TT-OAD2 free base

SKU:BHB21900734
Overview
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TT-OAD2 free base (CAS 1246826-07-2) is a glucagon-like peptide-1 agonist. Relevant to GPCR/G Protein research. Molecular formula C50H47Cl2N3O6, molecular weight 856.83 g/mol.
CAS Number 1246826-07-2
Molecular Weight 856.83 g/mol
Storage See Certificate of Analysis
Options selector
Catalog no. Size
HY-129658-50MG 50 mg
HY-129658-100MG 100 mg
HY-129658-250MG 250 mg
Available Options

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  • Options: Size: 50 mg, 100 mg, 250 mg
  • Lead time: confirmed on inquiry for every option.
  • Storage: Please store the product under the recommended conditions in the Certificate of Analysis.
  • Shipping: Room temperature in continental US; may vary elsewhere.
  • Upon receipt: store as stated on the Certificate of Analysis; contact us if you need the condition before ordering.
Field Specification
CAS no. 1246826-07-2
Applications
  • Functional Assay (In Vitro)
Molecular weight 856.83
Molecular formula C50H47Cl2N3O6
SMILES O=C(O)[C@H](CC1=CC=C(C2=C(C)C(C)=NC=C2)C=C1)NC([C@H]3N([C@H](C4=CC=CC=C4)CC)CC5=C(C=C(OC[C@H](C6=CC=C(OCC7=CC=C(Cl)C(Cl)=C7)C=C6)O8)C8=C5)C3)=O
Storage Refer to Certificate of Analysis (CoA) for storage conditions
Shipping Room temperature in continental US; may vary elsewhere.
Catalog no. (Mfr.) HY-129658
Main SKU BHB21900734
Agonists

Compound Overview

TT-OAD2 free base is a non-peptide agonist of the glucagon-like peptide-1 (GLP-1) receptor, with an EC50 of 5 nM, and has potential for use in the treatment of diabetes[1][2]. It has the molecular formula C50H47Cl2N3O6 and a molecular weight of 856.83 g/mol.

Physical & Chemical Properties

CAS Number 1246826-07-2
Molecular Formula C50H47Cl2N3O6
Molecular Weight 856.83 g/mol
SMILES O=C(O)[C@H](CC1=CC=C(C2=C(C)C(C)=NC=C2)C=C1)NC([C@H]3N([C@H](C4=CC=CC=C4)CC)CC5=C(C=C(OC[C@H](C6=CC=C(OCC7=CC=C(Cl)C(Cl)=C7)C=C6)O8)C8=C5)C3)=O
Signaling Pathway GPCR/G Protein
Storage Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping Room temperature in continental US; may vary elsewhere.

Biological Activity

Activity & Target

EC50: 5 nM (GLP-1 receptor)[2]

Literature Cited

Sources cited in this description and in the In Vitro & In Vivo Data tab. Peer-reviewed publications that used this product are listed under References.

[1]. Zhao P, et al. Activation of the GLP-1 receptor by a non-peptidic agonist. Nature. 2020 Jan;577(7790):432-436.

[2]. Transtech Pharma, et al. Substituted azoanthracene derivatives, pharmaceutical compositions, and methods of use thereof. WO2010114824A1.

Safety

For Research Use Only. Not for use in diagnostic or therapeutic procedures, and not for human or veterinary use. Handle in accordance with your institution's chemical hygiene plan.

In Vitro

In HEK293A cells, TT-OAD2 (0-10 μM) suppresses the cAMP, calcium, pERK1/2 and β-arrestin responses mediated by GLP-1 and oxyntomodulin, in a concentration-dependent manner[1].

In Vivo

In male human GLP-1 receptor knock-in and knockout mice, intravenous TT-OAD2 (3 mg/kg) induces plasma insulin during an acute IVGTT, in humanized GLP-1R knock-in (KI) and GLP-1R knockout (KO) mice[1].

Animal ModelMale human GLP-1 receptor knock-in and knockout mice (6-11 months of age) with intravenous glucose tolerance tests[1]
Dosage3 mg/kg
AdministrationIntravenous injection (Single dose)
ResultInduced plasma insulin.

Data provided by the manufacturer. Numbered citations refer to the Literature Cited list in the product description.

Q.Why is there no price listed?
A.Every size of this product is quoted on inquiry. Send us the size you need and we will come back with price and lead time.
Q.Can this be used in humans or for diagnostics?
A.No. This product is supplied For Research Use Only. It is not for diagnostic or therapeutic procedures and not for human or veterinary use.

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