EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	A0W351848Z
EPA CompTox	DTXSID001027198

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

A0W351848Z

EPA CompTox

DTXSID001027198


InChI Key	BOHCOUQZNDPURZ-UHFFFAOYSA-N
Smiles	CCC(C)C1NC(=O)CNC(=O)C2CC3=C(NC4=CC=CC=C34)S(=O)CC(NC(=O)CNC1=O)C(=O)NC(CC(N)=O)C(=O)N1CC(O)CC1C(=O)NC(C(C)C(O)CO)C(=O)N2
InChI	InChI=1S/C39H54N10O13S/c1-4-17(2)31-36(59)42-12-29(54)43-25-16-63(62)38-21(20-7-5-6-8-22(20)46-38)10-23(33(56)41-13-30(55)47-31)44-37(60)32(18(3)27(52)15-50)48-35(58)26-9-19(51)14-49(26)39(61)24(11-28(40)53)45-34(25)57/h5-8,17-19,23-27,31-32,46,50-52H,4,9-16H2,1-3H3,(H2,40,53)(H,41,56)(H,42,59)(H,43,54)(H,44,60)(H,45,57)(H,47,55)(H,48,58)

InChI Key

BOHCOUQZNDPURZ-UHFFFAOYSA-N

Smiles

CCC(C)C1NC(=O)CNC(=O)C2CC3=C(NC4=CC=CC=C34)S(=O)CC(NC(=O)CNC1=O)C(=O)NC(CC(N)=O)C(=O)N1CC(O)CC1C(=O)NC(C(C)C(O)CO)C(=O)N2

InChI

InChI=1S/C39H54N10O13S/c1-4-17(2)31-36(59)42-12-29(54)43-25-16-63(62)38-21(20-7-5-6-8-22(20)46-38)10-23(33(56)41-13-30(55)47-31)44-37(60)32(18(3)27(52)15-50)48-35(58)26-9-19(51)14-49(26)39(61)24(11-28(40)53)45-34(25)57/h5-8,17-19,23-27,31-32,46,50-52H,4,9-16H2,1-3H3,(H2,40,53)(H,41,56)(H,42,59)(H,43,54)(H,44,60)(H,45,57)(H,47,55)(H,48,58)

Property Name	Value
Molecular Formula	C39H54N10O13S1
Molecular Weight	902.36
AlogP	1.31
Hydrogen Bond Acceptor	13.0
Hydrogen Bond Donor	13.0
Number of Rotational Bond	7.0
Polar Surface Area	386.07
Heavy Atoms	63.0

Property Name

Value

Molecular Formula

C39H54N10O13S1

Molecular Weight

902.36

AlogP

1.31

Hydrogen Bond Acceptor

13.0

Hydrogen Bond Donor

13.0

Number of Rotational Bond

7.0

Polar Surface Area

386.07

Heavy Atoms

63.0

Resources	Reference
CAS NUMBER	58311-65-2
NORMAN SUSDAT
FDA SRS	A0W351848Z

Resources

Reference

CAS NUMBER

58311-65-2

NORMAN SUSDAT

FDA SRS

A0W351848Z

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, Volume 54, Issue D1, 6 January 2026, Pages D1397–D1404, https://doi.org/10.1093/nar/gkaf1251

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

Last update: Monday, 3 November 2025

AMANINAMIDE

Structure

Physicochemical Descriptors

Cross References