Harmine - Moligand™, ≥98% , Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 1A;Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 1B, CAS No.442-51-3, Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 1A;Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 1B

CAS: 442-51-3 Cat. No.: H107067 Molecular Weight: 212.25 Beilstein Registry Number: 178813 EC Number: 207-131-4
AVAILABLE TO ORDER
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. ≥98%
Synonyms
7-Methoxy-1-methyl-9H-pyrido[3,4-b]indole | HARMINE | HMS3885E10 | Spectrum5_001914 | 9H-Pyrido(3,4-b)indole, 7-methoxy-1-methyl- | HY-N0737A | Spectrum_001128 | 5-23-12-00237 (Beilstein Handbook Reference) | NCGC00016435-01 | NCGC00016435-03 | SMR0012332
Storage
Room temperature
Shipped In
Normal
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Size
Status
Price
Qty
250mg
H107067-250mg
1
$30.90
1g
H107067-1g
5
$93.90
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Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

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Quality documents

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

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Literature proof

Cited in 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Synonyms
7-Methoxy-1-methyl-9H-pyrido[3, 4-b]indole | HARMINE | HMS3885E10 | Spectrum5_001914 | 9H-Pyrido(3, 4-b)indole, 7-methoxy-1-methyl- | HY-N0737A | Spectrum_001128 | 5-23-12-00237 (Beilstein Handbook Reference) | NCGC00016435-01 | NCGC00016435-03 | SMR0012332
Specifications & Purity
Moligand™, ≥98%
Biochemical and Physiological Mechanisms
Potent and selective inhibitor of DYRK1A (dual specificity tyrosine-phosphorylated and -regulated kinase). (IC 50 values are 0.08 (DYRK1A), 0.9 (DYRK2), 0.8 (DYRK3), 4.3 (PIM3) and 1.5 μM (CK1)). 5-HT antagonist and MAO inhibitor.
Storage
Room temperature
Shipped In
Normal
Grade
Moligand™
Action Type
INHIBITOR
Mechanism of action
Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 1A;Inhibitor of dual specificity tyrosine phosphorylation regulated kinase 1B
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Purity
≥98%
Names and Identifiers
Pubchem Sid504763320
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504763320
Canonical SmilesCC1=NC=CC2=C1NC3=C2C=CC(=C3)OC
IUPAC Name7-methoxy-1-methyl-9H-pyrido[3,4-b]indole
InChIKeyBXNJHAXVSOCGBA-UHFFFAOYSA-N
INCHI1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3
Isomeric SMILES CC1=NC=CC2=C1NC3=C2C=CC(=C3)OC
WGK Germany 3
RTECS UV0175000
Alternate CAS 442-51-3
MeSH Entry Terms 9H-Pyrido(3,4-b)indole, 7-methoxy-1-methyl-;Banisterine;Harmine;Leucoharmine;Telepathine;Yageine
Molecular Weight 212.25
Beilstein 178813
Reaxy-Rn 178813
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=178813&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
SuperclassAlkaloids and derivatives
ClassHarmala alkaloids
SubclassNot available
Intermediate Tree Nodes Not available
Direct ParentHarmala alkaloids
Alternative Parents Beta carbolines  Indoles  Anisoles  Methylpyridines  Alkyl aryl ethers  Pyrroles  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteropolycyclic compounds
Substituents Harman - Beta-carboline - Pyridoindole - Indole - Indole or derivatives - Anisole - Methylpyridine - Alkyl aryl ether - Benzenoid - Pyridine - Heteroaromatic compound - Pyrrole - Ether - Azacycle - Organoheterocyclic compound - Organopnictogen compound - Organic nitrogen compound - Organic oxygen compound - Hydrocarbon derivative - Organonitrogen compound - Organooxygen compound - Aromatic heteropolycyclic compound
DescriptionThis compound belongs to the class of organic compounds known as harmala alkaloids. These are compounds with a structure based on harmaline, harmine, harmalol, harman or a derivative of those parents. These parents are beta-carbolines, consisting of a pyrimidine fused to the pyrrole moiety of an indole to form a pyrido[3,4-b]indole.
External Descriptors an alkaloid
3D Structure
Interactive Chemical Structure Model





