1-PALMITOYL-2-(3-TRANS)-HEXADECENOYL-SN-GLYCERO-3-PHOSPHOGLYCEROL


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	BIABMEZBCHDPBV-UHFFFAOYSA-N
Smiles	CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCC(O)CO)OC(=O)CCCCCCCCCCCCCCC
InChI	InChI=1S/C38H75O10P/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-37(41)45-33-36(34-47-49(43,44)46-32-35(40)31-39)48-38(42)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h35-36,39-40H,3-34H2,1-2H3,(H,43,44)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C38H75O10P
Molecular Weight	722.97
AlogP	11.46
Hydrogen Bond Acceptor	10.0
Hydrogen Bond Donor	3.0
Number of Rotational Bond	40.0
Polar Surface Area	158.63
Molecular species	ACID
Aromatic Rings	0.0
Heavy Atoms	49.0

Assay Description	Organism	Bioactivity
Insecticidal activity against Aphis gossypii (cotton aphid) infested fourth-leaf stage cucumber seedlings followed by compound exposure at 1000 ug/ml assessed as induction of insect death on leaves after 48 hr post compound treatment relative to untreated control	Aphis gossypii	None
Insecticidal activity against Aphis gossypii (cotton aphid) infested fourth-leaf stage cucumber seedlings followed by compound exposure assessed as insect control after 48 hr post compound treatment relative to untreated control	Aphis gossypii	None
Insecticidal activity against Aphis gossypii (cotton aphid) infested fourth-leaf stage cucumber seedlings followed by compound exposure at 250 to 1000 ug/ml assessed as insect control after 48 hr post compound treatment relative to untreated control	Aphis gossypii	45.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2286758
PubChem	65144
SureChEMBL	SCHEMBL13587396

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).