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ALLOCRYPTOPINE

Basic information Safety Supplier Related

ALLOCRYPTOPINE Basic information

Product Name:
ALLOCRYPTOPINE
Synonyms:
  • ALPHA-ALLOCRYPTOPINE
  • ALLOCRYPTOPINE, ALPHA-
  • ALLOCRYPTOPINE
  • 3,4-DIMETHOXY-6-METHYL-5,7,8,15-TETRAHYDRO-6H-BENZO[C][1,3]DIOXOLO[4',5':4,5]BENZO[1,2-G]AZECIN-14-ONE
  • .beta.-Allocryptopine
  • .gamma.-Homochelidonine
  • Benzo[E][1,3]dioxolo[4,5-K][3]benzazecin-14(6H)-one, 5,7,8,15-tetrahydro-3,4-dimethoxy-6-methyl-
  • Fagarine i
CAS:
24240-04-8
MF:
C21H23NO5
MW:
369.41
Mol File:
24240-04-8.mol
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ALLOCRYPTOPINE Chemical Properties

Melting point:
169-170 °C
Boiling point:
552.7±50.0 °C(Predicted)
Density 
1.216±0.06 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
form 
Powder
pka
7.86±0.20(Predicted)
biological source
plant
Water Solubility 
water: slightly soluble
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ALLOCRYPTOPINE Usage And Synthesis

Uses

It is a natural product derived from plant source th at finds application in compound screening libraries, metabolomics, phytochemical, and pharmaceutical research.

Definition

ChEBI: Allocryptopine is a dibenzazecine alkaloid, an organic heterotetracyclic compound, a tertiary amino compound, a cyclic ketone, a cyclic acetal and an aromatic ether.

Biological Activity

Allocryptopine has been reported to possess strong antibacterial, anti-inflammatoty, antiparasitic, antineoplastic and anti-addictive activities. Allocryptopine inhibits human acetylcholinesterase and butyrylcholinesterase. It blocks hERG current in HEK293 cells. Allocryptopine strongly enhanced the I(peak) of the T353I channel by enhancing the plasma membrane (PM) expression of Nav1.5 and rescued defective trafficking after co-incubation with HEK293 cells th at carry mutation channel 24 h.

target

cAMP | P450 (e.g. CYP17)

ALLOCRYPTOPINESupplier

Chembest Research Laboratories Limited
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BioBioPha Co., Ltd.
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ALB Technology Limited
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18607101326 15172504745
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