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6-BENZOOXAZOL-2-YL-BENZOTHIAZOL-2-YLAMINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

301321-03-9

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301321-03-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 301321-03-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,1,3,2 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 301321-03:
(8*3)+(7*0)+(6*1)+(5*3)+(4*2)+(3*1)+(2*0)+(1*3)=59
59 % 10 = 9
So 301321-03-9 is a valid CAS Registry Number.

301321-03-9Downstream Products

301321-03-9Relevant academic research and scientific papers

Discovery of 2-(2-aminobenzo[d]thiazol-6-yl) benzo[d]oxazol-5-amine derivatives that regulated HPV relevant cellular pathway and prevented cervical cancer from abnormal proliferation

Jiao, Peili,Wang, Yuxi,Mao, Beibei,Wang, Bingding,Zhong, Yi,Jin, Hongwei,Zhang, Lihe,Zhang, Liangren,Liu, Zhenming

, (2020)

Human papillomavirus (HPV) is a well-established etiological factor for cervical cancer, and the expression of oncogenic protein E7 is crucial for carcinogenesis. Herein, virtual screening was performed and 2-(2-aminobenzo[d]thiazol-6-yl) benzo[d]oxazol-5-amine derivatives were designed, synthesized as antineoplastic agents, and evaluated for their anti-tumor activities. Among them, the most promising compound H1 showed specific anti-proliferation ability against HeLa cells (IC50 = 380 nM) as well as excellent inhibition of tumor growth in the HeLa xenograft model without inducing obvious side effects. It is interesting that compound H1 displayed significant inhibition against HPV18-positive cervical cell lines (HeLa) but not for HPV16-positive cervical cell lines (SiHa). Further study demonstrated that a low concentration of compound H1 could lead to a cell cycle blockage at the G1 phase and promote cell apoptosis slightly (8.77%). Compound H1 also exhibited transcription repression, especially those associated with the oncoprotein E7 cellular pathway like E7/Rb/E2F-1/DNMT1, which were essential in tumorigenesis. Proteomics analysis revealed that E7 might be degraded through E3 ubiquitin ligases, which aligned with decreasing expression of E7 following the treatment of compound H1. Taken together, it indicated that compound H1 could be a promising potential agent for cervical cancer treatment.

Synthesis and antitumor activity evaluation of NEW 2-(4-aminophenyl) benzothiazole/oxazole/imidazole derivatives

El-Arab, Elham Ezz,El-Said,Amine,Moharram

, p. 967 - 984 (2017/04/17)

A NEW series of 2-(4-aminophenyl)benzothiazole and related structure compounds, bearing thiocyanate, thiol in the 3'postion as well as new condensed benzothiazoles and related structure compounds having thiazolones,tetrazole, oxadiazole have been synthesized. All the newly synthesized compounds were screened for their anti-tumor activities. The results revealed promising effects against most of the cancer cell lines.

Synthesis and Antitumor Activity Evaluation of New 2-(4-aminophenyl) benzothiazole/oxazole/imidazole Derivatives

El-Arab, Elham Ezz,El-Said,Amine,Moharram

, p. 967 - 984 (2017/04/17)

A NEW series of 2-(4-aminophenyl)benzothiazole and related structure compounds, bearing thiocyanate, thiol in the 3′postion as well as new condensed benzothiazoles and related structure compounds having thiazolones, tetrazole, oxadiazole have been synthesized. All the newly synthesized compounds were screened for their anti-tumor activities. The results revealed promising effects against most of the cancer cell lines.

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