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

Details

Stereochemistry ABSOLUTE
Molecular Formula C37H41N2O6
Molecular Weight 609.7312
Optical Activity UNSPECIFIED
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 1

SHOW SMILES / InChI
Structure of TUBOCURARINE

SMILES

COC1=CC2=C3C=C1OC4=CC(C[C@@H]5C6=C(OC7=CC=C(C[C@@H]3N(C)CC2)C=C7)C(O)=C(OC)C=C6CC[N+]5(C)C)=CC=C4O

InChI

InChIKey=JFJZZMVDLULRGK-URLMMPGGSA-O
InChI=1S/C37H40N2O6/c1-38-14-12-24-19-32(42-4)33-21-27(24)28(38)16-22-6-9-26(10-7-22)44-37-35-25(20-34(43-5)36(37)41)13-15-39(2,3)29(35)17-23-8-11-30(40)31(18-23)45-33/h6-11,18-21,28-29H,12-17H2,1-5H3,(H-,40,41)/p+1/t28-,29+/m0/s1

HIDE SMILES / InChI

Molecular Formula C37H40N2O6
Molecular Weight 608.7233
Charge 0
Count
Stereochemistry EPIMERIC
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 14:59:55 UTC 2023
Edited
by admin
on Fri Dec 15 14:59:55 UTC 2023
Record UNII
W9YXS298BM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TUBOCURARINE
HSDB   VANDF   WHO-DD  
Common Name English
13H-4,6:21,24-DIETHENO-8,12-METHENO-1H-PYRIDO(3',2':14,15)(1,11)DIOXACYCLOEICOSINO(2,3,4-IJ)ISOQUINOLINIUM, 2,3,13A,14,15,16,25,25A-OCTAHYDRO-9,19-DIHYDROXY-18,29-DIMETHOXY-1,14,14-TRIMETHYL-, (13AR,25AS)-
Common Name English
Tubocurarine [WHO-DD]
Common Name English
TUBOCURARINE [HSDB]
Common Name English
TUBOCURARINE ION
Common Name English
D-TUBOCURARINE
Common Name English
(+)-TUBOCURARINE
Common Name English
TUBOCURARINE CATION
Common Name English
TUBOCURARANIUM, 7',12'-DIHYDROXY-6,6'-DIMETHOXY-2,2',2'-TRIMETHYL-
Common Name English
TUBOCURARINE [VANDF]
Common Name English
Classification Tree Code System Code
WHO-ATC M03AA02
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
WHO-VATC QM03AA02
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
Code System Code Type Description
DAILYMED
W9YXS298BM
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
EVMPD
SUB15635MIG
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
PUBCHEM
6000
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
DRUG BANK
DB01199
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
HSDB
2152
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
RXCUI
10917
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY RxNorm
CAS
57-95-4
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
MESH
D014403
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
DRUG CENTRAL
2781
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
SMS_ID
100000077304
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
CHEBI
9774
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
IUPHAR
2294
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
FDA UNII
W9YXS298BM
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
WIKIPEDIA
Tubocurarine
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
EPA CompTox
DTXSID0048393
Created by admin on Fri Dec 15 14:59:55 UTC 2023 , Edited by admin on Fri Dec 15 14:59:55 UTC 2023
PRIMARY
Related Record Type Details
TRANSPORTER -> INHIBITOR
TARGET -> INHIBITOR
TARGET -> INHIBITOR
BINDER->LIGAND
Related Record Type Details
ACTIVE MOIETY