356568-70-2
356568-70-2
Chemical Structure
Barbadin
- CAS No.: 356568-70-2
- Formula:C19H15N3OS
- Molecular Weight:333.41
IUPAC Name: 3-amino-5-(4-benzylphenyl)thieno[2,3-d]pyrimidin-4(3H)-one
InChIKey: OCBXPCSXEQQADU-UHFFFAOYSA-N
SMILES: O=C1C(C(C2=CC=C(CC3=CC=CC=C3)C=C2)=CS4)=C4N=CN1N
Biological Activity: Barbadin is a novel and selective β-arrestin/β2-adaptin interaction inhibitor, has IC50 values of 19.1 μM for β-arrestin1 and 15.6 μM for β-arrestin2. Barbadin blocks agonist-promoted endocytosis of the prototypical β2-adrenergic, V2-vasopressin and angiotensin-II type-1 receptors. Barbadin can induce apoptosis[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Barbadin | 98.93% | Barbadin is a novel and selective β-arrestin/β2-adaptin interaction inhibitor, has IC50 values of 19.1 μM for β-arrestin1 and 15.6 μM for β-arrestin2. Barbadin blocks agonist-promoted endocytosis of the prototypical β2-adrenergic, V2-vasopressin and angiotensin-II type-1 receptors. Barbadin can induce apoptosis. | ||||||||||||||||||||
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Barbadin (Standard) | ≥98% | Barbadin (Standard) is the analytical standard of Barbadin (HY-119706). This product is intended for research and analytical applications. Barbadin is a novel and selective β-arrestin/β2-adaptin interaction inhibitor, has IC50 values of 19.1 μM for β-arrestin1 and 15.6 μM for β-arrestin2. Barbadin blocks agonist-promoted endocytosis of the prototypical β2-adrenergic, V2-vasopressin and angiotensin-II type-1 receptors. Barbadin can induce apoptosis. | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.58
HY-W027340ARM1 -
Similarity Score 0.54
HY-16693LDN-27219 -
Similarity Score 0.54
HY-153090Transketolase-IN-4 -
Similarity Score 0.53
HY-U00177GDP366 -
Similarity Score 0.53
HY-169573Casein kinase 1δ-IN-16 -
Similarity Score 0.52
HY-146100GABAA receptor agent 8 -
Similarity Score 0.52
![5-Phenylthieno[2,3-d]pyrimidin-4-amine Chemical Structure](//file.medchemexpress.com/product_pic/hy-w079315.gif)
HY-W0793155-Phenylthieno[2,3-d]pyrimidin-4-amine -
Similarity Score 0.51
HY-187055Antiproliferative agent-79 -
Similarity Score 0.50
HY-144906THP104c -
Explore the MedChemAI to find more analogs
![5-Phenylthieno[2,3-d]pyrimidin-4-amine Chemical Structure](http://file.medchemexpress.com/product_pic/hy-w079315.gif)
References
- [1]. Beautrait A, et al. A new inhibitor of the β-arrestin/AP2 endocytic complex reveals interplay between GPCR internalization and signalling. Nat Commun. 2017 Apr 18;8:15054. doi: 10.1038/ncomms15054. [Content Brief]
- [2]. Thoria Donia, et al. β-Arrestin inhibition induces autophagy, apoptosis, G0/G1 cell cycle arrest in agonist-activated V2R receptor in breast cancer cells. Med Oncol. 2021 Mar 15;38(4):38. [Content Brief]