Associated Targets(Human)
CYP1A2 Tchem Cytochrome P450 1A2 (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
DYRK1B Tchem Dual specificity tyrosine-phosphorylation-regulated kinase 1B (2 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
DYRK1A Tchem Dual specificity tyrosine-phosphorylation-regulated kinase 1A (6 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
MAOA Tclin Amine oxidase [flavin-containing] A (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
CLK1 Tchem Dual specificity protein kinase CLK1 (4 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NISCH Tclin Nischarin (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
Certificates(CoA,COO,BSE/TSE and Analysis Chart)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

4 results found

Lot NumberCertificate TypeDateItem
L2115107Certificate of AnalysisSep 17, 2025 H107067
L2115116Certificate of AnalysisSep 17, 2025 H107067
E1916020Certificate of AnalysisMar 08, 2023 H107067
G2319530Certificate of AnalysisDec 20, 2021 H107067
Chemical and Physical Properties
Melt Point(°C)262-264°C
Molecular Weight212.250 g/mol
XLogP33.600
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count2
Rotatable Bond Count1
Exact Mass212.095 Da
Monoisotopic Mass212.095 Da
Topological Polar Surface Area37.900 Ų
Heavy Atom Count16
Formal Charge0
Complexity258.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Documents & Articles
Citations of This Product
References
1. Yuanyuan Li, Guangmei Yang, Yuting Wang, Yahong Li, Shu Zhang, Ruyi Li, Linxin Yang, Jian Wang, Xibo Pei, Qianbing Wan, Junyu Chen.  (2023)  Osteoimmunity-regulating nanosilicate-reinforced hydrogel for enhancing osseointegration.  Journal of Materials Chemistry B,      [PMID:37822156] [10.1039/D3TB01509B]
2. Peijian Sun, Yipeng Wang, Song Yang, Xuehui Sun, Bin Peng, Lining Pan, Yunzhen Jia, Xiaobing Zhang, Cong Nie.  (2023)  Molecularly Imprinted Polymer Nanospheres with Hydrophilic Shells for Efficient Molecular Recognition of Heterocyclic Aromatic Amines in Aqueous Solution.  MOLECULES,  28  (5): (2052).  [PMID:36903298] [10.3390/molecules28052052]
3. Miao Jiefei, Meng Chi, Wu Hongmei, Shan Wenpei, Wang Haoran, Ling Changchun, Zhang Jinlin, Yang Tao.  (2021)  Novel Hybrid CHC from β-carboline and N-Hydroxyacrylamide Overcomes Drug-Resistant Hepatocellular Carcinoma by Promoting Apoptosis, DNA Damage, and Cell Cycle Arrest.  Frontiers in Pharmacology,      [PMID:33536926] [10.3389/fphar.2020.626065]
4. Gaofeng Cui, Haiqi Yuan, Zhiyan Jiang, Jing Zhang, Zhipeng Sun, Guohua Zhong.  (2019)  Natural harmine negatively regulates the developmental signaling network of Drosophila melanogaster (Drosophilidae: Diptera) in vivo.  ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY,      [PMID:31901541] [10.1016/j.ecoenv.2019.110134]
5. Shijiao Tian, Wenming Jia, Mei Lu, Juan Zhao, Xiulian Sun.  (2019)  Dual-specificity tyrosine phosphorylation-regulated kinase 1A ameliorates insulin resistance in neurons by up-regulating IRS-1 expression.  JOURNAL OF BIOLOGICAL CHEMISTRY,  294  (52): (20164-20176).  [PMID:31723029] [10.1074/jbc.RA119.010809]
6. Zhang Chunhua, Wu Huiqin, Huang Xiaolan, Zhu Zhixin, Luo Huitai, Huang Fang, Lin Xiaoshan.  (2012)  Simultaneous Determination of Toxic Alkaloids in Blood and Urine by HPLC–ESI–MS/MS.  CHROMATOGRAPHIA,  75  (9): (499-511).  [PMID:] [10.1007/s10337-012-2216-6]
Solution Calculators
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