Atipamezole - ≥98% (HPLC), high purity , CAS No.104054-27-5, Antagonist of α 2A-adrenoceptor;Antagonist of α 2B-adrenoceptor;Antagonist of α 2C-adrenoceptor

In stock
Item Number
A132977
Grouped product items
SKUSizeAvailabilityPrice Qty
A132977-5mg
5mg
9
$34.90
A132977-25mg
25mg
6
$123.90
A132977-100mg
100mg
6
$343.90
A132977-250mg
250mg
≥10
$686.90
A132977-1g
1g
9
$1,716.90

Basic Description

SynonymsMPV1248 | MPV 1248 | PDSP2_001566 | antipamezole | CAS_104054-27-5 | PDSP1_001582 | Atipamezolum (Latin) | Aurin No. 555 | BDBM81807 | AC-1614 | DTXSID2049135 | 4-(2-ethyl-2-indanyl)imidazole. | NCGC00182707-02 | NSC_71310 | Vioxx Dolor | D03002 | FT-0603
Specifications & PurityMoligand™, ≥98%(HPLC)
Storage TempRoom temperature
Shipped InNormal
GradeMoligand™
Action TypeANTAGONIST
Mechanism of actionAntagonist of α 2A-adrenoceptor;Antagonist of α 2B-adrenoceptor;Antagonist of α 2C-adrenoceptor
Product Description

Atipamezole(MPV1248) is an alpha-adrenoceptor antagonist with high affinity and selectivity for the alpha 2-receptor.

Associated Targets(Human)

ADRA2B Tclin Alpha-2B adrenergic receptor (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADRA2C Tclin Alpha-2C adrenergic receptor (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADRA2A Tclin Alpha-2A adrenergic receptor (3 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2B Tclin Alpha-2b adrenergic receptor (4412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2C Tclin Alpha-2c adrenergic receptor (4876 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Galc Galactocerebrosidase (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Adra1b Adrenergic receptor alpha-1 (5652 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Adra2c Adrenergic receptor alpha-2 (3313 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

Pubchem Sid488184646
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488184646
IUPAC Name 5-(2-ethyl-1,3-dihydroinden-2-yl)-1H-imidazole
INCHI InChI=1S/C14H16N2/c1-2-14(13-9-15-10-16-13)7-11-5-3-4-6-12(11)8-14/h3-6,9-10H,2,7-8H2,1H3,(H,15,16)
InChi Key HSWPZIDYAHLZDD-UHFFFAOYSA-N
Canonical SMILES CCC1(CC2=CC=CC=C2C1)C3=CN=CN3
Isomeric SMILES CCC1(CC2=CC=CC=C2C1)C3=CN=CN3
WGK Germany 3
Alternate CAS 104054-27-5
PubChem CID 71310
MeSH Entry Terms 1H-imidazole, 4-(2-ethyl-2,3-dihydro-1H-inden-2-yl)-;antipamezole;atipamezole;MPV 1248;MPV-1248
Molecular Weight 212.29

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.

9 results found

Lot NumberCertificate TypeDateItem
E2315572Certificate of AnalysisFeb 11, 2025 A132977
J2211560Certificate of AnalysisJul 19, 2024 A132977
J2211540Certificate of AnalysisJul 19, 2024 A132977
J2211552Certificate of AnalysisJul 19, 2024 A132977
J2211559Certificate of AnalysisJul 19, 2024 A132977
J2211569Certificate of AnalysisJul 19, 2024 A132977
G1605067Certificate of AnalysisNov 20, 2023 A132977
A1824001Certificate of AnalysisJun 08, 2023 A132977
A1824010Certificate of AnalysisJun 08, 2023 A132977

Chemical and Physical Properties

Melt Point(°C)129 °C
Molecular Weight212.290 g/mol
XLogP33.000
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count1
Rotatable Bond Count2
Exact Mass212.131 Da
Monoisotopic Mass212.131 Da
Topological Polar Surface Area28.700 Ų
Heavy Atom Count16
Formal Charge0
Complexity237.000
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

Safety and Hazards(GHS)

WGK Germany 3
Merck Index 861

Specifications

Citations of This Product

1. Rongzong Qiu, Weifeng Yao, Haocong Ji, Dongdong Yuan, Xiaofeng Gao, Weiping Sha, Fei Wang, Pinjie Huang, Ziqing Hei.  (2018)  Dexmedetomidine restores septic renal function via promoting inflammation resolution in a rat sepsis model.  LIFE SCIENCES,  204  (1).  [PMID:29733849] [10.1016/j.lfs.2018.05.001]

References

1. Rongzong Qiu, Weifeng Yao, Haocong Ji, Dongdong Yuan, Xiaofeng Gao, Weiping Sha, Fei Wang, Pinjie Huang, Ziqing Hei.  (2018)  Dexmedetomidine restores septic renal function via promoting inflammation resolution in a rat sepsis model.  LIFE SCIENCES,  204  (1).  [PMID:29733849] [10.1016/j.lfs.2018.05.001]

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