147819-32-7

JB-1 Chemical Structure
147819-32-7

Chemical Structure

JB-1

  • CAS. Nr.: 147819-32-7
  • Formula:C55H88N14O15S2
  • Molecular Weight:1249.50

IUPAC Name: (6S,9S,12S,15R,20R,23S,26S,29S,31aS,37S,40S,42aS)-15-amino-26,37-bis(4-aminobutyl)-12-(4-hydroxybenzyl)-23-(hydroxymethyl)-40-isobutyl-6,9,29-trimethyl-5,8,11,14,22,25,28,31,36,39,42-undecaoxooctatriacontahydro-1H,19H-dipyrrolo[2,1-p:2',1'-y][1,2]dithia[5,8,11,14,17,20,23,26,29,32,35]undecaazacyclooctatriacontine-20-carboxylic acid

InChIKey: MPUVBZQBFGGAAS-XHGDPFBQSA-N

SMILES: O=C1N2[C@@](C(N[C@H](C(N[C@H](C(N[C@H](C(N[C@@H](CSSC[C@@H](C(N[C@H](C(N[C@H](C(N[C@H](C(N3[C@](CCC3)([H])C(N[C@H](C(N[C@H]1CCCCN)=O)CC(C)C)=O)=O)C)=O)C)=O)CC4=CC=C(C=C4)O)=O)N)C(O)=O)=O)CO)=O)CCCCN)=O)C)=O)([H])CCC2

Biological Activity: JB-1, an IGF-I analog, is a selective IGF-I receptor inhibitor that does not interact with IGF-II. JB-1 competes with IGF-I for binding to IGF-1R and blocks receptor autophosphorylation. JB-1 increases the level of sVEGFR-1. JB-1 normalizes retinal abnormalities, including reducing retinal neovascularization. JB-1 is applicable to studies related to oxygen-induced retinopathy[1].

Art. -Nr. Produktname Reinheit Beschreibung Pricing
HY-P3226
JB-1 99.63% JB-1, an IGF-I analog, is a selective IGF-I receptor inhibitor that does not interact with IGF-II. JB-1 competes with IGF-I for binding to IGF-1R and blocks receptor autophosphorylation. JB-1 increases the level of sVEGFR-1. JB-1 normalizes retinal abnormalities, including reducing retinal neovascularization. JB-1 is applicable to studies related to oxygen-induced retinopathy.
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This product is a controlled substance and not for sale in your territory.

This product is not for sale in your territory.

This compound is listed in the SVHC (Substances of Very High Concern) candidate list of ECHA (European Chemicals Agency).

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References