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17α-Digitoxigenin is a naturally occurring cardiac glycoside derived from the Digitalis plant, which is known for its medicinal properties. It is a key component in the synthesis of the pharmaceutical drug digitoxin, which is used to treat heart conditions such as atrial fibrillation and heart failure. 17α-Digitoxigenin works by inhibiting the sodium-potassium ATPase enzyme, which leads to an increase in the concentration of calcium ions within cardiac muscle cells, thereby enhancing the force of cardiac contractions. Due to its potent effects, it is used in medicine at carefully controlled doses to ensure therapeutic efficacy and safety.

6788-34-7

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6788-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6788-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,8 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6788-34:
(6*6)+(5*7)+(4*8)+(3*8)+(2*3)+(1*4)=137
137 % 10 = 7
So 6788-34-7 is a valid CAS Registry Number.

6788-34-7Relevant academic research and scientific papers

BIOTRANSFORMATION OF DIGITOXIGENIN BY CELL SUSPENSION CULTURES OF STROPHANTHUS DIVARICATUS

Kawaguchi, Kiichiro,Hirotani, Masao,Furuya, Tsutomu

, p. 1503 - 1506 (2007/10/02)

Eight compounds, including a new compound (3-epi-17βH-gitoxigenin) were isolated as biotransformation products of digitoxigenin by cell suspension cultures of Strophanthus divaricatus.At the same time, three products were identified by TLC and HPLC. 16β-Hydroxylation and isomerization of the 17β-butenolide ring of digitoxigenin molecule were demonstrated using this cell suspension culture. Key Word Index - Strophanthus divaricatus; Apocynaceae; biotransformation; 16β-hydroxylation; isomerization of 17β-butenolide ring; cardenolides; digitoxigenin; 17βH-gitoxigenin; 3-epi-17βH-gitoxigenin.

BIOTRANSFORMATION OF DIGITOXIGENIN BY GINSENG HAIRY ROOT CULTURES

Kawaguchi, Kiichiro,Hirotani, Masao,Yoshikawa, Takafumi,Furuya, Tsutomu

, p. 837 - 843 (2007/10/02)

Five new compounds (three esters and two glycosides) and seven previously reported compounds were isolated as biotransformation products of digitoxigenin by ginseng hairy root cultures.The new esters and glycosides were elucidated as digitoxigenin stearate, digitoxigenin palmitate, digitoxigenin myristate, 3-epidigitoxigenin β-D-gentiobioside and digitoxigenin β-D-sophoroside using 1H and 13C NMR and FAB mass spectral data.Biotransformations involving esterification (of stearic acid, palmitic acid, myristic acid and lauric acid) and glycosylation (of gentiobiose and sophorose) of digitoxigenin have been demonstrated for the first time in the plant cell and tissue cultures.The hairy roots showed high glycosylation ability to the digitoxigenin molecule.

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