4-METHYL-2-[2-(3-METHYLBUTAN-2-YLIDENE)HYDRAZINO]BENZO[D]THIAZOLE


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	USSSDGIHKDXNMQ-XNTDXEJSSA-N
Smiles	CC(C)\C(=N\Nc1nc2c(C)cccc2s1)\C
InChI	InChI=1S/C13H17N3S/c1-8(2)10(4)15-16-13-14-12-9(3)6-5-7-11(12)17-13/h5-8H,1-4H3,(H,14,16)/b15-10+

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C13H17N3S
Molecular Weight	247.36
AlogP	4.0
Hydrogen Bond Acceptor	3.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	3.0
Polar Surface Area	65.52
Molecular species	NEUTRAL
Aromatic Rings	2.0
Heavy Atoms	17.0

Assay Description	Organism	Bioactivity
Fungicidal activity against Rhizoctonia solani assessed as inhibition rate of circle mycelium growth at 500 ug/ml	Rhizoctonia solani	60.0 %
Fungicidal activity against Ustilaginoidea oryzae assessed as inhibition rate of circle mycelium growth at 500 ug/ml	Ustilaginoidea	5.0 %
Fungicidal activity against Alternaria alternata assessed as inhibition rate of circle mycelium growth at 500 ug/ml	Alternaria alternata	56.5 %
Fungicidal activity against Phytophthora capsici assessed as inhibition rate of circle mycelium growth at 500 ug/ml	Phytophthora capsici	0.0 %
Fungicidal activity against Fusarium graminearum assessed as inhibition rate of circle mycelium growth at 500 ug/ml	Fusarium graminearum	0.0 %
Fungicidal activity against Botryotinia fuckeliana assessed as inhibition rate of circle mycelium growth at 500 ug/ml	Botryotinia fuckeliana	70.8 %
Fungicidal activity against Sclerotinia sclerotiorum assessed as inhibition rate of circle mycelium growth at 500 ug/ml	Sclerotinia sclerotiorum	90.6 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2268719
PubChem	76330422

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).