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253 179 fiches documentées

( E )-SB-590885
chemical entity

An N -{5-[2-{4-[2-(dimethylamino)ethoxy]phenyl}-4-(pyridin-4-yl)-1 H -imidazol-5-yl]-2,3-dihydro-1 H -inden-1-ylidene}hydroxylamine in which the oxime group has E configuration.

( E )-ascladiol
chemical entity

A butenolide that is furan-2(5 H )-one which is substituted by a hydroxymethyl group at position 4 and a 2-hydroxyethylidene group at position 5 (the 5 E isomer). A direct precursor of patulin in cell-free preparations of Penicillium urticae patulin-minus mutants J1 and S11, but not S15.

( E )-buprofezin
chemical entity

A 2-( tert -butylimino)-5-phenyl-3-(propan-2-yl)-1,3,5-thiadiazinan-4-one in which the C=N double bond has E configuration.

( E )-chlorprothixene
chemical entity

A chlorprothixene in which the double bond adopts an ( E )-configuration.

( E )-cinnamaldehyde
chemical entity

The E ( trans ) stereoisomer of cinnamaldehyde, the parent of the class of cinnamaldehydes.

( E )-cinnamoyl-CoA(4−)
chemical entity

Tetraanion of ( E )-cinnamoyl-CoA arising from deprotonation of the phosphate and diphosphate OH groups.

( E )-clothianidin
chemical entity

A clothiadin that has E configuration at the C=N bond of the nitroguanidine moiety.

( E )-dacarbazine
chemical entity

A dacarbazine in which the N=N double bond adopts a trans -configuration.

( E )-dec-3-en-2-ol
chemical entity

A fatty alcohol that is (3 E )-dec-3-ene substituted by a hydroxy group at position 2.

( E )-dehydrocyclopeptine
chemical entity

A geoisomer of dehydrocyclopeptine in which the C=C bond of the benzylidene substituent has E -configuration.

( E )-dimethomorph
chemical entity

An enamide resulting from the formal condensation of (2 E )-3-(4-chlorophenyl)-3-(3,4-dimethoxyphenyl)acrylic acid with the amino group of morpholine. The agricultural fungicide dimethomorph is a mixture of ( E )- and ( Z )-dimethomorph; only the Z isomer has fungicidal activity.

( E )-dodec-2-enal
chemical entity

A trans -2,3-unsaturated fatty aldehyde that is ( E )-dodec-2-ene in which the allylic methyl group has been oxidised to the corresponding aldehyde.