NAD(1−)
chemical compound
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NAD(1−)
Summary
NAD(1−) is a group of stereoisomers[1].
Key Facts
- NAD(1−)'s instance of is recorded as group of stereoisomers[2].
- NAD(1−)'s CAS Registry Number is recorded as 76961-04-1[3].
- NAD(1−)'s canonical SMILES is recorded as NC(=O)c1cccn+c1n+c1">[4].
- NAD(1−)'s InChI is recorded as InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/p-1/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1[5].
- NAD(1−)'s InChIKey is recorded as BAWFJGJZGIEFAR-NNYOXOHSSA-M[6].
- NAD(1−)'s chemical formula is recorded as C₂₁H₂₆N₇O₁₄P₂[7].
- NAD(1−)'s subclass of is recorded as chemical compound[8].
- NAD(1−)'s part of is recorded as glycerophosphate shuttle[9].
- NAD(1−)'s part of is recorded as NAD metabolic process[10].
- NAD(1−)'s part of is recorded as NAD+ binding[11].
- NAD(1−)'s PubChem CID is recorded as 15938971[12].
- NAD(1−)'s ChEBI ID is recorded as 57540[13].
- NAD(1−)'s isomeric SMILES is recorded as NC(=O)c1cccn+[C@@H]1OC@HC@@H[C@H]1On+[C@@H]1OC@HC@@H[C@H]1O">[14].
- NAD(1−)'s mass is recorded as {'unit': 'http://www.wikidata.org/entity/Q483261', 'amount': '+662.1018453519099'}[15].
- NAD(1−)'s subject has role is recorded as primary metabolite[16].
- NAD(1−)'s DSSTox substance ID is recorded as DTXSID201016357[17].
- NAD(1−)'s UniChem compound ID is recorded as 1103750[18].