UCSF

ZINC24629762

Substance Information

In ZINC since Heavy atoms Benign functionality
January 19th, 2009 7 No

Other Names:

34156-56-4; D02267; Foscarnet sodium hydrate (JAN); Foscavir (TN); Trisodium phosphonoformate hexahydrate

34156-56-4; Foscarnet; Prestwick_1024

4428-95-9; C06456; Foscarmet; Foscarnet; Phosphonoformate

A-29622

BAN

Carboxyphosphonic acid

Carboxyphosphonic acid;Dihydroxyphosphinecarboxylic acid oxide;Phgosphonocarboxylic acid;Phosphonoformate;Phosphonoformic acid

CHEBI:45085; CHEBI:8158

CPD-11735; phosphonoformate

Dihydroxyphosphinecarboxylic acid oxide

Dihydroxyphosphinecarboxylic acid oxide trisodium salt hexahydrate; Formic acid, phosphono-, trisodium salt, hexahydrate; LS-105953; Phosphinecarboxylic acid, dihydroxy-, oxide, trisodium salt, hexahydrate; Phosphonoformic acid, trisodium salt, hexahydrat

EHB-776

FDA

FDA)

Forscarnet sodium

fos-

Foscarmet

Foscarnet

foscarnet sodique; foscarnet sodium; foscarneto sodico; foscarnetum natricum

Foscarnet Sodium

Foscarnet Sodium (BAN

Foscarnet Sodium (FDA

Foscarnet sodium hexahydrate

FOSCARNET SODIUM; foscarnet sodium; trisodium carboxyphosphate; trisodium carboxyphosphate (anhydrous); trisodium dioxidophosphinecarboxylate oxide; trisodium phosphonoformate; trisodium phosphonoformate (anhydrous)

foscarnet(3-)

FOSCARNET; carboxyphosphonic acid; foscarnet; phosphonomethanoic acid

Foscavir

INN

LS-187063

LS-187793

MFCD00150176

PFA

Phgosphonocarboxylic acid

phosphonatoformate

Phosphonoformate

Phosphonoformic acid

Phosphonoformic acid trisodium salt hexahydrate

Phosphonoformic acid, PF

Sodium dioxidophosphinecarboxylate oxide hydrate

Sodium phosphonoformate hexahydrate

Sodium phosphonoformate hexahydrate, 98+%

Triapten

trisodium phosphonoformate

USAN

USAN)

Virudin

Download: MOL2 SDF SMILES Flexibase

Physical Representations

Type pH range xlogP Des A‑Pol Apolar desolvation (kcal/mol) Des Pol Polar desolvation (kcal/mol) H Don H-bond donors H Acc H-bond acceptors Chg Net charge tPSA (Ų) MWT Molecular weight (g/mol) RB Rotatable bonds DL
Ref Reference (pH 7) -1.71 -2.5 -120.9 1 5 -2 100 123.988 1

Vendor Notes

Note Type Comments Provided By
ALOGPS_SOLUBILITY 1.68e+01 g/l DrugBank-approved
Therapy antiviral SMDC MicroSource
UniProt Database Links AR6P6_HUMAN; LSMD1_HUMAN; N42L2_HUMAN; N42L2_MOUSE; N42L2_RAT; PCAT1_HUMAN; PHNHY_PSEFL; PSMD6_HUMAN ChEBI

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
DPOL-3-V Human Herpesvirus 6 DNA Polymerase (cluster #3 Of 4), Viral Viruses 280 1.31 Binding ≤ 10μM
Q72547-6-V Human Immunodeficiency Virus Type 1 Reverse Transcriptase (cluster #6 Of 6), Viral Viruses 2030 1.14 Binding ≤ 10μM
Z50613-1-O Avian Myeloblastosis Virus (cluster #1 Of 1), Other Other 9310 1.01 Binding ≤ 10μM
Z50530-5-O Human Herpesvirus 5 (cluster #5 Of 5), Other Other 7000 1.03 Functional ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
DPOL_VZVD P09252 DNA Polymerase, Vzvd 280 1.31 Binding ≤ 1μM
Z50613 Z50613 Avian Myeloblastosis Virus 9310 1.01 Binding ≤ 10μM
DPOL_VZVD P09252 DNA Polymerase, Vzvd 280 1.31 Binding ≤ 10μM
DPOL_HCMVA P08546 Human Herpesvirus 5 DNA Polymerase, Hcmva 2500 1.12 Binding ≤ 10μM
Q72547_9HIV1 Q72547 Human Immunodeficiency Virus Type 1 Reverse Transcriptase, 9hiv1 2030 1.14 Binding ≤ 10μM
Z50530 Z50530 Human Herpesvirus 5 7000 1.03 Functional ≤ 10μM

Analogs ( Draw Identity 99% 90% 80% 70% )