Cart
sales@molnova.com
Home - Products - Others - Other Targets - 4-Hydroxyindole

4-Hydroxyindole

CAS No. 2380-94-1

4-Hydroxyindole( —— )

Catalog No. M37709 CAS No. 2380-94-1

4-Hydroxyindole is an aromatic heterocyclic compound that is widely studied in both scientific research and laboratory experiments.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1G 26 In Stock
Get Quotation Bulk Inquiry Add to Cart

Biological Information

  • Product Name
    4-Hydroxyindole
  • Note
    Research use only, not for human use.
  • Brief Description
    4-Hydroxyindole is an aromatic heterocyclic compound that is widely studied in both scientific research and laboratory experiments.
  • Description
    4-Hydroxyindole is a member of the class of hydroxyindoles that is 1H-indole substituted by a hydroxy group at position 4. 4-Hydroxyindole is an important raw material or intermediate in the synthesis of pharmaceutical products and industrial polymers.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    Others
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2380-94-1
  • Formula Weight
    133.15
  • Molecular Formula
    C8H7NO
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 15.71 mg/mL (117.99 mM; Ultrasonic ) H2O : 1.43 mg/mL (10.74 mM; Ultrasonic)
  • SMILES
    OC1=C2C=CNC2=CC=C1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Nenad Manevski, et al. Glucuronidation of psilocin and 4-hydroxyindole by the human UDP-glucuronosyltransferases. Drug Metab Dispos. 2010 Mar;38(3):386-95.?
Calculator

Molecular Weight Calculator

Dilution Calculator

Molarity Calculator

molnova catalog
related products

  • Bunaftide

    Bunaftide (Bunaphtid) has antiarrhythmic effects and inhibits aconitine-induced ventricular tachycardia.

  • CRSP-1

    Endogenous central calcitonin (CT) receptor agonist that stimulates cAMP formation at a potency 350-fold greater than CT (ED50 values are 0.2 and 71 nM respectively). Displays no activity at calcitonin-gene related peptide (CGRP) and adrenomedullin receptors. Inhibits formation of multinuclear osteoclasts with similar efficacy to CT in vitro. Suppresses food intake and increases body temperature in free-feeding rats, and significantly decreases plasma calcium levels in vivo.

  • Rilmenidine Phosphat...

    Rilmenidine Phosphate is a selective I(1) imidazoline receptor agonist, used to treat hypertension.

Sign In Join Free