Misplaced Pages

Telomestatin: Difference between revisions

Article snapshot taken from Wikipedia with creative commons attribution-sharealike license. Give it a read and then ask your questions in the chat. We can research this topic together.
Browse history interactively
Page 1
Page 2
← Previous editContent deleted Content addedVisualWikitext
Revision as of 16:28, 6 December 2010 editCitation bot (talk | contribs)Bots5,424,102 editsm Citations: added: doi, pmid. Rjwilmsi← Previous edit Latest revision as of 16:00, 28 November 2024 edit undoAnomieBOT (talk | contribs)Bots6,568,448 editsm Dating maintenance tags: {{Cn}} 
(16 intermediate revisions by 12 users not shown)
Line 1: Line 1:
{{Chembox {{Chembox
| Verifiedfields = changed
| verifiedrevid = 400875358
| ImageFile = Telomestatin.png | ImageFile = Telomestatin.png
| ImageSize = 200px | ImageSize = 200px
| ImageAlt = | ImageAlt =
| PIN = (8<sup>4</sup>''R'')-6<sup>5</sup>,7<sup>5</sup>-Dimethyl-8<sup>4</sup>,8<sup>5</sup>-dihydro-1(2,4),2,3,4,5,6,7(4,2)-heptakis(oxazolo)-8(2,4)-thiazolocyclooctaphane
| IUPACName =
| OtherNames = | OtherNames =
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 265114-54-3
| PubChem = 11954679 | CASNo = 265114-54-3
| PubChem = 11954679
| SMILES = CC1=C(C2=NC(C3=NC(C4=NC(C5=NC(C6=NC(C7=NC(C8=N9()CS8)=CO7)=CO6)=CO5)=CO4)=CO3)=C(C)O2)N=C9O1
| ChEMBL_Ref = {{ebicite|changed|EBI}}
| ChEMBL = 443683
| SMILES = CC1=C(C2=NC(C3=NC(C4=NC(C5=NC(C6=NC(C7=NC(C8=N9()CS8)=CO7)=CO6)=CO5)=CO4)=CO3)=C(C)O2)N=C9O1
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| C=26 | H=14 | N=8 | O=7 | S=1 | C=26 | H=14 | N=8 | O=7 | S=1
| Appearance = | Appearance =
| Density = | Density =
| MeltingPt = | MeltingPt =
| BoilingPt = | BoilingPt =
| Solubility = }} | Solubility = }}
| Section3 = {{Chembox Hazards |Section3={{Chembox Hazards
| MainHazards = | MainHazards =
| FlashPt = | FlashPt =
| Autoignition = }} | AutoignitionPt = }}
}} }}


'''Telomestatin''' is a ] ] that acts by inhibiting the ] activity of the cancer cells.<ref name=Shin-ya>{{cite journal | doi = 10.1021/ja005780q | author = Shin-ya, Kazuo; Wierzba, Konstanty; Matsuo, Ken-ichi; Ohtani, Toshio; Yamada, Yuji; Furihata, Kazuo; Hayakawa, Yoichi; Seto, Haruo | title = Telomestatin, a novel telomerase inhibitor from Streptomyces anulatus | journal = Journal of the American Chemical Society | year = 2001 | volume = 123 | issue = 6 | pages = 1262–1263 | pmid = 11456694}}</ref> It was first isolated from the bacteria '']''.<ref name=Shin-ya/> Telomestatin induces the formation of basket-type ] (G4) structures from hybrid-type G-quadruplexes in the ]. Upon formation of G4 structure there will be a decrease in the activity of the telomerase, which is involved in the replication of the telomeres and as a result the cell dies due to ] type ]. '''Telomestatin''' is a ] ] that acts by inhibiting the ] activity of ''in vitro'' cancer cells.<ref name=Shin-ya>{{cite journal | doi = 10.1021/ja005780q |author1=Shin-ya, Kazuo |author2=Wierzba, Konstanty |author3=Matsuo, Ken-ichi |author4=Ohtani, Toshio |author5=Yamada, Yuji |author6=Furihata, Kazuo |author7=Hayakawa, Yoichi |author8=Seto, Haruo | title = Telomestatin, a novel telomerase inhibitor from Streptomyces anulatus | journal = Journal of the American Chemical Society | year = 2001 | volume = 123 | issue = 6 | pages = 1262–1263 | pmid = 11456694}}</ref> It was first isolated from the bacteria '']''.<ref name=Shin-ya/> Telomestatin induces the formation of basket-type ] (G4) structures from hybrid-type G-quadruplexes in the ]. Upon formation of G4 structure there will be a decrease in the activity of the telomerase, which is involved in the replication of the telomeres and as a result the cell dies due to ] type ].{{cn|date=November 2024}}


==References== ==References==
Line 30: Line 35:
] ]
] ]
] ]
]