Equilin

CAS No. 474-86-2

Equilin( —— )

Catalog No. M33216 CAS No. 474-86-2

Equilin (7-Dehydroestrone) is a neurotrophic estrogenic steroid with vasodilatory activity that increases monocyte-endothelial adhesion through NF-κB signalling.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 105 Get Quote
5MG 59 Get Quote
10MG 97 Get Quote
100MG Get Quote Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Equilin
  • Note
    Research use only, not for human use.
  • Brief Description
    Equilin (7-Dehydroestrone) is a neurotrophic estrogenic steroid with vasodilatory activity that increases monocyte-endothelial adhesion through NF-κB signalling.
  • Description
    Equilin (7-Dehydroestrone) is an important member of the large group of oestrogenic substances and is chemically related to menformon (oestrone). Equilin increases the growth of cortical neurons via an NMDA receptor-dependent mechanism.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    GPCR/G Protein
  • Target
    Calcium Channel
  • Recptor
    Calcium Channel
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    474-86-2
  • Formula Weight
    268.35
  • Molecular Formula
    C18H20O2
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 100 mg/mL (372.65 mM; Ultrasonic )
  • SMILES
    [H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])C2=CCc2cc(O)ccc12
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. David K, et al. Some biological properties of equilin. Biochem J. 1935;29(2):371-377.?
molnova catalog
related products
  • Cronidipine

    Cronidipine (LF 20254), a calcium channel antagonist, is used potentially for the treatment of hypertension and myocardia ischemia.

  • SAK3

    SAK3 (T-VGCC enhancer SAK3) is a potent, orally acitve enhancer of T-type voltage-gated Ca2+ channel (T-VGCC).

  • CRAC intermediate 1

    CRAC intermediate 1 is a key intermediate in the chemical synthesis of a series of CRAC channel inhibitors.