UCSF

ZINC12405084

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Substance Information

In ZINC since Heavy atoms Benign functionality
May 13th, 2008 27 No

Popular Name: IDP IDP

Find On: PubMed — Wikipedia — Google

CAS Numbers: 54735-61-4 , 81012-88-6 , 86-04-4 , [54735-61-4]

Other Names:

'Inosine-5''-diphosphate disodium salt'

5'-IDP; EINECS 201-648-9; IDP; Inosine 5'-(trihydrogen diphosphate); Inosine 5'-(trihydrogen pyrophosphate); Inosine 5'-diphosphate; Inosine 5'-pyrophosphate; Inosine diphosphate; Inosine pyrophosphate; LS-84008; Riboxin; Riboxine

5'-IDP; IDP; Inosine 5'-(trihydrogen diphosphate); Inosine 5'-(trihydrogen pyrophosphate) ; Inosine 5'-diphosphate; Inosine 5'-pyrophosphate; Inosine diphosphate; Inosine pyrophosphate; Riboxin; Riboxine

5'-IDP; IDP; Inosine 5'-(trihydrogen diphosphate); Inosine 5'-(trihydrogen pyrophosphate); Inosine 5'-diphosphate; Inosine 5'-pyrophosphate; Inosine diphosphate; Inosine pyrophosphate; Riboxin; Riboxine

5'-IDP; IDP; Inosine 5'-(trihydrogen diphosphate); Inosine 5'-(trihydrogen pyrophosphate); Inosine 5'-diphosphate; Inosine 5'-pyrophosphate; Inosine diphosphate; Inosine pyrophosphate; Riboxine

5'-IDP;IDP;Inosine 5'-(trihydrogen diphosphate);Inosine 5'-(trihydrogen pyrophosphate) ;Inosine 5'-diphosphate;Inosine 5'-pyrophosphate;Inosine diphosphate;Inosine pyrophosphate;Riboxin;Riboxine

5'-OO-[(phosphonatooxy)phosphinato]inosine; IDP; IDP trianion; inosine 5'-diphosphate(3-)

86-04-4; C00104; IDP; Inosine 5'-diphosphate; Inosine diphosphate

CHEBI:43252; CHEBI:5848; CHEBI:13371; CHEBI:19270

IDP(3-)

Inosine 5'-(trihydrogen diphosphate), disodium salt

Inosine 5'-pyrophosphate

Inosine-5'-diphosphate disodium salt

Inosine-5'-diphosphate trisodium salt

Inosine-5'-diphosphoric acid disodium salt

MFCD00043058

MFCD00211028

{[(2R,3S,4R)-3,4-dihydroxy-5-(6-oxo-3H-purin-9-yl)oxolan-2-yl]methoxy(hydroxy)phosphoryl}oxyphosphonic acid

Download: MOL2 SDF SMILES Flexibase

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
Ref Reference (pH 7) -3.49 -2.36 -259.56 3 15 -3 235 425.163 6 ↓
Hi High (pH 8-9.5) -3.04 -4.43 -320.42 2 15 -4 238 424.155 6 ↓
Mid Mid (pH 6-8) -3.49 -3.51 -139.61 4 15 -2 232 426.171 6 ↓

Vendor Notes

Note Type Comments Provided By
UniProt Database Links ADPRM_ARATH; ADPRM_BOVIN; ADPRM_DANRE; ADPRM_HUMAN; ADPRM_MOUSE; ADPRM_ORYSJ; ADPRM_RAT; ADPRM_XENLA; ADPRM_XENTR; ENTP5_AILME; ENTP5_BOVIN; ENTP5_CHICK; ENTP5_HUMAN; ENTP5_MESAU; ENTP5_MOUSE; ENTP5_RAT; ENTP6_HUMAN; ENTP6_RAT; IDH1_CANTR; IDH1_COLMA; IDH ChEBI
PUBCHEM_PATENT_ID EP0346865A2; EP0781851A3; EP1008657A2; EP1009854A1; US4587044; US4826824; US4845028; US5219732; US5891702; US5952203; US6103487; WO1991000346A1; WO1992001781A1; WO1998046784A1; WO1999010523A1; WO1999010524A1; WO2000016626A1; WO2000025789A1; WO2000059930A1 IBM Patent Data
Reactome Database Links REACT_150396 ChEBI

Activity (Go SEA)

Direct Reactome Annotations (via ChEBI)

Description Species
Phosphate bond hydrolysis by NUDT proteins

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