User user73910

11 votes

1 answer

551 views

Do quaternary sulfur dications exist?

asked May 6, 2019 at 1:02

10 votes

2 answers

899 views

AChE Aging time of organophosphorus compounds containing hydroxyl groups

asked Feb 21, 2020 at 7:18

9 votes

1 answer

199 views

How are unstable transition states determined? [closed]

asked Feb 25, 2020 at 4:47

7 votes

2 answers

714 views

What happens to boiled (BMIM)PF6?

asked Jul 9, 2020 at 3:09

6 votes

1 answer

74 views

Does the mechanism of AChE inhibition by Isoparathion depend on chirality?

asked Jan 20, 2021 at 2:48

5 votes

0 answers

69 views

Why are S-thiocarbamates less toxic than carbamates?

asked Dec 27, 2020 at 7:30

5 votes

1 answer

1k views

Nitro as a leaving group in an aromatic ring

asked Oct 29, 2021 at 6:45

5 votes

0 answers

346 views

Interaction of trifluoroacetates with acetylcholinesterase

asked Jun 25, 2020 at 4:41

4 votes

2 answers

132 views

What is the mechanism of AChE inhibition by Onchidal?

asked Jul 20, 2020 at 14:52

4 votes

0 answers

73 views

Can bis-quaternary aromatic compounds act directly on acetylcholine receptors?

asked Dec 20, 2020 at 22:57

4 votes

1 answer

167 views

Why are isomers of parathion less active acetylcholinesterase inhibitors than paraoxon?

asked Jan 12, 2021 at 19:30

3 votes

1 answer

175 views

Effect of competitive inhibitor on substrate inhibition

asked Jul 30, 2023 at 3:03

3 votes

1 answer

108 views

Effect of presence of competitive inhibitor on observed reaction constant

asked Aug 7, 2023 at 4:44

3 votes

0 answers

76 views

Halogenation of organic acid derivatives

asked Dec 11, 2022 at 5:40

3 votes

0 answers

43 views

Reaction of BTNA, DMSO, and phosphate?

asked Jan 13, 2023 at 20:48

3 votes

0 answers

34 views

Differences in AChE inhibition kinetics between VX and VR

asked Mar 5, 2021 at 14:28

3 votes

1 answer

68 views

Differences in AChE inhibition kinetics between paraoxon and methyl paraoxon

asked Mar 14, 2021 at 5:36

3 votes

1 answer

107 views

Can aged acetylcholinesterase be reactivated?

asked Jul 3, 2020 at 8:29

2 votes

1 answer

206 views

Why is methyl parathion less toxic than ethyl parathion?

asked Jul 3, 2020 at 23:38

2 votes

0 answers

38 views

Isomerization of phosphorylated 2-imino-1,3-dioxalanes into phosphorylated cyclic carbamates

asked Jul 6, 2020 at 3:18

2 votes

0 answers

419 views

Differences in Novichok agent mass spectra

asked Jun 27, 2020 at 18:40

2 votes

0 answers

86 views

Differences in efficacy of oxime reactivators in organophosphate poisoning

asked Mar 6, 2020 at 4:37

2 votes

0 answers

50 views

Why are carbamates capable of inhibiting acetylcholinesterase?

asked Jun 7, 2020 at 7:59

2 votes

0 answers

27 views

Reaction rate constants for the inhibition of cholinesterases by various carbamates

asked Dec 20, 2020 at 7:15

2 votes

0 answers

38 views

How do structural differences between neostigmine and TL-599 contribute to differences in toxicity?

asked Dec 28, 2020 at 3:31

2 votes

0 answers

37 views

Why is Chlormephos highly toxic despite requiring metabolic activation?

asked Feb 6, 2021 at 2:17

2 votes

0 answers

25 views

Reason for differences in AChE aging/reactivation kinetics between neutral and charged organophosphorus inhibitors

asked Feb 26 at 2:41

2 votes

0 answers

39 views

How are enzyme inhibition constants assayed for "multi-inhibitors"?

asked Jul 25, 2023 at 0:03

1 vote

0 answers

40 views

Does HI-6 form a covalent adduct with acetylcholinesterase?

asked Aug 26, 2020 at 20:35

1 vote

1 answer

52 views

Do phosphoryl thiocholines, their uncharged analogs, and other organophosphates, interact differently with Acetylcholinesterase?

asked Apr 12, 2021 at 3:41

Stack Exchange Network

39 Questions

Do quaternary sulfur dications exist?

AChE Aging time of organophosphorus compounds containing hydroxyl groups

How are unstable transition states determined? [closed]

What happens to boiled (BMIM)PF6?

Does the mechanism of AChE inhibition by Isoparathion depend on chirality?

Why are S-thiocarbamates less toxic than carbamates?

Nitro as a leaving group in an aromatic ring

Interaction of trifluoroacetates with acetylcholinesterase

What is the mechanism of AChE inhibition by Onchidal?

Can bis-quaternary aromatic compounds act directly on acetylcholine receptors?

Why are isomers of parathion less active acetylcholinesterase inhibitors than paraoxon?

Effect of competitive inhibitor on substrate inhibition

Effect of presence of competitive inhibitor on observed reaction constant

Halogenation of organic acid derivatives

Reaction of BTNA, DMSO, and phosphate?

Differences in AChE inhibition kinetics between VX and VR

Differences in AChE inhibition kinetics between paraoxon and methyl paraoxon

Can aged acetylcholinesterase be reactivated?

Why is methyl parathion less toxic than ethyl parathion?

Isomerization of phosphorylated 2-imino-1,3-dioxalanes into phosphorylated cyclic carbamates

Differences in Novichok agent mass spectra

Differences in efficacy of oxime reactivators in organophosphate poisoning

Why are carbamates capable of inhibiting acetylcholinesterase?

Reaction rate constants for the inhibition of cholinesterases by various carbamates

How do structural differences between neostigmine and TL-599 contribute to differences in toxicity?

Why is Chlormephos highly toxic despite requiring metabolic activation?

Reason for differences in AChE aging/reactivation kinetics between neutral and charged organophosphorus inhibitors

How are enzyme inhibition constants assayed for "multi-inhibitors"?

Does HI-6 form a covalent adduct with acetylcholinesterase?

Do phosphoryl thiocholines, their uncharged analogs, and other organophosphates, interact differently with Acetylcholinesterase?