NAP

Molecular formula
C21 H28 N7 O17 P3
Molecular weight (g/mol)
743.41
Classification
COFACTOR

Related PDB structures · 1

Names & identifiers

IUPAC name
NADP NICOTINAMIDE-ADENINE-DINUCLEOTIDE PHOSPHATE
SMILES
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
Isomeric SMILES
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)OP(=O)(O)O)O)O)O)C(=O)N
InChI
InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
XJLXINKUBYWONI-NNYOXOHSSA-N
CAS
53-59-8

Chemical & physical properties

HBA
19
HBD
8
TPSA (Ų)
367.62
cLogP
-3.53
Chiral atoms
9
Molar refractivity
148.07
Rings
5
Aromatic rings
3
Fraction Csp³
0.48
Formal charge
0

Calculated properties

QED0.062
Low High
0.062
NPScore0.10521115
Low High
0.105
SAScore8.792109442
Easy Difficult
8.792

Related databases

Experimental bioactivity

Activity against NPIM proteins

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Protein / UniProtOrganismActivityCommentSourceReferenceDetails

Activity against other proteins

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Protein / UniProtOrganismActivityCommentSourceReferenceDetails