UCSF

ZINC95617495

Draw Identity 99% 90% 80% 70%

Substance Information

In ZINC since Heavy atoms Benign functionality
January 16th, 2014 0 No

Popular Name: Uridine triphosphate Uridine triphosphate

Find On: PubMed — Wikipedia — Google

CAS Numbers: 108321-53-5 , 116295-90-0 , 19817-92-6 , 285978-18-9 , 63-39-8 , [19817-92-6] , [285978-18-9]

Other Names:

({[(2R,3S,4R,5R)-5-(2,4-dioxo-3H-pyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methoxy(hydroxy)phosphoryl}oxy(hydroxy)phosphoryl)oxyphosphonic acid

5'-UTP; BRN 0071520; C9H15N2O15P3; EINECS 200-558-7; INS316; INS365 Ophthalmic Solution; LS-160841; UTP; Uridine 5'-(tetrahydrogen triphosphate); Uridine 5'-triphosphate; Uridine 5'-triphosphoric acid; Uridine triphosphate; Uridine, 5'-(tetrahydrogen trip

5'-UTP; BRN 0071520; URIDINE 5'-TRIPHOSPHATE; UTP; Uridine 5'-(tetrahydrogen triphosphate); Uridine 5'-triphosphoric acid; Uridine triphosphate; Uteplex; bmse000295

5'-UTP; H4utp; uridine 5'-triphosphoric acid

5'-UTP; Uridine 5'-triphosphate; Uridine mono(tetrahydrogen triphosphate); Uridine triphosphate; Uridine triphosphic acid; Uteplex; UTP

5'-UTP; UTP; Uridine 5'-triphosphate; Uridine mono(tetrahydrogen triphosphate); Uridine triphosphate; Uteplex

5'-UTP;Uridine 5'-triphosphate;Uridine mono(tetrahydrogen triphosphate);Uridine triphosphate;Uteplex;UTP

5'-UTP;UTP;Uridine 5'-triphosphate;Uridine mono(tetrahydrogen triphosphate);Uridine triphosphate;Uteplex

63-39-8; C00075; UTP; Uridine 5'-triphosphate; Uridine triphosphate

63-39-8; UTP; uridine-5'-triphosphate; uridine-triphosphate

CHEBI:13510; CHEBI:9850; CHEBI:27233

MFCD00044310

MFCD00058360

MFCD00150714

MFCD00274571

MFCD11101450

QB-2953

SS-7954

Uridine 5'-triphosphate

Uridine 5'-triphosphate tris salt

Uridine 5'-triphosphate, trisodium salt, hydrate, 90%

URIDINE-13C9, 15N2-5 TRIPHOSPHATE SODI U

URIDINE-13C9,15N2-5TRIPHOSPHATESODIU

Uridine-5'-triphosphate disodium salt

Uridine-5'-triphosphate trisodium salt

Uridine-5'-triphosphate trisodium salt dihydrate

Uridine-5'-triphosphoric acid trisodium salt

Uridine5'-(tetrahydrogen triphosphate)

UTP

UTP (3-); UTP trianion

UTP(3-)

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
Mp [°C] >140 Acros Organics
UniProt Database Links ACKA_SALTY; ACKA_THEMA; ACTH_THEAC; ACTH_THEVO; AGLF_HALVD; ARC_RHOER; CBACL_PSEUC; CDA_MYROD; CELA_GLUXY; COFE_METJA; DER_THEMA; DGK_BACSU; ENPP1_HUMAN; ENPP1_MOUSE; ENPP1_RAT; ENTP2_HUMAN; ENTP4_HUMAN; ENTP7_HUMAN; ENTP7_MOUSE; ENTP7_PONAB; ENTP7_XENTR ChEBI
Reactome Database Links REACT_1082; REACT_1094; REACT_1138; REACT_1160; REACT_1179; REACT_1374; REACT_1467; REACT_15538; REACT_1611; REACT_1638; REACT_1645; REACT_18287; REACT_18310; REACT_2030; REACT_2053; REACT_209; REACT_21273; REACT_21292; REACT_21305; REACT_21362; REACT_214 ChEBI
S phrase S24/25: Avoid contact with skin and eyes. Acros Organics
Patent Database Links US2007219224; WO2007089703 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
DNA replication initiation
Formation of the active cofactor, UDP-glucuronate
Formation of the Early Elongation Complex
G alpha (i) signalling events
Glycogen synthesis
P2Y receptors
RNA Polymerase I Chain Elongation
RNA Polymerase II Pre-transcription Events
RNA Polymerase II Promoter Escape
RNA Polymerase II Transcription Elongation
RNA Polymerase II Transcription Initiation
RNA Polymerase III Abortive And Retractive Initiation
RNA Polymerase III Chain Elongation
Synthesis and interconversion of nucleotide di- and triphosphates
Synthesis of UDP-N-acetyl-glucosamine
Telomere C-strand synthesis initiation

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

No pre-computed analogs available. Try a structural similarity search.