CAS 165108-07-6
:Avermectina A1a, 25-cicloesil-4-O-de(2,6-didesossi-3-O-metil-alfa-L-arabino-esopiranosil)-5-desmetossi-25-de(1-metilpropil)-22,23-diidro-5-(idrossimino)-
Descrizione:
Avermectina A1a, con il numero CAS 165108-07-6, è un membro della famiglia delle avermectine, che sono lattone macrocicliche derivate dalla fermentazione del batterio Streptomyces avermitilis. Questo composto presenta potenti proprietà antihelmintiche e insetticide, rendendolo prezioso in applicazioni agricole e veterinarie. Strutturalmente, presenta un complesso arrangiamento di anelli e gruppi funzionali, inclusa una moiety cicloesilica e un componente zuccherino unico, che contribuiscono alla sua attività biologica. L'Avermectina A1a agisce principalmente interferendo con la neurotrasmissione negli organismi bersaglio, portando a paralisi e morte dei parassiti. È anche nota per la sua bassa tossicità per i mammiferi, il che migliora il suo profilo di sicurezza per l'uso in vari ambienti. Il composto è tipicamente somministrato in formulazioni che consentono una consegna efficace agli organismi bersaglio, minimizzando l'impatto ambientale. In generale, l'Avermectina A1a è riconosciuta per la sua efficacia e specificità nel controllo di una gamma di specie parassitarie e di insetti.
Formula:C43H63NO11
InChI:InChI=1/C43H63NO11/c1-24-11-10-14-30-23-50-40-36(44-48)27(4)19-33(43(30,40)47)41(46)52-32-20-31(16-15-25(2)38(24)53-35-21-34(49-6)37(45)28(5)51-35)54-42(22-32)18-17-26(3)39(55-42)29-12-8-7-9-13-29/h10-11,14-15,19,24,26,28-29,31-35,37-40,45,47-48H,7-9,12-13,16-18,20-23H2,1-6H3/b11-10+,25-15+,30-14+,44-36-/t24-,26-,28-,31+,32-,33-,34-,35?,37?,38-,39-,40+,42+,43+/m0/s1
InChI key:InChIKey=AFJYYKSVHJGXSN-PBTBINGESA-N
SMILES:O[C@@]1/2[C@]3(C(=NO)C(C)=C[C@]1(C(=O)O[C@@]4(C[C@@]5(O[C@@]([C@@H](C)CC5)(C6CCCCC6)[H])O[C@@](C4)(C/C=C(\C)/[C@@H](O[C@H]7C[C@H](OC)[C@@H](O)[C@H](C)O7)[C@@H](C)\C=C\C=C2/CO3)[H])[H])[H])[H]
Sinonimi:- (2aE,4E,5'S,6S,6'S,7S,8E,11R,13R,15S,17aR,20Z,20aR,20bS)-6'-cyclohexyl-20b-hydroxy-20-(hydroxyimino)-5',6,8,19-tetramethyl-17-oxo-3',4',5',6,6',10,11,14,15,17,17a,20,20a,20b-tetradecahydro-2H,7H-spiro[11,15-methanofuro[4,3,2-pq][2,6]benzodioxacyclooctadecine-13,2'-pyran]-7-yl (4ξ)-2,6-dideoxy-3-O-methyl-L-threo-hexopyranoside
- (2aE,4E,5'S,6S,6'S,7S,8E,11R,13R,15S,17aR,20aR,20bS)-6'-cyclohexyl-7-((2,6-dideoxy-3-O-methyl-alpha-L-arabino-hexopyranosyl)oxy)-3',4',5',6,6',7,10,11,14,15,20a,20b-dodecahydro-20b-hydroxy-5',6,8,19-tetramethylspiro(11,15-methano-2H,13H,17H-furo(4,3,2-pq)(2,6)benzodioxacyclooctadecin-13,2'-(2H)pyran)-17,20(17aH)-dione 20-oxime
- (5'S,6S,6'S,7S,11R,13R,15S,17aR,20Z,20aR,20bS)-6'-cyclohexyl-20b-hydroxy-20-(hydroxyimino)-5',6,8,19-tetramethyl-17-oxo-3',4',5',6,6',10,11,14,15,17,17a,20,20a,20b-tetradecahydro-2H,7H-spiro[11,15-methanofuro[4,3,2-pq][2,6]benzodioxacyclooctadecine-13,2'-pyran]-7-yl 2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranoside
- 25-Cyclohexyl-4'-O-de(2,6-dideoxy-3-O-methyl-alpha-L-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-5-(hydroxyimino)-avermectin A1a
- 25-Cyclohexyl-4′-O-de(2,6-dideoxy-3-O-methyl-α-<span class="text-smallcaps">L</span>-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-5-(hydroxyimino)avermectin A<sub>1a</sub>
- 25-cyclohexyl-25-de(1-methylpropyl)-5-deoxy-22 23-dihydro-5-(hydroxyimino)-avermectin B1 monosaccharide
- Avermectin A1a, 25-cyclohexyl-4'-O-de(2,6-dideoxy-3-O-methyl-a-L-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-5-(hydroxyimino)-
- Avermectin A1a,25-cyclohexyl-4'-O-de(2,6-dideoxy-3-O-methyl-a-L-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-5-(hydroxyimino)-,(5Z)-
- Avermectin A<sub>1a</sub>, 25-cyclohexyl-4′-O-de(2,6-dideoxy-3-O-methyl-α-<span class="text-smallcaps">L</span>-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-5-(hydroxyimino)-
- Selamectin
- Selamectin [USAN:INN]
- Uk-124,114
- Unii-A2669Owx9N
- 25-Cyclohexyl-4′-O-de(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-5-(hydroxyimino)avermectin A1a
- Avermectin A1a, 25-cyclohexyl-4-O-de(2,6-dideoxy-3-O-methyl-.alpha.-L-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-5-(hydroxyimino)-
- Avermectin A1a,25-cyclohexyl-4'-O-de(2,6-dideoxy-3-O-methyl-a-L-arabino-hexopyranosyl)-5-demethoxy-25-de(1-methylpropyl)-22,23-dihydro-5-(hydroxyimino)-(9CI)
- Selamectina
- Selamectin for peak identification CRS
- SelaMectin(SelaMeerin)
- Vedi altri sinonimi
Ordinare per
Purezza (%)
0
100
|
0
|
50
|
90
|
95
|
100
6 prodotti.
UK-124114
CAS:<p>Selamectin, a derivative of ivermectin, is a macrocyclic lactone that enhances chloride channels in nematodes, inhibiting H. contortus larval growth.</p>Formula:C43H63NO11Purezza:99.31%Colore e forma:SolidPeso molecolare:769.96LC PestiMix 4 10 µg/mL in Acetonitrile
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- 86-50-0
- 86479-06-3
- 87237-48-7
- 87674-68-8
- 95617-09-7
- 98730-04-2
- 98886-44-3
- 99607-70-2
Colore e forma:MixtureSelamectin
CAS:Selamectin is a medicinal compound that acts as an inhibitor of protein kinases. It has been found to be effective in the treatment of tumors and cancer cells. Selamectin is an analog of other anticancer protein kinase inhibitors, and it has been shown to induce apoptosis in cancer cells. This compound has also been found to be effective against Chinese hamster ovary cells and human urine-derived cell lines. Selamectin works by inhibiting specific kinases that are involved in the growth and survival of cancer cells, making it a promising candidate for future cancer treatments.Formula:C43H63NO11Purezza:Min. 95%Peso molecolare:770 g/mol






