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2-(5-chlorobenzothiazol-2-yl)-4-methoxyphenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

30616-45-6

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30616-45-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 30616-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,6,1 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 30616-45:
(7*3)+(6*0)+(5*6)+(4*1)+(3*6)+(2*4)+(1*5)=86
86 % 10 = 6
So 30616-45-6 is a valid CAS Registry Number.

30616-45-6Downstream Products

30616-45-6Relevant academic research and scientific papers

2-(Benzothiazol-2-yl)-phenyl-β-d-galactopyranoside derivatives as fluorescent pigment dyeing substrates and their application for the assay of β-d-galactosidase activities

Otsubo, Tadamune,Minami, Akira,Fujii, Haruna,Taguchi, Risa,Takahashi, Tadanobu,Suzuki, Takashi,Teraoka, Fumiteru,Ikeda, Kiyoshi

, p. 2245 - 2249 (2013)

2-(Benzothiazol-2-yl)-phenyl-β-d-galactopyranoside derivatives were synthesized as novel artificial fluorescent pigment dyeing substrates for β-d-galactosidase. The substrates, which exhibited non-fluorescence or weak fluorescence in solution phase, were

Synthesis, and In Vitro and In Silico α-Glucosidase Inhibitory Studies of 5-Chloro-2-Aryl Benzo[d]thiazoles

Shah, Shazia,Arshia,Javaid, Kulsoom,Zafar, Humaira,Mohammed Khan, Khalid,Khalil, Ruqaiya,Ul-Haq, Zaheer,Perveen, Shahnaz,Iqbal Choudhary

, p. 269 - 279 (2018/04/05)

Twenty-five derivatives of 5-chloro-2-aryl benzo[d]thiazole (1–25) were synthesized and evaluated for their α-glucosidase (S. cerevisiae EC 3.2.1.20) inhibitory activity in vitro. Among them eight compounds showed potent activity with IC50 values between 22.1 ± 0.9 and 136.2 ± 5.7 μM, when compared with standard acarbose (IC50 = 840 ± 1.73 μM). The most potent compounds 4, 9, and 10 showed IC50 values in the range of 22.1 ± 0.9 to 25.6 ± 1.5 μM. Compounds 2, 5, 11, and 19 showed IC50 values within the range of 40.2 ± 0.5 to 60.9 ± 2.0 μM. Compounds 1 and 3 were also found to be good inhibitors with IC50 values 136.2 ± 5.7 and 104.8 ± 9.9 μM, respectively. Their activities were compared with α-glucosidase inhibitor drug acarbose (standard) (IC50 = 840 ± 1.73 μM). The remaining compounds were inactive. Structure-activity relationships (SAR) have also been established. Kinetics studies indicated compounds 2, 3, 10, 19, and 25 to be non-competitive, while 1, 5, 9, and 11 as competitive inhibitors of α-glucosidase enzyme. All the active compounds (1–5, 9–11, and 19) were also found to be non-cytotoxic, in comparison to the standard drug i.e., doxorubicin (IC50 = 0.80 ± 0.12 μM) in MTT assay. Furthermore, molecular interactions of active compounds with the enzyme binding sites were predicted through molecular modeling studies.

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