TargetMol

Lobelanidine

Product Code:
 
TAR-T32832
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20℃
1 / 1

No additional charges, what you see is what you pay! *

CodeSizePrice
TAR-T32832-1mg1mg£352.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
TAR-T32832-1mL1 mL * 10 mM (in DMSO)£619.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
TAR-T32832-5mg5mg£736.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
TAR-T32832-10mg10mg£978.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
TAR-T32832-25mg25mg£1,348.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
TAR-T32832-50mg50mg£1,661.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
TAR-T32832-100mg100mg£2,079.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
TAR-T32832-500mg500mg£4,006.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
Prices exclude any Taxes / VAT
Stay in control of your spending. These prices have no additional charges, not even shipping!
* Rare exceptions are clearly labelled (only 0.14% of items!).
Multibuy discounts available! Contact us to find what you can save.
This product comes from: United States.
Typical lead time: 10-14 working days.
Contact us for more accurate information.
  • Further Information
  • Documents
  • References
  • Show All

Further Information

Bioactivity:
Lobelanidine is a chemical analog of lobeline.
CAS:
552-72-7
Formula:
C22H29NO2
Molecular Weight:
339.479
Pathway:
Neuroscience
Purity:
0.98
SMILES:
CN1C(CC(O)c2ccccc2)CCCC1CC(O)c1ccccc1
Target:
AChR

References

1. Paz C, Becerra J, Silva M, Burgosa V, Heydenreich M, Schmidt B, Tran T, Vetter I. (-)-Pentylsedinine, a New Alkaloid from the Leaves of Lobelia tupa with Agonist Activity at Nicotinic Acetylcholine Receptor. Nat Prod Commun. 2015 Aug;10(8):1355-7. PubMed PMID: 26434115. 2. Ch?nevert R, Morin P. Synthesis of (-)-lobeline via enzymatic desymmetrization of lobelanidine. Bioorg Med Chem. 2009 Mar 1;17(5):1837-9. doi: 10.1016/j.bmc.2009.01.055. Epub 2009 Jan 31. PubMed PMID: 19217305. 3. Chen MW, Chen WR, Zhang JM, Long XY, Wang YT. Lobelia chinensis: chemical constituents and anticancer activity perspective. Chin J Nat Med. 2014 Feb;12(2):103-7. doi: 10.1016/S1875-5364(14)60016-9. PubMed PMID: 24636059. 4. Birman VB, Jiang H, Li X. Enantioselective synthesis of lobeline via nonenzymatic desymmetrization. Org Lett. 2007 Aug 16;9(17):3237-40. Epub 2007 Jul 20. PubMed PMID: 17658751.