UCSF

ZINC04228260

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Substance Information

In ZINC since Heavy atoms Benign functionality
November 15th, 2005 20 No

Popular Name: dUMP dUMP

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CAS Numbers: 42155-08-8 , 964-26-1 , [42155-08-8]

Other Names:

2'-Deoxy-5'-uridylate; 2'-Deoxy-5'-uridylic acid; 2'-Deoxyuridine 5'-monophosphate; 2'-Deoxyuridine 5'-phosphate; 2'-Deoxyuridylate; 2'-Deoxyuridylic acid; Deoxy-UMP; Deoxyuridine 5'-monophosphate; Deoxyuridine 5'-phosphate; Deoxyuridine monophosphate; De

2'-Deoxy-5'-uridylate;2'-Deoxy-5'-uridylic acid;2'-Deoxyuridine 5'-monophosphate;2'-Deoxyuridine 5'-phosphate;2'-Deoxyuridylate;2'-Deoxyuridylic acid;Deoxy-UMP;Deoxyuridine 5'-monophosphate;Deoxyuridine 5'-phosphate;Deoxyuridine monophosphate;Deoxyuridyla

2'-Deoxy-5'-uridylic acid; 2'-Deoxyuridine 5'-monophosphate; 2'-Deoxyuridine 5'-phosphate; 2'-Deoxyuridylate; 2'-Deoxyuridylic acid; 5'-Uridylic acid, 2'-deoxy-; BRN 0042143; Deoxy-ump; Deoxyuridine 5'-monophosphate; Deoxyuridine 5'-phosphate; Deoxyuridin

2'-deoxy-5'-uridylic acid; 2'-deoxyuridine-5'-phosphate; 2'-deoxyuridine-5-monophosphate; 2'-deoxyuridylic acid; 964-26-1; dUMP; deoxyurdine-phosphate; deoxyuridine-phosphate

2'-deoxyuridine 5'-monophosphate

2'-Deoxyuridine 5'-monophosphate disodium salt

2'-Deoxyuridine 5'-phosphate; 964-26-1; C00365; Deoxyuridine 5'-phosphate; Deoxyuridine monophosphate; Deoxyuridylic acid; dUMP

2'-Deoxyuridine-5'-monophosphate

2'-Deoxyuridine-5'-monophosphate disodium salt

2'-DEOXYURIDINE-5'-MONOPHOSPHATE, DISODIUM SALT

2'-deoxyuridylic acid

CHEBI:19263; CHEBI:10532; CHEBI:14094

dUMP(2-)

dUMP; dUMP dianion; deoxyuridine 5'-phosphate dianion; deoxyuridine 5'-phosphate(2-); deoxyuridylate

MFCD00065282

MFCD00870752

SS-9451

[(2R,3S,5R)-5-(2,4-dioxo-3H-pyrimidin-1-yl)-3-hydroxyoxolan-2-yl]methoxyphosphonic acid

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) -2.80 -6.63 -140.03 2 10 -2 156 306.167 4 ↓

Vendor Notes

Note Type Comments Provided By
UniProt Database Links 438L_IIV6; 5DNU_ECOLI; APHA_ECOLI; CMPK2_HUMAN; CMPK2_MOUSE; DCD_ACIAC; DCD_ACIAD; DCD_ACIAM; DCD_ACIB3; DCD_ACIB5; DCD_ACIBC; DCD_ACIBS; DCD_ACIBT; DCD_ACIBY; DCD_ACIC1; DCD_ACIC5; DCD_ACICJ; DCD_ACIET; DCD_ACIF2; DCD_ACIF5; DCD_ACISJ; DCD_ACTP2; DCD_ACT ChEBI
ALOGPS_SOLUBILITY 7.97e+00 g/l DrugBank-experimental
Purity 95% Fluorochem
Purity 99% Fluorochem
Patent Database Links EP1666092 ChEBI
Reactome Database Links REACT_1172; REACT_1389; REACT_150; REACT_1679; REACT_1691; REACT_273; REACT_358; REACT_636; REACT_879; REACT_982 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Pyrimidine biosynthesis
Pyrimidine catabolism
Pyrimidine salvage reactions
Synthesis and interconversion of nucleotide di- and triphosphates

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