| SUBSTRATE | PRODUCT | REACTION DIAGRAM | ORGANISM | UNIPROT ACCESSION NO. | COMMENTARY/ Substrate | LITERATURE/ Substrate | COMMENTARY/ Product | LITERATURE/ Product | Reversibility r=reversible ir=irreversible ?=not specified |
| 1-naphthyl acetate + H2O | 1-naphthol + acetate |
 | Dysdercus cingulatus | - | - | 708700 | - | - | ? |
| 1-naphthyl acetate + H2O | 1-naphthol + acetate |
 | Trichoplusia ni | - | 13% of the activity with juvenile hormone I | 23487 | - | - | - |
| 1-Naphthyl methylcarbonate + H2O | 1-Naphthol + methylcarbonate |
 | Trichoplusia ni | - | 6% of the activity with juvenile hormone I | 23487 | - | - | - |
| 4-nitrophenyl acetate + H2O | 4-nitrophenol + acetate |
 | Trichoplusia ni | - | 69% of the activity with juvenile hormone I, slightly more active than with juvenile hormone III | 23487 | - | - | - |
| 4-Nitrophenyl methylcarbonate + H2O | 4-Nitrophenol + methylcarbonate |
 | Trichoplusia ni | - | 5% of the activity with juvenile hormone I | 23487 | - | - | - |
| alpha-naphthyl acetate + H2O | alpha-naphthol + acetate |
 | Tenebrio molitor | - | - | 649497 | - | 649497 | ? |
| alpha-naphthyl acetate + H2O | alpha-naphthol + acetate |
 | Trichoplusia ni | - | - | 651510 | - | 651510 | ? |
| alpha-naphthyl acetate + H2O | alpha-naphthol + acetate |
 | Tenebrio molitor | Q8WRD8 | - | 651512 | - | 651512 | ? |
| alpha-naphthyl acetate + H2O | alpha-naphthol + acetate |
 | Manduca sexta | - | - | 707525 | - | - | ? |
| alpha-naphthyl acetate + H2O | alpha-naphthol + acetate |
 | Manduca sexta | - | activity decreases with increasing the chain length of the alpha-naphthyl substrates from acetate to octanoate | 651510 | - | 651510 | ? |
| alpha-naphthyl acetate + H2O | alpha-naphthol + acetate |
 | Tenebrio molitor, Heliothis virescens | - | lower activity than with alpha-naphthyl propionate | 651510 | - | 651510 | ? |
| alpha-naphthyl acetate + H2O | alpha-naphthol + acetate |
 | Ips typographus | - | specific activities of several developmental stages | 649497 | - | 649497 | ? |
| alpha-naphthyl acetate + H2O | ? |
 | Drosophila melanogaster | - | artificial substrate | 651500 | - | 651500 | ? |
| alpha-naphthyl butyrate + H2O | alpha-naphthol + butyrate |
 | Manduca sexta | - | activity decreases with increasing the chain length of the alpha-naphthyl substrates from acetate to octanoate | 651510 | - | 651510 | ? |
| alpha-naphthyl butyrate + H2O | alpha-naphthol + butyrate |
 | Tenebrio molitor, Heliothis virescens | - | activity decreases with increasing the chain length of the alpha-naphthyl substrates from propionate to octanoate | 651510 | - | 651510 | ? |
| alpha-naphthyl hexanoate + H2O | alpha-naphthol + hexanoate |
 | Manduca sexta | - | activity decreases with increasing the chain length of the alpha-naphthyl substrates from acetate to octanoate | 651510 | - | 651510 | ? |
| alpha-naphthyl hexanoate + H2O | alpha-naphthol + hexanoate |
 | Tenebrio molitor, Heliothis virescens | - | activity decreases with increasing the chain length of the alpha-naphthyl substrates from propionate to octanoate | 651510 | - | 651510 | ? |
| alpha-naphthyl octanoate + H2O | alpha-naphthol + octanoate |
 | Manduca sexta | - | activity decreases with increasing the chain length of the alpha-naphthyl substrates from acetate to octanoate | 651510 | - | 651510 | ? |
| alpha-naphthyl octanoate + H2O | alpha-naphthol + octanoate |
 | Tenebrio molitor, Heliothis virescens | - | activity decreases with increasing the chain length of the alpha-naphthyl substrates from propionate to octanoate | 651510 | - | 651510 | ? |
| alpha-naphthyl propionate + H2O | alpha-naphthol + propionate |
 | Manduca sexta | - | activity decreases with increasing the chain length of the alpha-naphthyl substrates from acetate to octanoate | 651510 | - | 651510 | ? |
| alpha-naphthyl propionate + H2O | alpha-naphthol + propionate |
 | Tenebrio molitor, Heliothis virescens | - | higher activity than with alpha-naphthyl acetate, activity decreases with increasing the chain length of the alpha-naphthyl substrates from propionate to octanoate | 651510 | - | 651510 | ? |
| HEPTAT + H2O | ? |
