Harmine hydrochloride structure
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Common Name | Harmine hydrochloride | ||
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CAS Number | 343-27-1 | Molecular Weight | 248.708 | |
Density | N/A | Boiling Point | 421.4ºC at 760mmHg | |
Molecular Formula | C13H13ClN2O | Melting Point | 265-270°C | |
MSDS | N/A | Flash Point | 139.8ºC |
Use of Harmine hydrochlorideHarmine Hydrochloride (Telepathine Hydrochloride) is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1]. |
Name | 7-methoxy-1-methyl-9H-pyrido[3,4-b]indole,hydrochloride |
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Synonym | More Synonyms |
Description | Harmine Hydrochloride (Telepathine Hydrochloride) is a natural dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) inhibitor with anticancer and anti-inflammatory activities. Harmine has a high affinity of 5-HT2A serotonin receptor, with an Ki of 397 nM[1]. |
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Related Catalog | |
Target |
Ki: 397 nM (5-HT2A serotonin receptor)[1], DYRK1A[2] |
In Vitro | Harmine inhibits tau phosphorylation by DYRK1A by selected DANDYs, with an IC50 of 190 nM[2]. Harmine negatively regulates homologous recombination (HR) by interfering Rad51 recruitment, resulting in severe cytotoxicity in hepatoma cells. Furthermore, NHEJ inhibitor Nu7441 markedly sensitizes Hep3B cells to the anti-proliferative effects of Harmine[3]. |
In Vivo | It is shown that brain water content is significantly increased in the TBI group. Treatment with Harmine significantly reduces the tissue water content at 1, 3 and 5 days, compared with the TBI group. Harmine treatment significantly reduces the escape latency at 3 and 5 days, compared with the TBI group. Post-TBI administration of Harmine significantly improves the motor function recovery of the rats at 1, 3 and 5 days following TBI, compared with the TBI group without Harmine treatment. The neuronal survival rate in the Harmine-treated group is significantly increased, compared with the TBI group. Administration of Harmine results in marked elevation in the expression of GLT-1, compared with the TBI group. The administration of Harmine significantly reduces the expression of caspase 3, compared with the TBI group[4]. |
References |
Boiling Point | 421.4ºC at 760mmHg |
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Melting Point | 265-270°C |
Molecular Formula | C13H13ClN2O |
Molecular Weight | 248.708 |
Flash Point | 139.8ºC |
Exact Mass | 248.071640 |
PSA | 37.91000 |
LogP | 3.83510 |
CHEMICAL IDENTIFICATION
HEALTH HAZARD DATAACUTE TOXICITY DATA
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Hazard Codes | Xn: Harmful; |
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Risk Phrases | R20/21/22 |
Safety Phrases | S22-S36 |
RIDADR | 1544 |
WGK Germany | 3 |
RTECS | MG9450000 |
Packaging Group | III |
Hazard Class | 6.1(b) |
HS Code | 2933990090 |
HS Code | 2933990090 |
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Summary | 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
7-Methoxy-1-methyl-9H-β-carbolinhydrochlorid |
7-Methoxy-1-methyl-9H-β-carboline hydrochloride |
Harmine.HCL |
EINECS 206-443-8 |
Harmine hydrochloride hydrate |
Harmine monohydrochloride |
MFCD00012641 |
9H-Pyrido[3,4-b]indole, 7-methoxy-1-methyl-, monohydrochloride |
HARMINE HYDROCHLORIDE |
7-Methoxy-1-methyl-9H-β-carboline hydrochloride (1:1) |
7-Méthoxy-1-méthyl-9H-β-carboline chlorhydrate |
9H-Pyrido[3,4-b]indole, 7-methoxy-1-methyl-, hydrochloride (1:1) |
Banisterine Hydrochloride |