5,5'-Dimethyl-2,2'-bipyridyl - ≥98% , Zinc sequestering agent, CAS No.1762-34-1, Zinc sequestering agent

CAS: 1762-34-1 Cat. No.: D154986 Molecular Weight: 184.24 EC Number: 629-235-2

GRADE & PURITY ≥98%

Synonyms

2,2 -Bis-(5-methylpyridyl) | HA44 | HA-44 | 6UO390AMFB | BDBM50401351 | abametapirum | YSSJ3184 | PTRATZCAGVBFIQ-UHFFFAOYSA-N | Abametapir [USAN:INN] | Abametapir (USAN/INN) | 5,5'-Dimethyl-2,2'-dipyridyl | ABAMETAPIR [USAN] | D10687 | DB11932 | 5,5 inver

Storage

Room temperature

Shipped In

Normal

Overview

5,5'-Dimethyl-2,2'-bipyridyl is a metalloproteinase (MMP) inhibitor which is able to target metalloproteinases critical to egg hatching and louse development. Abametapir can inhibit hatching of both head and body louse

Specifications

Synonyms

2, 2 -Bis-(5-methylpyridyl) | HA44 | HA-44 | 6UO390AMFB | BDBM50401351 | abametapirum | YSSJ3184 | PTRATZCAGVBFIQ-UHFFFAOYSA-N | Abametapir [USAN:INN] | Abametapir (USAN/INN) | 5, 5'-Dimethyl-2, 2'-dipyridyl | ABAMETAPIR [USAN] | D10687 | DB11932 | 5, 5 inver

Specifications & Purity

≥98%

Storage

Room temperature

Shipped In

Normal

Action Type

INHIBITOR

Mechanism of action

Zinc sequestering agent

Purity

≥98%

Product Properties

• ALogP: 2.2

Names and Identifiers

• Pubchem Sid: 504752692
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752692
• Canonical Smiles: CC1=CN=C(C=C1)C2=NC=C(C=C2)C
• IUPAC Name: 5-methyl-2-(5-methylpyridin-2-yl)pyridine
• InChIKey: PTRATZCAGVBFIQ-UHFFFAOYSA-N
• INCHI: 1S/C12H12N2/c1-9-3-5-11(13-7-9)12-6-4-10(2)8-14-12/h3-8H,1-2H3
• Isomeric SMILES: CC1=CN=C(C=C1)C2=NC=C(C=C2)C
• WGK Germany: 3
• RTECS: DW1766000
• Molecular Weight: 184.24
• Reaxy-Rn: 123183
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=123183&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Class Pyridines and derivatives
      • Subclass Bipyridines and oligopyridines

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Class: Pyridines and derivatives
• Subclass: Bipyridines and oligopyridines
• Intermediate Tree Nodes: Not available
• Direct Parent: Bipyridines and oligopyridines
• Alternative Parents: Methylpyridines Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
• Molecular Framework: Aromatic heteromonocyclic compounds
• Substituents: Bipyridine - Methylpyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteromonocyclic compound
• Description: This compound belongs to the class of organic compounds known as bipyridines and oligopyridines. These are organic compounds containing two pyridine rings linked to each other.
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

CCR1 Tchem C-C chemokine receptor type 1 (1730 Activities)

Discover Target: CCR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CCR5 Tclin C-C chemokine receptor type 5 (5640 Activities)

Discover Target: CCR5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CCR8 Tchem C-C chemokine receptor type 8 (339 Activities)

Discover Target: CCR8

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)

Discover Target: Hdac6

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

rep Replicase polyprotein 1ab (378 Activities)

Discover Target: rep

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Chemical and Physical Properties

• Melt Point(°C): 115 °C
• Molecular Weight: 184.240 g/mol
• XLogP3: 2.200
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 1
• Exact Mass: 184.1 Da
• Monoisotopic Mass: 184.1 Da
• Topological Polar Surface Area: 25.800 Ų
• Heavy Atom Count: 14
• Formal Charge: 0
• Complexity: 161.000
• 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

References

1. Yingying Xu, Xiaojin Huang, Yulan Wang, Weiyu Qu, Weiliang Guo, Bin Su, Zhihui Dai.  (2024)  Controllable and Low-Loss Electrochemiluminescence Waveguide Supported by a Micropipette Electrode.  Journal of the American Chemical Society,      [PMID:38354221] [10.1021/jacs.3c12913]

2. Can Fang, Zhouxian Wang, Jingxu Han, Ning Zhou, Tonghao Dai, Zhifeng Dai, Yubing Xiong.  (2025)  Facile Synthesis of Bifunctional Heterogeneous Catalysts Used for the Chemical Fixation of a Low Concentration of CO2.  INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH,      [PMID:] [10.1021/acs.iecr.5c00820]

3. Hu Wang, Pengxiao Guo, Chaochuang Yin, Yadong Zhou, Yizhu Lei, Tingting Wu, Yinyan Wang, Kang Chen, Li Sun, Ziao Zong, Huaijun Luo.  (2025)  Design, structural analysis, and biological evaluation of four mononuclear copper(II) complexes as potent urease inhibitors: Insights from experimental and theoretical studies.  JOURNAL OF MOLECULAR STRUCTURE,      [PMID:] [10.1016/j.molstruc.2025.143005]

4. Zhilei Dai, Jing Zhang, Yiling Tong, Ning Zhou, Songyao Liu, Zhifeng Dai, Yubing Xiong.  (2026)  Toward sustainable catalysis: Anion-engineered metal-/halogen-free catalysts for efficient chemical fixation of low concentration CO2.  Journal of CO2 Utilization,      [PMID:] [10.1016/j.jcou.2025.103308]