EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	V9LX869GRG

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

V9LX869GRG


InChI Key	XZDDTAKXLUVBPD-RVTZKUCMSA-N
Smiles	CC[C@H]1CCC[C@H](O[C@H]2CC[C@H](NC)[C@@H](C)O2)[C@@H](C)C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(C)=C[C@H]3[C@@H]2CC(=O)O1)O[C@@H]1O[C@@H](C)[C@H](OC)[C@@H](OC)[C@H]1OC
InChI	InChI=1S/C41H65NO10/c1-10-25-12-11-13-34(52-36-15-14-33(42-6)23(4)48-36)22(3)37(44)32-19-30-28(31(32)20-35(43)50-25)16-21(2)27-17-26(18-29(27)30)51-41-40(47-9)39(46-8)38(45-7)24(5)49-41/h16,19,22-31,33-34,36,38-42H,10-15,17-18,20H2,1-9H3/t22-,23-,24+,25+,26-,27+,28-,29-,30-,31+,33+,34+,36+,38+,39-,40-,41+/m1/s1

InChI Key

XZDDTAKXLUVBPD-RVTZKUCMSA-N

Smiles

CC[C@H]1CCC[C@H](O[C@H]2CC[C@H](NC)[C@@H](C)O2)[C@@H](C)C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(C)=C[C@H]3[C@@H]2CC(=O)O1)O[C@@H]1O[C@@H](C)[C@H](OC)[C@@H](OC)[C@H]1OC

InChI

InChI=1S/C41H65NO10/c1-10-25-12-11-13-34(52-36-15-14-33(42-6)23(4)48-36)22(3)37(44)32-19-30-28(31(32)20-35(43)50-25)16-21(2)27-17-26(18-29(27)30)51-41-40(47-9)39(46-8)38(45-7)24(5)49-41/h16,19,22-31,33-34,36,38-42H,10-15,17-18,20H2,1-9H3/t22-,23-,24+,25+,26-,27+,28-,29-,30-,31+,33+,34+,36+,38+,39-,40-,41+/m1/s1

Property Name	Value
Molecular Formula	C41H65N1O10
Molecular Weight	731.46
AlogP	5.54
Hydrogen Bond Acceptor	11.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	9.0
Polar Surface Area	120.01
Heavy Atoms	52.0

Property Name

Value

Molecular Formula

C41H65N1O10

Molecular Weight

731.46

AlogP

5.54

Hydrogen Bond Acceptor

11.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

9.0

Polar Surface Area

120.01

Heavy Atoms

52.0

Resources	Reference
CAS NUMBER	149439-70-3
NORMAN SUSDAT
FDA SRS	V9LX869GRG
PubChem	101145238

Resources

Reference

CAS NUMBER

149439-70-3

NORMAN SUSDAT

FDA SRS

V9LX869GRG

PubChem

101145238

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

N-DEMETHYLSPINOSYN D

Structure

Physicochemical Descriptors

Cross References