942997-00-4 Usage
Uses
Used in Pharmaceutical Industry:
Nigelloside C is used as a potential therapeutic agent for its anti-inflammatory properties, which can help in reducing inflammation and alleviating symptoms associated with various inflammatory conditions.
Nigelloside C is used as a potential anti-cancer agent for its ability to inhibit the growth of certain cancer cells. Its anti-cancer properties can be utilized in the development of novel cancer treatments and therapies.
Used in Nutraceutical Industry:
Nigelloside C is used as a natural antioxidant, which can help in protecting the body from oxidative stress and damage caused by free radicals. Its antioxidant properties can be incorporated into dietary supplements and functional foods for promoting overall health and well-being.
Used in Cosmetic Industry:
Nigelloside C is used as an ingredient in cosmetic products for its potential anti-inflammatory and antioxidant properties. It can be utilized in skincare formulations to provide anti-aging, soothing, and protective benefits to the skin.
Used in Immunomodulation:
Nigelloside C is used as an immunomodulatory agent for its ability to modulate the immune system. It can be employed in the development of immunotherapies and treatments for autoimmune diseases and other conditions where immune system regulation is required.
Check Digit Verification of cas no
The CAS Registry Mumber 942997-00-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,2,9,9 and 7 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 942997-00:
(8*9)+(7*4)+(6*2)+(5*9)+(4*9)+(3*7)+(2*0)+(1*0)=214
214 % 10 = 4
So 942997-00-4 is a valid CAS Registry Number.
942997-00-4Relevant academic research and scientific papers
Studies on the constituents of Hedera rhombea Bean. IV. On the hederagenin glycosides
Kizu,Hirabayashi,Suzuki,Tomimori
, p. 3473 - 3478 (2007/10/02)
On the basis of chemical and physicochemical evidence, the structures of two new hederagenin bisdesmosides, named Kizuta saponins K8 (X) and K11 (I), which were isolated from the stem and bark of Hedera rhombea Bean (Araliaceae), were established to be as follows: X, 3-O-α-L-arabinopyranosyl-hederagenin 28-O-α-L-rhamnopyranosyl-(1 →4)-6-O-acetyl-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl ester; I,3-O-α-L-rhamnopyranosyl-(1→2)-α-L-arabinopyranosyl-hederagenin 28-O-α-L-rhamnopyranosyl(1→4)-6-O-acetyl-β-D-glucopyranosyl-(1→6)-β-D -glucopyranosyl ester. A glucoside mixture (XIII) was considered to be a mixture of the β-D glucopyranosides of campesterol (trace), stigmasterol and β-sitosterol based on chemical and physicochemical evidence.
