Bio-Connect
Chemical Structure
Chemical Structure
Chemical Structure

Osthole

CDX-O0097
Chemodex
CAS Number484-12-8
Product group Chemicals
Estimated Purity>95%
Molecular Weight244.29
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    Chemodex
  • Product Name
    Osthole [484-12-8]
  • Delivery Days Customer
    10
  • CAS Number
    484-12-8
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Molecular Formula
    C15H16O3
  • Molecular Weight
    244.29
  • Scientific Description
    Chemical. CAS: 484-12-8. Formula: C15H16O3. MW: 244.29. Synthetic. Osthole is a natural coumarin that was first isolated from several medicinal plants, including C. monnieri and A. pubescens. Osthole exhibits immunomodulatory, antioxidative, and anti-inflammatory properties, by regulating the expression of TNF-alpha, NF-kappaB, TGF-beta, cyclooxygenases, leukotrienes, nitric oxide, ERK and JNK. Shows also anti-cancer, chemopherapeutic, analgesic, neuroprotective, antipruritic, anti-leishmania and anti-lipedemic activities. It is reported to induce a nonspecific elevation of cAMP and cGMP levels through its ability to inhibit phosphodiesterases, which leads to a modulation of calcium channel signaling and vasorelaxant effects. Selectively inhibits TRPV3 channels in skin. Induces apoptosis and cell cycle arrest in cancer cells. Suppression of fatty acid synthase expression in HER2-overexpressing breast cancer cells indicates osthole as a promising agent for chemotherapy. - Osthole is a natural coumarin that was first isolated from several medicinal plants, including C. monnieri and A. pubescens. Osthole exhibits immunomodulatory, antioxidative, and anti-inflammatory properties, by regulating the expression of TNF-alpha, NF-kappaB, TGF-beta, cyclooxygenases, leukotrienes, nitric oxide, ERK and JNK. Shows also anti-cancer, chemopherapeutic, analgesic, neuroprotective, antipruritic, anti-leishmania and anti-lipedemic activities. It is reported to induce a nonspecific elevation of cAMP and cGMP levels through its ability to inhibit phosphodiesterases, which leads to a modulation of calcium channel signaling and vasorelaxant effects. Selectively inhibits TRPV3 channels in skin. Induces apoptosis and cell cycle arrest in cancer cells. Suppression of fatty acid synthase expression in HER2-overexpressing breast cancer cells indicates osthole as a promising agent for chemotherapy.
  • SMILES
    O=C1OC2=C(C/C=C(C)/C)C(OC)=CC=C2C=C1
  • Storage Instruction
    RT
  • UNSPSC
    12352200

Related products

Osthole [484-12-8]
Product group Chemicals
TargetMol Chemicals
CAS Number484-12-8
Estimated Purity99.87%
Molecular Weight244.29
  • SizePrice
Product group Chemicals
RayBiotech
Osthole331-70249
  • SizePrice
Product group Chemicals
Santa Cruz Biotechnology
CAS Number484-12-8
  • SizePrice
Product group Chemicals
MedChem Express
OstholeHY-N0054
CAS Number484-12-8
Estimated Purity99.94
Molecular Weight244.29
  • SizePrice
Product group Chemicals
AbMole BioScience
OstholeM10391
CAS Number484-12-8
Molecular Weight244.29
  • SizePrice
Product group Chemicals
Biorbyt
OstholeORB703259
CAS Number484-12-8
Estimated Purity0.99
  • SizePrice
Product group Chemicals
Biosynth
CAS Number484-12-8
Molecular Weight244.29 g/mol
  • SizePrice