Metabolomics Structure Database

MDLMOL SDF CSV TSV

MW REGNO:	63787
Common Name:	Pictrelisib
Systematic Name:	2-(1H-indazol-4-yl)-6-{[4-(methylsulfonyl)piperazin-1-yl]methyl}-4-(morpholin-4-yl)thieno[3,2-d]pyrimidine
Synonyms:	GDC0941 [PubChem Synonyms]
Exact Mass:	513.1617 (neutral)    Calculate m/z: (Choose adduct) [M+H]+ [M+H-H2O]+ [M.]+ [M+2H]2+ [M+3H]3+ [M+4H]4+ [M+K]+ [M+2K]2+ [M-H+2K]+ [M+Na]+ [M+2Na]2+ [M-H+2Na]+ [M+Li]+ [M+2Li]2+ [M+NH4]+ [M-H]- [M-2H]2- [M-3H]3- [M-4H]4- [M+Cl]- [M+OAc]- [M+HCOO]- M(neutral)
Formula:	C23H27N7O3S2
InChIKey:	LHNIIDJUOCFXAP-UHFFFAOYSA-N
ClassyFire superclass:	Organoheterocyclic compounds [C0000002]
ClassyFire class:	Thienopyrimidines [C0002020]
ClassyFire subclass:	Thienopyrimidines [C0002020]
ClassyFire direct parent:	Aromatic heteropolycyclic compounds
SMILES:	CS(=O)(=O)N1CCN(CC1)Cc1cc2c(c(nc(c3cccc4c3cn[nH]4)n2)N2CCOCC2)s1
Studies:	-

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All Database Links Calculated Properties Human Pathways

External database links:

PubChem CID:	17755052
CHEBI ID:	65326
HMDB ID:	HMDB0252659
EPA CompTox DB:	DTXCID70164421

Calculated physicochemical properties (?):

Heavy Atoms:	35
Rings:	6
Aromatic Rings:	4
Rotatable Bonds:	4
van der Waals Molecular volume:	407.97 Å3 molecule-1
Toplogical Polar Sufrace Area:	109.62 Å2 molecule-1
Hydrogen Bond Donors:	1
Hydrogen Bond Acceptors:	9
logP:	5.35
Molar Refractivity:	141.12
Fraction sp3 Carbons:	0.43
sp3 Carbons:	10

Human Pathway links:

REACTOME pathways containing this metabolite

References

LIPID MAPS classification: "Update of the LIPID MAPS comprehensive classification system for lipids", Fahy E, Subramaniam S, Murphy RC, Nishijima M, Raetz CR, Shimizu T, Spener F, van Meer G, Wakelam MJ, and Dennis EA, J. Lipid Res. (2009) 50: S9-S14. DOI: 10.1194/jlr.R800095-JLR200
ClassyFire classification: "ClassyFire: automated chemical classification with a comprehensive, computable taxonomy", Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS, J. Cheminformatics (2016) 8:61. DOI: 10.1186/s13321-016-0174-y