In ZINC since | Heavy atoms | Benign functionality |
---|---|---|
November 10th, 2008 | 29 | No |
Popular Name: Uridine-5'-triphosphoric acid trisodium salt Uridine-5'-triphosphoric acid tr…
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]
"Uridine 5'-triphosphate trisodium salt hydrate, 95%"
5'-UTP; H4utp; uridine 5'-triphosphoric acid
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
Uridine 5'-triphosphate tris salt
Uridine 5'-Triphosphate Trisodium Salt Hydrate
Uridine 5'-triphosphate, trisodium salt, hydrate, 90%
uridine triphosphate trisodium
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
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) | -4.57 | -4.59 | -370.18 | 3 | 17 | -4 | 276 | 480.108 | 8 | ↓ |
Mid Mid (pH 6-8) | -4.57 | -5.75 | -234.35 | 4 | 17 | -3 | 273 | 481.116 | 8 | ↓ |
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 |
Therapy | psychostimulant | SMDC MicroSource |
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 |
Code | Description | Organism Class | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
P2RY2-1-E | Purinergic Receptor P2Y2 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 60 | 0.35 | Functional ≤ 10μM |
P2RY2-1-E | Purinergic Receptor P2Y2 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 130 | 0.33 | Functional ≤ 10μM |
P2RY4-1-E | Pyrimidinergic Receptor P2Y4 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 90 | 0.34 | Functional ≤ 10μM |
P2RY4-1-E | Pyrimidinergic Receptor P2Y4 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 90 | 0.34 | Functional ≤ 10μM |
P2RY6-1-E | Pyrimidinergic Receptor P2Y6 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 6000 | 0.25 | Functional ≤ 10μM |
P2RY6-1-E | Pyrimidinergic Receptor P2Y6 (cluster #1 Of 1), Eukaryotic | Eukaryotes | 6000 | 0.25 | Functional ≤ 10μM |
Uniprot | Swissprot | Description | Affinity (nM) | LE (kcal/mol/atom) | Type |
---|---|---|---|---|---|
P2RY2_MOUSE | P35383 | P2Y Purinoceptor 2, Mouse | 1260 | 0.28 | Functional ≤ 10μM |
P2RY2_RAT | P41232 | Purinergic Receptor P2Y2, Rat | 130 | 0.33 | Functional ≤ 10μM |
P2RY2_HUMAN | P41231 | Purinergic Receptor P2Y2, Human | 17.9 | 0.37 | Functional ≤ 10μM |
P2RY4_HUMAN | P51582 | Pyrimidinergic Receptor P2Y4, Human | 80 | 0.34 | Functional ≤ 10μM |
P2RY4_RAT | O35811 | Pyrimidinergic Receptor P2Y4, Rat | 2600 | 0.27 | Functional ≤ 10μM |
P2RY6_HUMAN | Q15077 | Pyrimidinergic Receptor P2Y6, Human | 6000 | 0.25 | Functional ≤ 10μM |
Description | Species |
---|---|
G alpha (i) signalling events | |
G alpha (q) signalling events | |
P2Y receptors |