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Details

Stereochemistry ABSOLUTE
Molecular Formula C43H51N3O11
Molecular Weight 785.8785
Optical Activity UNSPECIFIED
Defined Stereocenters 9 / 9
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of RIFAXIMIN

SMILES

CO[C@H]1\C=C\O[C@@]2(C)OC3=C(C2=O)C4=C(C(O)=C3C)C(O)=C(NC(=O)C(C)=C\C=C\[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)C5=C4N=C6C=C(C)C=CN56

InChI

InChIKey=NZCRJKRKKOLAOJ-XRCRFVBUSA-N
InChI=1S/C43H51N3O11/c1-19-14-16-46-28(18-19)44-32-29-30-37(50)25(7)40-31(29)41(52)43(9,57-40)55-17-15-27(54-10)22(4)39(56-26(8)47)24(6)36(49)23(5)35(48)20(2)12-11-13-21(3)42(53)45-33(34(32)46)38(30)51/h11-18,20,22-24,27,35-36,39,48-51H,1-10H3,(H,45,53)/b12-11+,17-15+,21-13-/t20-,22+,23+,24+,27-,35-,36+,39+,43-/m0/s1

HIDE SMILES / InChI

Approval Year

Unknown
86413
Name Type Language
RIFAXIMIN
EP   INN   MART.   MI   ORANGE BOOK   USAN   VANDF   WHO-DD  
USAN   INN  
Official Name English
(2S,16Z,18E,20S,21S,22R,23R,24R,25S,26R,27S,28E)-25-(ACETYLOXY)-5,6,21,23-TETRAHYDROXY-27-METHOXY-2,4,11,16,20,22,24,26-OCTAMETHYL-2,7-(EPOXYPENTADECA(1,11,13)TRIENIMINO)BENZOFURO(4,5-E)PYRIDO(1,2-A)BENZIMIDAZOLE-1,15(2H)-DIONE
Common Name English
RIFAXIMIN [USAN]
Common Name English
rifaximin [INN]
Common Name English
NSC-758957
Code English
RIFAXIMIN [VANDF]
Common Name English
RIFAXIMIN [EP IMPURITY]
Common Name English
RIFAXIMIN [ORANGE BOOK]
Common Name English
RIFAMYCIN L 105
Common Name English
RIFAXIDIN
Common Name English
L-105
Common Name English
RIFAXIMIN [EP MONOGRAPH]
Common Name English
Rifaximin [WHO-DD]
Common Name English
RIFAXIMIN [MART.]
Common Name English
RIFAXIMIN [MI]
Common Name English
XIFAXSAN
Brand Name English
2,7-(EPOXYPENTADECA(1,11,13)TRIENIMINO)BENZOFURO(4,5-E)PYRIDO(1,2-A)BENZIMIDAZOLE-1,15(2H)-DIONE, 25-(ACETYLOXY)-5,6,21,23-TETRAHYDROXY-27-METHOXY-2,4,11,16,20,22,24,26-OCTAMETHYL-, (2S,16Z,18E,20S,21S,22R,23R,24R,25S,26R,27S,28E)-
Systematic Name English
RIFAXIMIN [JAN]
Common Name English
4-DEOXY-4'-METHYLPYRIDO(1',2'-1,2)IMIDAZO(5,4-C)RIFAMYCIN SV
Common Name English
Classification Tree Code System Code
WHO-ATC D06AX11
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
NDF-RT N0000007911
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
NDF-RT N0000007911
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
WHO-VATC QD06AX11
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
FDA ORPHAN DRUG 778520
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
NDF-RT N0000007911
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
WHO-VATC QA07AA11
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
NCI_THESAURUS C258
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
FDA ORPHAN DRUG 109497
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
WHO-VATC QJ51XX01
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
WHO-VATC QG51AA06
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
NDF-RT N0000175500
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
WHO-ATC A07AA11
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
NDF-RT N0000007911
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
LIVERTOX NBK548082
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
Code System Code Type Description
SMS_ID
100000091946
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
INN
5244
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
RXCUI
35619
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY RxNorm
CAS
80621-81-4
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
LACTMED
Rifaximin
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
EVMPD
SUB10312MIG
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
FDA UNII
L36O5T016N
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
DAILYMED
L36O5T016N
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
MERCK INDEX
m9615
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY Merck Index
ChEMBL
CHEMBL1617
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
CHEBI
75246
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
USAN
EE-33
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
NCI_THESAURUS
C61926
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
NSC
758957
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
DRUG CENTRAL
2379
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
EPA CompTox
DTXSID7045998
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
DRUG BANK
DB01220
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
MESH
C042734
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
PUBCHEM
6436173
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
WIKIPEDIA
RIFAXIMIN
Created by admin on Fri Dec 15 15:44:56 UTC 2023 , Edited by admin on Fri Dec 15 15:44:56 UTC 2023
PRIMARY
ACTIVE MOIETY
Structure of RIFAXIMIN
NIH
NCATS
PRIVACY ACT
ACCESSIBILITY
DISCLAIMER
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