EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
EPA CompTox	DTXSID60988274

Keyword(s):

Human Metabolites

Molecule Category

Free-form

EPA CompTox

DTXSID60988274


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70


InChI Key	LVBSECZFJBGOCR-UHFFFAOYSA-N
Smiles	O=C([O-])C(CCCCCCCCCCCC)[N+](C)(C)C
InChI	InChI=1/C17H35NO2/c1-5-6-7-8-9-10-11-12-13-14-15-16(17(19)20)18(2,3)4/h16H,5-15H2,1-4H3

InChI Key

LVBSECZFJBGOCR-UHFFFAOYSA-N

Smiles

O=C([O-])C(CCCCCCCCCCCC)[N+](C)(C)C

InChI

InChI=1/C17H35NO2/c1-5-6-7-8-9-10-11-12-13-14-15-16(17(19)20)18(2,3)4/h16H,5-15H2,1-4H3

Property Name	Value
Molecular Formula	C17H36NO2
Molecular Weight	285.27
AlogP	3.12
Hydrogen Bond Acceptor	2.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	13.0
Polar Surface Area	40.13
Molecular species	None
Aromatic Rings	0.0
Heavy Atoms	20.0

Property Name

Value

Molecular Formula

C17H36NO2

Molecular Weight

285.27

AlogP

3.12

Hydrogen Bond Acceptor

2.0

Hydrogen Bond Donor

0.0

Number of Rotational Bond

13.0

Polar Surface Area

40.13

Molecular species

None

Aromatic Rings

0.0

Heavy Atoms

20.0

Resources	Reference
CAS NUMBER	686-83-9
NORMAN SUSDAT
PubChem	101833

Resources

Reference

CAS NUMBER

686-83-9

NORMAN SUSDAT

PubChem

101833


PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

(1-CARBOXYLATOTRIDECYL)TRIMETHYLAMMONIUM

Structure

Physicochemical Descriptors

Cross References