CARBAMOTHIOIC ACID,(1,2,3-THIADIAZOLE-4-YLCARBONYL)-,S-BUTYL ESTER


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	NTLMQMFVZSFMQU-UHFFFAOYSA-N
Smiles	CCCCSC(=O)NC(=O)c1csnn1
InChI	InChI=1S/C8H11N3O2S2/c1-2-3-4-14-8(13)9-7(12)6-5-15-11-10-6/h5H,2-4H2,1H3,(H,9,12,13)

Physicochemical Descriptors

Property Name	Value
Molecular Formula	C8H11N3O2S2
Molecular Weight	245.32
AlogP	2.33
Hydrogen Bond Acceptor	5.0
Hydrogen Bond Donor	1.0
Number of Rotational Bond	5.0
Polar Surface Area	125.49
Molecular species	NEUTRAL
Aromatic Rings	1.0
Heavy Atoms	15.0

Assay Description	Organism	Bioactivity
Fungistatic activity against Alternaria kikuchiana assessed as inhibition of mycelial growth measured at 5 ug/mL at 28 degC after 72 hr relative to control	Alternaria kikuchiana	32.0 %
Fungistatic activity against Alternaria kikuchiana assessed as inhibition of mycelial growth measured at 50 ug/mL at 28 degC after 72 hr relative to control	Alternaria kikuchiana	36.0 %
Fungistatic activity against Fusarium graminearum assessed as inhibition of mycelial growth measured at 5 ug/mL at 28 degC after 72 hr relative to control	Fusarium graminearum	0.0 %
Fungistatic activity against Fusarium graminearum assessed as inhibition of mycelial growth measured at 50 ug/mL at 28 degC after 72 hr relative to control	Fusarium graminearum	10.0 %

Cross References

Resources	Reference
ChEMBL	CHEMBL2252742
PubChem	11242026

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).