CAS 182234-02-2
:(3aS,5aS,14aR)-3,3a,11,12-Tetraidro-9,13-diidrossi-3a-metossi-11-metil-5a-[[(2S,5S,6S)-tetraidro-5-idrossi-6-metil-2H-pirano-2-il]ossi]-2H,5H-furo[2′′,3′′:4′,5′]furo[3′,4′:6,7]nafto[2,3-e]isoindolo-2,6,10,14(5aH)-tetrone
Descrizione:
La sostanza chimica con il nome "(3aS,5aS,14aR)-3,3a,11,12-Tetraidro-9,13-diidrossi-3a-metossi-11-metil-5a-[[(2S,5S,6S)-tetraidro-5-idrossi-6-metil-2H-pirano-2-il]ossi]-2H,5H-furo[2′′,3′′:4′,5′]furo[3′,4′:6,7]nafto[2,3-e]isoindolo-2,6,10,14(5aH)-tetrone" e numero CAS "182234-02-2" è un composto organico complesso caratterizzato dalla sua intricatissima struttura policiclica e da molteplici gruppi funzionali. Questa sostanza presenta una combinazione di moieties di tetraidrofurano e furofurano, indicando una potenziale attività biologica. La presenza di gruppi idrossilici suggerisce che potrebbe mostrare capacità di legame idrogeno, influenzando la sua solubilità e reattività. La stereochimica, denotata da configurazioni specifiche in vari centri chirali, è cruciale per le sue interazioni biologiche e proprietà farmacologiche. Composti di questo tipo hanno spesso applicazioni in chimica medicinale, potendo fungere da lead per lo sviluppo di farmaci grazie alla loro diversità strutturale e capacità di interagire con bersagli biologici. In generale, la complessità e la funzionalizzazione del composto suggeriscono un potenziale significativo per la ricerca in campi come la farmacologia e la sintesi organica.
Formula:C28H27NO12
InChI:InChI=1S/C28H27NO12/c1-11-15(30)4-5-18(39-11)41-26-10-38-27(37-3)8-17(32)40-28(26,27)24(35)21-13(23(26)34)6-12-7-16(31)20-14(19(12)22(21)33)9-29(2)25(20)36/h6-7,11,15,18,30-31,33H,4-5,8-10H2,1-3H3/t11-,15-,18-,26+,27-,28-/m0/s1
InChI key:InChIKey=XFQJOLWXLJXJSV-VUAGTGNDSA-N
SMILES:O([C@]12[C@]3([C@@](OC)(OC1)CC(=O)O3)C(=O)C=4C(C2=O)=CC=5C(C4O)=C6C(=C(O)C5)C(=O)N(C)C6)[C@@H]7O[C@@H](C)[C@@H](O)CC7
Sinonimi:- (3aS,5aS)-9,13-dihydroxy-5a-{[(2S,5S,6S)-5-hydroxy-6-methyltetrahydro-2H-pyran-2-yl]oxy}-3a-methoxy-11-methyl-3,3a,11,12-tetrahydro-2H,5H-furo[2'',3'':4',5']furo[3',4':6,7]naphtho[2,3-e]isoindole-2,6,10,14(5aH)-tetrone
- (3aS,5aS,14aR)-3,3a,11,12-Tetrahydro-9,13-dihydroxy-3a-methoxy-11-methyl-5a-[[(2S,5S,6S)-tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl]oxy]-2H,5H-furo[2′′,3′′:4′,5′]furo[3′,4′:6,7]naphth[2,3-e]isoindole-2,6,10,14(5aH)-tetrone
- 2H,5H-Furo(2'',3'':3',5')furo(3',4':6,7)naphth(2,3-e)isoindole-2,6,10,14(5aH)-tetrone, 3,3a,11,12-tetrahydro-9,13-dihydroxy-3a-methoxy-11-methyl-5a-((tetrahydro-5-hydroxy-6-2H-pyran-2-yl)oxy)-
- 2H,5H-Furo[2′′,3′′:4′,5′]furo[3′,4′:6,7]naphth[2,3-e]isoindole-2,6,10,14(5aH)-tetrone, 3,3a,11,12-tetrahydro-9,13-dihydroxy-3a-methoxy-11-methyl-5a-[(tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl)oxy]-
- 2H,5H-Furo[2′′,3′′:4′,5′]furo[3′,4′:6,7]naphth[2,3-e]isoindole-2,6,10,14(5aH)-tetrone, 3,3a,11,12-tetrahydro-9,13-dihydroxy-3a-methoxy-11-methyl-5a-[[(2S,5S,6S)-tetrahydro-5-hydroxy-6-methyl-2H-pyran-2-yl]oxy]-, (3aS,5aS,14aR)-
- (+)-Lactonamycin
- Lactonamycin
Ordinare per
Purezza (%)
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100
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0
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50
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90
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95
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100
2 prodotti.
Lactonamycin
CAS:<p>Lactonamycin is a linker that contains an oxygenated functional group. It can be found in some active natural products and has been synthesized in the laboratory. Lactonamycin is used as a model system for biosynthesis, where it was shown to efficiently produce glycosidic bonds when supplied with carbon sources such as glucose. The biological properties of Lactonamycin include its ability to inhibit microbial infection and inflammation, which may be due to its hydroxy group.</p>Formula:C28H27NO12Purezza:Min. 95%Peso molecolare:569.51 g/molLactonamycin
CAS:<p>Lactonamycin exhibits significant activity against Gram-positive bacteria, including Staphylococcus, Streptococcus, Enterococcus, MRSA (MIC of 0.39-0.78 μg/mL), and VRE (MIC of 0.39-0.78 μg/mL). It also demonstrates inhibitory effects on various tumor cell lines such as L-1210, P388, S180, FS-3, Ehrlich, and B16-BL5 (IC50 of 0.06-3.3 μg/mL).</p>Formula:C28H27NO12Colore e forma:SolidPeso molecolare:569.513

