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Compounds

COMPOUND NPA008843

STRUCTURE
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PROPERTIES
NPAID NPA008843
CLUSTER ID 1206
NODE ID 1025
NAME Thienamycin
FORMULA C11H16N2O4S
MOLECULAR WEIGHT (Da) 272.3260
ACCURATE MASS (Da) 272.0831
ORIGIN ORGANISM TYPE Bacterium
ORIGIN GENUS Streptomyces
ORIGIN SPECIES cattleya
InChIKey WKDDRNSBRWANNC-LPBDRPKESA-N
InChI InChI=1S/C11H16N2O4S/c1-5(14)8-6-4-7(18-3-2-12)9(11(16)17)13(6)10(8)15/h5-6,8,14H,2-4,12H2,1H3,(H,16,17)/t5-,6-,8?/m1/s1
SMILES C[C@H](C1[C@H]2CC(=C(N2C1=O)C(=O)O)SCCN)O
ORIGINAL ISOLATION REFERENCE
CITATION Kahan, J S; Kahan, F M; Goegelman, R; Currie, S A; Jackson, M; Stapley, E O; Miller, T W; Miller, A K; Hendlin, D; Mochales, S; Hernandez, S; Woodruff, H B; Birnbaum, J Thienamycin, a new β-lactam antibiotic. I. Discovery, taxonomy, isolation and physical properties Journal of Antibiotics 1979 32 (1) 1.
DOI 10.7164/antibiotics.32.1 PMID 761989
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 Salzmann TN; Ratcliffe RW; Bouffard FA; Christensen BG A stereocontrolled, enantiomerically specific total synthesis of thienamycin. Philosophical Transactions of the Royal Society B: Biological Sciences 1980 289 (1036) 191-5. DOI: 10.1098/rstb.1980.0037 PMID: 6109315
CITATION 2 Tatsuta K; Takahashi M; Tanaka N; Chikauchi K Novel synthesis of (+)-4-acetoxy-3-hydroxyethyl-2-azetidinone from carbohydrate. A formal total synthesis of (+)-thienamycin. Journal of Antibiotics 2000 53 (10) 1231-4. DOI: 10.7164/antibiotics.53.1231 PMID: 11132974
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