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Ebastine - ≥99%, high purity , Histamine H1 receptor inverse agonist, CAS No.90729-43-4, Histamine H1 receptor inverse agonist

  • ≥99%
Item Number
E129486
Grouped product items
SKUSizeAvailabilityPrice Qty
E129486-250mg
250mg
In stock
$24.90
E129486-1g
1g
In stock
$82.90
E129486-5g
5g
In stock
$296.90
E129486-25g
25g
In stock
$1,336.90
E129486-100g
100g
In stock
$4,811.90
View related series
Histamine receptor antagonists

Basic Description

Synonymsebastine|90729-43-4|Kestine|Ebastel|Ebastin|Bactil|Kestin|LAS W-090|RP 64305|LAS-W-090|1-(4-tert-butylphenyl)-4-[4-(diphenylmethoxy)piperidin-1-yl]butan-1-one|LAS-W 090;RP64305|RP64305|4-(4-benzhydryloxypiperidin-1-yl)-1-(4-tert-butylphenyl)butan-1-one|4-
Specifications & Purity≥99%
Storage TempStore at 2-8°C,Protected from light
Shipped InWet ice
Action TypeINVERSE AGONIST
Mechanism of actionHistamine H1 receptor inverse agonist

Product Properties

ALogP7.2

Associated Targets

DRD2 Tclin D(2) dopamine receptor 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HRH1 Tclin Histamine H1 receptor 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A2 Tclin Sodium-dependent noradrenaline transporter 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A3 Tclin Sodium-dependent dopamine transporter 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC6A4 Tclin Sodium-dependent serotonin transporter 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

DRD3 Tclin D(3) dopamine 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)

HTR2A Tclin 5-hydroxytryptamine receptor 2A 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CHRM1 Tclin Muscarinic acetylcholine receptor M1 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR1A Tclin 5-hydroxytryptamine receptor 1A 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 4 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 4-(4-benzhydryloxypiperidin-1-yl)-1-(4-tert-butylphenyl)butan-1-one
INCHI InChI=1S/C32H39NO2/c1-32(2,3)28-18-16-25(17-19-28)30(34)15-10-22-33-23-20-29(21-24-33)35-31(26-11-6-4-7-12-26)27-13-8-5-9-14-27/h4-9,11-14,16-19,29,31H,10,15,20-24H2,1-3H3
InChi Key MJJALKDDGIKVBE-UHFFFAOYSA-N
Canonical SMILES CC(C)(C)C1=CC=C(C=C1)C(=O)CCCN2CCC(CC2)OC(C3=CC=CC=C3)C4=CC=CC=C4
Isomeric SMILES CC(C)(C)C1=CC=C(C=C1)C(=O)CCCN2CCC(CC2)OC(C3=CC=CC=C3)C4=CC=CC=C4
WGK Germany 3
RTECS EL8140000
PubChem CID 3191
Molecular Weight 469.66
Reaxy-Rn 7522103

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

5 results found

Lot NumberCertificate TypeDateItem
G2220652Certificate of AnalysisMay 14, 2024 E129486
G2220653Certificate of AnalysisMay 14, 2024 E129486
G2220694Certificate of AnalysisMay 14, 2024 E129486
G2220695Certificate of AnalysisMay 14, 2024 E129486
G2220934Certificate of AnalysisMay 14, 2024 E129486

Chemical and Physical Properties

SolubilitySlightly soluble in chloroform, methanol
SensitivityLight sensitive
Melt Point(°C)85.0-89.0 °C

Safety and Hazards(GHS)

Hazard Statements

H413:May cause long lasting harmful effects to aquatic life

Precautionary Statements

P273:Avoid release to the environment.

P501:Dispose of contents/container to ...

WGK Germany 3
RTECS EL8140000
Reaxy-Rn 7522103

Related Documents

References

1. Li Q et al..  (2020)  Antihistamine Drug Ebastine Inhibits Cancer Growth by Targeting Polycomb Group Protein EZH2..  Mol Cancer Ther,  19  (10): (2023-2033).  [PMID:32855270]

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