5-METHOXY-2,2-DIMETHYL-2H-CHROMENE-8-CARBOXYLIC ACID METHYLESTER


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	BUWAHMOFPHKQKA-UHFFFAOYSA-N
Smiles	COC(=O)c1ccc(OC)c2C=CC(C)(C)Oc12
InChI	InChI=1S/C14H16O4/c1-14(2)8-7-9-11(16-3)6-5-10(12(9)18-14)13(15)17-4/h5-8H,1-4H3

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C14H16O4
Molecular Weight	248.27
AlogP	2.46
Hydrogen Bond Acceptor	4.0
Hydrogen Bond Donor	0.0
Number of Rotational Bond	3.0
Polar Surface Area	44.76
Molecular species	None
Aromatic Rings	1.0
Heavy Atoms	18.0

Assay Description	Organism	Bioactivity
Termiticidal activity against Coptotermes formosanus (third-instar worker and soldier) assessed as mortality at 0.5% wt/wt at 26.6 degC, 100% RH measured after 5 days	Coptotermes formosanus	100.0 %
Termiticidal activity against Coptotermes formosanus (third-instar worker and soldier) assessed as mortality at 1% wt/wt at 26.6 degC, 100% RH measured after 3 days (Rvb= 0%)	Coptotermes formosanus	2.5 %
Termiticidal activity against Coptotermes formosanus (third-instar worker and soldier) assessed as mortality at 1% wt/wt at 26.6 degC, 100% RH measured after 17 days (Rvb= 5 +/- 4.1%)	Coptotermes formosanus	100.0 %
Termiticidal activity against Coptotermes formosanus (third-instar worker and soldier) assessed as mortality at 1% wt/wt at 26.6 degC, 100% RH measured after 21 days (Rvb= 1.3 +/- 2.5 to 5 +/- 4.1%)	Coptotermes formosanus	100.0 %
Termiticidal activity against Coptotermes formosanus (third-instar worker and soldier) assessed as mortality at 1% wt/wt at 26.6 degC, 100% RH measured after 9 days (Rvb= 3.8 +/- 4.8%)	Coptotermes formosanus	61.3 %
Termiticidal activity against Coptotermes formosanus (third-instar worker and soldier) assessed as mortality at 1% wt/wt at 26.6 degC, 100% RH measured after 7 days (Rvb= 3.8 +/- 4.8%)	Coptotermes formosanus	30.0 %
Termiticidal activity against Coptotermes formosanus (third-instar worker and soldier) assessed as mortality at 1% wt/wt at 26.6 degC, 100% RH measured after 15 days (Rvb= 1.3 +/- 2.5 to 5 +/- 4.1%)	Coptotermes formosanus	96.3 %
Termiticidal activity against Coptotermes formosanus (third-instar worker and soldier) assessed as mortality at 1% wt/wt at 26.6 degC, 100% RH measured after 1 day (Rvb= 0%)	Coptotermes formosanus	0.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2287246
PubChem	76320145

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).