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Neobotogenin, also known as neobutoxin, is a synthetic chemical compound that is structurally similar to botulinum toxin, a neurotoxin produced by the bacterium Clostridium botulinum. It is designed to mimic the effects of botulinum toxin, which is commonly used in medical treatments for conditions such as muscle spasms and cosmetic procedures to reduce wrinkles. Neobotogenin works by inhibiting the release of acetylcholine, a neurotransmitter responsible for muscle contraction, thus relaxing the muscles and reducing their activity. neobotogenin has potential applications in various medical fields, but it is important to note that its safety, efficacy, and regulatory status may vary, and it should only be used under the guidance of a qualified healthcare professional.

467-57-2

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467-57-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 467-57-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,6 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 467-57:
(5*4)+(4*6)+(3*7)+(2*5)+(1*7)=82
82 % 10 = 2
So 467-57-2 is a valid CAS Registry Number.

467-57-2Upstream product

467-57-2Relevant academic research and scientific papers

The NMR studies on two new furostanol saponins from Agave sisalana leaves

Zou, Peng,Fu, Jing,Yu, He-Shui,Zhang, Jie,Kang, Li-Ping,Ma, Bai-Ping,Yan, Xian-Zhong

, p. 1090 - 1095 (2008/02/04)

The detailed NMR studies and full assignments of the 1H and 13C spectral data for two new furostanol saponins isolated from Agave sisalana leaves are described. Their structures were established using a combination of 1D and 2D NMR techniques including 1H, 13C, 1H-1H COSY, TOCSY, HSQC, HMBC and HSQC-TOCSY, and also FAB-MS spectrometry and chemical methods. The structures were established as (25S)-26-(β-D-glucopyranosyl)-22ξ-hydroxyfurost-12-one-3β-yl-O- α-L-rhamnopyranosyl-(1→4)-β-D-glucopyranosyl-(1→3) -O-[O-β-D-glucopyranosyl-(1→2)]-O-β-D-glucopyranosyl-(1→4) -β-D-galactopyranoside (1) and (25S)-26-(β-D-glucopyranosyl)-22ξ- hydroxyfurost-5-en-12-one-3ξ-yl-O-α-L-rhamnopyranosyl-(1→4) -β-D-glucopyranosyl-(1→3)-O-[O-β-D-glucopyranosyl-(1→2)] -O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranoside (2). Copyright

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