 | Tenebrio molitor | Q8WRD8 | synthetic juvenile hormone analog | 651512 | - | 651512 | ? |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | insecta, Manduca sexta | - | - | 23470 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Manduca sexta | - | - | 23471 | - | 23471 | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Manduca sexta | - | - | 23472 | - | 23472 | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Samia cynthia, Trichoplusia ni | - | - | 23470 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Trichoplusia ni | - | - | 23472 | - | 23472 | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Trichoplusia ni | - | - | 23484 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Galleria mellonella | - | - | 23470, 23483 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Periplaneta brunnea, Schistocerca nitens, Neobellieria bullata, Lymantria dispar | - | - | 23470 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Trichoplusia ni | - | juvenile hormone II | 23476, 23487 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Manduca sexta | - | juvenile hormone III | 23480 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Trichoplusia ni | - | juvenile hormone III | 23477, 23479, 23481, 23487 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Lymantria dispar | - | juvenile hormone III | 23474 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Schistocerca gregaria | - | C16 juvenile hormone-23H | 23485 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Trichoplusia ni | - | juvenile hormone I | 23477, 23479, 23481, 23487 | - | - | - |
| Juvenile hormone + H2O | Juvenile hormone acid + acid diol |
 | Galleria mellonella | - | juvenile hormone I | 23478 | - | - | - |
| juvenile hormone + H2O | ? |
 | Lymantria dispar | - | - | 651502 | - | 651502 | ? |
| juvenile hormone + H2O | ? |
 | Rhyparobia maderae | - | - | 651504 | - | 651504 | ? |
| juvenile hormone + H2O | ? |
 | Choristoneura fumiferana | - | juvenile hormone esterase activity | 653222 | - | 653222 | ? |
| juvenile hormone + H2O | ? |
 | Manduca sexta | - | selective enzyme, hydrolyzes the methyl ester of juvenile hormone | 651511 | - | 651511 | ? |
| juvenile hormone + H2O | ? |
 | Gryllus assimilis | - | endocrine regulator, degrades and inactivates a key developmental and reproductive hormone, juvenile hormone | 649644 | - | 649644 | ? |
| juvenile hormone + H2O | ? |
 | Leptinotarsa decemlineata | - | juvenile hormone degradation | 649498 | - | 649498 | ? |
| juvenile hormone + H2O | ? |
 | Manduca sexta | - | plays an important role in the regulation of metamorphosis in caterpillars, JHE is implicated in additional roles in development and reproduction | 651511 | - | 651511 | ? |
| juvenile hormone + H2O | ? |
 | Tenebrio molitor | Q8WRD8 | selective enzyme, juvenile hormone metabolism, alters the activity of juvenile hormone, which regulates development and reproduction | 651512 | - | 651512 | ? |
| juvenile hormone + H2O | juvenile hormone acid + methanol |
 | Tenebrio molitor, Manduca sexta, Trichoplusia ni, Heliothis virescens | - | - | 651510 | - | 651510 | ? |
| juvenile hormone + H2O | juvenile hormone acid + methanol |
 | Ips typographus | - | JHE catabolizes juvenile hormone | 649497 | - | 649497 | ? |
| juvenile hormone + H2O | juvenile hormone acid + methanol |
 | Bombyx mori | - | key enzyme in the regulation of juvenile hormone level | 670670 | - | - | ? |
| juvenile hormone + H2O | juvenile hormone acid + methanol |
 | Trichoplusia ni | - | key enzyme in the regulation of juvenile hormone level | 669746 | - | - | ? |
| juvenile hormone + H2O | juvenile hormone acid + methanol |
 | Manduca sexta | P19985, Q9GPG0 | key enzyme in the regulation of juvenile hormone level, degradation of juvenile hormone is required for proper insect development | 667723 | - | - | ? |
| juvenile hormone + H2O | juvenile hormone acid + methanol |
 | Bombyx mori Shogetu-Shunrei, Bombyx mori C108, Bombyx mori P22, Bombyx mori P21, Bombyx mori Bm-N, Bombyx mori 122 | - | key enzyme in the regulation of juvenile hormone level | 670670 | - | - | ? |
| juvenile hormone I + H2O | juvenile hormone I acid + methanol |
 | Tenebrio molitor, Manduca sexta | - | - | 651510 | - | 651510 | ? |
| juvenile hormone I + H2O | juvenile hormone I acid + methanol |
 | Trichoplusia ni | - | - | 23477, 23479, 23481 | - | - | - |
| juvenile hormone I + H2O | juvenile hormone I acid + methanol |
 | Galleria mellonella | - | - | 23478 | - | - | - |
| juvenile hormone I + H2O | juvenile hormone I acid + methanol |
 | Heliothis virescens | - | - | 651510 | - | 651510 | ? |
| juvenile hormone I + H2O | juvenile hormone I acid + methanol |
 | Drosophila melanogaster | A1ZA98 | - | 680156 | - | - | ? |
| juvenile hormone II + H2O | juvenile hormone II acid + methanol |
 | Manduca sexta | - | - | 707525 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori | D2KWC2 | - | 715173 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Tribolium castaneum | D7US45 | degradation | 715184 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Rhyparobia maderae | - | high affinity for juvenile hormone III | 651504 | - | 651504 | ? |
