MedKoo Cat#: 525487 | Name: LY 186126

Description:

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

LY 186126 is a potent cGI-PDE inhibitor. It exhibit reversible, high affinity (Ka = 6 nM) binding to a single class of SaR binding sites.

Chemical Structure

LY 186126
LY 186126
CAS#100644-00-6

Theoretical Analysis

MedKoo Cat#: 525487

Name: LY 186126

CAS#: 100644-00-6

Chemical Formula: C16H19N3O2

Exact Mass: 285.1477

Molecular Weight: 285.34

Elemental Analysis: C, 67.35; H, 6.71; N, 14.73; O, 11.21

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
Bulk Inquiry
Related CAS #
No Data
Synonym
LY 186126; LY186126; LY-186126.
IUPAC/Chemical Name
2H-Indol-2-one, 1,3-dihydro-1,3,3-trimethyl-5-(1,4,5,6-tetrahydro-4-methyl-6-oxo-3-pyridazinyl)-
InChi Key
KYKHXPMUZAMXTE-UHFFFAOYSA-N
InChi Code
InChI=1S/C16H19N3O2/c1-9-7-13(20)17-18-14(9)10-5-6-12-11(8-10)16(2,3)15(21)19(12)4/h5-6,8-9H,7H2,1-4H3,(H,17,20)
SMILES Code
O=C1N(C)C2=C(C=C(C(C(C)C3)=NNC3=O)C=C2)C1(C)C
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
>2 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
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 285.34 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
1: Ashikaga T, Robertson DW, Sportsman RJ, Strada SJ, Thompson WJ. Comparison of indolidan analog binding sites of drug antibody and sarcoplasmic reticulum with inhibition of cyclic AMP phosphodiesterase. J Recept Signal Transduct Res. 1996 Sep-Nov;16(5-6):315-37. PubMed PMID: 8968964. 2: Lugnier C, Muller B, Le Bec A, Beaudry C, Rousseau E. Characterization of indolidan- and rolipram-sensitive cyclic nucleotide phosphodiesterases in canine and human cardiac microsomal fractions. J Pharmacol Exp Ther. 1993 Jun;265(3):1142-51. PubMed PMID: 8389853. 3: Flawn P, Loten EG. Properties and distribution of cyclic AMP phosphodiesterase from rat liver. Int J Biochem. 1990;22(9):983-8. PubMed PMID: 1704319. 4: Artman M, Robertson DW, Mahony L, Thompson WJ. Analysis of the binding sites for the cardiotonic phosphodiesterase inhibitor [3H]LY186126 in ventricular myocardium. Mol Pharmacol. 1989 Aug;36(2):302-11. PubMed PMID: 2505059. 5: Robertson DW, Krushinski JH, Utterback BG, Kauffman RF. Synthesis of a tritium-labeled indolidan analogue and its use as a radioligand for phosphodiesterase-inhibitor cardiotonic binding sites. J Med Chem. 1989 Jul;32(7):1476-80. PubMed PMID: 2738882. 6: Kauffman RF, Utterback BG, Robertson DW. Characterization and pharmacological relevance of high affinity binding sites for [3H]LY186126, a cardiotonic phosphodiesterase inhibitor, in canine cardiac membranes. Circ Res. 1989 Jul;65(1):154-63. PubMed PMID: 2544318. 7: Kauffman RF, Utterback BG, Robertson DW. Specific binding of [3H]LY186126, an analogue of indolidan (LY195115), to cardiac membranes enriched in sarcoplasmic reticulum vesicles. Circ Res. 1989 May;64(5):1037-40. PubMed PMID: 2539921.