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(3S,4R,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-3,9-Bis-benzyloxy-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydro-picene-4-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

186415-74-7

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186415-74-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 186415-74-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,6,4,1 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 186415-74:
(8*1)+(7*8)+(6*6)+(5*4)+(4*1)+(3*5)+(2*7)+(1*4)=157
157 % 10 = 7
So 186415-74-7 is a valid CAS Registry Number.

186415-74-7Relevant academic research and scientific papers

Preventive effects of soyasapogenol B derivatives on liver injury in a concanavalin A-induced hepatitis model

Sasaki, Kazue,Minowa, Nobuto,Kuzuhara, Hiroyuki,Nishiyama, Shoji

, p. 4900 - 4911 (2007/10/03)

To shed light on the structure-activity relationship, various soyasapogenol B derivatives were synthesized and evaluated for preventive effects on liver injury in the concanavalin A (Con A)-induced hepatitis model in mice. Con A injection into mice induces some pathophysiology of human liver disease such as autoimmune or viral hepatitis. Two hydroxyl groups on the A ring of soyasapogenol B are required for amelioration of liver damage. Modification of the C-22 hydroxyl moiety with an acyloxy or alkyloxy group, or removal of the hydroxyl group, resulted in a greatly enhanced percentage of alleviation. Among the series of soyasapogenol B derivatives examined, six compounds exhibited preventive effects on liver damage.

Synthesis and hepatoprotective effects of soyasapogenol B derivatives

Sasaki, Kazue,Minowa, Nobuto,Kuzuhara, Hiroyuki,Nishiyama, Shoji,Omoto, Shoji

, p. 85 - 88 (2007/10/03)

Derivatives of soyasapogenol B (1), which is the aglycon moiety of soyasaponins from soybean, were synthesized and evaluated for their hepatoprotective effects in vitro.

Medicinal foodstuffs. VI. Histamine release inhibitors from kidney bean, the seeds of Phaseolus vulgaris L.: Chemical structures of sandosaponins A and B

Yoshikawa, Masayuki,Shimada, Hiromi,Komatsu, Hajime,Sakurama, Tetsuo,Nishida, Norihisa,Yamahara, Johji,Shimoda, Hiroshi,Matsuda, Hisashi,Tani, Tadato

, p. 877 - 882 (2007/10/03)

Two new olean-12-ene-type triterpene oligoglycosides, named sandsaponins A and B, were isolated from kidney bean, the seed of Phaseoulus vulgaris L., together with three known saponins, soyasaponins I and V and dehydrosoyasaponin I. The structures of sand

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