| juvenile hormone III + H2O | ? |
 | Tenebrio molitor | Q8WRD8 | hydrolyzes the methyl ester of juvenile hormone, highest specificity for juvenile hormone III | 651512 | - | 651512 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster | - | JHE is highly selective for JHIII and JHIII bisepoxide | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Leptinotarsa decemlineata | - | racemic | 649498 | - | 649498 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster | - | JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori | D2KWC2 | BmJHE is a juvenile hormone-selective esterase. Of the CCEs containing a GQSAG motif only BmJHE can function as a JH-specific degradation enzyme in the silkworm | 715173 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori | D2KWC2 | BmCCE-5 has the ability to degrade juvenile hormone, however, the protein might not function as a JH-specific esterase in vivo as it has a high Km value for juvenile hormone | 715173 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster MH19 | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster CuZn-SOD | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster Oregon K | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster Oregon R | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori Shogetu-Shunrei | - | BmJHE is a juvenile hormone-selective esterase. Of the CCEs containing a GQSAG motif only BmJHE can function as a JH-specific degradation enzyme in the silkworm | 715173 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori C108 | - | BmJHE is a juvenile hormone-selective esterase. Of the CCEs containing a GQSAG motif only BmJHE can function as a JH-specific degradation enzyme in the silkworm | 715173 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster Canton S | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster OregonR | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori P22 | - | BmJHE is a juvenile hormone-selective esterase. Of the CCEs containing a GQSAG motif only BmJHE can function as a JH-specific degradation enzyme in the silkworm | 715173 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori P21 | - | BmJHE is a juvenile hormone-selective esterase. Of the CCEs containing a GQSAG motif only BmJHE can function as a JH-specific degradation enzyme in the silkworm | 715173 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori Bm-N | - | BmJHE is a juvenile hormone-selective esterase. Of the CCEs containing a GQSAG motif only BmJHE can function as a JH-specific degradation enzyme in the silkworm | 715173 | - | - | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster S-2 | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster AANAT2 | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster Samarkand | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Drosophila melanogaster Oregon-R | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III + H2O | ? |
 | Bombyx mori 122 | - | BmJHE is a juvenile hormone-selective esterase. Of the CCEs containing a GQSAG motif only BmJHE can function as a JH-specific degradation enzyme in the silkworm | 715173 | - | - | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Bombyx mori | - | - | 651397 | - | 651397 | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Tenebrio molitor | Q8WRD8 | - | 651512 | - | - | - |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Tenebrio molitor, Manduca sexta | - | - | 651510 | - | 651510 | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Trichoplusia ni | - | - | 23477, 23479, 23481 | - | - | - |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Trichoplusia ni, Heliothis virescens | - | - | 651510 | - | 651510 | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Tribolium freemani | - | - | 651397 | - | 651397 | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Tenebrio molitor | - | highest specific activity | 649497 | - | 649497 | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Gryllus assimilis | - | racemic | 649644 | juvenile hormone acid is the sole product | 649644 | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Ips typographus | - | specific activities of several developmental stages, highest specific activity | 649497 | - | 649497 | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Drosophila melanogaster | A1ZA98 | 10R-juvenile hormone III is the natural isomer | 680156 | - | - | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Manduca sexta | - | juvenile hormone III fits very tightly within the substrate binding pocket of JHE. This tight fit places two noncatalytic amino acid residues, Phe-259 and Thr-314, within the appropriate distance and geometry to potentially interact with the R,beta-unsaturated ester and epoxide, respectively, of juvenile hormone III. Neither nucleophilic attack of the resonance-stabilized ester by the catalytic serine nor the availability of a water molecule for attack of the acyl-enzyme intermediate appears to be a rate-determining step in the hydrolysis. Release of the juvenile hormone III acid metabolite from the substrate binding pocket limits the catalytic cycle. Chemical bond strength does not necessarily correlate with how reactive the bond will be to metabolism | 707525 | - | - | ? |
