EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	T74307G2D9
EPA CompTox	DTXSID0036502

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

T74307G2D9

EPA CompTox

DTXSID0036502


InChI Key	ZGDZDAPCWHIIKB-LVYWIKMTSA-N
Smiles	C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2OC(=O)c1ccccc1
InChI	InChI=1S/C26H34O3/c1-25-14-12-19(27)16-18(25)8-9-20-21-10-11-23(26(21,2)15-13-22(20)25)29-24(28)17-6-4-3-5-7-17/h3-7,18,20-23H,8-16H2,1-2H3/t18-,20-,21-,22-,23-,25-,26-/m0/s1

InChI Key

ZGDZDAPCWHIIKB-LVYWIKMTSA-N

Smiles

C[C@]12CC[C@H]3[C@@H](CC[C@H]4CC(=O)CC[C@]34C)[C@@H]1CC[C@@H]2OC(=O)c1ccccc1

InChI

InChI=1S/C26H34O3/c1-25-14-12-19(27)16-18(25)8-9-20-21-10-11-23(26(21,2)15-13-22(20)25)29-24(28)17-6-4-3-5-7-17/h3-7,18,20-23H,8-16H2,1-2H3/t18-,20-,21-,22-,23-,25-,26-/m0/s1

Property Name	Value
Molecular Formula	C26H34O3
Molecular Weight	394.25
AlogP	5.82
Hydrogen Bond Acceptor	3.0
Number of Rotational Bond	2.0
Polar Surface Area	43.37
Heavy Atoms	29.0

Property Name

Value

Molecular Formula

C26H34O3

Molecular Weight

394.25

AlogP

5.82

Hydrogen Bond Acceptor

3.0

Number of Rotational Bond

2.0

Polar Surface Area

43.37

Heavy Atoms

29.0

Resources	Reference
CAS NUMBER	1057-07-4
NORMAN SUSDAT
FDA SRS	T74307G2D9
PubChem	13987
ChemSpider	13379.0

Resources

Reference

CAS NUMBER

1057-07-4

NORMAN SUSDAT

FDA SRS

T74307G2D9

PubChem

13987

ChemSpider

13379.0

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, 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

DIHYDROTESTOSTERONE BENZOATE

Structure

Physicochemical Descriptors

Cross References