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Burger, AM; Kaur, G; Hollingshead, M; Fischer, RT; Nagashima, K; Malspeis, L; Duncan, KL; Sausville, EA (March 1997). "Antiproliferative activity in vitro and in vivo of the spicamycin analogue KRN5500 with altered glycoprotein expression in vitro".
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InChI=1S/C30H51N7O7/c1-19(2)13-11-9-7-5-3-4-6-8-10-12-14-21(40)31-15-22(41)36-23-25(42)26(43)30(44-27(23)20(39)16-38)37-29-24-28(33-17-32-24)34-18-35-29/h17-20,23,25-27,30,38-39,42-43H,3-16H2,1-2H3,(H,31,40)(H,36,41)(H2,32,33,34,35,37)
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Suzuki, Tamotsu; Suzuki, Sayaka T.; Yamada, Iwao; Koashi, Yoshiaki; Yamada, Kazue; Chida, Noritaka (1 May 2002). "Total
Synthesis of Spicamycin".
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Suzuki, Tamotsu; Chida, Noritaka (February 2003). "The New and
Efficient Synthesis of a Heptose Moiety of Spicamycin".
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N(C1=C2C(N=CN2)=NC=N1)3O((CO)O)((NC(CNC(CCCCCCCCCCCCC(C)C)=O)=O)(O)3O)
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Except where otherwise noted, data are given for materials in their
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The Search for
Bioactive Compounds from Microorganisms
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40:N-amino]-2-oxoethyl]-14-methylpentadecanamide
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259:Key: YBZRLMLGUBIIDN-UHFFFAOYSA-N
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347:(at 25 °C , 100 kPa).
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337: g·mol
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351:Infobox references
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518:Chemistry Letters
501:10.1021/jo010925c
468:978-1-4612-4412-7
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54:Identifiers
46:Other names
608:Antibiotics
289:Properties
115:CHEBI:80079
17:Spicamycin
602:Categories
395:References
367:antibiotic
363:Spicamycin
330:Molar mass
146:ChemSpider
82:3D model (
71:87099-85-2
61:CAS Number
37:IUPAC name
623:Heptoses
509:11975540
613:Purines
423:9815705
335:621.780
187:PubChem
618:Amides
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365:is an
273:SMILES
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175:C15751
155:432387
126:ChEMBL
31:Names
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248:InChI
106:ChEBI
84:JSmol
559:stub
505:PMID
463:ISBN
419:PMID
166:KEGG
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217:EPA
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