(-)-Huperzine A - Moligand™,2mM in DMSO , CAS No.102518-79-6

CAS: 102518-79-6 Cat. No.: H420384 Peso molecular: 242.32 Número EC: 600-320-6
Disponible para pedir
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. 2mM in DMSO
Synonyms
Huperzine A|(-)-huperzine A|102518-79-6|HupA|Selagine|(-)-Selagine|Fordine|(-)- HUPPERZINE A|92138-20-0|HuperzineA|120786-18-7|C15H18N2O|(1R,9R)-1-amino-13-ethylidene-11-methyl-6-azatricyclo[7.3.1.02,7]trideca-2(7),3,10-trien-5-one|SR-01000781266|Isoselag
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1ml
H420384-1ml
2
29,90US$
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Moligand™,2mM in DMSO Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 17 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Descripción general

Acetylcholinesterase inhibitor; active enantiomer.

Specifications

Sinónimos
Huperzine A | (-)-huperzine A | 102518-79-6 | HupA | Selagine | (-)-Selagine | Fordine | (-)- HUPPERZINE A | 92138-20-0 | HuperzineA | 120786-18-7 | C15H18N2O | (1R, 9R)-1-amino-13-ethylidene-11-methyl-6-azatricyclo[7.3.1.02, 7]trideca-2(7), 3, 10-trien-5-one | SR-01000781266 | Isoselag
Especificaciones y pureza
Moligand™, 2mM in DMSO
Mecanismos bioquímicos y fisiológicos
Huperzine A, an active Lycopodium alkaloid extracted from traditional Chinese herb, is a potent, selective and reversible acetylcholinesterase (AChE) inhibitor and has been widely used in China for the treatment of Alzheimer's disease (AD). Huperzine A ex
Condiciones de almacenamiento de almacenamiento
Store at -80°C
Enviado en
Dry ice packs + Cold packs
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Grado
Moligand™
Nombres e identificadores
Sonrisas canónicasCC=C1C2CC3=C(C1(CC(=C2)C)N)C=CC(=O)N3
IUPAC Name(1R,9R)-1-amino-13-ethylidene-11-methyl-6-azatricyclo[7.3.1.02,7]trideca-2(7),3,10-trien-5-one
InChIKeyZRJBHWIHUMBLCN-ZUZCIYMTSA-N
INCHI1S/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)/t10-,15+/m0/s1
Isómeros SMILES CC=C1[C@@H]2CC3=C([C@]1(CC(=C2)C)N)C=CC(=O)N3
WGK Alemania 3
RTECS PB9185700
Número ONU 1544
Peso molecular 242.32
Reaxy-Rn 24107487
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24107487&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
ClaseQuinolines and derivatives
SubclassQuinolones and derivatives
Intermediate Tree Nodes Not available
Direct ParentQuinolones and derivatives
Alternative Parents Pyridinones  Aralkylamines  Heteroaromatic compounds  Lactams  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Quinolone - Pyridinone - Aralkylamine - Pyridine - Heteroaromatic compound - Lactam - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary amine - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Organic nitrogen compound - Aromatic heteropolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as quinolones and derivatives. These are compounds containing a quinoline moiety which bears a ketone group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ACHE Tclin Acetylcholinesterase (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Objetivos asociados (no humanos)
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
Propiedades químicas y físicas
Rotación específica [α]-147° (C=0.5,MeOH)
Punto de fusión (°C)232 °C
Peso molecular242.320 g/mol
XLogP30.000
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count2
Rotatable Bond Count0
Exact Mass242.142 Da
Monoisotopic Mass242.142 Da
Topological Polar Surface Area55.100 Ų
Heavy Atom Count18
Formal Charge0
Complexity551.000
Isotope Atom Count0
Defined Atom Stereocenter Count2
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count1
The total count of all stereochemical bonds1
Covalently-Bonded Unit Count1
Citations of This Product
Referencias
1. Jianjin GUO, Lu BAI, Chi-Tang HO, Sen GUO, Naisheng BAI.  (2023)  Chemical characterization, multivariate analysis and in vitro bioactivity evaluation of the roots of Fraxinus mandshurica.  CHINESE JOURNAL OF ANALYTICAL CHEMISTRY,      [PMID:] [10.1016/j.cjac.2023.100303]
2. Nan Zhao, Dan Liu, Yi Wang, Xiaozhe Zhang, Lihua Zhang.  (2022)  Screening and identification of anti-acetylcholinesterase ingredients from Tianzhi granule based on ultrafiltration combined with ultra-performance liquid chromatography-mass spectrometry and in silico analysis.  JOURNAL OF ETHNOPHARMACOLOGY,      [PMID:35973628] [10.1016/j.jep.2022.115641]
3. Peiqi Luo, Liping Wang, Lixia Jiang, Jie Sun, Yafeng Li, Huihui Liu, Caiqiao Xiong, Zongxiu Nie.  (2020)  Application of Graphdiyne in Surface-Assisted Laser Desorption Ionization Mass Spectrometry.  ACS Applied Materials & Interfaces,      [PMID:33378159] [10.1021/acsami.0c18280]
