TargetMol

Lupinine, (+)-

Product Code:
 
TAR-T32973
Product Group:
 
Inhibitors and Activators
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1
❮❯

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CodeSizePrice
TAR-T32973-5mg5mg£850.00
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This product comes from: United States.
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Further Information

Bioactivity:
Lupinine, (+)- is a bioactive chemical.
CAS:
7635-60-1
Formula:
C10H19NO
Molecular Weight:
169.268
Purity:
0.98
SMILES:
[H][C@@]12CCCCN1CCC[C@@H]2CO

References

1. Lee JA, An J, Kang TM, De D, Kim KK. Discovery of natural compounds promoting cardiomyocyte differentiation. Stem Cells Dev. 2018 Oct 25. doi: 10.1089/scd.2018.0153. [Epub ahead of print] PubMed PMID: 30358491. 2. Basilico N, Parapini S, Sparatore A, Romeo S, Misiano P, Vivas L, Yardley V, Croft SL, Habluetzel A, Lucantoni L, Renia L, Russell B, Suwanarusk R, Nosten F, Dondio G, Bigogno C, Jabes D, Taramelli D. In Vivo and In Vitro Activities and ADME-Tox Profile of a Quinolizidine-Modified 4-Aminoquinoline: A Potent Anti-P. falciparum and Anti-P. vivax Blood-Stage Antimalarial. Molecules. 2017 Dec 1;22(12). pii: E2102. doi: 10.3390/molecules22122102. PubMed PMID: 29194347. 3. Davies SG, Fletcher AM, Foster EM, Houlsby IT, Roberts PM, Schofield TM, Thomson JE. The asymmetric syntheses of pyrrolizidines, indolizidines and quinolizidines via two sequential tandem ring-closure/N-debenzylation processes. Org Biomol Chem. 2014 Dec 7;12(45):9223-35. doi: 10.1039/c4ob01737d. PubMed PMID: 25300749. 4. Koley D, Krishna Y, Srinivas K, Khan AA, Kant R. Organocatalytic asymmetric Mannich cyclization of hydroxylactams with acetals: total syntheses of (-)-epilupinine, (-)-tashiromine, and (-)-trachelanthamidine. Angew Chem Int Ed Engl. 2014 Nov 24;53(48):13196-200. doi: 10.1002/anie.201407185. Epub 2014 Sep 26. PubMed PMID: 25264221.