24006-62-0 Usage
Uses
1. Used in Cellular Process Regulation:
D-ERYTHRO-C20-DIHYDROSPHINGOSINE is used as a regulator for cellular processes, including cell growth, survival, and differentiation, due to its role as a precursor and substrate in the production of ceramide, sphingosine, and sphingosine-1-phosphate.
2. Used in Heat Stress Adaptation:
In the application industry of cellular response to stress, D-ERYTHRO-C20-DIHYDROSPHINGOSINE is used as an adaptogen for heat stress, as its levels increase 10.8-fold in S. cerevisiae in response to heat stress, indicating its involvement in heat stress adaptation.
3. Used in Response to Mycotoxins:
In the field of mycotoxin research, D-ERYTHRO-C20-DIHYDROSPHINGOSINE is used as a biomarker for exposure to certain mycotoxins, such as fumonisins, as its levels increase significantly in response to these toxins.
4. Used in Cancer Research:
In the oncology research industry, D-ERYTHRO-C20-DIHYDROSPHINGOSINE is used as a biomarker for certain cancers, as its levels rise in response to some cancerous conditions. Additionally, it may be investigated for its potential role in cancer cell signaling and response to treatment.
5. Used in Protein Kinase C Activation Research:
In the field of cellular signaling, D-ERYTHRO-C20-DIHYDROSPHINGOSINE is used as a research tool to study its effects on protein kinase C activation, as it can block this activation in some cases but not others.
Check Digit Verification of cas no
The CAS Registry Mumber 24006-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,0 and 6 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 24006-62:
(7*2)+(6*4)+(5*0)+(4*0)+(3*6)+(2*6)+(1*2)=70
70 % 10 = 0
So 24006-62-0 is a valid CAS Registry Number.
24006-62-0Relevant articles and documents
A general, efficient and stereospecific route to sphingosine, sphinganines, phytosphingosines and their analogs
Cai, Ye,Ling, Chang-Chun,Bundle, David R.
, p. 1140 - 1146 (2008/02/03)
Sphingosine, sphinganines and phytosphingosines and their analogs were synthesized by an aldol condensation between an iminoglycinate bearing a (+)-(1R,2R,5R)-2-hydroxy-3-pinanone group as chiral auxiliary and an appropriate aldehyde. All condensations proceeded with excellent enantioselectivity to generate the (2S,3R)-d-erythro structures in good yields. The Royal Society of Chemistry 2006.
