Chemical Compound

J1.150.617H

J1.150.617H chemical structure
Primary Record

J1.150.617H

In stock
550 g
Purity
98.1 %

Compound Identifiers & Properties

PubChem CID
100983435
SMILES
CC[C@H](C)[C@@H](C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCS(=O)C)C(=O)N)NC(=O)[C@H](CC1=CC=CC=C1)NC(=O)[C@H](C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@@H]2CCCN2C(=O)[C@@H]3CCC(=O)N3
Canonical SMILES
CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)[C@H](C)NC(=O)[C@H](CC(=O)O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@@H]1CCCN1C(=O)[C@@H]1CCC(=O)N1)C(=O)NCC(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCS(C)=O)C(N)=O

Names & Synonyms

  • J1.150.617H
  • pGlu-Pro-Ser-Lys-Asp-Ala-Phe-Ile-Gly-Leu-4-(Methylsulfinyl)-L-Abu-NH2
  • (3S)-3-[(2S)-6-amino-2-[(2S)-3-hydroxy-2-{[(2S)-1-[(2S)-5-oxopyrrolidine-2-carbonyl]pyrrolidin-2-yl]formamido}propanamido]hexanamido]-3-{[(1S)-1-{[(1S)-1-{[(1S,2S)-1-[({[(1S)-1-{[(1S)-1-carbamoyl-3-methanesulfinylpropyl]carbamoyl}-3-methylbutyl]carbamoyl}methyl)carbamoyl]-2-methylbutyl]carbamoyl}-2-phenylethyl]carbamoyl}ethyl]carbamoyl}propanoic acid