5-HYDROXYLANSOPRAZOLE

Details

Stereochemistry	RACEMIC
Molecular Formula	C16H14F3N3O3S
Molecular Weight	385.361
Optical Activity	( + / - )
Defined Stereocenters	0 / 1
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

CC1=C(OCC(F)(F)F)C=CN=C1C[S+]([O-])C2=NC3=C(N2)C=CC(O)=C3

InChI

InChIKey=IDCLTMRSSAXUNY-UHFFFAOYSA-N

InChI=1S/C16H14F3N3O3S/c1-9-13(20-5-4-14(9)25-8-16(17,18)19)7-26(24)15-21-11-3-2-10(23)6-12(11)22-15/h2-6,23H,7-8H2,1H3,(H,21,22)

HIDE SMILES / InChI

Molecular Formula	C16H14F3N3O3S
Molecular Weight	385.361
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 21:56:54 GMT 2025` Edited by `admin` on `Mon Mar 31 21:56:54 GMT 2025`
Record UNII	N5ROU3WS91
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

AG-1908

Preferred Name

English

5-HYDROXYLANSOPRAZOLE

Common Name

English

M-VI

Code

English

1H-BENZIMIDAZOL-6-OL, 2-(((3-METHYL-4-(2,2,2-TRIFLUOROETHOXY)-2-PYRIDINYL)METHYL)SULFINYL)-

Systematic Name

English

Code System Code Type Description

PUBCHEM

9800271

Created by admin on Mon Mar 31 21:56:54 GMT 2025 , Edited by admin on Mon Mar 31 21:56:54 GMT 2025

PRIMARY

FDA UNII

N5ROU3WS91

Created by admin on Mon Mar 31 21:56:54 GMT 2025 , Edited by admin on Mon Mar 31 21:56:54 GMT 2025

PRIMARY

CAS

131926-98-2

Created by admin on Mon Mar 31 21:56:54 GMT 2025 , Edited by admin on Mon Mar 31 21:56:54 GMT 2025

PRIMARY

Related Record Type Details


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LANSOPRAZOLE

PARENT -> METABOLITE

Comments:

the 5-hydroxylation of lansoprazole is primarily catalyzed by CYP2C19.


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LANSOPRAZOLE

PARENT -> METABOLITE

Comments:

These metabolites have very little or no antisecretory activity.