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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H28N4O7
Molecular Weight 436.4589
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FR-144633

SMILES

CC(C)[C@H](NC(=O)[C@H](CC(O)=O)NC(=O)CCCOC1=CC=C(C=C1)C(N)=N)C(O)=O

InChI

InChIKey=JFCXCBBSUORTNS-YOEHRIQHSA-N
InChI=1S/C20H28N4O7/c1-11(2)17(20(29)30)24-19(28)14(10-16(26)27)23-15(25)4-3-9-31-13-7-5-12(6-8-13)18(21)22/h5-8,11,14,17H,3-4,9-10H2,1-2H3,(H3,21,22)(H,23,25)(H,24,28)(H,26,27)(H,29,30)/t14-,17-/m0/s1

HIDE SMILES / InChI

Molecular Formula C20H28N4O7
Molecular Weight 436.4589
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Pharmacologic platelet anesthesia by glycoprotein IIb/IIIa complex antagonist and argatroban during in vitro extracorporeal circulation.
2003 Aug
Efficacy of FK633, an ultra-short acting glycoprotein IIb/IIIa antagonist on platelet preservation during and after cardiopulmonary bypass.
2004 Aug
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:28:33 GMT 2023
Edited
by admin
on Sat Dec 16 18:28:33 GMT 2023
Record UNII
9SP2H336UF
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FR-144633
Code English
FR144633
Code English
FK-633
Code English
N-(4-(4-(AMINOIMINOMETHYL)PHENOXY)-1-OXOBUTYL)-L-.ALPHA.-ASPARTYL-L-VALINE
Systematic Name English
FK633
Code English
L-VALINE, N-(N-(4-(4-(AMINOIMINOMETHYL)PHENOXY)-1-OXOBUTYL)-L-.ALPHA.-ASPARTYL)-
Systematic Name English
(2S)-2-((2S)-2-(4-(4-CARBAMIMIDOYLPHENOXY)BUTANAMIDO)-3-CARBOXYPROPANAMIDO)-3-METHYLBUTANOIC ACID
Systematic Name English
Code System Code Type Description
MANUFACTURER PRODUCT INFORMATION
FK-633
Created by admin on Sat Dec 16 18:28:33 GMT 2023 , Edited by admin on Sat Dec 16 18:28:33 GMT 2023
PRIMARY
CAS
147865-49-4
Created by admin on Sat Dec 16 18:28:33 GMT 2023 , Edited by admin on Sat Dec 16 18:28:33 GMT 2023
PRIMARY
EPA CompTox
DTXSID00163821
Created by admin on Sat Dec 16 18:28:33 GMT 2023 , Edited by admin on Sat Dec 16 18:28:33 GMT 2023
PRIMARY
PUBCHEM
132814
Created by admin on Sat Dec 16 18:28:33 GMT 2023 , Edited by admin on Sat Dec 16 18:28:33 GMT 2023
PRIMARY
FDA UNII
9SP2H336UF
Created by admin on Sat Dec 16 18:28:33 GMT 2023 , Edited by admin on Sat Dec 16 18:28:33 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY