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(-)-Huperzine A

(-)-Huperzine A Structure
CAS No.
102518-79-6
Chemical Name:
(-)-Huperzine A
Synonyms
Huperizine A;HUPERZINE A 1%;HupA;Haboyin;Hupzine A;HUPERIZINE;Kimpukan A;Isoselagine;(-)-Selagine;HUPERZINE A(P)
CBNumber:
CB9173024
Molecular Formula:
C15H18N2O
Molecular Weight:
242.32
MOL File:
102518-79-6.mol
MSDS File:
SDS
Modify Date:
2024/7/11 9:50:51

(-)-Huperzine A Properties

Melting point 211-216oC
alpha D -147° (c = 0.36 in CH3OH) (Ayer); D24.5 -150.4° (c = 0.498 in MeOH) (Liu)
Boiling point 505.0±50.0 °C(Predicted)
Density 1.20±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility insoluble in H2O; ≥12.12 mg/mL in DMSO; ≥23.13 mg/mL in EtOH
pka 12.25±0.60(Predicted)
form Solid
color White to Almost white
optical activity [α]/D -153±5°, c = 0.5 in methanol
InChI InChI=1S/C15H18N2O/c1-3-11-10-6-9(2)8-15(11,16)12-4-5-14(18)17-13(12)7-10/h3-6,10H,7-8,16H2,1-2H3,(H,17,18)/b11-3+/t10-,15+/m0/s1
InChIKey ZRJBHWIHUMBLCN-YQEJDHNASA-N
SMILES C12C[C@@]3([H])/C(=C\C)/[C@@](N)(C=1C=CC(=O)N2)CC(C)=C3
LogP 0.833 (est)
CAS DataBase Reference 102518-79-6(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H300+H310+H330
Precautionary statements  P262-P280-P301+P310+P330-P302+P352+P310-P304+P340+P310
Hazard Codes  T+
Risk Statements  26/27/28-36/37/38
Safety Statements  26-36/37/39-45
RIDADR  UN 1544 6.1/PG 2
WGK Germany  3
RTECS  PB9185700
HS Code  29339900
NFPA 704
0
4 0

(-)-Huperzine A price More Price(4)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 42643 (−)-Huperzine A analytical standard 102518-79-6 25MG ₹21444.33 2022-06-14 Buy
TCI Chemicals (India) H1700 (-)-Huperzine A 102518-79-6 10MG ₹2600 2022-05-26 Buy
TCI Chemicals (India) H1700 (-)-Huperzine A 102518-79-6 100MG ₹7800 2022-05-26 Buy
ottokemi H 1438 (-)-Huperzine A+ 98% 102518-79-6 25mg ₹18009 2022-05-26 Buy
Product number Packaging Price Buy
42643 25MG ₹21444.33 Buy
H1700 10MG ₹2600 Buy
H1700 100MG ₹7800 Buy
H 1438 25mg ₹18009 Buy

(-)-Huperzine A Chemical Properties,Uses,Production

Description

Huperzine A is obtained from Huperzia serrata, which is the perennial fern. It shows activities in antipyretic, hemostasis, and dehumidification and is used for the treatment in folk of pneumonia, lung abscess, hematemesis, hematochezia, traumatic injury, etc.

Chemical Properties

Pale Brown Solid

Physical properties

Appearance: white crystalline powder. Bitter with hygroscopicity. Solubility: easily soluble in chloroform, soluble in methanol and ethanol, and slightly soluble in water. Melting point: 211–216?°C.

Uses

Huperzine A is a potential therapeutic agent for Alzheimer disease that reversible alkaloid inhibitor of AChE which crosses the blood-brain barrier. It reduces cell death induced by glutamate in primary cultures derived from forebrain, hippocampus, cortex and cere.
In China, it is approved for use in the treatment of Alzheimer’s disease (AD). Huperzine A was classified as a dietary supplement by the FDA in 1997. As a nutraceutical, it is available in American health food stores or via the Internet, labeled as a memory aid.

Definition

ChEBI: Huperzine A is a sesquiterpene alkaloid isolated from a club moss Huperzia serrata that has been shown to exhibit neuroprotective activity. It is also an effective inhibitor of acetylcholinesterase and has attracted interest as a therapeutic candidate for Alzheimer's disease. It has a role as an EC 3.1.1.7 (acetylcholinesterase) inhibitor, a neuroprotective agent, a plant metabolite and a nootropic agent. It is a sesquiterpene alkaloid, a pyridone, a primary amino compound and an organic heterotricyclic compound. It is a conjugate base of a huperzine A(1+).

Indications

Huperzine A is purified from Chinese club moss and has been traditionally used in China for the treatment of swelling, fever, inflammation, blood disorders, and schizophrenia. It was mainly applied to age-related memory dysfunction and Alzheimer and has a good effect on improving memory function. It can be used to treat various types of Alzheimer's disease and also myasthenia gravis.

Preparation

(-)-Huperzine A, a Lyco-podium alkaloid isolated in 1986 from the club moss Huperzia serrata, has drawn considerable attention after it was revealed to be a potent, selective, and reversible AChE inhibitor.
synthesis of  (?)-huperzine A
The total synthesis of Lycopodium alkaloid (-)-huperzine A has been accomplished in 10 steps with 17% overall yield from commercially abundant (R)-pulegone. The synthetic route features an efficient synthesis of 4 via a Buchwald–Hartwig coupling reaction, a dianion-mediated highly stereoselective alkylation of 4, and a rare example of an intramolecular Heck reaction of an enamine-type substrate. The stereoselective β-elimination and the accompanying Wagner–Meerwein rearrangement are of particular interest.
[1] RUI DING Guo Q L Bing Feng Sun*. An Efficient Total Synthesis of (-)-Huperzine A [J]. Organic Letters, 2012, 14 17: 4446-4449. DOI:10.1021/ol301951r.
[2] RUI DING. Divergent Total Synthesis of the Lycopodium Alkaloids Huperzine A, Huperzine B, and Huperzine U[J]. The Journal of Organic Chemistry, 2013, 79 1: 240-250. DOI:10.1021/jo402419h.
[3] TUN M K M, WüSTMANN D J, HERZON S B. A robust and scalable synthesis of the potent neuroprotective agent (-)-huperzine A [J]. Chemical Science, 2011, 11: 2251-2253. DOI:10.1039/C1SC00455G.

Pharmacology

Huperzine A has the ability to enhance learning and memory, improve spatial memory, and can be used for age-related dementia, vascular dementia, and other neurodegenerative diseases. Compared with the current anti-AD drugs, huperzine A can go through the blood-brain barrier, with a high oral bioavailability and longer time inhibition on AChE.
As a highly selective AChE reversible inhibitor, huperzine A can inhibit AChE, reduce acetylcholine hydrolysis, and improve the level of acetylcholine in the synaptic gap. This inhibition is reversible, lasts for a long time, shows no drug dependence if repeated administration, and does not induce significant liver toxicity. X-ray diffraction results show that the direct binding of huperzine A to AChE active sites inhibits the binding of AChE to its substrate.
In addition to the potent inhibition on AChE, huperzine A only shows a weak inhibitory effect on the butyrylcholinesterase; also protects neurons by inhibiting oxidative stress, reducing somatostatin, reducing the content of glutamate, decreasing the increased intracellular calcium, and inhibiting neuronal apoptosis; further improves AD-related cognitive function and reduces the symptoms of AD patients.

Clinical Use

Since 1994, huperzine A has been approved for clinical use in improving memory and cognitive impairment in old patients with memory loss and dementia. A large number of domestic clinical studies have found that huperzine A shows therapeutic effect on learning and cognitive dysfunction of vascular dementia, mental retardation, and schizophrenia patients with mild adverse reactions.

(-)-Huperzine A Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 501)Suppliers
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CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
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Henan Bao Enluo International TradeCo.,LTD +86-17331933971 +86-17331933971 China 2503 58 Inquiry
Huperzine-A1-5% (5r-(5-alpha,9-beta,11e))-ydro-7-methyl 5,9-methanocycloocta(b)pyridin-2(1h)-one,5-amino-11-ethylidene-5,6,9,10-tetrah HUPERIZINE (-)-HUPERZINE A FROM HUPERZIA SERRATA HuperziaSerrateP.E120786-18-7/ (5R,9R,E)-5-AMino-11-ethylidene-7-Methyl-5,6,9,10-tetrahydro-5,9-Methanocycloocta[b]pyridin-2(1H)-one (-)-Huperzine A (HupA) Huperzine Serrate Extract (-)-Huperzine A (HupA) (-)-Selagine Huperzia Serrate P.E./Huperzine-A HUP, [5R-(5a,911E)]-5-Amino-11-ethylidene-5,6,9,10-tetrahydro-7-methyl-5,9-methanocycloocta[b]pyridin-2-(1H)-one, Selagine, 5,9-Methanocyclooctabpyridin-2(1H)-one, 5-amino-11-ethylidene-5,6,9,10-tetrahydro-7-methyl-, (5R,9R,11E)- Huperzine A ( Selagine ) (-)-HUPERZINE A, 99% HPLC (-)-Huperzine A (-)-Selagine [5R-(5α,9β,11E)]-5-Amino-11-ethylidene- 5,6,9,10-tetrahydro-7-methyl-5,9-methanocycloocta[b]pyridin-2(1H)-one (5R,11E)-5β-Amino-11-ethylidene-5,6,9,10-tetrahydro-7-methyl-5α,9α-methanocycloocta[b]pyridin-2(1H)-one Kimpukan A SynonyMs (-)-Selagine HUPERZINE A(P) (-)- Hupperzine A Isoselagine Hupzine A Haboyin (1R,9S,13E)- 1-AMINO- 13-ETHYLIDENE- 11-METHYL- 6-AZATRICYCLO[7.3.1.02,7] TRIDECA- 2(7),3,10- TRIEN- 5-ONE Huperzine A, 98%, from Huperzia serrata (Thunb.) Trevis. (-)-HUPERZINE A (HUPERZINE A) Huperzine A 102518-79-6 (+-)-huperzine A,Huperzine-a,Huperzine A HupA (-)-Huperzine A USP/EP/BP Huperzia Serrate Plant Exrtact - Huperzine A Melaleuca extract/Huperzine A TIANFU-CHEM CAS:102518-79-6 (-)-Huperzine A (-)- Hupperzine A HUPERZINE A 1% Huperizine A Huperzia Serrata Extract / Huperzine A (1R,9R)-1-amino-13-ethylidene-11-methyl-6-azatricyclo[7.3.1.0^{2,7}]trideca-2(7),3,10-trien-5-one 102518-79-6 102517-79-6 Inhibitor chemical reagent pharmaceutical intermediate phytochemical reference standards from Chinese medicinal herbs (TCM). standardized herbal extract Nutritional Ingredients reference substance Inhibitors Intermediates & Fine Chemicals Pharmaceuticals Acetylcholine receptor API Alkaloids