UCSF

ZINC19735373

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
November 8th, 2008 11 No

Popular Name: Glufosinate ammonium Glufosinate ammonium

Find On: PubMed — Wikipedia — Google

CAS Numbers: 51276-47-2 , 77182-82-2 , [51276-47-2]

Other Names:

( -)-phosphinothricin; (+-)-2-Amino-4-(hydroxymethylphosphinyl)butanoic acid; (+-)-2-Amino-4-(hydroxymethylphosphinyl)butanoic acid (9CI); (2S)-2-amino-4-(hydroxy-methylphosphoryl)butanoic acid; 2-Amino-4-(hydroxy-methyl-phosphoryl)butanoic acid; 2-Amino-

( -)-Phosphinothricin; 2-Amino-4-(hydroxymethylphosphinyl)butyric acid; 2-amino-4-methylphosphinobutyric acid; 3-Amino-3-carboxypropylmethylphosphinic acid; Basta; Butanoic acid, 2-amino-4-(hydroxymethylphosphinyl)-; C5H12NO2P; DL-2-Amino-4-(methylphosphi

(S)-2-amino-4-(hydroxymethylphosphinyl)butyric acid; (S)-4-[hydroxy(methyl)phosphinyl]-2-aminobutyric acid; (S)-phosphinothricin; L-PHOSPHINOTHRICIN; L-glufosinate; L-phophinothricin; phosphinothricine

2-Amino-4-(hydroxymethylphosphinyl)butanoic acid monoammonium salt; Ammonium (3-amino-3-carboxypropyl)methylphosphinate; Ammonium (DL-homoalanine-4-yl)methylphosphinate; Ammonium 2-amino-4-(hydroxymethylphosphinyl)butanoate; Ammonium 2-amino-4-(hydroxymet

2-Amino-4-(hydroxymethylphosphinyl)butanoic acid, monoammonium salt

2-Amino-4-(hydroxymethylphosphinyl)butanoic acid; 51276-47-2; C05042; Glufosinate; Phosphinothricin

2-ammonio-4-(methylphosphinato)butanoate; phosphinothricin

3-Amino-3-carboxypropylmethylphosphinic acid; DL-2-Amino-4-(methylphosphino)butanoic acid; glufosinate

CHEBI:45066; CHEBI:8139

DL-Phosphinothricin monoammonium salt solution

DL-Phosphinotricin; (PPT)

DL-PHOSPHINOTRICIN; [51276-47-2]

Glufosinate

Glufosinate-ammonium

MFCD00055562

MFCD00211362

phosphinothricin

phosphinothricin(1-)

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) -3.70 -0.02 -65.9 3 5 -1 108 180.12 4 ↓

Vendor Notes

Note Type Comments Provided By
MP 215° Oakwood Chemical
BP 519° Oakwood Chemical
Purity 97% Fluorochem
UniProt Database Links GLNA1_ALNGL; GLNA1_CHLRE; GLNA1_MEDSA; GLNA1_PEA; GLNA1_PHAVU; GLNA1_SOYBN; GLNA2_MEDSA; GLNA2_PEA; GLNA2_PHAVU; GLNA3_PEA; GLNA3_PHAVU; GLNA4_PEA; GLNA4_PHAVU; GLNA_LACSA; GLNA_NICPL; GLNA_PINSY; HEPD_STRVR; HPPE_PSESX; HPPE_STRWE; PAT_ALCFA; PAT_STRCO ChEBI

Activity (Go SEA)

Clustered Target Annotations
Code Description Organism Class Affinity (nM) LE (kcal/mol/atom) Type
GLNA-1-B Glutamine Synthetase (cluster #1 Of 1), Bacterial Bacteria 600 0.79 Binding ≤ 10μM
ChEMBL Target Annotations
Uniprot Swissprot Description Affinity (nM) LE (kcal/mol/atom) Type
GLNA_ECOLI P0A9C5 Glutamine Synthetase, Ecoli 600 0.79 Binding ≤ 1μM
GLNA_ECOLI P0A9C5 Glutamine Synthetase, Ecoli 1200 0.75 Binding ≤ 10μM

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