Atiprimod

Atiprimod
Clinical data
ATC code	none;
Identifiers
	IUPAC name 3-(8,8-dipropyl-3-azaspiro[4.5]decan-3-yl)-N,N- diethylpropan-1-amine;
CAS Number	123018-47-3 ;
PubChem CID	129869;
ChemSpider	114962 ;
UNII	MG7D3QD743;
KEGG	D03003 ;
ChEMBL	ChEMBL103735 ;
CompTox Dashboard (EPA)	DTXSID10153834 ;
Chemical and physical data
Formula	C22H44N2
Molar mass	336.608 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES N(CC)(CC)CCCN2CCC1(CCC(CC1)(CCC)CCC)C2;
	InChI InChI=1S/C22H44N2/c1-5-10-21(11-6-2)12-14-22(15-13-21)16-19-24(20-22)18-9-17-23(7-3)8-4/h5-20H2,1-4H3 ; Key:SERHTTSLBVGRBY-UHFFFAOYSA-N ;
	(what is this?) (verify)

Atiprimod (INN, codenamed SK&F106615) is a substance being studied in the treatment of certain multiple myelomas and other advanced cancers. It may block the growth of tumors and the growth of blood vessels from surrounding tissue to the tumor. This drug is also being researched as a potential treatment for various autoimmune diseases. It was first developed by GlaxoSmithKline as a potential treatment for rheumatoid arthritis.[1] The substance is also known as azaspirane, although this more properly refers to the class of chemicals to which atiprimod belongs.

This compound has also been shown to kill mantle cell lymphoma cells in vitro.[2]

Mechanism of action

Atiprimod has been shown to inhibit angiogenesis (growth of blood vessels) in a blood vessel model using chicken eggs. It is thought to inhibit the secretion of vascular endothelial growth factor (VEGF), a growth factor that promotes angiogenesis.

Chemistry

Atiprimod is an amphiphilic compound and a cation at neutral pH.

Synthesis

Atiprimod synthesis: Anormed Inc. Dagger, R. E.; Grady, C. W.; 1999, U.S. Patent 5,952,365.

gollark: What people want it to be might be more accurate, I suppose.

gollark: I mostly think of it as the second one. It's possible palaiologos is trying to move it toward the first, and I don't like this.

gollark: It's possible that this stems partly from differences in perception of what esolangs actually is; esoteric programming language discussion place which happens to have a somewhat weird community in it versus weird community which happens to exist in something nominally for esolang discussion.

gollark: Ah, sinthÖrion.

gollark: I figure people are mostly prompted by *something* instead of just bringing it up entirely at random, and a ControversialEsolangs server would lack many of those prompts if it's purely for that.

References

Jacobs GS (Spring 2004). "Atiprimod: A New Drug Candidate in Early-Stage Development for Myeloma". Myeloma Today. International Myeloma Foundation. 5 (10). Archived from the original on 2011-07-18. Retrieved 2010-09-30.
Wang, M.; Zhang, L.; Han, X.; Yang, J.; Qian, J.; Hong, S.; Samaniego, F.; Romaguera, J.; Yi, Q. (2007). "Atiprimod inhibits the growth of mantle cell lymphoma in vitro and in vivo and induces apoptosis via activating the mitochondrial pathways". Blood. 109 (12): 5455. doi:10.1182/blood-2006-12-063958. PMID 17317853.

External links

Atiprimod entry in the public domain NCI Dictionary of Cancer Terms

This article incorporates public domain material from the U.S. National Cancer Institute document: "Dictionary of Cancer Terms".

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Jacobs GS (Spring 2004). "Atiprimod: A New Drug Candidate in Early-Stage Development for Myeloma". Myeloma Today. International Myeloma Foundation. 5 (10). Archived from the original on 2011-07-18. Retrieved 2010-09-30.

[2] Wang, M.; Zhang, L.; Han, X.; Yang, J.; Qian, J.; Hong, S.; Samaniego, F.; Romaguera, J.; Yi, Q. (2007). "Atiprimod inhibits the growth of mantle cell lymphoma in vitro and in vivo and induces apoptosis via activating the mitochondrial pathways". Blood. 109 (12): 5455. doi:10.1182/blood-2006-12-063958. PMID 17317853.