U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C20H19NO5
Molecular Weight 353.3686
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of UDONITRECTAG

SMILES

OC(=O)[C@H]1O[C@H]2O[C@@H]1C(=O)N(CC3=CC=CC=C3)[C@@H]2CC4=CC=CC=C4

InChI

InChIKey=SEKGLVUAECPQQM-NHAYFPRASA-N
InChI=1S/C20H19NO5/c22-18-16-17(19(23)24)26-20(25-16)15(11-13-7-3-1-4-8-13)21(18)12-14-9-5-2-6-10-14/h1-10,15-17,20H,11-12H2,(H,23,24)/t15-,16+,17+,20-/m1/s1

HIDE SMILES / InChI

Approval Year

Name Type Language
UDONITRECTAG
INN  
Official Name English
(1S,4R,5R,7S)-2-OXO-3,4-BIS(PHENYLMETHYL)-6,8-DIOXA-3-AZABICYCLO(3.2.1)OCTANE-7-CARBOXYLATE
Systematic Name English
REC-0559 (NERVE GROWTH FACTOR MIMETIC)
Common Name English
6,8-DIOXA-3-AZABICYCLO(3.2.1)OCTANE-7-CARBOXYLIC ACID, 2-OXO-3,4-BIS(PHENYLMETHYL)-, (1S,4R,5R,7S)-
Systematic Name English
REC-0559
Code English
3, 4-DIBENZYL-2-OXO-6, 8-DIOXA-3-AZABICYCLO (3.2.1) OCTANE-7-CARBOXYLIC ACID, (1S,4R,5R,7S)-
Systematic Name English
Udonitrectag [WHO-DD]
Common Name English
udonitrectag [INN]
Common Name English
(1S,4R,5R,7S)-3, 4-DIBENZYL-2-OXO-6, 8-DIOXA-3-AZABICYCLO (3.2.1) OCTANE-7-CARBOXYLIC ACID
Systematic Name English
Classification Tree Code System Code
EU-Orphan Drug EU/3/14/1400
Created by admin on Sat Dec 16 14:30:01 GMT 2023 , Edited by admin on Sat Dec 16 14:30:01 GMT 2023
Code System Code Type Description
SMS_ID
100000183259
Created by admin on Sat Dec 16 14:30:01 GMT 2023 , Edited by admin on Sat Dec 16 14:30:01 GMT 2023
PRIMARY
FDA UNII
2GOW9TT6AD
Created by admin on Sat Dec 16 14:30:01 GMT 2023 , Edited by admin on Sat Dec 16 14:30:01 GMT 2023
PRIMARY
PUBCHEM
86287629
Created by admin on Sat Dec 16 14:30:01 GMT 2023 , Edited by admin on Sat Dec 16 14:30:01 GMT 2023
PRIMARY
INN
11045
Created by admin on Sat Dec 16 14:30:01 GMT 2023 , Edited by admin on Sat Dec 16 14:30:01 GMT 2023
PRIMARY
NCI_THESAURUS
C175205
Created by admin on Sat Dec 16 14:30:01 GMT 2023 , Edited by admin on Sat Dec 16 14:30:01 GMT 2023
PRIMARY
EVMPD
SUB197644
Created by admin on Sat Dec 16 14:30:01 GMT 2023 , Edited by admin on Sat Dec 16 14:30:01 GMT 2023
PRIMARY
CAS
1458063-04-1
Created by admin on Sat Dec 16 14:30:01 GMT 2023 , Edited by admin on Sat Dec 16 14:30:01 GMT 2023
PRIMARY