CIM-0216
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 563652

CAS#: 1031496-06-6

Description: CIM-0216 is a selective TRPM3 agonist.


Chemical Structure

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CIM-0216
CAS# 1031496-06-6

Theoretical Analysis

MedKoo Cat#: 563652
Name: CIM-0216
CAS#: 1031496-06-6
Chemical Formula: C21H21N3O2
Exact Mass: 347.16
Molecular Weight: 347.410
Elemental Analysis: C, 72.60; H, 6.09; N, 12.10; O, 9.21

Price and Availability

Size Price Availability Quantity
1mg USD 210 2 Weeks
5mg USD 385 2 Weeks
10mg USD 625 2 Weeks
25mg USD 1000 2 Weeks
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Synonym: CIM-0216; CIM 0216; CIM0216;

IUPAC/Chemical Name: 3,4-Dihydro-N-(5-methyl-3-isoxazolyl)-a-phenyl-1(2H)-quinolineacetamide

InChi Key: KSEXDSJYVSEVGF-UHFFFAOYSA-N

InChi Code: InChI=1S/C21H21N3O2/c1-15-14-19(23-26-15)22-21(25)20(17-9-3-2-4-10-17)24-13-7-11-16-8-5-6-12-18(16)24/h2-6,8-10,12,14,20H,7,11,13H2,1H3,(H,22,23,25)

SMILES Code: O=C(NC1=NOC(C)=C1)C(C2=CC=CC=C2)N3CCCC4=C3C=CC=C4

Appearance: Solid powder

Purity: >95% (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 347.41 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: Held K, Gruss F, Aloi VD, Janssens A, Ulens C, Voets T, Vriens J. Mutations in the voltage-sensing domain affect the alternative ion permeation pathway in the TRPM3 channel. J Physiol. 2018 Jun;596(12):2413-2432. doi: 10.1113/JP274124. Epub 2018 Apr 25. PubMed PMID: 29604058; PubMed Central PMCID: PMC6002228.

2: Badheka D, Yudin Y, Borbiro I, Hartle CM, Yazici A, Mirshahi T, Rohacs T. Inhibition of Transient Receptor Potential Melastatin 3 ion channels by G-protein βγ subunits. Elife. 2017 Aug 15;6. pii: e26147. doi: 10.7554/eLife.26147. PubMed PMID: 28829742; PubMed Central PMCID: PMC5593506.

3: Thiel G, Rubil S, Lesch A, Guethlein LA, Rössler OG. Transient receptor potential TRPM3 channels: Pharmacology, signaling, and biological functions. Pharmacol Res. 2017 Oct;124:92-99. doi: 10.1016/j.phrs.2017.07.014. Epub 2017 Jul 16. Review. PubMed PMID: 28720517.

4: Rubil S, Thiel G. Activation of gene transcription via CIM0216, a synthetic ligand of transient receptor potential melastatin-3 (TRPM3) channels. Channels (Austin). 2017 Jan 2;11(1):79-83. doi: 10.1080/19336950.2016.1207026. Epub 2016 Jun 29. PubMed PMID: 27356187; PubMed Central PMCID: PMC5279878.

5: Held K, Kichko T, De Clercq K, Klaassen H, Van Bree R, Vanherck JC, Marchand A, Reeh PW, Chaltin P, Voets T, Vriens J. Activation of TRPM3 by a potent synthetic ligand reveals a role in peptide release. Proc Natl Acad Sci U S A. 2015 Mar 17;112(11):E1363-72. doi: 10.1073/pnas.1419845112. Epub 2015 Mar 2. PubMed PMID: 25733887; PubMed Central PMCID: PMC4371942.