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2-Amino-4-picoline - 98%, high purity , CAS No.695-34-1, Inhibitor of Inducible NOS

1 Citations COA COA
In stock
Item Number
A107214
Grouped product items
SKU Size
Availability
 Price Qty
A107214-25g
25g
3
$15.90
A107214-100g
100g
2
$48.90
A107214-250g
250g
2
$108.90
A107214-500g
500g
2
$195.90
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Bulk Order  SDS  DATASHEET  Specification Sheet
View related series
Immunology/Inflammation (1929) Inducible NOS Inhibitor (7) NO Synthase (134)

Basic Description

Synonyms A0402 | BRD-K74039237-001-01-7 | WLN: T6NJ BZ D1 | AKOS000119085 | FT-0661940 | Tocris-1020 | W-45 | 4-methylpyridyl amine | STK385035 | 4M2AP | DTXCID9024720 | Ascensil | DTXSID1044720 | Methyl-4 amino-2-pyridine | NSC-176165 | 4-METHYLPYRIDIN-2-AMINE, 6
Specifications & Purity Moligand™, ≥98%
Biochemical and Physiological Mechanisms 2-Amino-4-methylpyridine inhibits the activity of inducible NO synthase isolated from mouse RAW 264.7 cells in vitro.
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade Moligand™
Action Type INHIBITOR
Mechanism of action Inhibitor of Inducible NOS
Product Description

Product Description：

2-Amino-4-methylpyridine acts as ligand and forms methoxo-bridged copper(II) complexes.


Product Application：

2-Amino-4-methylpyridine has been used in the synthesis of 2-amino-4-methyl-pyridinium 2-hy¬droxy¬benzoate.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Pyridines and derivatives
Subclass Aminopyridines and derivatives
Intermediate Tree Nodes Not available
Direct Parent Aminopyridines and derivatives
Alternative Parents Methylpyridines  Imidolactams  Heteroaromatic compounds  Azacyclic compounds  Primary amines  Organopnictogen compounds  Hydrocarbon derivatives  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents Methylpyridine - Aminopyridine - Imidolactam - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as aminopyridines and derivatives. These are organic heterocyclic compounds containing an amino group attached to a pyridine ring.
External Descriptors Not available

Associated Targets(Human)

NOS2 Tchem Nitric oxide synthase, inducible (5 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
NOS1 Tchem Nitric oxide synthase, brain (4 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
NOS3 Tchem Nitric oxide synthase, endothelial (4 Activities)
Activity Type Activity Value -log(M) Mechanism of Action Activity Reference Publications (PubMed IDs)
NOS1 Tchem Nitric-oxide synthase, brain (1786 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2D6 Tclin Cytochrome P450 2D6 (33882 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NOS3 Tchem Nitric-oxide synthase, endothelial (1452 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP1A2 Tchem Cytochrome P450 1A2 (26471 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2C9 Tchem Cytochrome P450 2C9 (32119 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP2C19 Tchem Cytochrome P450 2C19 (29246 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CYP3A4 Tclin Cytochrome P450 3A4 (53859 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM4E Tchem Lysine-specific demethylase 4D-like (40243 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MEN1 Tchem Menin/Histone-lysine N-methyltransferase MLL (48157 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
NOS1 Tchem Nitric oxide sythases; iNOS & nNOS (685 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Mus musculus (284745 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name 4-methylpyridin-2-amine
INCHI InChI=1S/C6H8N2/c1-5-2-3-8-6(7)4-5/h2-4H,1H3,(H2,7,8)
InChIKey ORLGLBZRQYOWNA-UHFFFAOYSA-N
Smiles CC1=CC(=NC=C1)N
Isomeric SMILES CC1=CC(=NC=C1)N
WGK Germany 3
RTECS TJ5150000
UN Number 2811
Molecular Weight 108.14
Beilstein 107066
Reaxy-Rn 107066
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=107066&ln=

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.

3 results found

Lot Number Certificate Type Date Item
A2330396 Certificate of Analysis Nov 18, 2022 A107214
A2330397 Certificate of Analysis Nov 18, 2022 A107214
A2330405 Certificate of Analysis Nov 18, 2022 A107214

Chemical and Physical Properties

Solubility Soluble in water (41 mg/ml at 20 °C), lower alcohols (slightly), chloroform, ethyl acetate, and DMF.
Sensitivity Moisture sensitive
Flash Point(°F) 244.4 °F
Flash Point(°C) 118 °C
Boil Point(°C) 230°C
Melt Point(°C) 96-101°C
Molecular Weight 108.140 g/mol
XLogP3 0.600
Hydrogen Bond Donor Count 1
Hydrogen Bond Acceptor Count 2
Rotatable Bond Count 0
Exact Mass 108.069 Da
Monoisotopic Mass 108.069 Da
Topological Polar Surface Area 38.900 Ų
Heavy Atom Count 8
Formal Charge 0
Complexity 72.900
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Citations of This Product

How to Cite Aladdin Scientific Products?
1. Xiaopeng Wei, Shuang Chen, Guoyuan Zheng, Qiule Zhao, Shuyi Mo, Jilin Wang, Disheng Yao, Nan Tian, Fei Long.  (2024)  Synthesis, crystal structure, thermal stability, and photovoltaic properties of organic-inorganic hybridized copper-based perovskite single crystals modulated by organics.  JOURNAL OF MOLECULAR STRUCTURE,  1304  (137634). 

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