2D Structure

3D Structure

Benzothiazole


Properties
PID PID00105
Mol. Weight 135.184 g/mol
LogP 2.01
Water solubility slightly soluble in water
Hydrogen Bond Donor 0
Hydrogen Bond Acceptor 2
Rotatable Bonds 0
XLogP3 2.0

Benzothiazole

Identifiers
Formula C7H5NS
PubChem CID 7222
FEMA 3256
Flavor Profile Odor Similar To That Of Quinoline, Unpleasant Odor; Nut, Rubber
Smiles c1ccc2scnc2c1
InChl Key IOJUPLGTWVMSFF-UHFFFAOYSA-N
InChl InChI=1S/C7H5NS/c1-2-4-7-6(3-1)8-5-9-7/h1-5H
CAS Registry Number 95-16-9
IUPAC Systematic Name 1,3-benzothiazole

Organ Location Map/System Distribution of Pungent Flavor Compounds’ Targets


Note: Known Targets (Gene) from 6952 literatures, DrugBank (http://www.drugbank.ca/), STITCH (http://stitch.embl.de/), ChEMBL (https://www.ebi.ac.uk/chembl/), Therapeutic Target Database (http://bidd.nus.edu.sg/group/ttd/), and Comparative Toxicogenomics Database (CTD, http://ctdbase.org/)


Related Pungent TCM

English Name Pinyin Name (Chinese Name) Latin Name Properties in TCM merdians View Graph
Rhizoma TyphoniiBai Fu Zi(白附子)rhizome of Giant TyphoniumWarm,Pungent,SweetSpleen,Liver,HeartView Graph
SafflowerHong Hua (红花)Carthami FlosWarm,PungentSpleen, Stomach, Kidney, LungView Graph
Odoriferous RosewoodJiang Xiang (降香)Dalbergiae odoriferae LignumWarm, PungentLung, Spleen, StomachView Graph
PLATYCODONIS RADIXJu Gen(桔梗)Radix Citri reticulataeNeural,Bitter,PungentLungView Graph
Fresh Common GingerSheng Jiang (生姜)Zingiber Rhizoma RecensWarm, PungentLung, Spleen, StomachView Graph
Chinese ClematisWei Ling Xian (威灵仙)Clematidis Radix Et RhizomaWarm, Pungent, SaltyBladderView Graph

Pharmacological action

Benzothiazole is an aromatic heterocyclic compound with the chemical formula C7H5NS. It is colorless, slightly viscous liquid. Although the parent compound, benzothiazole is not widely used, many of its derivatives are found in commercial products or in nature. Firefly luciferin can be considered a derivative of benzothiazole. Benzothiazole has potential activity against malarial and microbial infections.Benzothiazole is antimycobacterial agent of control the Sclerotinia sclerotiorum, Ditylenchus destructor, and Tribolium castaneum.



Note: Click anywhere in the blank, you can drag the whole dynamic diagram. Click on a node, you can drag his location to see it more clearly. The blue circle represents pharmacology, toxicology, or daily use. Orange hexagon represents the pungent compounds.

References

1. Thakkar, S. S., Thakor, P., Ray, A., Doshi, H., & Thakkar, V. R. Benzothiazole analogues: synthesis, characterization, MO calculations with PM6 and DFT, in silico studies and in vitro antimalarial as DHFR inhibitors and antimicrobial activities[J]. Bioorganic & medicinal chemistry, 2017, 25(20): 5396-5406.

2. Landge, S., Mullick, A. B., Nagalapur, K., Neres, J., Subbulakshmi, V., Murugan, K., Mahadevaswamy, J. Discovery of benzothiazoles as antimycobacterial agents: synthesis, structure–activity relationships and binding studies with Mycobacterium tuberculosis decaprenylphosphoryl-β-d-ribose 2′-oxidase[J]. Bioorganic & medicinal chemistry, 2015, 23(24): 7694-7710.

3. Reshma, R. S., Jeankumar, V. U., Kapoor, N., Saxena, S., Bobesh, K. A., Vachaspathy, A. R., Sriram, D. Mycobacterium tuberculosis lysine-ɛ-aminotransferase a potential target in dormancy: Benzothiazole based inhibitors[J]. Bioorganic & medicinal chemistry, 2017, 25(10): 2761-2771.

4. Zhao, Y., Cui, K., Xu, C., Wang, Q., Wang, Y., Zhang, Z., Mu, W. Proteomic profile of the Bradysia odoriphaga in response to the microbial secondary metabolite benzothiazole[J]. Scientific reports, 2016, 6: 37730.

5. Peng, X., Xie, G., Wang, Z., Lin, H., Zhou, T., Xiang, P., Zhao, Y. SKLB-163, a new benzothiazole-2-thiol derivative, exhibits potent anticancer activity by affecting RhoGDI/JNK-1 signaling pathway[J]. Cell death & disease, 2014, 5(3): e1143.

6. Fernando, W. D., Ramarathnam, R., Krishnamoorthy, A. S., & Savchuk, S. C. Identification and use of potential bacterial organic antifungal volatiles in biocontrol[J]. Soil Biology and Biochemistry, 2005, 37(5): 955-964.

7. Liu, W., Ji, J., Wang, C., Mu, W., & Liu, F. Evaluation and identification of the potential nematicidal volatiles produced by Bacillus subtilis[J]. Acta Phytopathologica Sinica, 2009, 39(3): 304-309.

8. Zhao, L. J., Yang, X. N., Li, X. Y., Wei, M. U., & Feng, L. I. U. Antifungal, insecticidal and herbicidal properties of volatile components from Paenibacillus polymyxa strain BMP-11[J]. Agricultural Sciences in China, 2011, 10(5): 728-736.