| juvenile hormone III + H2O | juvenile hormone III acid + methanol |
 | Bombyx mori Shogetu-Shunrei, Bombyx mori C108, Bombyx mori P22, Bombyx mori P21, Bombyx mori Bm-N, Bombyx mori 122 | - | - | 651397 | - | 651397 | ? |
| juvenile hormone III + H2O | juvenile hormone acid + methanol |
 | Apis mellifera | - | JH esterase hydrolyzes the methyl ester to produce juvenile hormone acid | 715819 | - | - | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster MH19 | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster CuZn-SOD | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster Oregon K | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster Oregon R | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster Canton S | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster OregonR | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster S-2 | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster AANAT2 | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster Samarkand | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III bisepoxide + H2O | ? |
 | Drosophila melanogaster Oregon-R | - | JHE is highly selective for JHIII and JHIII bisepoxide, JHE is highly selective for JHIII and JHIII bisepoxide, both may be in vivo substrates | 651500 | - | 651500 | ? |
| juvenile hormone III diol + H2O | ? |
 | Manduca sexta | - | although hydrogen bonding appears not to occur between juvenile hormone III diol and Thr-314, the hydroxyls of the diol (at C10 and C11) are within hydrogen bonding distance of the main chain carbonyl oxygen atoms of Phe-259 and Phe-311 | 707525 | - | - | ? |
| methyl (2E,6E)-(10R,11S)-10,11-epoxy-3,7,11-trimethyltrideca-2,6-dienoate + H2O | (2E,6E)-(10R,11S)-10,11-epoxy-3,7,11-trimethyltrideca-2,6-dienoate + methanol |
 | Aedes aegypti | Q17AV1 | juvenile hormone esterase plays an important role in regulating juvenile hormone titers | 680159 | - | - | ? |
| methyl farnesoate + H2O | methanol + farnesoic acid |
 | Drosophila melanogaster | A1ZA98 | - | 680156 | - | - | ? |
| methyl hepthylthioacetothioate + H2O | ? |
 | Bombyx mori | D2KWC2 | a synthetic substrate | 715173 | - | - | ? |
| methyl hepthylthioacetothioate + H2O | ? |
 | Tribolium castaneum | D7US45 | the recombinant JHE has a strong ability to degrade methyl hepthylthioacetothioate, HEPTAT, as a synthetic substrate | 715184 | - | - | ? |
| methyl hexylthio acetothioate + H2O | ? |
 | Tenebrio molitor | - | putative surrogate substrate for juvenile hormone | 649497 | - | 649497 | ? |
| p-nitrophenyl acetate + H2O | p-nitrophenol + acetate |
 | Trichoplusia ni | - | - | 651510 | - | 651510 | ? |
| p-nitrophenyl acetate + H2O | p-nitrophenol + acetate |
 | Tenebrio molitor | Q8WRD8 | - | 651512 | - | 651512 | ? |
| p-nitrophenyl acetate + H2O | p-nitrophenol + acetate |
 | Tenebrio molitor, Manduca sexta, Heliothis virescens | - | higher specific activity than for p-nitrophenyl valerate | 651510 | - | 651510 | ? |
| p-nitrophenyl valerate + H2O | p-nitrophenol + valerate |
 | Tenebrio molitor, Manduca sexta, Heliothis virescens | - | lower specific activity than for p-nitrophenyl acetate | 651510 | - | 651510 | ? |
| saturated juvenile hormone III + H2O | saturated juvenile hormone III acid + methanol |
 | Manduca sexta | - | alpha,beta-saturated methyl ester | 707525 | - | - | ? |
| methyl hexylthio acetothioate + H2O | ? |
 | Ips typographus | - | putative surrogate substrate for juvenile hormone, specific activities of several developmental stages | 649497 | - | 649497 | ? |
| additional information | ? | - | Trichoplusia ni | - | low activity with hydroprene and methoprene | 23479 | - | - | - |
| additional information | ? | - | Spodoptera frugiperda | - | effectiveness of thioester compounds as surrogate substrates | 23491 | - | - | - |
| additional information | ? | - | insecta, Manduca sexta, Samia cynthia, Trichoplusia ni, Galleria mellonella, Periplaneta brunnea, Schistocerca nitens, Neobellieria bullata, Lymantria dispar | - | demethylates the insect juvenile hormones, JH1 and JH3, but does not hydrolyze the analogous ethyl or isopropyl esters | 23470 | - | - | - |
