CAS 165108-07-6
: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)-
Description:
Avermectin A1a, with the CAS number 165108-07-6, is a member of the avermectin family, which are macrocyclic lactones derived from the fermentation of the bacterium Streptomyces avermitilis. This compound exhibits potent anthelmintic and insecticidal properties, making it valuable in agricultural and veterinary applications. Structurally, it features a complex arrangement of rings and functional groups, including a cyclohexyl moiety and a unique sugar component, which contribute to its biological activity. Avermectin A1a acts primarily by interfering with neurotransmission in target organisms, leading to paralysis and death of pests. It is also known for its low toxicity to mammals, which enhances its safety profile for use in various environments. The compound is typically administered in formulations that allow for effective delivery to the target organisms while minimizing environmental impact. Overall, Avermectin A1a is recognized for its efficacy and specificity in controlling a range of parasitic and pest species.
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]
Synonyms:- (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)
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
SELAMECTIN CRS
CAS:<p>SELAMECTIN CRS</p>Formula:C43H63NO11Color and Shape:Powder.Molecular weight:769.9604UK-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:C43H63NO11Purity:99.31%Color and Shape:SolidMolecular weight:769.96LC PestiMix 4 10 µg/mL in Acetonitrile
CAS:- 103055-07-8
- 10311-84-9
- 103112-35-2
- 113614-08-7
- 114-26-1
- 114369-43-6
- 1172134-12-1
- 117428-22-5
- 117704-25-3
- 120983-64-4
- 1216-44-0
- 122836-35-5
- 123997-26-2
- 125225-28-7
- 126833-17-8
- 129558-76-5
- 129630-19-9
- 13067-93-1
- 13141-86-1
- 131983-72-7
- 135590-91-9
- 13684-63-4
- 137641-05-5
- 14255-72-2
- 142891-20-1
- 143807-66-3
- 149961-52-4
- 163520-33-0
- 165108-07-6
- 179101-81-6
- 189278-12-4
- 19044-88-3
- 203313-25-1
- 220899-03-6
- 2274-67-1
- 229977-93-9
- 2303-17-5
- 23031-36-9
- 2314-09-2
- 24353-61-5
- 2439-01-2
- 24691-80-3
- 2600-69-3
- 2655-15-4
- 26644-46-2
- 30558-43-1
- 31251-03-3
- 33399-00-7
- 35256-85-0
- 35575-96-3
- 3761-41-9
- 38083-17-9
- 39184-27-5
- 39184-59-3
- 40487-42-1
- 42509-80-8
- 50512-35-1
- 50563-36-5
- 51218-49-6
- 5131-24-8
- 54406-48-3
- 555-37-3
- 56425-91-3
- 581809-46-3
- 60-51-5
- 60207-31-0
- 60238-56-4
- 6132-17-8
- 6552-21-2
- 69581-33-5
- 70124-77-5
- 70288-86-7
- 71751-41-2
- 7292-16-2
- 76674-21-0
- 78-34-2
- 79622-59-6
- 81406-37-3
- 83121-18-0
- 83657-24-3
- 86-50-0
- 86479-06-3
- 87237-48-7
- 87674-68-8
- 95617-09-7
- 98730-04-2
- 98886-44-3
- 99607-70-2
Color and Shape:MixtureSelamectin
CAS:<p>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.</p>Formula:C43H63NO11Purity:Min. 95%Molecular weight:770 g/mol






