| In ZINC since | Heavy atoms | Benign functionality |
|---|---|---|
| May 16th, 2008 | 28 | No |
Popular Name: Deoxyuridine triphosphate Deoxyuridine triphosphate
Find On: PubMed — Wikipedia — Google
CAS Numbers: 102814-08-4 , 1173-82-6 , 93858-62-9 , [102814-08-4]
1173-82-6; 2'-deoxyuridine-5'-triphosphate; dUTP; deoxy-UTP; deoxyuridine-triphosphate
2'-Deoxyuridine 5'-triphosphate tetralithium salt
2'-deoxyuridine 5'-triphosphate trianion; 2'-deoxyuridine 5'-triphosphate(3-); dUTP trianion
2'-Deoxyuridine 5'-triphosphate; C00460; dUTP
2'-Deoxyuridine-5'-triphosphate sodium salt
2'-Deoxyuridine-5'-triphosphate trisodium salt
2'-Deoxyuridine-5'-triphosphatetrisodiumsalt
2'-Deoxyuridine-5'-triphosphoric acid = dUTP
| 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) | -4.59 | -2.7 | -373.25 | 2 | 16 | -4 | 255 | 464.109 | 8 | ↓ |
| Mid Mid (pH 6-8) | -4.59 | -3.86 | -237.61 | 3 | 16 | -3 | 253 | 465.117 | 8 | ↓ |
| Note Type | Comments | Provided By |
|---|---|---|
| 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 |
|---|---|
| Pyrimidine biosynthesis | |
| Synthesis and interconversion of nucleotide di- and triphosphates |
|
