OSELTAMIVIR

U.S. Department of Health & Human Services Divider Arrow

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ABSOLUTE
Molecular Formula	C16H28N2O4
Molecular Weight	312.4045
Optical Activity	UNSPECIFIED
Defined Stereocenters	3 / 3
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of OSELTAMIVIR

Structure Search

SMILES

CCOC(=O)C1=C[C@@H](OC(CC)CC)[C@H](NC(C)=O)[C@@H](N)C1

InChI

InChIKey=VSZGPKBBMSAYNT-RRFJBIMHSA-N

InChI=1S/C16H28N2O4/c1-5-12(6-2)22-14-9-11(16(20)21-7-3)8-13(17)15(14)18-10(4)19/h9,12-15H,5-8,17H2,1-4H3,(H,18,19)/t13-,14+,15+/m0/s1

HIDE SMILES / InChI

Molecular Formula	C16H28N2O4
Molecular Weight	312.4045
Charge	0
Count

Stereochemistry	ABSOLUTE
Additional Stereochemistry	No
Defined Stereocenters	3 / 3
E/Z Centers	0
Optical Activity	UNSPECIFIED

Approval Year

Substance Class	Chemical Created by `admin` on `Fri Dec 15 15:44:25 UTC 2023` Edited by `admin` on `Fri Dec 15 15:44:25 UTC 2023`
Record UNII	20O93L6F9H
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

OSELTAMIVIR

Official Name

English

oseltamivir [INN]

Common Name

English

GS4104

Code

English

OSELTAMIVIR [EMA EPAR]

Common Name

English

OSELTAMIVIR [VANDF]

Common Name

English

RO-640796

Code

English

RO 640796

Code

English

Oseltamivir [WHO-DD]

Common Name

English

RO-64-0796

Code

English

GS-4104

Code

English

ETHYL (3R,4R,5S)-4-ACETAMIDO-5-AMINO-3-(1-ETHYLPROPOXY)-1-CYCLOHEXENE-1-CARBOXYLATE

Systematic Name

English

RO64-0796

Code

English

OSELTAMIVIR [HSDB]

Common Name

English

GS-4071 ETHYL ESTER

Code

English

GS 4104

Code

English

OSELTAMIVIR [MI]

Common Name

English

Classification Tree Code System Code

NCI_THESAURUS

C281

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

WHO-ATC

J05AH02

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

WHO-ESSENTIAL MEDICINES LIST

6.4.3

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

LIVERTOX

NBK548268

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

NDF-RT

N0000175436

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

NDF-RT

N0000175524

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

WHO-VATC

QJ05AH02

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

Code System Code Type Description

CHEBI

7798

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

DRUG CENTRAL

2001

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

DRUG BANK

DB00198

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

LACTMED

Oseltamivir

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

CAS

196618-13-0

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

MERCK INDEX

m8256

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

Merck Index

ChEMBL

CHEMBL1229

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

EVMPD

SUB03553MIG

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

HSDB

7433

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

INN

7793

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

FDA UNII

20O93L6F9H

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

WIKIPEDIA

OSELTAMIVIR

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

PUBCHEM

65028

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

DAILYMED

20O93L6F9H

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

NCI_THESAURUS

C62061

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

MESH

D053139

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

EPA CompTox

DTXSID9044291

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

SMS_ID

100000089424

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

RXCUI

260101

Created by admin on Fri Dec 15 15:44:25 UTC 2023 , Edited by admin on Fri Dec 15 15:44:25 UTC 2023

PRIMARY

RxNorm

Related Record Type Details


					XSC4R7KWN6

OSELTAMIVIR HYDROCHLORIDE

SALT/SOLVATE -> PARENT

Amount:


					1314JZ2X6W

INFLUENZA B VIRUS WHOLE

TARGET ORGANISM->INHIBITOR


					R9HH0NDE2E

INFLUENZA A VIRUS WHOLE

TARGET ORGANISM->INHIBITOR


					6D53G0FD0Z

PLASMA PROTEIN FRACTION (HUMAN)

BINDER->LIGAND

Interaction Type:

BINDING

Amount:


					4A3O49NGEZ

OSELTAMIVIR PHOSPHATE

SALT/SOLVATE -> PARENT


					HPN66MJEK8

LIVER CARBOXYLESTERASE 1

METABOLIC ENZYME -> SUBSTRATE

Amount:

Related Record Type Details


					VM7P2DST6J

OSELTAMIVIR-1-CARBOXYLIC ACID

METABOLITE -> PARENT

Related Record Type Details


					K6106LV5Q8

OSELTAMIVIR ACID

ACTIVE MOIETY

Name	Property Type	Amount	Referenced Substance	Defining	Parameters	References
Tmax	PHARMACOKINETIC				FASTED STATE ORAL ADMINISTRATION SINGLE DOSE IN HEALTHY VOLUNTEERS

Volume of Distribution	PHARMACOKINETIC

Biological Half-life	PHARMACOKINETIC

Tmax	PHARMACOKINETIC				SINGLE DOSE ORAL ADMINISTRATION IN HEALTHY VOLUNTEERS FED CONDITION