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TAS-108

From Wikipedia, the free encyclopedia
Chemical compound

Pharmaceutical compound
TAS-108
Clinical data
Other names17β-[2-[4-[(diethylamino)methyl]-2-methoxyphenoxy]ethyl]-7α-methylestra-1,3,5(10)-trien-3-ol; 17β-[2-[4-[(diethylamino)methyl]-2-methoxyphenoxy]ethyl]-7α-methylestradiol
Routes of
administration
By mouth[1]
ATC code
Identifiers
  • (1S,9R,10S,11S,14R,15R)-14-(2-{4-[(diethylamino)methyl]-2-methoxyphenoxy}ethyl)-9,15-dimethyltetracyclo[8.7.0.02,7.011,15]heptadeca-2(7),3,5-trien-5-ol
CAS Number
PubChemCID
ChemSpider
UNII
CompTox Dashboard(EPA)
Chemical and physical data
FormulaC33H47NO3
Molar mass505.743 g·mol−1
3D model (JSmol)
  • CCN(CC)CC1=CC(=C(C=C1)OCC[C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3[C@@H](CC5=C4C=CC(=C5)O)C)C)OC

  • Citrate: CCN(CC)CC1=CC(=C(C=C1)OCC[C@H]2CC[C@@H]3[C@@]2(CC[C@H]4[C@H]3[C@@H](CC5=C4C=CC(=C5)O)C)C)OC.C(C(=O)O)C(CC(=O)O)(C(=O)O)O
  • InChI=1S/C33H47NO3/c1-6-34(7-2)21-23-8-13-30(31(19-23)36-5)37-17-15-25-9-12-29-32-22(3)18-24-20-26(35)10-11-27(24)28(32)14-16-33(25,29)4/h8,10-11,13,19-20,22,25,28-29,32,35H,6-7,9,12,14-18,21H2,1-5H3/t22-,25-,28-,29+,32-,33-/m1/s1 checkY
  • Key:OHCPNHFLPCVWRG-MWSJHZLTSA-N checkY

  • Citrate: InChI=1S/C33H47NO3.C6H8O7/c1-6-34(7-2)21-23-8-13-30(31(19-23)36-5)37-17-15-25-9-12-29-32-22(3)18-24-20-26(35)10-11-27(24)28(32)14-16-33(25,29)4;7-3(8)1-6(13,5(11)12)2-4(9)10/h8,10-11,13,19-20,22,25,28-29,32,35H,6-7,9,12,14-18,21H2,1-5H3;13H,1-2H2,(H,7,8)(H,9,10)(H,11,12)/t22-,25-,28-,29+,32-,33-;/m1./s1
  • Key:VOHOCSJONOJOSD-SCIDSJFVSA-N

TAS-108, also known asSR-16234, is a drug discovered byMasato Tanabe and under development bySRI International andTaiho Pharmaceutical. It is asteroid hormone that has shown signs of treating and preventingbreast cancer, even in patients wheretamoxifen has failed.[2][3]

Development

[edit]

Masato Tanabe's team at SRI has focused on the development of steroid hormones. A compound discovered in a previous SRI contract from theNational Institutes of Health showed potential – it acted like "anti-estrogen" in the breasts and uterus but like normal estrogen elsewhere in the body, and was more "tissue-selective".[4] A contract was proposed toTaiho Pharmaceutical in July 1996, and within six years and slightly under $3 million (an unusually short amount of time), two new drugs were discovered and tested on people (particularly people for whichtamoxifen has failed): SR-16234 and SR-16287.[4]

The first of those, SR-16234, also inhibited the growth of blood vesselsangiogenesis and accelerated the death of cancer cellsapoptosis and thus was particularly well suited to be an anti-cancer drug.[4] As of August 2010, the drug had been through five Phase I and two Phase II studies,[5] and Phase III studies are being planned.[6]

See also

[edit]

References

[edit]
  1. ^Yamamoto Y, Shibata J, Yonekura K, Sato K, Hashimoto A, Aoyagi Y, et al. (January 2005). "TAS-108, a novel oral steroidal antiestrogenic agent, is a pure antagonist on estrogen receptor alpha and a partial agonist on estrogen receptor beta with low uterotrophic effect".Clinical Cancer Research.11 (1):315–322.doi:10.1158/1078-0432.315.11.1.PMID 15671561.
  2. ^Yamamoto Y, Wada O, Takada I, Yogiashi Y, Shibata J, Yanagisawa J, et al. (December 2003). "Both N- and C-terminal transactivation functions of DNA-bound ERalpha are blocked by a novel synthetic estrogen ligand".Biochemical and Biophysical Research Communications.312 (3):656–662.doi:10.1016/j.bbrc.2003.10.178.PMID 14680815.
  3. ^"Alumni Hall of Fame 2004: Masato Tanabe".SRI International. Archived fromthe original on 2013-01-04. Retrieved2013-02-10.
  4. ^abcNielson D (2006).A Heritage of Innovation: SRI's First Half Century.Menlo Park, California: SRI International. pp. 10–15.ISBN 978-0-9745208-1-0.
  5. ^"SRI International to Advance Clinical Development of TAS-108, a Late-Stage Breast Cancer Drug" (Press release).SRI International. Archived fromthe original on 2013-04-03. Retrieved2013-02-24.
  6. ^Buzdar AU (January 2005)."TAS-108: a novel steroidal antiestrogen".Clinical Cancer Research.11 (2 Pt 2):906s –908s.doi:10.1158/1078-0432.906s.11.2.PMID 15701885.

External links

[edit]
ERTooltip Estrogen receptor
Agonists
Mixed
(SERMsTooltip Selective estrogen receptor modulators)
Antagonists
GPERTooltip G protein-coupled estrogen receptor
Agonists
Antagonists
Unknown
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