EcoDrugPlus


Keyword(s):	Natural Toxins
Molecule Category	Free-form
EPA CompTox	DTXSID20930259

Keyword(s):

Natural Toxins

Molecule Category

Free-form

EPA CompTox

DTXSID20930259


InChI Key	FVFQELHSZVFPDZ-VIFPVBQESA-N
Smiles	CC(C)([C@@H]1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)O
InChI	InChI=1S/C14H14O5/c1-14(2,17)9-6-8-5-7-3-4-10(15)19-12(7)11(16)13(8)18-9/h3-5,9,16-17H,6H2,1-2H3/t9-/m0/s1

InChI Key

FVFQELHSZVFPDZ-VIFPVBQESA-N

Smiles

CC(C)([C@@H]1CC2=C(O1)C(=C3C(=C2)C=CC(=O)O3)O)O

InChI

InChI=1S/C14H14O5/c1-14(2,17)9-6-8-5-7-3-4-10(15)19-12(7)11(16)13(8)18-9/h3-5,9,16-17H,6H2,1-2H3/t9-/m0/s1

Property Name	Value
Molecular Formula	C14H14O5
Molecular Weight	262.08
AlogP	1.57
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	1.0
Polar Surface Area	79.9
Heavy Atoms	19.0

Property Name

Value

Molecular Formula

C14H14O5

Molecular Weight

262.08

AlogP

1.57

Hydrogen Bond Acceptor

5.0

Hydrogen Bond Donor

2.0

Number of Rotational Bond

1.0

Polar Surface Area

79.9

Heavy Atoms

19.0

Resources	Reference
CAS NUMBER	13895-92-6
NORMAN SUSDAT
PubChem	44146779
ChemSpider	29365150.0

Resources

Reference

CAS NUMBER

13895-92-6

NORMAN SUSDAT

PubChem

44146779

ChemSpider

29365150.0

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

9-HYDROXY-2-(2-HYDROXYPROPAN-2-YL)-2,3-DIHYDRO-7H-FURO[3,2-G][1]BENZOPYRAN-7-ONE (RUTARETIN)

Structure

Physicochemical Descriptors

Cross References