BVT.13
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 563369

CAS#: 756813-87-3

Description: BVT.13 is a selective PPAR-gamma activator.

Chemical Structure

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BVT.13
CAS# 756813-87-3
Instruction

Theoretical Analysis

MedKoo Cat#: 563369
Name: BVT.13
CAS#: 756813-87-3
Chemical Formula: C18H11Cl2N3O4
Exact Mass: 403.01
Molecular Weight: 404.200
Elemental Analysis: C, 53.49; H, 2.74; Cl, 17.54; N, 10.40; O, 15.83

Price and Availability

Size Price Availability Quantity
5mg USD 370
25mg USD 1060
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Synonym: BVT.13; BVT 13; BVT-13; BVT13;

IUPAC/Chemical Name: 2-[(2,4-Dichlorobenzoyl)amino]-5-(2-pyrimidinyloxy)-benzoic acid

InChi Key: VNDRRWBKNSHALL-UHFFFAOYSA-N

InChi Code: InChI=1S/C18H11Cl2N3O4/c19-10-2-4-12(14(20)8-10)16(24)23-15-5-3-11(9-13(15)17(25)26)27-18-21-6-1-7-22-18/h1-9H,(H,23,24)(H,25,26)

SMILES Code: O=C(O)C1=CC(OC2=NC=CC=N2)=CC=C1NC(C3=CC=C(Cl)C=C3Cl)=O

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.03.00

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 404.20 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1: Ostberg T, Svensson S, Selén G, Uppenberg J, Thor M, Sundbom M, Sydow-Bäckman M, Gustavsson AL, Jendeberg L. A new class of peroxisome proliferator-activated receptor agonists with a novel binding epitope shows antidiabetic effects. J Biol Chem. 2004 Sep 24;279(39):41124-30. Epub 2004 Jul 15. PubMed PMID: 15258145.