CC-90001

CAS No. 1403859-14-2

CC-90001( —— )

Catalog No. M28833 CAS No. 1403859-14-2

CC-90001 is an orally administered c-Jun N-terminal kinase (JNK) inhibitor with bias for JNK1 over JNK2.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 305 Get Quote
10MG 483 Get Quote
25MG 782 Get Quote
50MG 1071 Get Quote
100MG 1431 Get Quote
200MG Get Quote Get Quote
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Biological Information

  • Product Name
    CC-90001
  • Note
    Research use only, not for human use.
  • Brief Description
    CC-90001 is an orally administered c-Jun N-terminal kinase (JNK) inhibitor with bias for JNK1 over JNK2.
  • Description
    CC-90001 is an orally administered c-Jun N-terminal kinase (JNK) inhibitor with bias for JNK1 over JNK2.(In Vitro):CC-90001 is 12.9-fold more potent for JNK1 inhibition over JNK2 in knockout fibroblasts. CC-90001 blocks LPS-induced c-jun phosphorylation (EC50 = 480 nM).(In Vivo):CC-90001 decreases multiple measures of lung collagen and reduces disease induced increases in α-SMA to nearly baseline levels in a house dust mite model of lung fibrosis. CC-90001 (3 mg/kg b.i.d.) reduces the development of fibrosis, as evidenced by a 48% reduction in collagen and a 53% reduction in α-smooth muscle actin (α-SMA) in a steatohepatitis model.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    MAPK/ERK Signaling
  • Target
    JNK
  • Recptor
    Antioxidant
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    1403859-14-2
  • Formula Weight
    321.42
  • Molecular Formula
    C16H27N5O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (388.90 mM)
  • SMILES
    C[C@H](CC[C@H](C1)Nc(nc(NC(C)(C)C)nc2)c2C(N)=O)[C@@H]1O
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Boubaker J, et al. Isorhamnetin 3-O-robinobioside from Nitraria retusa leaves enhance antioxidant and antigenotoxic activity in human chronic myelogenous leukemia cell line K562. BMC Complement Altern Med. 2012 Aug 22;12:135.
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