MedKoo Cat#: 407978 | Name: TTT20171

Description:

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

TTT20171 is a SDHC inhibitor. TTT20171 displays nanomolar inhibition of CII but lacks cellular potency. In cell assays, the most sensitive cells (22Rv1 prostate cancer cells) are inhibited at an IC50=5.4 uM, a value well above the suggested use concentration of 2 uM and the criterion of 1 uM for a quality chemical probe.

Chemical Structure

TTT20171
TTT20171
CAS#2110408-47-2

Theoretical Analysis

MedKoo Cat#: 407978

Name: TTT20171

CAS#: 2110408-47-2

Chemical Formula: C20H33NO5

Exact Mass: 367.2359

Molecular Weight: 367.49

Elemental Analysis: C, 65.37; H, 9.05; N, 3.81; O, 21.77

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.
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Related CAS #
No Data
Synonym
TTT20171; TTT-20171; TTT 20171;
IUPAC/Chemical Name
4-hydroxy-5,6-dimethoxy-3-tridecanoylpyridin-2(1H)-one
InChi Key
CZKPAGLXQOQNEI-UHFFFAOYSA-N
InChi Code
InChI=1S/C20H33NO5/c1-4-5-6-7-8-9-10-11-12-13-14-15(22)16-17(23)18(25-2)20(26-3)21-19(16)24/h4-14H2,1-3H3,(H2,21,23,24)
SMILES Code
COC1=C(OC)NC(C(C(CCCCCCCCCCCC)=O)=C1O)=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
2934.99.9001
More Info
Mitochondrial complex II (CII) is an emerging target for numerous human diseases.

Preparing Stock Solutions

The following data is based on the product molecular weight 367.49 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: Wang H, Huwaimel B, Verma K, Miller J, Germain TM, Kinarivala N, Pappas D, Brookes PS, Trippier PC. Synthesis and Antineoplastic Evaluation of Mitochondrial Complex II (Succinate Dehydrogenase) Inhibitors Derived from Atpenin A5. ChemMedChem. 2017 Jul 6;12(13):1033-1044. doi: 10.1002/cmdc.201700196. Epub 2017 Jun 12. PubMed PMID: 28523727; PubMed Central PMCID: PMC5557372.