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spinetoram

Identification (Source:EPA,EU)

ID	1448
Name	spinetoram
CAS	187166-40-1 + 187166-15-0
IUPAC
Inchi	InChI=1S/C42H69NO10/c1-10-27-13-12-14-35(53-37-18-17-34(43(6)7)24(4)49-37)23(3)38(45)33-21-31-29(32(33)22-36(44)51-27)16-15-26-19-28(20-30(26)31)52-42-41(47-9)40(48-11-2)39(46-8)25(5)50-42/h21,23-32,34-35,37,39-42H,10-20,22H2,1-9H3/t23-,24-,25+,26-,27+,28-,29-,30-,31-,32+,34+,35+,37+,39+,40-,41-,42+/m1/s1
CIPAC	None allocated
EPA Code
Formula	C42H69NO10 + C43H69NO10
SMILES	O([C@]1([H])[C@]([H])([C@]([H])([C@@]([H])([C@@]([H])(C([H])([H])[H])O1)OC([H])([H])[H])OC([H])([H])C([H])([H])[H])OC([H])([H])[H])[C@@]([H])(C([H])([H])[C@]([H])(C([H])([H])C([H])([H])[C@]([H])([C@@]([H])(C([H])([H])C2=O)C(C([C@@]([H])(C([H])([H])[H])[C@@]([H])(C([H])([H])C([H])([H])C([H])([H])[C@@]([H])(C([H])([H])C([H])([H])[H])O2)O[C@]3([H])C([H])([H])C([H])([H])[C@]([H])([C@]([H])(C([H])([H])[H])O3)N(C([H])([H])[H])C([H])([H])[H])=O)=C4[H])[C@]45[H])[C@@]56[H])C6([H])[H]
Status	PENDING

Classification

Mode of Action	Acts through a novel site in the nicotinic receptor. Shows high residual, contact and ingestion activity
Pesticide Type	Insecticide
Chemical Group	Unclassified
Classification	spinosyn insecticides

Properties (Source:PubChem)

Molecular Weight	748.01 / 760.03
Physical State	Off-white solid
AlogP	5.404
H-Bond Donor	0
H-Bond Acceptor	11
Surface Area	741.56
Polar Surface Area	111.22

Structure

Ecotoxicology (Source:PPDB,IPM)

Species	Method	Study Time	Dose Type	Value
Aquatic invertebrates	Acute	48 hour	EC50	3.17 mg l-1
Aquatic plants	Acute	7 day	EC50, biomass	14.2 mg l-1
Birds	Acute		LD50	2250 mg kg-1
Earthworms	Acute	14 day	LD50	1000 mg kg-1
Fish	Acute	96 hour	LC50	3.46 mg l-1
Mammals	Acute oral		LD50	> 5000 mg kg-1
Sediment dwelling organisms	Chronic	28 day	NOEC, sediment	0.000375 mg kg-1

Related targets

Target Name	RScore (About this table)
acetylcholine receptors (protein family or complex)	2(0,0,0,2)	Details

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