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Compounds

COMPOUND NPA006938

STRUCTURE
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PROPERTIES
NPAID NPA006938
CLUSTER ID 3161
NODE ID 2408
NAME Telomestatin
FORMULA C26H14N8O7S
MOLECULAR WEIGHT (Da) 582.5140
ACCURATE MASS (Da) 582.0706
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES anulatus
InChIKey YVSQVYZBDXIXCC-INIZCTEOSA-N
InChI InChI=1S/C26H14N8O7S/c1-9-17-24-30-14(6-39-24)21-28-12(4-37-21)19-27-11(3-35-19)20-29-13(5-36-20)22-31-15(7-38-22)26-32-16(8-42-26)23-33-18(10(2)40-23)25(34-17)41-9/h3-7,16H,8H2,1-2H3/t16-/m0/s1
SMILES CC1=C2N=C(O1)C1=C(C)OC(=N1)[C@@H]1CSC(=N1)C1=COC(=N1)C1=COC(=N1)C1=COC(=N1)C1=COC(=N1)C1=COC2=N1
ORIGINAL ISOLATION REFERENCE
CITATION Shin-ya, Kazuo; Wierzba, Konstanty; Matsuo, Ken-ichi; Ohtani, Toshio; Yamada, Yuji; Furihata, Kazuo; Hayakawa, Yoichi; Seto, Haruo Telomestatin, a Novel Telomerase Inhibitor from Streptomyces anulatus Journal of the American Chemical Society 2001 123 (6) 1262-1263.
DOI 10.1021/ja005780q PMID 11456694
ORIGINAL ISOLATION TAXONOMY
RANK NAME DB LINK NCBI
Domain Bacteria LPSN 2
Phylum Actinobacteria LPSN 201174
Class Actinobacteria LPSN -
Order Streptomycetales LPSN 85011
Family Streptomycetaceae LPSN 2062
Genus Streptomyces LPSN 1883
SYNTHESES
CITATION 1 Doi T; Yoshida M; Shin-ya K; Takahashi T Total synthesis of (R)-telomestatin. Organic Letters 2006 8 (18) 4165-7. DOI: 10.1021/ol061793i PMID: 16928100
CITATION 2 Doi T; Shibata K; Yoshida M; Takagi M; Tera M; Nagasawa K; Shin-ya K; Takahashi T (S)-stereoisomer of telomestatin as a potent G-quadruplex binder and telomerase inhibitor. Organic & Biomolecular Chemistry 2011 9 (2) 387-93. DOI: 10.1039/c0ob00513d PMID: 20967317
REVISIONS
VERSION SMILES CITATION
Original Isolation CC1=C2C3=NC(=C(O3)C)C4=NC(=CO4)C5=NC(=CO5)C6=NC(=CO6)C7=NC(=CO7)C8=NC(=CO8)C9=NC(CS9)C(=N2)O1 Shin-ya, Kazuo; Wierzba, Konstanty; Matsuo, Ken-ichi; Ohtani, Toshio; Yamada, Yuji; Furihata, Kazuo; Hayakawa, Yoichi; Seto, Haruo Telomestatin, a Novel Telomerase Inhibitor from Streptomyces anulatus Journal of the American Chemical Society 2001 123 (6) 1262-1263. DOI: 10.1021/ja005780q PMID: 11456694
2 CC1=C2N=C(O1)C1=C(C)OC(=N1)[C@@H]1CSC(=N1)C1=COC(=N1)C1=COC(=N1)C1=COC(=N1)C1=COC(=N1)C1=COC2=N1 Doi T; Yoshida M; Shin-ya K; Takahashi T Total synthesis of (R)-telomestatin. Organic Letters 2006 8 (18) 4165-7. DOI: 10.1021/ol061793i PMID: 16928100
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