In ZINC since | Heavy atoms | Benign functionality |
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March 21st, 2014 | 0 | No |
Popular Name: Deoxyuridine triphosphate Deoxyuridine triphosphate
Find On: PubMed — Wikipedia — Google
CAS Numbers: 102814-08-4 , 1173-82-6 , [102814-08-4]
2'-deoxyuridine 5'-triphosphate trianion; 2'-deoxyuridine 5'-triphosphate(3-); dUTP trianion
2'-Deoxyuridine-5'-triphosphate sodium salt
2'-Deoxyuridine-5'-triphosphate trisodium salt
2'-Deoxyuridine-5'-triphosphatetrisodiumsalt
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 |
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Note Type | Comments | Provided By |
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UniProt Database Links | 438L_IIV6; 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_ACTP7; DCD_ACTPJ; DCD_ACTSZ | ChEBI |
Reactome Database Links | REACT_150; REACT_21273; REACT_21292; REACT_21362; REACT_21416 | ChEBI |
Patent Database Links | US2002106674; US2007197538 | ChEBI |
Description | Species |
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Pyrimidine biosynthesis | |
Synthesis and interconversion of nucleotide di- and triphosphates |
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No pre-computed analogs available. Try a structural similarity search.