-8, Inquire Ask
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