Allomatrine

Modify Date: 2025-08-23 16:08:01

Allomatrine Structure
Allomatrine structure
Common Name Allomatrine
CAS Number 641-39-4 Molecular Weight 347.364
Density 1.4±0.1 g/cm3 Boiling Point 638.7±55.0 °C at 760 mmHg
Molecular Formula C15H24N2O Melting Point 106-107 ℃
MSDS N/A Flash Point 340.1±31.5 °C

 Use of Allomatrine


Allomatrine ((+)-Allomatrine) is an alkaloid from the bark of Sophora japonica. Allomatrine has antinociceptive properties mediated mainly through the activation ofκ-opioid receptors[1][2].

 Names

Name 4-(2-Biphenylyl)-1-(hydroxymethyl)-10-oxa-4-azatricyclo[5.2.1.02,6]dec-8-ene-3,5-dione
Synonym More Synonyms

 Allomatrine Biological Activity

Description Allomatrine ((+)-Allomatrine) is an alkaloid from the bark of Sophora japonica. Allomatrine has antinociceptive properties mediated mainly through the activation ofκ-opioid receptors[1][2].
Related Catalog
References

[1]. Long Pan, et al. Chemical Constituents of Alkaloids From the Bark of Sophora Japonica. Zhong Yao Cai. 2016 Sep;39(9):2027-9.

[2]. Seiichi Kobashi , et al. Antinociceptive Effects of 1-acyl-4-dialkylaminopiperidine and 1-alkyl-4-dialkylaminopiperidine in Mice: Structure-Activity Relation Study of Matrine-Type Alkaloids. Biol Pharm Bull. 2002 Aug;25(8):1030-4.

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 638.7±55.0 °C at 760 mmHg
Melting Point 106-107 ℃
Molecular Formula C15H24N2O
Molecular Weight 347.364
Flash Point 340.1±31.5 °C
Exact Mass 347.115753
PSA 66.84000
LogP 2.09
Vapour Pressure 0.0±2.0 mmHg at 25°C
Index of Refraction 1.666
InChIKey ZSBXGIUJOOQZMP-KYEXWDHISA-N
SMILES O=C1CCCC2C3CCCN4CCCC(CN12)C34
Storage condition 2-8C

 Synthetic Route

 AllomatrineBioassay

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Name: Antiviral activity against HBV infected in human HepG2.2.15 cells assessed as inhibit...
Source: ChEMBL
Target: Hepatitis B virus
External Id: CHEMBL4202361
Name: Inhibition of HBeAg release against HBV in HepG2 2.2.15 cell line at 0.1 umol/mL
Source: ChEMBL
Target: Hepatitis B virus
External Id: CHEMBL866534
Name: Inhibition of HBeAg release against HBV in HepG2 2.2.15 cell line at 0.2 umol/mL
Source: ChEMBL
Target: Hepatitis B virus
External Id: CHEMBL866533
Name: Inhibition of HBsAg release against HBV in HepG2 2.2.15 cell line at 0.1 umol/mL
Source: ChEMBL
Target: Hepatitis B virus
External Id: CHEMBL866532
Name: Inhibition of HBsAg release against HBV in HepG2 2.2.15 cell line at 0.2 umol/mL
Source: ChEMBL
Target: Hepatitis B virus
External Id: CHEMBL866531
Name: Cytotoxicity against human HepG2.2.15 cells assessed as growth inhibition at 0.8 mM b...
Source: ChEMBL
Target: HepG2 2.2.15
External Id: CHEMBL4202369
Name: Cytotoxicity against HepG2 2.2.15 cell line at 0.4 umol/mL by MTT assay
Source: ChEMBL
Target: HepG2
External Id: CHEMBL866535
Name: Antiviral activity against HBV infected in human HepG2.2.15 cells assessed as inhibit...
Source: ChEMBL
Target: Hepatitis B virus
External Id: CHEMBL4202365
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 Synonyms

13S-HYDROXY-6Z,9Z,11E-OCTADECATRIENOIC ACID
4-(2-Biphenylyl)-1-(hydroxymethyl)-10-oxa-4-azatricyclo[5.2.1.0]dec-8-ene-3,5-dione
13-hydroxy-(6Z,9Z,11E,13S)-6,9,11-octadecatrienoic acid
13(S)-HYDROXY-9(Z),11(E),15(Z)-OCTADECATRIENOIC ACID
(13S,6Z,9Z,11E)-hydroxyoctadeca-6,9,11-trienoic acid
Allomatrine
13-hydroxy-6,9,11-octadecatrienoic acid
(+)-Allomatrin
13(S)-HOT
13(S)-HYDROXYOCTADECA-6Z,9Z,11E-TRIENOIC ACID
13(S)-HOTE
(6Z,9Z,11E)-13(S)-hydroxyoctadeca-6,9,11-trienoic acid
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