TargetMol

Indanamin

Product Code:
 
TAR-T32153
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1
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CodeSizePrice
TAR-T32153-5mg5mg£850.00
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Further Information

Bioactivity:
Indanamin is a biochemical.
CAS:
1506-17-8
Formula:
C13H16ClN
Molecular Weight:
221.73
Purity:
0.98
SMILES:
Cl.CN(CC#C)C1CCc2ccccc12

References

1. Pati ML, Abate C, Contino M, Ferorelli S, Luisi R, Carroccia L, Niso M, Berardi F. Deconstruction of 6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline moiety to separate P-glycoprotein (P-gp) activity from ?2 receptor affinity in mixed P-gp/?2 receptor agents. Eur J Med Chem. 2015 Jan 7;89:691-700. doi: 10.1016/j.ejmech.2014.11.001. Epub 2014 Nov 4. PubMed PMID: 25462276. 2. Silva LF Jr, Siqueira FA, Pedrozo EC, Vieira FY, Doriguetto AC. Iodine(III)-promoted ring contraction of 1,2-dihydronaphthalenes: a diastereoselective total synthesis of (+/-)-indatraline. Org Lett. 2007 Apr 12;9(8):1433-6. Epub 2007 Mar 20. PubMed PMID: 17371034. 3. Gardner EL, Liu X, Paredes W, Giordano A, Spector J, Lepore M, Wu KM, Froimowitz M. A slow-onset, long-duration indanamine monoamine reuptake inhibitor as a potential maintenance pharmacotherapy for psychostimulant abuse: effects in laboratory rat models relating to addiction. Neuropharmacology. 2006 Oct;51(5):993-1003. Epub 2006 Aug 8. PubMed PMID: 16901516. 4. McConathy J, Owens MJ, Kilts CD, Malveaux EJ, Votaw JR, Nemeroff CB, Goodman MM. Synthesis and biological evaluation of trans-3-phenyl-1-indanamines as potential norepinephrine transporter imaging agents. Nucl Med Biol. 2005 Aug;32(6):593-605. PubMed PMID: 16026706.