Antide

CAS No. 112568-12-4

Antide( ——— )

Catalog No. M40004 CAS No. 112568-12-4

Antide (D-21074) is a potent LHRH antagonist. Antide also can be used for the research of prostatic cancer.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 171 In Stock
10MG 283 In Stock
25MG Get Quote In Stock
50MG Get Quote In Stock
100MG Get Quote In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Antide
  • Note
    Research use only, not for human use.
  • Brief Description
    Antide (D-21074) is a potent LHRH antagonist. Antide also can be used for the research of prostatic cancer.
  • Description
    Antide (D-21074) is a potent LHRH antagonist. Antide also can be used for the research of prostatic cancer.
  • In Vitro
    ———
  • In Vivo
    Animal Model:Cynomolgus monkey and rat Dosage:1, 3, 6, 10 and 15 mg/kg Administration:Subcutaneous, once or on 5 consecutive days Result:Had a dose-dependent inhibitory effect on serum concentration of LH (only rat) and testosterone and on the weights of the testes, prostates and seminal vesicles.Achieved long-lasting castration-like effects at concentrations between 6 (less than or equal to 8 weeks) and 15 mg/kg (greater than 8 weeks) in the rat. Induced a prolonged inhibitory effect only at 15 mg/kg and the duration was only 2-3 weeks in the cynomolgus monkey.
  • Synonyms
    ———
  • Pathway
    Others
  • Target
    Other Targets
  • Recptor
    ———
  • Research Area
    ———
  • Indication
    ———

Chemical Information

  • CAS Number
    112568-12-4
  • Formula Weight
    1591.29
  • Molecular Formula
    C82H108ClN17O14
  • Purity
    >98% (HPLC)
  • Solubility
    H2O : 10 mg/mL (6.28 mM; ultraphonic)
  • SMILES
    ———
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. U F Habenicht, et al. Effect of the new potent LHRH antagonist antide. J Steroid Biochem Mol Biol. 1990 Dec 20;37(6):937-42. ?
molnova catalog
related products
  • AdTx1

    Selective, high affinity, non-competitive α1A adrenoceptor antagonist (Ki = 0.35 nM). Exhibits no significant activity against a range of other GPCRs, including α2A, β1 and β2 adrenoceptors. Antagonizes effects of phenylephrine on isolated rabbit prostate muscle in vitro and on intra-urethral pressure in rats.

  • 3,5-Dimethoxy-1-[(6-...

    3,5-Dimethoxy-1-[(6-O-β-D-xylopyranosyl-β-D-glucopyranosyl)oxy]-9H-xanthen-9-one

  • ms48107

    MS48107 is a potent and selective positive allosteric modulator of G protein-coupled receptor 68 (GPR68). It is selective for GPR68 over the closely related proton GPCRs, neurotransmitter transporters, and hERG ion channels. It can readily cross the blood-brain barrier (BBB) in mice.