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allo-Isopteropodine
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allo-Isopteropodine

CAS: 5171-37-9

Ref. 3D-FI137502

1mg
217.00 €
2mg
325.00 €
5mg
542.00 €
10mg
775.00 €
25mg
1,572.00 €
Estimated delivery in United States, on Wednesday 15 Jan 2025

Product Information

Name:
allo-Isopteropodine
Synonyms:
  • Uncarine E
  • 7-Isopteropodine
  • Formosanan-16-carboxylic acid, 19-methyl-2-oxo-, methyl ester, (7α,19α,20α)-
  • Isopteropodin
  • Isopteropodine
  • Spiro[3H-indole-3,6'(10'H)-[1H]pyrano[3,4-f]indolizine]-4'-carboxylic acid, 1,2,4'a,5',5'a,7',8',10'a-octahydro-1'-methyl-2-oxo-, methyl ester, (1'R,4a'R,10a'R)-
  • Spiro[3H-indole-3,6′(4′aH)-[1H]pyrano[3,4-f]indolizine]-4′-carboxylic acid, 1,2,5′,5′a,7′,8′,10′,10′a-octahydro-1′-methyl-2-oxo-, methyl ester, (1′S,3S,4′aS,5′aS,10′aS)-
  • Spiro[3H-indole-3,6′(4′aH)-[1H]pyrano[3,4-f]indolizine]-4′-carboxylic acid, 1,2,5′,5′a,7′,8′,10′,10′a-octahydro-1′-methyl-2-oxo-, methyl ester, [1′S-(1′α,4′aα,5′aα,6′α,10′aα)]-
Description:

Allo-isopteropodine is a monoterpenoid indole alkaloid that belongs to the group of acetate extract. It has been shown to have strong anti-cancer effects on skin cancer cells, as well as potential for treatment of cervical cancer. Allo-isopteropodine was found to inhibit 5-HT2 receptors and produce a locomotor activity in rats. This compound also inhibits the production of acetylcholine by binding to muscarinic receptors and has been shown to have a variety of physiological effects such as reducing blood pressure, increasing urine output, and lowering heart rate. Allo-isopteropodine can also be used as an analgesic and antipyretic agent.

Notice:
Our products are intended for lab use only. For any other use, please contact us.
Brand:
Biosynth
Long term storage:
Notes:

Chemical properties

Molecular weight:
368.43 g/mol
Formula:
C21H24N2O4
Purity:
Min. 95%
Color/Form:
White Powder
MDL:
Melting point:
Boiling point:
Flash point:
Density:
Concentration:
EINECS:
Merck:
HS code:

Hazard Info

UN Number:
EQ:
Class:
H Statements:
P Statements:
Forbidden to fly:
Hazard Info:
Packing Group:
LQ:

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