UCSF

ZINC08215945

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
July 4th, 2006 28 No

Popular Name: dCTP dCTP

Find On: PubMed — Wikipedia — Google

CAS Numbers: 102783-51-7 , 109909-44-6 , 2056-98-6 , [102783-51-7]

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

Vendor Notes

Note Type Comments Provided By
UniProt Database Links 438L_IIV6; 5DNU_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_ACTP7; DCD_ACTP ChEBI
Patent Database Links EP1806400; US2007224611; US2008268462 ChEBI
Reactome Database Links REACT_21273; REACT_21292; REACT_21362; REACT_21416; REACT_7985; REACT_8004; REACT_8019; REACT_8029; REACT_9039; REACT_91 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Assembly of telomerase and telomere extension
DNA replication initiation
Minus-strand DNA synthesis
Mismatch repair (MMR) directed by MSH2:MSH3 (MutSbeta)
Mismatch repair (MMR) directed by MSH2:MSH6 (MutSalpha)
Processive synthesis on the C-strand of the telomere
Synthesis and interconversion of nucleotide di- and triphosphates
Telomere C-strand synthesis initiation
Telomere Extension By Telomerase

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