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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
Urban particulate matter activates Akt in human lung cells.
2012-01
Molecular modeling: a search for a calpain inhibitor as a new treatment for cataractogenesis.
2011-11-10
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.
2009-06-16
Endothelial gap junctions are down-regulated by arsenic trioxide.
2007-08-13
Regulation of adipocyte lipolysis by degradation of the perilipin protein: nelfinavir enhances lysosome-mediated perilipin proteolysis.
2007-07-27
Defective hepatocyte aquaporin-8 expression and reduced canalicular membrane water permeability in estrogen-induced cholestasis.
2007-03
Activation and enzymatic characterization of recombinant human kallikrein 8.
2006-06
Transforming growth factor-beta1 inhibits all-trans retinoic acid-induced apoptosis.
2006-05
Proteasomal degradation of caspase-6 in 17beta-estradiol-treated neurons.
2004-05
Inhibition of proteolysis by a cyclooxygenase inhibitor, indomethacin.
2000-11
Characterization of cytochrome P4502E1 turnover in transfected HepG2 cells expressing human CYP2E1.
1997-05-01
Cryptosporidium parvum metalloaminopeptidase inhibitors prevent in vitro excystation.
1996-12
Efficacy of serine protease inhibitors against Cryptosporidium parvum infection in a bovine fallopian tube epithelial cell culture system.
1996-08
Antiviral effect of oryzacystatin, a proteinase inhibitor in rice, against herpes simplex virus type 1 in vitro and in vivo.
1995-04
Peptide aldehydes as inhibitors of HIV protease.
1993-03-22
Purification and biochemical characterization of recombinant simian immunodeficiency virus protease and comparison to human immunodeficiency virus type 1 protease.
1991-08-27
Inhibition of the growth of human coronavirus 229E by leupeptin.
1985-02
Drug-induced lysosomal changes and nephrotoxicity in rats.
1978-11
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:18:31 GMT 2025
Edited
by admin
on Mon Mar 31 23:18:31 GMT 2025
Record UNII
2Y77S7IT1P
Record Status Validated (UNII)
Record Version
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Name Type Language
L-LEUCINE, D-PHENYLALANYL-L-PROLYL-5-AMINOPENTANOYL-5-AMINOPENTANOYL-L-.ALPHA.-ASPARTYL-L-PHENYLALANYL-L-.ALPHA.-GLUTAMYL-L-PROLYL-L-ISOLEUCYL-L-PROLYL-
Preferred Name English
BCH-2763
Common Name English
Code System Code Type Description
CAS
204641-27-0
Created by admin on Mon Mar 31 23:18:31 GMT 2025 , Edited by admin on Mon Mar 31 23:18:31 GMT 2025
PRIMARY
PUBCHEM
72941757
Created by admin on Mon Mar 31 23:18:31 GMT 2025 , Edited by admin on Mon Mar 31 23:18:31 GMT 2025
PRIMARY
FDA UNII
2Y77S7IT1P
Created by admin on Mon Mar 31 23:18:31 GMT 2025 , Edited by admin on Mon Mar 31 23:18:31 GMT 2025
PRIMARY
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