Ptaquiloside
CAS: 87625-62-5
Ref. 3D-FP159309
1mg | 615.00 € | ||
2mg | 896.00 € | ||
5mg | 1,321.00 € | ||
10mg | 2,269.00 € | ||
25mg | 5,063.00 € |
Product Information
- (2′R,3′aR,4′S,7′aR)-7′a-(β-<span class="text-smallcaps">D</span>-Glucopyranosyloxy)-1′,3′a,4′,7′a-tetrahydro-4′-hydroxy-2′,4′,6′-trimethylspiro[cyclopropane-1,5′-[5H]inden]-3′(2′H)-one
- Braxin C
- Spiro(cyclopropane-1,5'-(5H)indan)-3'(2'H)-one, 7'a-(beta-D-glucopyranosyloxy)-1',3'a,4',7'a-tetrahydro-4'-hydroxy-2',4',6'-trimethyl-, (2'R,3'aR,4'S,7'aR)-
- Spiro[cyclopropane-1,5′-[5H]inden]-3′(2′H)-one, 7′a-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-1′,3′a,4′,7′a-tetrahydro-4′-hydroxy-2′,4′,6′-trimethyl-, (2′R,3′aR,4′S,7′aR)-
- Spiro[cyclopropane-1,5′-[5H]inden]-3′(2′H)-one, 7′a-(β-<span class="text-smallcaps">D</span>-glucopyranosyloxy)-1′,3′a,4′,7′a-tetrahydro-4′-hydroxy-2′,4′,6′-trimethyl-, [2′R-(2′α,3′aα,4′β,7′aα)]-
- spiro[cyclopropane-1,5'-[5H]inden]-3'(2'H)-one, 7'a-(beta-D-glucopyranosyloxy)-1',3'a,4',7'a-tetrahydro-4'-hydroxy-2',4',6'-trimethyl-, (2'R,3a'R,4'S,7a'R)-
- Spiro[cyclopropane-1,5′-[5H]inden]-3′(2′H)-one, 7′a-(β-D-glucopyranosyloxy)-1′,3′a,4′,7′a-tetrahydro-4′-hydroxy-2′,4′,6′-trimethyl-, [2′R-(2′α,3′aα,4′β,7′aα)]-
- Spiro[cyclopropane-1,5′-[5H]inden]-3′(2′H)-one, 7′a-(β-D-glucopyranosyloxy)-1′,3′a,4′,7′a-tetrahydro-4′-hydroxy-2′,4′,6′-trimethyl-, (2′R,3′aR,4′S,7′aR)-
- (2′R,3′aR,4′S,7′aR)-7′a-(β-D-Glucopyranosyloxy)-1′,3′a,4′,7′a-tetrahydro-4′-hydroxy-2′,4′,6′-trimethylspiro[cyclopropane-1,5′-[5H]inden]-3′(2′H)-one
Ptaquiloside is a potent inducer of cancer that belongs to the class of plant compounds. It has been shown to be genotoxic and carcinogenic in experimental models. Ptaquiloside can be found in the roots and stems of Angelica dahurica, a plant grown in China and Russia. This compound has also been identified as an active ingredient in traditional Chinese medicines used for the treatment of various disorders including fever, pain, and inflammation. Ptaquiloside has been observed to inhibit DNA synthesis by binding to its template or primer strand, preventing DNA replication and transcription. The drug has also been shown to cause cell cycle arrest at G1 phase in CD-1 mice following chronic oral administration. Ptaquiloside was identified using LC-MS/MS method with a detection limit of 1 ng/mL in humans with normal hepatic function. Histological analysis showed no significant changes following oral administration at doses up to 50 mg/kg
Chemical properties
Technical inquiry about: 3D-FP159309 Ptaquiloside
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