EcoDrugPlus


Molecule Category	Free-form
UNII	0CV8D1DR96
EPA CompTox	DTXSID1020649
Source	Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...

Molecule Category

Free-form

UNII

EPA CompTox

DTXSID1020649

Source

Gaulton A, Kale N, van Westen GJ, Bellis LJ, Bento AP, Davies M, Hersey A, Papadatos G, Forster M, Wege P, Overington JP. A large-scale crop protection bioassay data set. Sci Data. 2015 Jul 7;2:150032. Read more ...


InChI Key	LNISAMDQAWTXQV-DUFIIWHPSA-N
Smiles	CC(=O)O[C@@H]1C[C@@H](O)[C@H]2O[C@@H]3C=C(C)C(=O)[C@@H](O)[C@]3(CO)[C@]1(C)[C@@]24CO4
InChI	InChI=1S/C18H24O8/c1-8-4-12-17(6-19,14(23)13(8)22)16(3)11(25-9(2)20)5-10(21)15(26-12)18(16)7-24-18/h4,10-12,14-15,19,21,23H,5-7H2,1-3H3/t10-,11-,12-,14-,15-,16-,17-,18-/m1/s1

InChI Key

LNISAMDQAWTXQV-DUFIIWHPSA-N

Smiles

CC(=O)O[C@@H]1C[C@@H](O)[C@H]2O[C@@H]3C=C(C)C(=O)[C@@H](O)[C@]3(CO)[C@]1(C)[C@@]24CO4

InChI

InChI=1S/C18H24O8/c1-8-4-12-17(6-19,14(23)13(8)22)16(3)11(25-9(2)20)5-10(21)15(26-12)18(16)7-24-18/h4,10-12,14-15,19,21,23H,5-7H2,1-3H3/t10-,11-,12-,14-,15-,16-,17-,18-/m1/s1

Property Name	Value
Molecular Formula	C18H24O8
Molecular Weight	368.38
AlogP	-1.64
Hydrogen Bond Acceptor	8.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	3.0
Polar Surface Area	125.82
Molecular species	NEUTRAL
Aromatic Rings	0.0
Heavy Atoms	26.0

Property Name

Value

Molecular Formula

C18H24O8

Molecular Weight

368.38

AlogP

-1.64

Hydrogen Bond Acceptor

8.0

Hydrogen Bond Donor

3.0

Number of Rotational Bond

3.0

Polar Surface Area

125.82

Molecular species

NEUTRAL

Aromatic Rings

0.0

Heavy Atoms

26.0

Resources	Reference
CAS NUMBER	23255-69-8
ChEMBL	CHEMBL2251641
FDA SRS	0CV8D1DR96
PubChem	76329955

Resources

Reference

CAS NUMBER

ChEMBL

FDA SRS

PubChem

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

4-ACETYLNIVALENOL

Structure

Physicochemical Descriptors

Cross References