PERENNIPORIDE C

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Search structure


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 ...


Active Pharmaceutical Ingredients Bioactive chemicals	Exact Similarity SubStructure	Threshold (%) >= 70

Structure


InChI Key	OQWJPFFTMZHPBR-FSPWUOQZSA-N
Smiles	CCc1c(O)c2C(=O)C[C@@]3(OC)O[C@H](C[C@@]3(O)c2cc1OC)C(=O)OC
InChI	InChI=1S/C18H22O8/c1-5-9-12(23-2)6-10-14(15(9)20)11(19)7-18(25-4)17(10,22)8-13(26-18)16(21)24-3/h6,13,20,22H,5,7-8H2,1-4H3/t13-,17-,18-/m1/s1

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C18H22O8
Molecular Weight	366.36
AlogP	1.11
Hydrogen Bond Acceptor	8.0
Hydrogen Bond Donor	2.0
Number of Rotational Bond	5.0
Polar Surface Area	111.52
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	26.0

Assay Description	Organism	Bioactivity	Reference
Antifungal activity against Alternaria longipes CGMCC 3.2875 at 20 ug/ml after 48 hr by Alamar blue assay	Alternaria longipes	None
Antifungal activity against Fusarium graminearum CGMCC 3.2873 at 20 ug/ml after 48 hr by Alamar blue assay	Fusarium graminearum	None
Antifungal activity against Fusarium oxysporum CGMCC 3.2830 at 20 ug/ml after 48 hr by Alamar blue assay	Fusarium oxysporum	None
Antifungal activity against Verticillium albo-atrum CGMCC 3.4306 at 20 ug/ml after 48 hr by Alamar blue assay	Verticillium albo-atrum	None
Antifungal activity against Fusarium verticillioides CGMCC 3.2835 at 20 ug/ml after 48 hr by Alamar blue assay	Fusarium verticillioides	None

Cross References

Resources	Reference
ChEMBL	CHEMBL2253039
PubChem	60199565

CONTENTS

PREMIER has received funding from the 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 this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).