EcoDrugPlus


Keyword(s):	Human Metabolites
Molecule Category	Free-form
UNII	CQ2F5O6YIY
EPA CompTox	DTXSID40956057

Keyword(s):

Human Metabolites

Molecule Category

Free-form

UNII

CQ2F5O6YIY

EPA CompTox

DTXSID40956057


InChI Key	BNMGUJRJUUDLHW-UHFFFAOYSA-N
Smiles	CC1CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO)C5C(O)CC34C)C2C1C)C(=O)OC6OC(COC7OC(CO)C(OC8OC(C)C(O)C(O)C8O)C(O)C7O)C(O)C(O)C6O
InChI	InChI=1S/C48H78O20/c1-19-10-11-48(13-12-46(6)22(28(48)20(19)2)8-9-27-44(4)14-24(52)39(61)45(5,18-50)38(44)23(51)15-47(27,46)7)43(62)68-42-35(59)32(56)30(54)26(66-42)17-63-40-36(60)33(57)37(25(16-49)65-40)67-41-34(58)31(55)29(53)21(3)64-41/h8,19-21,23-42,49-61H,9-18H2,1-7H3

InChI Key

BNMGUJRJUUDLHW-UHFFFAOYSA-N

Smiles

CC1CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO)C5C(O)CC34C)C2C1C)C(=O)OC6OC(COC7OC(CO)C(OC8OC(C)C(O)C(O)C8O)C(O)C7O)C(O)C(O)C6O

InChI

InChI=1S/C48H78O20/c1-19-10-11-48(13-12-46(6)22(28(48)20(19)2)8-9-27-44(4)14-24(52)39(61)45(5,18-50)38(44)23(51)15-47(27,46)7)43(62)68-42-35(59)32(56)30(54)26(66-42)17-63-40-36(60)33(57)37(25(16-49)65-40)67-41-34(58)31(55)29(53)21(3)64-41/h8,19-21,23-42,49-61H,9-18H2,1-7H3

Property Name	Value
Molecular Formula	C48H78O20
Molecular Weight	974.51
AlogP	-2.06
Hydrogen Bond Acceptor	20.0
Hydrogen Bond Donor	13.0
Number of Rotational Bond	9.0
Polar Surface Area	335.44
Heavy Atoms	68.0

Property Name

Value

Molecular Formula

C48H78O20

Molecular Weight

974.51

AlogP

-2.06

Hydrogen Bond Acceptor

20.0

Hydrogen Bond Donor

13.0

Number of Rotational Bond

9.0

Polar Surface Area

335.44

Heavy Atoms

68.0

Resources	Reference
CAS NUMBER	34540-22-2
NORMAN SUSDAT
FDA SRS	CQ2F5O6YIY

Resources

Reference

CAS NUMBER

34540-22-2

NORMAN SUSDAT

FDA SRS

CQ2F5O6YIY

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

MADECASSOSIDE

Structure

Physicochemical Descriptors

Cross References