CAS 165108-07-6
:Avermectina A1a, 25-ciclohexil-4-O-de(2,6-didesoxi-3-O-metil-alfa-L-arabino-hexopiranosil)-5-desmetoxi-25-de(1-metilpropil)-22,23-diidro-5-(hidroximino)-
Descrição:
Avermectina A1a, com o número CAS 165108-07-6, é um membro da família das avermectinas, que são lactonas macrocíclicas derivadas da fermentação da bactéria Streptomyces avermitilis. Este composto exibe potentes propriedades anti-helmínticas e inseticidas, tornando-o valioso em aplicações agrícolas e veterinárias. Estruturalmente, apresenta uma disposição complexa de anéis e grupos funcionais, incluindo um grupo ciclohexila e um componente de açúcar único, que contribuem para sua atividade biológica. A Avermectina A1a atua principalmente interferindo na neurotransmissão em organismos-alvo, levando à paralisia e morte de pragas. Também é conhecida por sua baixa toxicidade para mamíferos, o que melhora seu perfil de segurança para uso em vários ambientes. O composto é tipicamente administrado em formulações que permitem uma entrega eficaz aos organismos-alvo, minimizando o impacto ambiental. No geral, a Avermectina A1a é reconhecida por sua eficácia e especificidade no controle de uma variedade de espécies parasitárias e de pragas.
Fórmula: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
Chave InChI: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]
Sinónimos:- (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)
- Ver mais sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
6 produtos.
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>Fórmula:C43H63NO11Pureza:99.31%Cor e Forma:SolidPeso molecular:769.96LC PestiMix 4 10 µg/mL in Acetonitrile
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Cor 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.Fórmula:C43H63NO11Pureza:Min. 95%Peso molecular:770 g/mol