4. Liping Zhao, Ge Yang, Linsen Li, Chao Zhu, Yao Ma, Feng Qu.  (2020)  Aptamer-functionalized magnetic nanoparticles conjugated organic framework for immobilization of acetylcholinesterase and its application in inhibitors screening.  ANALYTICA CHIMICA ACTA,      [PMID:33218485] [10.1016/j.aca.2020.10.024]
5. Xiao Tian, Sen Guo, Shanshan Zhang, Peisheng Li, Tianyi Wang, Chi-Tang Ho, Min-Hsiung Pan, Naisheng Bai.  (2019)  Chemical characterization of main bioactive constituents in Paeonia ostii seed meal and GC-MS analysis of seed oil.  JOURNAL OF FOOD BIOCHEMISTRY,  44  (1): (e13088).  [PMID:31646682] [10.1111/jfbc.13088]
6. Sen Guo, Li Liu, Shanshan Zhang, Chuang Yang, Wenping Yue, Haoan Zhao, Chi-Tang Ho, Junfeng Du, Hai Zhang, Naisheng Bai.  (2019)  Chemical characterization of the main bioactive polyphenols from the roots of Morus australis (mulberry).  Food & Function,  10  (10): (6915-6926).  [PMID:31588440] [10.1039/C9FO01457H]
7. Wei Li, Qian Liu, Shimian Cheng, Shanren Li, Yongbiao Zheng.  (2019)  New Sesquiterpenoids from the Fermented Broth of Termitomyces albuminosus and Their Anti-Acetylcholinesterase Activity.  MOLECULES,  24  (16): (2980).  [PMID:31426402] [10.3390/molecules24162980]
8. Jiqing Yang, Xiaotong Hu, Jia Xu, Xin Liu, Li Yang.  (2018)  Single-Step In Situ Acetylcholinesterase-Mediated Alginate Hydrogelation for Enzyme Encapsulation in CE.  ANALYTICAL CHEMISTRY,      [PMID:29469571] [10.1021/acs.analchem.7b05353]
9. Qiang Fu, Jun Tang, Meng Cui, Zhong Zheng, Zhiqiang Liu, Shuying Liu.  (2015)  Development of ESI-MS-based continuous enzymatic assay for real-time monitoring of enzymatic reactions of acetylcholinesterase.  JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES,      [PMID:25875590] [10.1016/j.jchromb.2015.03.022]
10. Yong-Hao Ye, Cong Li, Jun Yang, Liang Ma, Yu Xiao, Jun Hu, Nasir Ahmed Rajput, Cong-Fen Gao, Ying-Ying Zhang, Ming-Hua Wang.  (2014)  Construction of an immobilised acetylcholinesterase column and its application in screening insecticidal constituents from Magnolia officinalis.  PEST MANAGEMENT SCIENCE,  71  (4): (607-615).  [PMID:25228142] [10.1002/ps.3908]
11. Min Wenao, Wang Weiping, Chen Jianrong, Wang Aijun, Hu Zhide.  (2012)  On-line immobilized acetylcholinesterase microreactor for screening of inhibitors from natural extracts by capillary electrophoresis.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,  404  (8): (2397-2405).  [PMID:22932810] [10.1007/s00216-012-6333-8]
12. Jianjin Guo, Jing Gao, Yan Guo, Lu Bai, Chi-Tang Ho, Naisheng Bai.  (2024)  Characterization, multivariate analysis and bioactivity evaluation of coumarins in the bark of Fraxinus mandshurica.  FITOTERAPIA,      [PMID:38382892] [10.1016/j.fitote.2024.105865]
13. Jianjin Guo, Shaojing Liu, Yan Guo, Lu Bai, Chi-Tang Ho, Naisheng Bai.  (2024)  Chemical characterization, multivariate analysis and comparison of biological activities of different parts of Fraxinus mandshurica.  BIOMEDICAL CHROMATOGRAPHY,  38  (6): (e5861).  [PMID:38501361] [10.1002/bmc.5861]
14. Zhao Fengju, Guo Hui, Yang Wei, Guo Lili, Li Jiaxin, Chen Hanqi.  (2024)  Determination of Acetylcholinesterase Activity Based on Ratiometric Fluorescence Signal Sensing.  JOURNAL OF FLUORESCENCE,      [PMID:38613708] [10.1007/s10895-024-03703-y]
15. Lv Jie, He Chengcai, Cao Jingcheng, Shuai Qiuyan, Liu Xifang, Li Meng, Lin Yulong.  (2024)  Gold nanoclusters/manganese dioxide nanosheets hybrid nanozyme with fluorescence and oxidase-like activity for dual-mode detection of acetylcholinesterase and inhibitors screening.  ANALYTICAL AND BIOANALYTICAL CHEMISTRY,      [PMID:39733176] [10.1007/s00216-024-05712-z]
16. Dai-Xu Wei, Duanfang Cai, Youguo Tan, Kezhi Liu, Jin-Wei Dao, Xiang Li, Aikeremujiang Muheremu.  (2024)  Poly(3-hydroxybutyrate-co-3-hydroxyvalerate-co-3-hydroxyhexanoate)-based microspheres as a sustained platform for Huperzine A delivery for alzheimer's disease therapy.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:39447780] [10.1016/j.ijbiomac.2024.136582]
17. Xin Liu, Irfan Azhar, Habib Khan, Qishu Qu, Miaomiao Tian, Li Yang.  (2019)  Capillary electrophoresis-immobilized enzyme microreactors for acetylcholinesterase assay with surface modification by highly-homogeneous microporous layer.  JOURNAL OF CHROMATOGRAPHY A,      [PMID:31443966] [10.1016/j.chroma.2019.460454]
Calculadoras de soluciones
Reseñas

Reseñas de cliente

Need help choosing the grade?

Our grade selection guide covers purity, stabilizer status, and application suitability for all variants in our catalog.

View Moligand™ grade guide →

Shall we send you a message when we have discounts available?

Remind me later

Thank you! Please check your email inbox to confirm.

Oops! Notifications are disabled.