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145033-48-3

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145033-48-3 Usage

General Description

Digalactosyldiacylglycerol (DGDG) is a type of glycolipid found in the thylakoid membrane of chloroplasts in plants. It consists of two galactose molecules linked to a diacylglycerol backbone and is an important component of the photosynthetic machinery. DGDG plays a crucial role in the structural organization and stability of the thylakoid membrane, and it also participates in the transfer of electrons during the light reactions of photosynthesis. Additionally, DGDG has been linked to the maintenance of membrane fluidity and the response to environmental stress in plants, making it a significant molecule for plant adaptation and survival.

Check Digit Verification of cas no

The CAS Registry Mumber 145033-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,0,3 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145033-48:
(8*1)+(7*4)+(6*5)+(5*0)+(4*3)+(3*3)+(2*4)+(1*8)=103
103 % 10 = 3
So 145033-48-3 is a valid CAS Registry Number.

145033-48-3Upstream product

145033-48-3Downstream Products

145033-48-3Relevant articles and documents

Synthesis of digalactosyl diacylglycerols and their structure-inhibitory activity on human lanosterol synthase

Tanaka, Rie,Sakano, Yuichi,Nagatsu, Akito,Shibuya, Masaaki,Ebizuka, Yutaka,Goda, Yukihiro

, p. 159 - 162 (2007/10/03)

Digalactosyl and monogalactocyl diacylglycerols, were synthesized. DGDG with two myristoyl groups at both sn-1 and sn-2 positions showed the most potent inhibitory activity on human lanosterol synthase. Digalactosyl and monogalactocyl diacylglycerols (DGDG and MGDG), which were identified as anti-hyperlipemia active components in Colocasia esculenta (Taro), were synthesized. The inhibitory activity of DGDG, MGDG and related compounds on human lanosterol synthase was evaluated as anti-hyperlipemic activity. DGDG with two myristoyl groups at both sn-1 and sn-2 positions and with an oleoyl group at the sn-1 position showed the most potent activity.

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