Kelatorphan

Kelatorphan Suppliers list
Company Name: Fan De(Beijing) Biotechnology Co., Ltd.  
Tel: 15911056312
Email: liming@bio-fount.com
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: Beijing Jin Ming Biotechnology Co., Ltd.  
Tel: 010-60605840
Email: psaitong@jm-bio.com
Company Name: TargetMol Chemicals Inc.  
Tel: 4008200310 15002144251
Email: marketing@tsbiochem.com
Company Name: TargetMol Chemicals Inc.  
Tel: 13564774135
Email: marketing@targetmol.com

Kelatorphan manufacturers

  • Kelatorphan
  • Kelatorphan pictures
  • $1820.00
  • 2026-07-27
  • CAS:92175-57-0
  • Purity:
  • Supply Ability: 10g
Kelatorphan Basic information
Product Name:Kelatorphan
Synonyms:Kelatorphan;N-[(R)-4-(Hydroxyamino)-1,4-dioxo-2-(phenylmethyl)butyl]-L-alanine;OJCFZTVYDSKXNM-GXSJLCMTSA-N;(2S)-2-[[(2R)-2-benzyl-4-(hydroxyamino)-4-oxobutanoyl]amino]propanoic acid;L-Alanine, N-[(2R)-4-(hydroxyamino)-1,4-dioxo-2-(phenylmethyl)butyl]-
CAS:92175-57-0
MF:C14H18N2O5
MW:294.3
EINECS:
Product Categories:
Mol File:92175-57-0.mol
Kelatorphan Structure
Kelatorphan Chemical Properties
density 1.301±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility Soluble in DMSO
form Solid
pka3.58±0.10(Predicted)
color White to off-white
Safety Information
MSDS Information
Kelatorphan Usage And Synthesis
UsesKelatorphan is a full inhibitor of enkephalin degrading enzymes.
in vivo

The administration of Kelatorphan alone (50 μg) could result in a strong increase of intact [3H]enkephalin content corresponding to 80±11% of total recovered radioactivity[2]. In normal awake rats, Kelatorphan (10±20 mg/kg i.v.) increases minute-volume. The increase in ventilation is due to a dose-dependent increase in breathing frequency. In arthritic rats Kelatorphan (20 mg/kg i.v.) increases ventilation and there is no significant difference between arthritic and non-arthritic rats. In pentobarbital-anesthetized rats, a slight (116%) but significant increase of respiration is also produced by Kelatorphan (20 mg/kg, n=6) 10±15 min after administration. The effects of Kelatorphan are not antagonized by a pretreatment with a small dose of naloxone (0.2 mg/kg i.v., 15 min before Kelatorphan), but a larger dose (1 mg/kg) significantly antagonized Kelatorphan (20 mg/kg) at 5 and 10 min in awake rats[3].

References[1] Waksman G, et al. Kelatorphan: a full inhibitor of enkephalin degrading enzymes. Biochemical and pharmacological properties, regional distribution of enkephalinase in rat brain by use of a tritiated derivative. Neuropeptides. 1985 Feb;5(4-6):529-32. DOI:10.1016/0143-4179(85)90071-x
[2] Waksman G, et al. In vitro and in vivo effects of kelatorphan on enkephalin metabolism in rodent brain. Eur J Pharmacol. 1985 Nov 5;117(2):233-43.
[3] Boudinot E, et al. Effects of the potent analgesic enkephalin-catabolizing enzyme inhibitors RB101 and kelatorphan on respiration. Pain. 2001 Feb 1;90(1-2):7-13. DOI:10.1016/s0304-3959(00)00382-1
Kelatorphan Preparation Products And Raw materials
Tag:Kelatorphan(92175-57-0) Related Product Information
5-Azabicyclo[11.3.1]heptadeca-1(17),13,15-triene-6-carboxylic acid, 3-(mercaptomethyl)-4-oxo-, (3S,6S)- N-Ac-R-(2-Indanyl)glycine D-KLVFFA L-Glutamic acid, N-(1-oxo-4-phenylbutyl)- L-Leucine, N,N'-[1,4-phenylenebis(1-oxo-2,1-ethanediyl)]bis- (9CI) Kelatorphan