EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	5UDJ46528K
EPA CompTox	DTXSID90883122

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

5UDJ46528K

EPA CompTox

DTXSID90883122


InChI Key	MDWNFWDBQGOKNZ-XYUDZHFQSA-N
Smiles	CC(=O)N[C@H]1[C@H](O[C@H]2[C@@H](O)[C@@H](NC(C)=O)[C@H](O[C@@H]3[C@@H](CO)[C@@H]4OC(N(C)C)=N[C@@H]4[C@H]3O)O[C@@H]2CO)O[C@H](CO)[C@@H](O)[C@H]1O
InChI	InChI=1S/C25H42N4O14/c1-8(33)26-14-17(36)16(35)11(6-31)39-23(14)42-22-12(7-32)40-24(15(19(22)38)27-9(2)34)41-21-10(5-30)20-13(18(21)37)28-25(43-20)29(3)4/h10-24,30-32,35-38H,5-7H2,1-4H3,(H,26,33)(H,27,34)/t10-,11+,12+,13+,14+,15+,16+,17-,18+,19-,20-,21+,22+,23-,24-/m0/s1

InChI Key

MDWNFWDBQGOKNZ-XYUDZHFQSA-N

Smiles

CC(=O)N[C@H]1[C@H](O[C@H]2[C@@H](O)[C@@H](NC(C)=O)[C@H](O[C@@H]3[C@@H](CO)[C@@H]4OC(N(C)C)=N[C@@H]4[C@H]3O)O[C@@H]2CO)O[C@H](CO)[C@@H](O)[C@H]1O

InChI

InChI=1S/C25H42N4O14/c1-8(33)26-14-17(36)16(35)11(6-31)39-23(14)42-22-12(7-32)40-24(15(19(22)38)27-9(2)34)41-21-10(5-30)20-13(18(21)37)28-25(43-20)29(3)4/h10-24,30-32,35-38H,5-7H2,1-4H3,(H,26,33)(H,27,34)/t10-,11+,12+,13+,14+,15+,16+,17-,18+,19-,20-,21+,22+,23-,24-/m0/s1

Property Name	Value
Molecular Formula	C25H42N4O14
Molecular Weight	622.27
AlogP	-4.37
Hydrogen Bond Acceptor	16.0
Hydrogen Bond Donor	9.0
Number of Rotational Bond	9.0
Polar Surface Area	268.54
Heavy Atoms	43.0

Property Name

Value

Molecular Formula

C25H42N4O14

Molecular Weight

622.27

AlogP

-4.37

Hydrogen Bond Acceptor

16.0

Hydrogen Bond Donor

9.0

Number of Rotational Bond

9.0

Polar Surface Area

268.54

Heavy Atoms

43.0

Resources	Reference
CAS NUMBER	103782-08-7
NORMAN SUSDAT
FDA SRS	5UDJ46528K
PubChem	119339

Resources

Reference

CAS NUMBER

103782-08-7

NORMAN SUSDAT

FDA SRS

5UDJ46528K

PubChem

119339

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

ALLOSAMIDIN

Structure

Physicochemical Descriptors

Cross References