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Cyclamiretin A is a naturally occurring chemical compound belonging to the family of retinoids, which are derived from vitamin A. It is primarily found in the seeds of the plant Cyclamia, and exhibits a unique chemical structure characterized by a cyclopropane ring fused to a retinoid backbone. Cyclamiretin A has garnered interest due to its potential biological activities, including anti-inflammatory and anti-cancer properties. Research is ongoing to explore its therapeutic potential, particularly in the context of cancer treatment, as it may modulate cellular signaling pathways and influence gene expression. However, further studies are required to fully understand its mechanisms of action and to assess its safety and efficacy in clinical settings.

5172-34-9

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5172-34-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5172-34-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,7 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5172-34:
(6*5)+(5*1)+(4*7)+(3*2)+(2*3)+(1*4)=79
79 % 10 = 9
So 5172-34-9 is a valid CAS Registry Number.
InChI:InChI=1/C30H48O4/c1-24(2)19-7-11-27(5)20(26(19,4)10-9-22(24)32)8-12-30-21-15-25(3,17-31)13-14-29(21,18-34-30)23(33)16-28(27,30)6/h17,19-23,32-33H,7-16,18H2,1-6H3/t19-,20+,21+,22-,23+,25-,26-,27+,28-,29+,30-/m0/s1

5172-34-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Oleanan-29-al,13,28-epoxy-3,16-dihydroxy-,(3beta,16alpha,20beta)

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:5172-34-9 SDS

5172-34-9Downstream Products

5172-34-9Relevant academic research and scientific papers

New Triterpenoid Pentasaccharides from Androsace saxifragifolia

Pal, Bikas C.,Mahato, Shashi B.

, p. 1963 - 1968 (2007/10/02)

Two new triterpenoid pentasaccharides, saxifragifolins C and D, isolated from the aerial part of Androsace saxifragifolia were characterized as androsacenol 3-O-2)-β-D-glucopyranosyl-(1--->4)-4)-β-D-glucopyranosyl-(1--->2)>-α-L-arabinopyranoside> (6) and cyclamiretin A 3-O-2)-β-D-glucopyranosyl-(1--->4)-4)-β-D-glucopyranosyl-(1--->2)>-α-L-arabinoside> (7).The structures were elucidated by a combination of field desorption mass spectrometry, chemical degradation, and 1H and 13C n.m.r. spectroscopy.

Structure Elucidation of Two Triterpenoid Tetrasaccharides from Androsace saxifragifolia

Waltho, Jonathan P.,Williams, Dudley H.,Mahato, Shashi B.,Pal, Bikas C.,Barna, Jennifer C. J.

, p. 1527 - 1532 (2007/10/02)

Saxifragifolins A and B, two new triterpenoid tetrasaccharides isolated from the aerial part of Androsace saxifragifolia, were respectively shown to be androsacenol-3-O-2)-β-D-glucopyranosyl-(1-->4)-(β-D-glucopyranosyl-(1-->2))-α-L-arabinopyranoside> (1) and cyclamiretin A 3-O-2)-β-D-glucopyranosyl-(1-->4)-(β-D-glucopyranosyl-(1-->2))-α-L-arabinopyranoside> (2).The structural details were elucidated by a combination of fast atom-bombardment mass spectrometry, chemical degradation, and one- and two-dimensional n.m.r. spectroscopy.

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