In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
November 4th, 2008 | 8 | No |
Popular Name: Fosfomycin Fosfomycin
Find On: PubMed — Wikipedia — Google
CAS Numbers: 23155-02-4 , 26016-98-8 , 26016-99-9 , 26472-47-9 , 26472-47-9, 23112-90-5(acid) , 78964-85-9 , [26016-98-8] , [26016-99-9]
(-)-(1R,2S)-(1,2-Epoxypropyl)phosphonic acid
(1R,2S)(-)-(1,2-Epoxypropyl)phosphonic acid disodium salt
(1R,2S)-epoxypropylphosphonate
(1R,2S)-epoxypropylphosphonate(1-)
(1R,2S)-Epoxypropylphosphonate; 23155-02-4; C06454; Fosfomycin; Phosphonomycin
(1R,2S)-epoxypropylphosphonate; fosfomycin; fosfomycin(1-)
(1R,2S)-epoxypropylphosphonic acid
(2R-cis)-(3-Methyloxiranyl)phosphonic acid disodium salt
(3-methyloxiran-2-yl)phosphonate
(_)-(1R,2S)-(1,2-Epoxypropyl)phosphonic acid
)-(1R,2S)-(1,2-Epoxypropyl)phosphonic acid
23155-02-4; D04253; FCM; Fosfomycin (USAN/INN); Phosphonomycin
26016-98-8; D07995; Fosfocin (TN); Fosfomycin calcium
26016-99-9; D02188; Fosfomycin sodium (JP16); Fosmicin S (TN)
6F066DFF-696A-4A94-AF78-A28430EBE5BA
calcium (3-methyloxiran-2-yl)phosphonate
CHEBI:42503; CHEBI:8159; CHEBI:24100
Disodium (1R,2S)-(1,2-epoxypropyl)phosphonate
disodium [(2R,3S)-3-methyloxiran-2-yl]-dioxido-oxo-
disodium [(2R,3S)-3-methyloxiran-2-yl]phosphonate
disodium[(2r,3s)-3-methyloxiran-2-yl]phosphonate
fosfomicina; fosfomycin; fosfomycine; fosfomycinum
Fosfomycin Calciumfor culture media
Fosfomycin disodium salt, Antibiotic for Culture Media Use Only
L-cis-1,2-epoxypropylphosphonic acid
Phosphonic acid, (1,2-epoxypropyl)-, disodium salt (1R,2S) (-)-
Phosphonic acid, (3-methyloxiranyl)-, disodium salt, (2R-cis)-
Phosphonic acid, (3-methyloxiranyl)-, disodium salt, (2R-cis)- (9CI)
USAN); Fosfomycin Calcium (JAN); Fosfomycin Sodium (JAN)
USAN); Fosfomycin Calcium (JAN); Fosfomycin Sodium (JAN); Fosfomycin Tromethamine (FDA
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) | -0.76 | -2.22 | -39.02 | 1 | 4 | -1 | 73 | 137.051 | 1 | ↓ |
Note Type | Comments | Provided By |
---|---|---|
ALOGPS_SOLUBILITY | 4.69e+01 g/l | DrugBank-approved |
purity | 9.500000000000000e+001 | Enamine Building Blocks Enamine Building Blocks |
therap | antibacterial | MicroSource Spectrum |
Indications | Antibiotic | KeyOrganics Bioactives |
Therapy | antimicrobial | SMDC MicroSource |
UniProt Database Links | DRP35_STAAN; DRP35_STAAU; FMTA_STAA8; FMTA_STAAC; FMTA_STAAU; FOSA_PSEAE; FOSA_SERMA; FOSB1_BACAA; FOSB1_BACAC; FOSB1_BACAN; FOSB2_BACAA; FOSB2_BACAC; FOSB2_BACAN; FOSB_BACA2; FOSB_BACAH; FOSB_BACC0; FOSB_BACC1; FOSB_BACC2; FOSB_BACC3; FOSB_BACC4; FOSB_BA | ChEBI |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
MURA-1-B | UDP-N-acetylglucosamine 1-carboxyvinyltransferase (cluster #1 Of 2), Bacterial | Bacteria | 118 | 1.21 | Binding ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
MURA_ECOLI | P0A749 | UDP-N-acetylglucosamine 1-carboxyvinyltransferase, Ecoli | 118 | 1.21 | Binding ≤ 1μM |
MURA_ECOLI | P0A749 | UDP-N-acetylglucosamine 1-carboxyvinyltransferase, Ecoli | 118 | 1.21 | Binding ≤ 10μM |