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Details

Stereochemistry ABSOLUTE
Molecular Formula C21H41N7O12
Molecular Weight 583.5899
Optical Activity UNSPECIFIED
Defined Stereocenters 15 / 15
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIHYDROSTREPTOMYCIN

SMILES

[H][C@]2(O[C@@H]1O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1NC)[C@H](O[C@@]3([H])[C@H](O)[C@@H](O)[C@H](NC(N)=N)[C@@H](O)[C@@H]3NC(N)=N)O[C@@H](C)[C@]2(O)CO

InChI

InChIKey=ASXBYYWOLISCLQ-HZYVHMACSA-N
InChI=1S/C21H41N7O12/c1-5-21(36,4-30)16(40-17-9(26-2)13(34)10(31)6(3-29)38-17)18(37-5)39-15-8(28-20(24)25)11(32)7(27-19(22)23)12(33)14(15)35/h5-18,26,29-36H,3-4H2,1-2H3,(H4,22,23,27)(H4,24,25,28)/t5-,6-,7+,8-,9-,10-,11+,12-,13-,14+,15+,16-,17-,18-,21+/m0/s1

HIDE SMILES / InChI
Molecular Formula C21H41N7O12
Molecular Weight 583.5899
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 15 / 15
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Sat Dec 16 16:00:17 UTC 2023
Edited
by admin
on Sat Dec 16 16:00:17 UTC 2023
Record UNII
P2I6R8W6UA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIHYDROSTREPTOMYCIN
INN   MI   WHO-DD  
INN  
Official Name English
ABIOCINE
Common Name English
DIHYDROSTREPTOMYCIN [MI]
Common Name English
VIBRIOMYCIN
Common Name English
D-STREPTAMINE, O-2-DEOXY-2-(METHYLAMINO)-.ALPHA.-L-GLUCOPYRANOSYL-(1->2)-O-5-DEOXY-3-C-(HYDROXYMETHYL)-.ALPHA.-L-LYXOFURANOSYL-(1->4)-N1,N3-BIS(AMINOIMINOMETHYL)-
Systematic Name English
Dihydrostreptomycin [WHO-DD]
Common Name English
STREPTOMYCIN, DIHYDRO-
Common Name English
dihydrostreptomycin [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QJ51GA90
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
WHO-VATC QJ01GA90
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
WHO-ATC S01AA15
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
WHO-VATC QA07AA90
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
WHO-VATC QJ51RC04
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
WHO-VATC QS01AA15
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
WHO-VATC QG51AG01
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
CFR 21 CFR 556.200
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
CFR 21 CFR 526.1696B
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
NCI_THESAURUS C2363
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
WHO-VATC QG51AG02
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
Code System Code Type Description
RXCUI
1549540
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY RxNorm
WIKIPEDIA
DIHYDROSTREPTOMYCIN
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
ChEMBL
CHEMBL1950576
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
EVMPD
SUB07140MIG
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
INN
1574
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
EPA CompTox
DTXSID0022937
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
CHEBI
38291
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
SMS_ID
100000082626
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
CAS
128-46-1
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
ECHA (EC/EINECS)
204-888-2
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
PUBCHEM
439369
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
MERCK INDEX
m4467
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY Merck Index
NCI_THESAURUS
C61724
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
DAILYMED
P2I6R8W6UA
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
FDA UNII
P2I6R8W6UA
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
DRUG BANK
DB11512
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
DRUG CENTRAL
890
Created by admin on Sat Dec 16 16:00:19 UTC 2023 , Edited by admin on Sat Dec 16 16:00:19 UTC 2023
PRIMARY
Related Record Type Details
Structure of DIHYDROSTREPTOMYCIN PANTOTHENATE
SALT/SOLVATE -> PARENT
Structure of PASOMYCIN
SALT/SOLVATE -> PARENT
Structure of DIHYDROSTREPTOMYCIN DIHYDROCHLORIDE
SALT/SOLVATE -> PARENT
Structure of DIHYDROSTREPTOMYCIN TRIHYDROCHLORIDE
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of DIHYDROSTREPTOMYCIN
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