KL001

CAS No. 309928-48-1

KL001( KL-001 | KL 001 )

Catalog No. M13992 CAS No. 309928-48-1

KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 85 In Stock
5MG 76 In Stock
10MG 110 In Stock
25MG 188 In Stock
50MG 272 In Stock
100MG 407 In Stock
200MG Get Quote In Stock
500MG 914 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    KL001
  • Note
    Research use only, not for human use.
  • Brief Description
    KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock.
  • Description
    KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock; prevents SCFFBXL3-mediated ubiquitination and degradation of CRY, resulting in lengthening of the circadian period, interacts directly with CRY1 and CRY2 and stabilizes CRY proteins; KL001-mediated CRY stabilization inhibited glucagon-induced gluconeogenesis in primary hepatocytes; KL001 is the first-in-class cryptochrome-targeting circadian modulator and substrate-targeting ubiquitination antagonist.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    KL-001 | KL 001
  • Pathway
    Proteasome/Ubiquitin
  • Target
    DUB
  • Recptor
    DUB
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    309928-48-1
  • Formula Weight
    398.477
  • Molecular Formula
    C21H22N2O4S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 5 mg/mL (12.55 mM助)
  • SMILES
    CS(=O)(N(CC(O)CN1C2=C(C3=C1C=CC=C3)C=CC=C2)CC4=CC=CO4)=O
  • Chemical Name
    N-[3-(9H-Carbazol-9-yl)-2-hydroxypropyl]-N-(2-furanylmethyl)-methanesulfonamide

Shipping & Storage Information

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

Reference

1. Hirota T, et al. Science. 2012 Aug 31;337(6098):1094-7. 2. Nangle S, et al. Cell Res. 2013 Dec;23(12):1417-9. 3. St John PC, et al. Proc Natl Acad Sci U S A. 2014 Feb 4;111(5):2040-5. 4. Oshima T, et al. Angew Chem Int Ed Engl. 2015 Jun 8;54(24):7193-7.
molnova catalog
related products
  • SJB3-019A B

    SJB3-019A is a potent, potent and novel ubiquitin-specific protease 1 (USP1) inhibitor, which promotes ID1 degradation and cytotoxicity in K562 cells 5 times more than SJB2-043, with IC50 of 0.0781 μM. SJB3-019A inhibits cell proliferation and causes cell apoptosis.

  • HBX 28258

    HBX 28258 is a potent, selective USP7 inhibitor with IC50 of 22.6 uM.

  • OTUB1/USP8-IN-1

    OTUB1/USP8-IN-1 is a potent OTUB1/USP8 inhibitor with potential anticancer activity, demonstrating IC50 values of 0.17 nM for OTUB1 and 0.28 nM for USP8.