EcoDrugPlus


Keyword(s):	Natural Toxins
Molecule Category	Free-form
EPA CompTox	DTXSID00989846

Keyword(s):

Natural Toxins

Molecule Category

Free-form

EPA CompTox

DTXSID00989846


InChI Key	DFDVWAJDFYYBAC-UHFFFAOYSA-N
Smiles	C[C@@H]1[C@@H]([C@@H](C[C@@H](O1)O[C@H]2CC[C@]3([C@@H](C2)CC[C@]45[C@@H]3CC[C@@](C4=O)([C@H](CC5)C6=CC(=O)OC6)C)C)OC)O
InChI	InChI=1S/C30H44O7/c1-17-26(32)22(34-4)15-25(36-17)37-20-6-9-28(2)19(14-20)5-11-30-12-7-21(18-13-24(31)35-16-18)29(3,27(30)33)10-8-23(28)30/h13,17,19-23,25-26,32H,5-12,14-16H2,1-4H3

InChI Key

DFDVWAJDFYYBAC-UHFFFAOYSA-N

Smiles

C[C@@H]1[C@@H]([C@@H](C[C@@H](O1)O[C@H]2CC[C@]3([C@@H](C2)CC[C@]45[C@@H]3CC[C@@](C4=O)([C@H](CC5)C6=CC(=O)OC6)C)C)OC)O

InChI

InChI=1S/C30H44O7/c1-17-26(32)22(34-4)15-25(36-17)37-20-6-9-28(2)19(14-20)5-11-30-12-7-21(18-13-24(31)35-16-18)29(3,27(30)33)10-8-23(28)30/h13,17,19-23,25-26,32H,5-12,14-16H2,1-4H3

Property Name	Value
Molecular Formula	C30H44O7
Molecular Weight	516.31
AlogP	4.35
Hydrogen Bond Acceptor	7.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	4.0
Polar Surface Area	91.29
Heavy Atoms	37.0

Property Name

Value

Molecular Formula

C30H44O7

Molecular Weight

516.31

AlogP

4.35

Hydrogen Bond Acceptor

7.0

Hydrogen Bond Donor

1.0

Number of Rotational Bond

4.0

Polar Surface Area

91.29

Heavy Atoms

37.0

Resources	Reference
CAS NUMBER	69686-84-6
NORMAN SUSDAT
PubChem	434211
ChemSpider	384004.0

Resources

Reference

CAS NUMBER

69686-84-6

NORMAN SUSDAT

PubChem

434211

ChemSpider

384004.0

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, 2025, gkaf1251 Read...

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

Last update: Monday, 3 November 2025

10,12B-DIMETHYL-13-OXO-9-(5-OXO-2,5-DIHYDROFURAN-3-YL)TETRADECAHYDRO-1H-6A,10-METHANOCYCLOOCTA[A]NAPHTHALEN-3-YL 2,6-DIDEOXY-3-O-METHYLHEXOPYRANOSIDE (OLEASIDE A)

Structure

Physicochemical Descriptors

Cross References