COCHLIOQUINONE B


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	NTPNSKLZWVYKGK-WWURSIHSSA-N
Smiles	CC[C@H](C)C(=O)[C@@H](C)C1=CC(=O)C2=C(O[C@]3(C)CC[C@H]4O[C@H](CC[C@]4(C)[C@H]3C2)C(C)(C)O)C1=O
InChI	InChI=1S/C28H40O6/c1-8-15(2)23(30)16(3)17-13-19(29)18-14-20-27(6)11-9-21(26(4,5)32)33-22(27)10-12-28(20,7)34-25(18)24(17)31/h13,15-16,20-22,32H,8-12,14H2,1-7H3/t15-,16-,20+,21+,22+,27+,28+/m0/s1

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C28H40O6
Molecular Weight	472.61
AlogP	4.03
Hydrogen Bond Acceptor	6.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	5.0
Polar Surface Area	89.9
Molecular species	NEUTRAL
Aromatic Rings	0.0
Heavy Atoms	34.0

Assay Description	Organism	Bioactivity
Inhibition of Solanum tuberosum (potato) tuber electron transport protein complex 4 activity	Solanum tuberosum	None
Inhibition of Solanum tuberosum (potato) tuber electron transport protein complex 3 activity	Solanum tuberosum	None
Inhibition of Solanum tuberosum (potato) tuber electron transport protein complex 2 activity	Solanum tuberosum	None
Inhibition of Solanum tuberosum (potato) tuber succinate oxidase activity at 3600 nmol/mg protein	Solanum tuberosum	None
Inhibition of Solanum tuberosum (potato) tuber proton-pump NADH dehydrogenase activity assessed per mg protein	Solanum tuberosum	3000.0 nM
Inhibition of Bos taurus (bovine) heart mitochondrial electron transport protein complex 4 assessed per mg protein	Bos taurus	3600.0 nM
Inhibition of Bos taurus (bovine) heart mitochondrial electron transport protein complex 2 assessed per mg protein	Bos taurus	3600.0 nM
Inhibition of Bos taurus (bovine) heart mitochondrial electron transport protein complex 3 assessed per mg protein	Bos taurus	3600.0 nM
Inhibition of Bos taurus (bovine) heart mitochondrial electron transport protein complex 2/3 assessed per mg protein	Bos taurus	3600.0 nM
Inhibition of Bos taurus (bovine) heart mitochondrial NADPH oxidase activity assessed per mg protein	Bos taurus	83.0 nM
Inhibition of Bos taurus (bovine) heart mitochondrial electron transport protein complex 1 assessed per mg protein	Bos taurus	370.0 nM
Octanol-water partition coefficient, log K of the compound by reversed-phase HPLC	None	0.437
Phytotoxicity in Oryza sativa (rice) seedlings assessed as assessed as inhibition of root growth at 100 ppm at 26 degC for 72 hr	Oryza sativa	None
Phytotoxicity against Lolium multiflorum (Italian ryegrass) seedlings assessed as inhibition of root growth at 100 ppm at 26 degC for 72 hr	Lolium multiflorum	None

Cross References

Resources	Reference
ChEMBL	CHEMBL2288169

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).

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).