yingweiwo
  1. Home
  2. Products
  3. Signaling Pathways
  4. MAPK
  5. JNK

JNK

JNK

JNK related products

Structure Cat No. Product Name CAS No. Product Description
8-羟基依法韦伦 V51559 8-Hydroxy-efavirenz 205754-33-2 major metabolite of Efavirenz
BI-78D3 V2665 BI-78D3 883065-90-5 BI-78D3 (also known as JNK Inhibitor X) is a novel, potent and competitive JNK inhibitor with IC50 of 280nM.
CC-401 V2078 CC-401 395104-30-0 CC-401 (CC401) is a potent, specific, 2nd generation and ATP-competitive anthrapyrazolone c-Jun N terminal kinase (JNK) inhibitor with potential antineoplastic activity.
CC-401盐酸盐 V2978 CC-401 HCl 1438391-30-0 CC-401 HCl (CC401 hydrochloride) is an anthrapyrazolone-based inhibitor of c-Jun N terminal kinase (JNK) with potential anticancer activity.
CC-90001 V2263 CC-90001 1403859-14-2 CC-90001 (CC90001; CC 90001) is a novel, potent and selective inhibitor of c-Jun N-terminal kinase (JNK) with potential anti-fibrotic activity.
CMX-8933 V87071 CMX-8933 146877-90-9 CMX-8933 is an octapeptide fragment of the goldfish brain neurotrophic factor ependymin.
ICA-1S V137776 ICA-1S ICA-1S is a specific PKC-1 inhibitor.
JIP-1 (153-163) V51553 JIP-1 (153-163) 438567-88-5 peptide-based JNK inhibitor
JIP-1(153-163) TFA V87072 JIP-1(153-163) TFA JIP-1(153-163) TFA (TI-JIP TFA) is a peptide inhibitor of c-JNK.
JNK-IN-15, Cell-Permeable, Negative Control V85683 JNK-IN-15, Cell-Permeable, Negative Control
JNK1 degrader-1 V138271 JNK1 degrader-1 JNK1 degrader-1 is a JNK1 HyT degrader.
JNK抑制剂5a V0473 TCS JNK 5a 312917-14-9 TCS JNK 5a (alsoknown asJNK Inhibitor IX; TCS JNK-5a) is a novel, highly selective and potent JNK (c-Jun N-terminal Kinase) inhibitor with potential antineoplastic activity.
JNK抑制剂8 V0472 JNK-IN-8 1410880-22-6 JNK-IN-8 (JNK Inhibitor XVI; JNK-IN8) is the first irreversible/covalent inhibitor of pan-JNK (c-Jun N-terminal Kinase) with potential antitumor activity.
n-Butyl α-D-fructofuranoside V74394 n-Butyl α-D-fructofuranoside 80971-59-1 n-Butyl α-D-fructofuranoside is extracted from the root bark of Ulmus davidiana var.
Ro 31-8220 formic V144257 Ro 31-8220 formic Ro 31-8220 formic is a potent PKC inhibitor with IC50 values of 5, 24, 14, 27, 24, and 23 nM for PKCα, PKCβI, PKCβII, PKCγ, PKCε, and rat brain PKC, respectively.
Saquinavir-13C6 V144578 Saquinavir-13C6 Saquinavir-13C6 is 13C-labeled saquinavir.
Tanzisertib (CC-930) V1565 Tanzisertib (CC-930) 899805-25-5 Tanzisertib (formerly known as CC-930,JNK-930, JNKI-1,CC 930) is a potent, specific andand orally bioavailable JNK1/JNK2/JNK3 inhibitor that has the potential to be used for the treatment of fibrotic and infammatory indications.
Wnt/β-catenin-IN-6 V147130 Wnt/β-catenin-IN-6 Wnt/β-catenin-IN-6 is an orally effective inhibitor of the Wnt/β-catenin pathway.
α-Neoendorphin (porcine) V147549 α-Neoendorphin (porcine) 77739-20-9 α-Neoendorphin (porcine) is a peptide.
吡唑蒽酮 V0471 SP600125 (SP600125; NSC75890) 129-56-6 SP600125 (SP6-00125; NSC-75890) is a cell-permeable, broad-spectrum, reversible and ATP-competitive JNK (c-Jun N-terminal Kinase) inhibitor with potential anticancer and anti-inflammatory activity.
Contact Us
Tel: 1-708-310-1919 Fax: 1-708-557-7486 Email: [email protected] Frequently Asked Questions
Subscribe to our E-newsletter
Name
E-mail

Products are for research use only; We do not sell to patients
Copyright 2020 InvivoChem LLC | All Rights Reserved

linkedin facebook
Contact Us
Home Product Cart Member