| additional information | ? | - | Drosophila melanogaster | - | structural features promoting substrate binding at the active site of JHE | 651500 | - | 651500 | ? |
| additional information | ? | - | Bombyx mori | - | likely to be involved in elimination of intracellular juvenile hormone from the target tissues in the preparation for metamorphosis | 23492 | - | - | - |
| additional information | ? | - | Manduca sexta | - | likely to be involved in elimination of intracellular juvenile hormone from the target tissues in the preparation for metamorphosis | 23471, 23492 | - | - | - |
| additional information | ? | - | Trichoplusia ni, Heliothis virescens, Helicoverpa zea | - | likely to be involved in elimination of intracellular juvenile hormone from the target tissues in the preparation for metamorphosis | 23492 | - | - | - |
| additional information | ? | - | insecta, Manduca sexta, Samia cynthia, Trichoplusia ni, Galleria mellonella, Periplaneta brunnea, Schistocerca nitens, Neobellieria bullata, Lymantria dispar | - | demethylates the insect juvenile hormones, JH1 and JH3, major role in regulation of juvenile hormone titer and may be necessary for the removal of all traces of juvenile hormone at periods critical to further development | 23470 | - | - | - |
| additional information | ? | - | Choristoneura fumiferana | - | hormonal regulation of enzyme | 653222 | - | 653222 | ? |
| additional information | ? | - | Dysdercus cingulatus | - | the enzyme plays a profound role in metamorphosis and reproduction | 680125 | - | - | - |
| additional information | ? | - | Drosophila melanogaster | A1ZA98 | there is probably only one physiologically functional JHE in Drosophila melanogaster but multiple esterases with JH esterase activity, no activity with juvenile hormone II | 680156 | - | - | - |
| additional information | ? | - | Apis mellifera | Q76LA5 | clearance of juvenile hormone during larval-pupal metamorphosis | 697457 | - | - | - |
| additional information | ? | - | Apis mellifera | Q76LA5 | deficiency in Amjhe-like results in 6fold increase in juvenile hormone titer (adult, 4 day-old worker bee) | 697457 | - | - | - |
| additional information | ? | - | Reticulitermes flavipes | D8UUL2 | the enzyme is also active on alpha-naphthyl propionate, alpha-naphthyl butyrate, and 2-carbon substrate alpha-naphthyl acetate | 713975 | - | - | - |
| additional information | ? | - | Bombyx mori | D2KWC2 | the enzymes encoded by genes Bmcce-1-4 are not active on juvenile hormone | 715173 | - | - | - |
| additional information | ? | - | Drosophila melanogaster MH19, Drosophila melanogaster CuZn-SOD | - | structural features promoting substrate binding at the active site of JHE | 651500 | - | 651500 | ? |
| additional information | ? | - | Spodoptera frugiperda Sf9 | - | effectiveness of thioester compounds as surrogate substrates | 23491 | - | - | - |
| additional information | ? | - | Drosophila melanogaster Oregon K, Drosophila melanogaster Oregon R | - | structural features promoting substrate binding at the active site of JHE | 651500 | - | 651500 | ? |
| additional information | ? | - | Bombyx mori Shogetu-Shunrei | - | likely to be involved in elimination of intracellular juvenile hormone from the target tissues in the preparation for metamorphosis | 23492 | - | - | - |
| additional information | ? | - | Spodoptera frugiperda Sf-21 | - | effectiveness of thioester compounds as surrogate substrates | 23491 | - | - | - |
| additional information | ? | - | Bombyx mori C108 | - | likely to be involved in elimination of intracellular juvenile hormone from the target tissues in the preparation for metamorphosis | 23492 | - | - | - |
| additional information | ? | - | Drosophila melanogaster Canton S, Drosophila melanogaster OregonR | - | structural features promoting substrate binding at the active site of JHE | 651500 | - | 651500 | ? |
| additional information | ? | - | Bombyx mori P22, Bombyx mori P21, Bombyx mori Bm-N | - | likely to be involved in elimination of intracellular juvenile hormone from the target tissues in the preparation for metamorphosis | 23492 | - | - | - |
| additional information | ? | - | Drosophila melanogaster S-2, Drosophila melanogaster AANAT2, Drosophila melanogaster Samarkand, Drosophila melanogaster Oregon-R | - | structural features promoting substrate binding at the active site of JHE | 651500 | - | 651500 | ? |
| additional information | ? | - | Bombyx mori 122 | - | likely to be involved in elimination of intracellular juvenile hormone from the target tissues in the preparation for metamorphosis | 23492 | - | - | - |