MedKoo Cat#: 562077 | Name: Bax-activator-106

Description:

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

Bax-activator-106 is a specific Bax agonist. It acts by promoting Bax-dependent but not Bak-dependent apoptosis.

Chemical Structure

Bax-activator-106
Bax-activator-106
CAS#1638526-94-9

Theoretical Analysis

MedKoo Cat#: 562077

Name: Bax-activator-106

CAS#: 1638526-94-9

Chemical Formula: C29H36N4O3

Exact Mass: 488.2787

Molecular Weight: 488.63

Elemental Analysis: C, 71.28; H, 7.43; N, 11.47; O, 9.82

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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Synonym
Bax-activator-106; Baxactivator106; Bax activator 106;
IUPAC/Chemical Name
(R)-(5-(3,4-dimethylbenzyl)-1-(3-methoxybenzyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-3-yl)(3-hydroxypiperidin-1-yl)methanone
InChi Key
OLNVSYZSZXRLCF-XMMPIXPASA-N
InChi Code
InChI=1S/C29H36N4O3/c1-20-9-10-23(14-21(20)2)16-31-13-11-27-26(19-31)28(29(35)32-12-5-7-24(34)18-32)30-33(27)17-22-6-4-8-25(15-22)36-3/h4,6,8-10,14-15,24,34H,5,7,11-13,16-19H2,1-3H3/t24-/m1/s1
SMILES Code
O=C(C1=NN(CC2=CC=CC(OC)=C2)C3=C1CN(CC4=CC=C(C)C(C)=C4)CC3)N5C[C@H](O)CCC5
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 488.63 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: Shivakumar S, Kurylowicz M, Hirmiz N, Manan Y, Friaa O, Shamas-Din A, Masoudian P, Leber B, Andrews DW, Fradin C. The proapoptotic protein tBid forms both superficially bound and membrane-inserted oligomers. Biophys J. 2014 May 20;106(10):2085-95. doi: 10.1016/j.bpj.2014.03.049. PubMed PMID: 24853737; PubMed Central PMCID: PMC4052270. 2: Pan B, Yang L, Wang J, Wang Y, Wang J, Zhou X, Yin X, Zhang Z, Zhao D. C-Abl tyrosine kinase mediates neurotoxic prion peptide-induced neuronal apoptosis via regulating mitochondrial homeostasis. Mol Neurobiol. 2014 Apr;49(2):1102-16. doi: 10.1007/s12035-014-8646-4. Epub 2014 Feb 8. PubMed PMID: 24510275. 3: Jeong JK, Moon MH, Lee YJ, Seol JW, Park SY. Autophagy induced by the class III histone deacetylase Sirt1 prevents prion peptide neurotoxicity. Neurobiol Aging. 2013 Jan;34(1):146-56. doi: 10.1016/j.neurobiolaging.2012.04.002. Epub 2012 May 9. PubMed PMID: 22575359. 4: Sun CK, Chang CL, Lin YC, Kao YH, Chang LT, Yen CH, Shao PL, Chen CH, Leu S, Yip HK. Systemic administration of autologous adipose-derived mesenchymal stem cells alleviates hepatic ischemia-reperfusion injury in rats. Crit Care Med. 2012 Apr;40(4):1279-90. doi: 10.1097/CCM.0b013e31823dae23. PubMed PMID: 22336724. 5: Leu S, Lin YC, Yuen CM, Yen CH, Kao YH, Sun CK, Yip HK. Adipose-derived mesenchymal stem cells markedly attenuate brain infarct size and improve neurological function in rats. J Transl Med. 2010 Jun 28;8:63. doi: 10.1186/1479-5876-8-63. PubMed PMID: 20584315; PubMed Central PMCID: PMC2913939.