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19896-54-9

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19896-54-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19896-54-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,8,9 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 19896-54:
(7*1)+(6*9)+(5*8)+(4*9)+(3*6)+(2*5)+(1*4)=169
169 % 10 = 9
So 19896-54-9 is a valid CAS Registry Number.

19896-54-9Downstream Products

19896-54-9Relevant articles and documents

The chemistry of the West and Central African Penianthus zenkeri Diels (Menispermaceae)

Akak, Carine Mvot,Azebaze, Anatole Guy Blaise,Frese, Marcel,Happi, Gervais Mouthé,Langat, Moses K.,Lenta, Bruno N.,Neumann, Beate,Nkengfack, Augustin E.,Sewald, Norbert,Stammler, Hans-Georg,Tabekoueng, Georges Bellier,Vardamides, Juliette Catherine,Waffo, Alain Fran?ois Kamdem,Wansi, Jean Duplex

, p. 12 - 18 (2020)

A phytochemical investigation of the roots and twigs of Penianthus zenkeri Diels led to the identification of twenty four compounds including one previously undescribed C-28 ecdysteroid (1) and previously described phytosteroids (2–5, 20, 22, 23), phenolic compounds (6–8, 12), diterpenoids (9–11), alkaloids (13,14, 18, 19), a dipeptide (15), ursane type triterpenoids (16–17), a carbohydrate (21) and a fatty alcohol (24). Three semi-synthetic derivatives (5b, 5a, 17a) obtained from acetylation and acetonidation of rubrosterone (5), and allylation of ursolic acid (17), respectively, are also reported. The chemical structures of the compounds were determined using 1D and 2D NMR spectral data, mass spectrometry and by comparison with the data reported in the literature. The absolute configuration of compound 9 was established using X-Ray and ECD analysis. Different extracts of the twigs and roots, compounds 2–4, 6–11, 15, and 17–21 were evaluated for their antibacterial, and cytotoxic activities. The twigs extract showed an antibacterial activity with an MIC of 62.5 μg/mol against Staphylococcus aureus ATCC 4300, while ursolic acid exhibited a moderate cytotoxicity with an IC50 of 50.9 μM. The chemotaxonomic relevance of the isolated compounds is discussed.

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