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Omilancor (BT-11)

Cat.No.S6419

Omilancor (BT-11) is an orally active compound that binds to lanthionine synthetase C-like 2 (LANCL2) for treating inflammatory bowel disease (IBD), with a Kd value of 7.7 µM.
Omilancor (BT-11) Chemical Structure

Chemical Structure

Molecular Weight: 528.56

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 528.56 Formula

C30H24N8O2

Storage (From the date of receipt) 3 years -20°C powder
CAS No. 1912399-75-7 -- Storage of Stock Solutions

Synonyms N/A Smiles C1CN(CCN1C(=O)C2=CC=CC(=N2)C3=NC4=CC=CC=C4N3)C(=O)C5=CC=CC(=N5)C6=NC7=CC=CC=C7N6

Solubility

In vitro
Batch:

DMSO : 4 mg/mL (7.56 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : Insoluble

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
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Mechanism of Action

Targets/IC50/Ki
LANCL2 [1]
In vitro

In vitro measurement of cAMP in mouse splenocytes extracted from either WT or LANCL2−/− mice and treated with increasing doses of Omilancor (BT-11) demonstrates that it stimulates cAMP production by activating the LANCL2 pathway[1].

In vivo

Oral treatment with Omilancor (BT-11) at 8 mg/kg/day ameliorates colitis in mice. Safety assessment in rats indicateds that oral treatment with this compound at high doses has an excellent safety profile up to 1000 mg/kg/day. In a dextran sodium sulfate colitis mouse model, its oral administration upregulates the expression of IL-10 and downregulates the expression of TNF-α mRNA. It also upregulates LANCL2 expression in the gastrointestinal tract[1].

References

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