FOSARILATE

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

National Institutes of Health Divider Arrow

NCATS

Details

Stereochemistry	ACHIRAL
Molecular Formula	C17H28ClO5P
Molecular Weight	378.828
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure of FOSARILATE

Structure Search

SMILES

CCOP(=O)(CCCCCCOC1=CC=C(OC)C=C1Cl)OCC

InChI

InChIKey=QDGWHHFJDHIIOS-UHFFFAOYSA-N

InChI=1S/C17H28ClO5P/c1-4-22-24(19,23-5-2)13-9-7-6-8-12-21-17-11-10-15(20-3)14-16(17)18/h10-11,14H,4-9,12-13H2,1-3H3

HIDE SMILES / InChI

Molecular Formula	C17H28ClO5P
Molecular Weight	378.828
Charge	0
Count

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

Description
Sources: Elks J., The Dictionary of Drugs: Chemical Data: Chemical Data, Structures, retrieved from: https://books.google.ru/books?id=0vXTBwAAQBAJ&pg=PA256&lpg=PA256&dq=FOSARILATE&source=bl&ots=6JUir9UAsr&sig=ACfU3U1a_6-0ckNPRNXYWjGTk_SfWqXLXw&hl=ru&sa=X&ved=2ahUKEwi_wuf649zjAhWOfZoKHUjWCfw4ChDoATAHegQICBAB#v=onepage&q=FOSARILATE&f=false

Fosarilate was studied as an antiviral agent. Information about the current use of this compound is not available.

Approval Year

PubMed

PubMed

Title	Date	PubMed
Synthesis of some phosphonates with antiherpetic activity.	1984-05	6325695

Patents

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 18:20:35 GMT 2025` Edited by `admin` on `Mon Mar 31 18:20:35 GMT 2025`
Record UNII	GM8PQW6Q2J
Record Status	`Validated (UNII)`
Record Version

Download

Name

Type

Language

WIN-42202

Preferred Name

English

FOSARILATE

Official Name

English

FOSARILATE [USAN]

Common Name

English

WIN 42,202

Code

English

fosarilate [INN]

Common Name

English

PHOSPHONIC ACID, (6-(2-CHLORO-4-METHOXYPHENOXY)HEXYL)-, DIETHYL ESTER

Common Name

English

Diethyl [6-(2-chloro-4-methoxyphenoxy)hexyl]phosphonate

Systematic Name

English

Classification Tree Code System Code

NCI_THESAURUS

C281

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

Code System Code Type Description

FDA UNII

GM8PQW6Q2J

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

USAN

W-26

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

PUBCHEM

71756

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

INN

5734

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

EVMPD

SUB07790MIG

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

EPA CompTox

DTXSID70223729

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

NCI_THESAURUS

C65757

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

CAS

73514-87-1

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

SMS_ID

100000080436

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

ChEMBL

CHEMBL161350

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

ECHA (EC/EINECS)

277-523-8

Created by admin on Mon Mar 31 18:20:35 GMT 2025 , Edited by admin on Mon Mar 31 18:20:35 GMT 2025

PRIMARY

Related Record Type Details


					GM8PQW6Q2J

ACTIVE MOIETY