Doramectin structure
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Common Name | Doramectin | ||
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CAS Number | 117704-25-3 | Molecular Weight | 899.114 | |
Density | 1.3±0.1 g/cm3 | Boiling Point | 967.4±65.0 °C at 760 mmHg | |
Molecular Formula | C50H74O14 | Melting Point | 116 - 119ºC | |
MSDS | Chinese USA | Flash Point | 274.4±27.8 °C | |
Symbol |
GHS06, GHS09 |
Signal Word | Danger |
Use of DoramectinDoramectin is an antiparasitic agent.IC50 Value:Target: AntiparasiticDoramectin (Dectomax) is a veterinary drug approved by the Food and Drug Administration (FDA) for the treatment of parasites such as gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice and mange mites in cattle. Mutational biosynthetic antiparasitic antibiotic structurally related to the avermectins. |
Name | doramectin |
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Synonym | More Synonyms |
Description | Doramectin is an antiparasitic agent.IC50 Value:Target: AntiparasiticDoramectin (Dectomax) is a veterinary drug approved by the Food and Drug Administration (FDA) for the treatment of parasites such as gastrointestinal roundworms, lungworms, eyeworms, grubs, sucking lice and mange mites in cattle. Mutational biosynthetic antiparasitic antibiotic structurally related to the avermectins. |
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Related Catalog | |
References |
Density | 1.3±0.1 g/cm3 |
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Boiling Point | 967.4±65.0 °C at 760 mmHg |
Melting Point | 116 - 119ºC |
Molecular Formula | C50H74O14 |
Molecular Weight | 899.114 |
Flash Point | 274.4±27.8 °C |
Exact Mass | 898.507874 |
PSA | 170.06000 |
LogP | 7.16 |
Vapour Pressure | 0.0±0.6 mmHg at 25°C |
Index of Refraction | 1.580 |
Storage condition | 0-6°C |
Water Solubility | methanol: soluble |
Symbol |
GHS06, GHS09 |
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Signal Word | Danger |
Hazard Statements | H301-H410 |
Precautionary Statements | P273-P301 + P310-P501 |
Personal Protective Equipment | Eyeshields;Faceshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
Hazard Codes | T,N,Xi |
Risk Phrases | R25 |
Safety Phrases | 33-45-60-61-36/37-26 |
RIDADR | UN 2811 6.1/PG 3 |
Anthelmintic resistance in a herd of alpacas (Vicugna pacos).
Can. Vet. J. 53(12) , 1310-3, (2012) A herd of alpacas was examined because of a history of severe endoparasitism, anemia, hypoproteinemia, and weight loss. Resistance of gastrointestinal nematodes to albendazole, fenbendazole, and doram... |
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Reversal of P-glycoprotein-mediated multidrug resistance in vitro by doramectin and nemadectin.
J. Pharm. Pharmacol. 62(3) , 393-9, (2010) Multidrug resistance (MDR) is a serious obstacle encountered in cancer treatment. This study was performed to explore the reversal of MDR by doramectin from the avermectin family and nemadectin belong... |
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The influence of gastrointestinal parasitism on fecal elimination of doramectin, in lambs.
Ecotoxicol. Environ. Saf. 73(8) , 2017-21, (2010) A study was done to investigate the effect of parasitism on patterns of doramectin (DRM) fecal elimination in lambs. Fourteen Suffolk Down parasitized lambs (26.9 ± 1.5 kg body weight: bw) were purpos... |
Doromectin |
extended von Baeyer nomenclature: (10E,14E,16E)-(1R,4S,5’S,6S,6’R,8R,12S,13S,20R,21R,24S)-6’-cyclohexyl-21,24-dihydroxy-5’,11,13,22-tetramethyl-2-oxo-(3,7,19-trioxatetracyclo[15.6.1.14,8.020,24]pentacosa-10,14,16,22-tetraene)-6-spiro-2’-(5’,6’-dihydro-2’H-pyran)-12-yl 2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranoside |
Doramectina |
Doramectin |
25-cyclohexyl-avermectin B1 |
DONGGUAI.P.E |
bridged fused ring systems nomenclature: (2aE,4E,8E)-(5’S,6S,6’R,7S,11R,13S,15S,17aR,20R,20aR,20bS)-6’-cyclohexyl-5’,6,6’,7,10,11,14,15,17a,20,20a,20b-dodecahydro-20,20b-dihydroxy-5’,6,8,19-tetramethyl-17-oxospiro[11,15-methano-2H,13H,17H-furo[4,3,2-pq][2,6]benzodioxacyclooctadecin-13,2’-[2H]pyran]-7-yl 2,6-dideoxy-4-O-(2,6-dideoxy-3-O-methyl-α-L-arabino-hexopyranosyl)-3-O-methyl-α-L-arabino-hexopyranoside |
Dectoma |
Dectomax |
25-cyclohexyl-5-O-demethyl-25-de(1-methylpropyl)avermectin A1a |
Doramecin |