EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	49M19XFI8B
EPA CompTox	DTXSID7044893

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

49M19XFI8B

EPA CompTox

DTXSID7044893


InChI Key	JMOLZNNXZPAGBH-UHFFFAOYSA-N
Smiles	CCCCCCCCC(CCCCCC)C(O)=O
InChI	InChI=1S/C16H32O2/c1-3-5-7-9-10-12-14-15(16(17)18)13-11-8-6-4-2/h15H,3-14H2,1-2H3,(H,17,18)

InChI Key

JMOLZNNXZPAGBH-UHFFFAOYSA-N

Smiles

CCCCCCCCC(CCCCCC)C(O)=O

InChI

InChI=1S/C16H32O2/c1-3-5-7-9-10-12-14-15(16(17)18)13-11-8-6-4-2/h15H,3-14H2,1-2H3,(H,17,18)

Property Name	Value
Molecular Formula	C16H32O2
Molecular Weight	256.24
AlogP	5.41
Hydrogen Bond Acceptor	1.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	13.0
Polar Surface Area	37.3
Heavy Atoms	18.0

Property Name

Value

Molecular Formula

C16H32O2

Molecular Weight

256.24

AlogP

5.41

Hydrogen Bond Acceptor

1.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

13.0

Polar Surface Area

37.3

Heavy Atoms

18.0

Resources	Reference
CAS NUMBER	25354-97-6
NORMAN SUSDAT
FDA SRS	49M19XFI8B
PubChem	32912
ChemSpider	30486.0

Resources

Reference

CAS NUMBER

25354-97-6

NORMAN SUSDAT

FDA SRS

49M19XFI8B

PubChem

32912

ChemSpider

30486.0

EcoDrug+ was developed under the PREMIER 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 EcoDrug+ contains.

Elements of EcoDrug+ were developed under the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT Center for Science Ltd is thanked for providing computational resources. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

Content of EcoDrug+ is provided without guarantee for correctness.

Cite Us:

Ashenafi Legehar, Siobhán Monaghan, Mael Briand, Akseli Niemelä, Leo Ghemtio, Ziaurrehman Tanoli, A Ross Brown, Charles R Tyler, Henri Xhaard, EcoDrug PLUS: an advanced database for drug target conservation analysis and environmental risk assessment, Nucleic Acids Research, 2025, gkaf1251 Read...

This work is licensed under Creative Commons Attribution-ShareAlike 4.0 International License

Last update: Monday, 3 November 2025

2-HEXYLDECANOIC ACID

Structure

Physicochemical Descriptors

Cross References