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1,2-epoxy-3-(4-nitrophenoxy)propane
2-mercaptoethanol
-
10.55% inhibition at 10 mM
alpha-Diazo-p-bromoacetophenone
Penicillium duponti
-
in presence of Cu2+
Benzyloxycarbonyl-Gln-Tyr
-
-
Benzyloxycarbonyl-Glu
-
-
Benzyloxycarbonyl-Val-Tyr
-
-
Ca2+
Penicillium candidum
-
23% residual activity at 10 mM
Diazoacetyl DL-norleucine methyl ester
Diazoacetyl-DL-norleucine methyl ester
Diazoacetylglycine ethyl ester
Penicillium duponti
-
in presence of Cu2+
Difluorostatine- and difluorostatone-containing peptides
-
-
-
EDTA
Penicillium candidum
-
7% residual activity at 10 mM
Fe3+
Penicillium candidum
-
complete inhibition at 10 mM
isovaleryl-Val-statine-ethoxy
pepstatin analogue
Isovaleryl-Val-Val-statyl ethyl ester
-
-
Isovaleryl-Val-Val-statyl-Ala ethyl ester
-
-
K+
Penicillium candidum
-
85% residual activity at 10 mM
KMnO4
Penicillium duponti
-
-
Leu-Gly-Leu
-
inhibits trypsinogen activation, activates cleavage of Leu-Tyr amide
methyl (2S)-2-({hydroxy[({N-[(naphthalen-1-yl)acetyl]-L-valyl}amino)methyl]phosphoryl}oxy)-3-phenylpropanoate
-
-
methyl (2S)-2-({[(4S,7R)-2,5-dioxo-4-(propan-2-yl)-2,3,4,5,6,7-hexahydro-1H-8,10-etheno-3,6-benzodiazacycloundecin-7-yl](hydroxy)phosphoryl}oxy)-3-phenylpropanoate
-
-
methyl (2S)-2-({[(R)-[(N-formyl-L-valyl)amino](naphthalen-2-yl)methyl](hydroxy)phosphoryl}oxy)-3-phenylpropanoate
-
-
methyl 10-hydroxy-6-[[N-(3-methylbutanoyl)valyl]amino]-9-(2-methylpropyl)-4,7-dioxo-11-oxa-3,8-diaza-10-phosphabicyclo[12.3.1]octadeca-1(18),14,16-triene-12-carboxylate 10-oxide
methyl cyclo[(2S)-2-[[(1R)-1-(N-(l-N-(3-methylbutanoyl)valyl-L-aspartyl)amino)-3-methylbutyl]hydroxyphosphinyloxy]-3-(3-aminomethyl)] phenylpropanoate
phosphonate-based macrocycle PPi4, macrocyclic pentapeptide inhibitor
methyl cyclo[(2S)-2-[[(1R)-1-(N-(l-N-(3-methylbutanoyl)valyl-L-aspartyl)amino)-3-methylbutyl]ydroxyphosphinyloxy]-3-(3-aminomethyl)] phenylpropanoate
-
Mg2+
Penicillium candidum
-
31% residual activity at 10 mM
Mn2+
Penicillium candidum
-
98% residual activity at 10 mM
N-(3-methylbutanoyl)valyl-N1-(1-[hydroxy[(1-methoxy-1-oxo-3-phenylpropan-2-yl)oxy]phosphoryl]-3-methylbutyl)aspartamide
-
N-bromosuccinimide
Penicillium duponti
-
-
pepstatin A
-
55.08% inhibition at 10 mM
phenylmethylsulfonyl fluoride
-
complete inhibition at 10 mM
Phosphorus-based peptide analogues
-
-
-
SDS
Penicillium candidum
-
33% residual activity at 10 mM
sodium lauryl sulfate
Penicillium duponti
-
-
Specific pepsin inhibitor produced by Streptomyces naniwaensis
Penicillium duponti
-
-
-
Streptomycin inhibitor
-
weak
-
Zn2+
Penicillium candidum
-
92% residual activity at 10 mM
1,2-epoxy-3-(4-nitrophenoxy)propane
-
-
1,2-epoxy-3-(4-nitrophenoxy)propane
-
enzyme previously inactivated with diazoacetylnorleucine methyl ester does not react, pH-dependence of inhibition
1,2-epoxy-3-(4-nitrophenoxy)propane
-
-
Diazoacetyl DL-norleucine methyl ester
Penicillium duponti
-
in presence of Cu2+
Diazoacetyl DL-norleucine methyl ester
-
in presence of Cu2+
Diazoacetyl DL-norleucine methyl ester
-
-
Diazoacetyl-DL-norleucine methyl ester
-
i.e. DAN, active-site directed inhibitor
Diazoacetyl-DL-norleucine methyl ester
Penicillium duponti
-
i.e. DAN, active-site directed inhibitor, inactivation, also by related compounds
Diazoacetyl-DL-norleucine methyl ester
i.e. DAN, active-site directed inhibitor
methyl 10-hydroxy-6-[[N-(3-methylbutanoyl)valyl]amino]-9-(2-methylpropyl)-4,7-dioxo-11-oxa-3,8-diaza-10-phosphabicyclo[12.3.1]octadeca-1(18),14,16-triene-12-carboxylate 10-oxide
-
-
methyl 10-hydroxy-6-[[N-(3-methylbutanoyl)valyl]amino]-9-(2-methylpropyl)-4,7-dioxo-11-oxa-3,8-diaza-10-phosphabicyclo[12.3.1]octadeca-1(18),14,16-triene-12-carboxylate 10-oxide
includes a methylene bridge between the Asn(P2) and Phe(P1') side chains
additional information
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not inhibited by EDTA and iodoacetic acid
-
additional information
Penicillium candidum
-
not inhibited by phenylmethylsulfonyl fluoride
-
additional information
Penicillium duponti
-
p-bromophenacylbromide
-
additional information
Penicillium duponti
-
chelating agents; potato inhibitor
-
additional information
-
benzyloxycarbonyl-Phe; not: benzyloxycarbonyl-Tyr; p-bromophenacylbromide
-
additional information
-
investigation of the protonation state penicillopepsin in complex with phosphinate and phosphonate inhibitors
-
additional information
-
p-bromophenacylbromide
-