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Details

Stereochemistry ABSOLUTE
Molecular Formula C64H93N11O16
Molecular Weight 1272.4873
Optical Activity UNSPECIFIED
Defined Stereocenters 10 / 10
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of BCH-2763

SMILES

CC[C@H](C)[C@H](NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC2=CC=CC=C2)NC(=O)[C@H](CC(O)=O)NC(=O)CCCCN)C(=O)N3CCC[C@H]3C(=O)N([C@@H](CC(C)C)C(O)=O)C(=O)CCCCNC(=O)[C@@H]4CCCN4C(=O)[C@H](N)CC5=CC=CC=C5

InChI

InChIKey=VKIPOMGKUAJAEY-GEPLSBMPSA-N
InChI=1S/C64H93N11O16/c1-5-40(4)55(71-59(85)48-24-17-33-73(48)61(87)44(28-29-53(78)79)69-56(82)45(37-42-21-10-7-11-22-42)70-57(83)46(38-54(80)81)68-51(76)26-12-14-30-65)63(89)74-34-18-25-49(74)62(88)75(50(64(90)91)35-39(2)3)52(77)27-13-15-31-67-58(84)47-23-16-32-72(47)60(86)43(66)36-41-19-8-6-9-20-41/h6-11,19-22,39-40,43-50,55H,5,12-18,23-38,65-66H2,1-4H3,(H,67,84)(H,68,76)(H,69,82)(H,70,83)(H,71,85)(H,78,79)(H,80,81)(H,90,91)/t40-,43+,44-,45-,46-,47-,48-,49-,50-,55-/m0/s1

HIDE SMILES / InChI

Molecular Formula C64H93N11O16
Molecular Weight 1272.4873
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 10 / 10
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Drug-induced lysosomal changes and nephrotoxicity in rats.
1978 Nov
Inhibition of the growth of human coronavirus 229E by leupeptin.
1985 Feb
Purification and biochemical characterization of recombinant simian immunodeficiency virus protease and comparison to human immunodeficiency virus type 1 protease.
1991 Aug 27
Peptide aldehydes as inhibitors of HIV protease.
1993 Mar 22
Antiviral effect of oryzacystatin, a proteinase inhibitor in rice, against herpes simplex virus type 1 in vitro and in vivo.
1995 Apr
Efficacy of serine protease inhibitors against Cryptosporidium parvum infection in a bovine fallopian tube epithelial cell culture system.
1996 Aug
Cryptosporidium parvum metalloaminopeptidase inhibitors prevent in vitro excystation.
1996 Dec
Characterization of cytochrome P4502E1 turnover in transfected HepG2 cells expressing human CYP2E1.
1997 May 1
Inhibition of proteolysis by a cyclooxygenase inhibitor, indomethacin.
2000 Nov
Proteasomal degradation of caspase-6 in 17beta-estradiol-treated neurons.
2004 May
Activation and enzymatic characterization of recombinant human kallikrein 8.
2006 Jun
Transforming growth factor-beta1 inhibits all-trans retinoic acid-induced apoptosis.
2006 May
Endothelial gap junctions are down-regulated by arsenic trioxide.
2007 Aug 13
Regulation of adipocyte lipolysis by degradation of the perilipin protein: nelfinavir enhances lysosome-mediated perilipin proteolysis.
2007 Jul 27
Defective hepatocyte aquaporin-8 expression and reduced canalicular membrane water permeability in estrogen-induced cholestasis.
2007 Mar
2,2',4,4',5,5'-hexachlorobiphenyl (PCB 153) induces degradation of adherens junction proteins and inhibits beta-catenin-dependent transcription in liver epithelial cells.
2009 Jun 16
Molecular modeling: a search for a calpain inhibitor as a new treatment for cataractogenesis.
2011 Nov 10
Urban particulate matter activates Akt in human lung cells.
2012 Jan
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:31:48 GMT 2023
Edited
by admin
on Sat Dec 16 10:31:48 GMT 2023
Record UNII
2Y77S7IT1P
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
BCH-2763
Common Name English
L-LEUCINE, D-PHENYLALANYL-L-PROLYL-5-AMINOPENTANOYL-5-AMINOPENTANOYL-L-.ALPHA.-ASPARTYL-L-PHENYLALANYL-L-.ALPHA.-GLUTAMYL-L-PROLYL-L-ISOLEUCYL-L-PROLYL-
Systematic Name English
Code System Code Type Description
CAS
204641-27-0
Created by admin on Sat Dec 16 10:31:48 GMT 2023 , Edited by admin on Sat Dec 16 10:31:48 GMT 2023
PRIMARY
PUBCHEM
72941757
Created by admin on Sat Dec 16 10:31:48 GMT 2023 , Edited by admin on Sat Dec 16 10:31:48 GMT 2023
PRIMARY
FDA UNII
2Y77S7IT1P
Created by admin on Sat Dec 16 10:31:48 GMT 2023 , Edited by admin on Sat Dec 16 10:31:48 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY