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Details

Stereochemistry ABSOLUTE
Molecular Formula C23H45N5O14.H2O4S
Molecular Weight 713.707
Optical Activity UNSPECIFIED
Defined Stereocenters 19 / 19
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PAROMOMYCIN SULFATE

SMILES

OS(O)(=O)=O.[H][C@@]3(O[C@@H]1[C@@H](O)[C@H](N)C[C@H](N)[C@@]1([H])O[C@H]2O[C@H](CO)[C@@H](O)[C@H](O)[C@H]2N)O[C@H](CO)[C@@H](O[C@@]4([H])O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]4N)[C@H]3O

InChI

InChIKey=LJRDOKAZOAKLDU-UDXJMMFXSA-N
InChI=1S/C23H45N5O14.H2O4S/c24-2-7-13(32)15(34)10(27)21(37-7)41-19-9(4-30)39-23(17(19)36)42-20-12(31)5(25)1-6(26)18(20)40-22-11(28)16(35)14(33)8(3-29)38-22;1-5(2,3)4/h5-23,29-36H,1-4,24-28H2;(H2,1,2,3,4)/t5-,6+,7+,8-,9-,10-,11-,12+,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23+;/m1./s1

HIDE SMILES / InChI
Molecular Formula C23H45N5O14
Molecular Weight 615.6285
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 19 / 19
E/Z Centers 0
Optical Activity UNSPECIFIED
Molecular Formula H2O4S
Molecular Weight 98.078
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:07:06 UTC 2023
Edited
by admin
on Fri Dec 15 15:07:06 UTC 2023
Record UNII
845NU6GJPS
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PAROMOMYCIN SULFATE
JAN   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
Common Name English
METALCAPTASE
Common Name English
GABBROMYCIN
Brand Name English
AMINOSIDINE
Brand Name English
HUMATIN
Brand Name English
GABBROMICINA
Brand Name English
PAROMOMYCIN SULFATE [JAN]
Common Name English
FARMINOSIDIN
Brand Name English
PAROMOMYCIN SULPHATE IS THE SULPHATE SALT OF AN ANTIBIOTIC SUBSTANCE OR SUBSTANCES PRODUCED BY THE GROWTH OF STREPTOMYCES RIMOSUS VAR. PAROMOMYCINUS, OR A MIXTURE OF TWO OR MORE SUCH SALTS
Common Name English
PENICILLAMINUM [WHO-IP LATIN]
Common Name English
FARMIGLUCIN
Brand Name English
1600 ANTIBIOTIC
Code English
D-STREPTAMINE, O-2-AMINO-2-DEOXY-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-O-(O-2,6-DIAMINO-2,6-DIDEOXY-.BETA.-L-IDOPYRANOSYL-(1->3)-.BETA.-D-RIBOFURANOSYL-(1->5))-2-DEOXY-, SULPHATE (SALT)
Common Name English
NSC-758421
Code English
PARGONYL
Brand Name English
SINOSID
Brand Name English
FI-5853
Code English
PAROMOMYCIN SULFATE [USP MONOGRAPH]
Common Name English
PAROMOMYCIN SULFATE [ORANGE BOOK]
Common Name English
O-2,6-DIAMINO-2,6-DIDEOXY-.BETA.-L-IDOPYRANOSYL-(1->3)-O-.BETA.-D-RIBOFURANOSYL-(1->5)-O-(2-AMINO-2-DEOXY-.ALPHA.-D-GLUCOPYRANOSYL-(1->4))-2-DEOXYSTREPTAMINE SULPHATE (SALT)
Common Name English
PAROMOMYCIN SULFATE [VANDF]
Common Name English
PARAMICINA
Brand Name English
PENICILLAMINE [WHO-IP]
Common Name English
HUMAGEL
Brand Name English
O-2,6-DIAMINO-2,6-DIDEOXY-.BETA.-L-IDOPYRANOSYL-(1->3)-O-.BETA.-D-RIBOFURANOSYL-(1->5)-O-(2-AMINO-2-DEOXY-.ALPHA.-D-GLUCOPYRANOSYL-(1->4))-2-DEOXYSTREPTAMINE SULFATE (SALT)
Common Name English
PAROMOMYCIN SULFATE [MI]
Common Name English
D-STREPTAMINE, O-2-AMINO-2-DEOXY-.ALPHA.-D-GLUCOPYRANOSYL-(1->4)-O-(O-2,6-DIAMINO-2,6-DIDEOXY-.BETA.-L-IDOPYRANOSYL-(1->3)-.BETA.-D-RIBOFURANOSYL-(1->5))-2-DEOXY-, SULFATE (SALT)
Common Name English
PAROMOMYCIN SULFATE [USP-RS]
Common Name English
PAROMOMYCIN SULFATE IS THE SULFATE SALT OF AN ANTIBIOTIC SUBSTANCE OR SUBSTANCES PRODUCED BY THE GROWTH OF STREPTOMYCES RIMOSUS VAR. PAROMOMYCINUS, OR A MIXTURE OF TWO OR MORE SUCH SALTS
Common Name English
D-STREPTAMINE, O-2,6-DIAMINO-2,6-DIDEOXY-.BETA.-L-IDOPYRANOSYL-(1->3)-O-.BETA.-D-RIBOFURANOSYL-(1->5)-O-(2-AMINO-2-DEOXY-.ALPHA.-D-GLUCOPYRANOSYL-(1->4))-2-DEOXY-, SULFATE (1:1)
Systematic Name English
AMINOXIDIN
Brand Name English
PAROMOMYCIN SULFATE [WHO-IP]
Common Name English
Paromomycin sulfate [WHO-DD]
Common Name English
PAROMOMYCIN SULFATE [MART.]
Common Name English
PAROMOMYCINI SULFAS [WHO-IP LATIN]
Common Name English
PAROMOMYCIN SULPHATE
Common Name English
GABBRORAL
Brand Name English
PARICINA
Brand Name English
Classification Tree Code System Code
FDA ORPHAN DRUG 77193
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
FDA ORPHAN DRUG 231206
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
FDA ORPHAN DRUG 83194
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
NCI_THESAURUS C2363
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
FDA ORPHAN DRUG 74693
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
EU-Orphan Drug EU/3/05/271
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
FDA ORPHAN DRUG 201705
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
Code System Code Type Description
NSC
758421
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
SMS_ID
100000085520
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
NCI_THESAURUS
C47652
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
DRUG BANK
DBSALT000265
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
CAS
7205-49-4
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
DAILYMED
845NU6GJPS
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
EPA CompTox
DTXSID5047829
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
MERCK INDEX
m8416
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY Merck Index
CHEBI
7935
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
CAS
1263-89-4
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
ChEMBL
CHEMBL370143
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
ECHA (EC/EINECS)
215-031-7
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
CHEBI
7934
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
FDA UNII
845NU6GJPS
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
PUBCHEM
441375
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
EVMPD
SUB03654MIG
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
RXCUI
66912
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY RxNorm
WHO INTERNATIONAL PHARMACOPEIA
PAROMOMYCIN SULFATE
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY Description: A creamy white to light yellow powder; odourless or almost odourless. Solubility: Very soluble in water; practically insoluble in ethanol (~750 g/l) TS and ether R. Category: Antiamoebic drug. Storage: Paromomycin sulfate should be kept in a tightly closed container, protected from light. Additional information: Paromomycin sulfate is very hygroscopic. Even in the absence of light, it is gradually degraded onexposure to a humid atmosphere, the decomposition being faster at higher temperatures. Definition: Paromomycin sulfate contains not less than 675 International Units of paromomycin per mg, calculated with referenceto the dried substance.
RS_ITEM_NUM
1500003
Created by admin on Fri Dec 15 15:07:06 UTC 2023 , Edited by admin on Fri Dec 15 15:07:06 UTC 2023
PRIMARY
Related Record Type Details
Structure of PAROMOMYCIN
PARENT -> SALT/SOLVATE
Related Record Type Details
Structure of PAROMOMYCIN
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