CAS 19683-98-8

(3S,4R,5S)-4-Idrossi-5-metossi-4-[(2S,3R)-2-metil-3-(3-metil-2-buten-1-il)-2-ossiranil]-1-ossaspiro[2.5]ottan-6-one

Descrizione:

La sostanza chimica nota come (3S,4R,5S)-4-Idrossi-5-metossi-4-[(2S,3R)-2-metil-3-(3-metil-2-buten-1-il)-2-ossiranil]-1-ossaspiro[2.5]ottan-6-one, con il numero CAS 19683-98-8, è un composto organico complesso caratterizzato dalla sua struttura spirociclica, che include un framework ossaspiro. Questo composto presenta più stereocentri, contribuendo alla sua natura chirale, ed espone gruppi funzionali come idrossile (-OH), metossile (-OCH3) e un gruppo epossido. La presenza di questi gruppi funzionali suggerisce una reattività e un'attività biologica potenziale, rendendolo di interesse in campi come la chimica medicinale e la sintesi di prodotti naturali. La stereochimica indicata dai descrittori (3S,4R,5S) e (2S,3R) è cruciale per comprendere le sue interazioni e proprietà. Inoltre, la struttura molecolare del composto può influenzare la sua solubilità, stabilità e potenziali applicazioni in prodotti farmaceutici o agrochimici. In generale, questa sostanza esemplifica la complessità e la diversità dei composti organici nella ricerca chimica.

Formula: C₁₆H₂₄O₅

InChI: InChI=1S/C16H24O5/c1-10(2)5-6-12-14(3,21-12)16(18)13(19-4)11(17)7-8-15(16)9-20-15/h5,12-13,18H,6-9H2,1-4H3/t12-,13-,14+,15+,16+/m1/s1

InChI key: InChIKey=NESRXFGQJARQNM-OWYFMNJBSA-N

SMILES: O[C@]1([C@@]2(CO2)CCC(=O)[C@H]1OC)[C@]3(C)[C@@H](CC=C(C)C)O3

Sinonimi:

• (3R,4S,5S)-5-methoxy-4-[(3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one
• (3S,4R,5S)-4-Hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-1-oxaspiro[2.5]octan-6-one
• (3S,4R,5S)-4-hydroxy-5-methoxy-4-[(2R,3R)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one
• (3S,4R,5S)-4-hydroxy-5-methoxy-4-[(2S)-2-methyl-3-(3-methylbut-2-en-1-yl)oxiran-2-yl]-1-oxaspiro[2.5]octan-6-one
• 1-Oxaspiro[2.5]octan-6-one, 4-(1,2-epoxy-1,5-dimethyl-4-hexenyl)-4-hydroxy-5-methoxy-, (1S,2R,3S,4R,5S)-(-)-
• 1-Oxaspiro[2.5]octan-6-one, 4-hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methyl-2-buten-1-yl)-2-oxiranyl]-, (3S,4R,5S)-
• 1-Oxaspiro[2.5]octan-6-one, 4-hydroxy-5-methoxy-4-[(2S,3R)-2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-, (3S,4R,5S)-
• 1-Oxaspiro[2.5]octan-6-one, 4-hydroxy-5-methoxy-4-[2-methyl-3-(3-methyl-2-butenyl)oxiranyl]-, [3S-[3α,4β,4(2R*,3S*),5β]]-
• 7-Hydroxy-8-Methoxy-7-[2-Methyl-3-(3-Methylbut-2-En-1-Yl)Oxiran-2-Yl]-4-Oxaspiro[2.5]Octan-1-One
• 7-Hydroxy-8-Methoxy-7-[2-Methyl-3-(3-Methylbut-2-Enyl)Oxiran-2-Yl]-4-Oxaspiro[2.5]Octan-2-One
• Graphinone

Ovalicin

CAS: 19683-98-8

Formula: C₁₆H₂₄O₅

Purezza: 99.81%

Colore e forma: Whitish. Solid

Peso molecolare: 296.0

Ref: 8R-AD0081

Ovalicin-d4

CAS: 19683-98-8

Formula: C₁₆H₂₀D₄O₅

Peso molecolare: 300.39

Ref: 4Z-F-113003

Ovalicin

CAS: 19683-98-8

Formula: C₁₆H₂₄O₅

Peso molecolare: 296.36

Ref: 4Z-F-113002

Ovalicin

CAS: 19683-98-8

Ovalicin is a peptide that has been used in research as an activator. It is a potent and specific inhibitor of voltage-gated ion channels, such as nicotinic acetylcholine receptors. Ovalicin also interacts with other proteins, including receptor and ligand interactions, which have led to its use as a research tool for investigating protein interactions. Ovalicin can be used in pharmacology to study the effects of drugs on cells by measuring the change in ion channel activity.

Formula: C₁₆H₂₄O₅

Purezza: Min. 95%

Peso molecolare: 296.36 g/mol

Ref: 3D-UAA68398