Details
Stereochemistry | ACHIRAL |
Molecular Formula | C10H19ClNO5P |
Molecular Weight | 299.688 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 1 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CCN(CC)C(=O)C(\Cl)=C(\C)OP(=O)(OC)OC
InChI
InChIKey=RGCLLPNLLBQHPF-CMDGGOBGSA-N
InChI=1S/C10H19ClNO5P/c1-6-12(7-2)10(13)9(11)8(3)17-18(14,15-4)16-5/h6-7H2,1-5H3/b9-8+
Originator
Approval Year
Targets
Primary Target | Pharmacology | Condition | Potency |
---|---|---|---|
Target ID: acetylcholinesterase of hen brain Sources: https://www.ncbi.nlm.nih.gov/pubmed/7495383 |
2.9 µM [IC50] |
Conditions
Condition | Modality | Targets | Highest Phase | Product |
---|---|---|---|---|
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7495383
The LD50 value of phosphamidon p.o. for hens was 9 mg/kg
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/7495383
Phosphamidon (PSM) was a potent inhibitor of acetylcholinesterase (AChE), with an I50 of 2.9 microM and second-order rate constant (ka) of 1.2 x 10(4) M-1 min-1 at 37 degrees C. PSM-inhibited AChE aged rapidly (t1/2 = 1.9 h).
Name | Type | Language | ||
---|---|---|---|---|
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
3033834
Created by
admin on Fri Dec 15 15:56:03 GMT 2023 , Edited by admin on Fri Dec 15 15:56:03 GMT 2023
|
PRIMARY | |||
|
54VR7A0BQD
Created by
admin on Fri Dec 15 15:56:03 GMT 2023 , Edited by admin on Fri Dec 15 15:56:03 GMT 2023
|
PRIMARY | |||
|
297-99-4
Created by
admin on Fri Dec 15 15:56:03 GMT 2023 , Edited by admin on Fri Dec 15 15:56:03 GMT 2023
|
PRIMARY | |||
|
DTXSID5058357
Created by
admin on Fri Dec 15 15:56:03 GMT 2023 , Edited by admin on Fri Dec 15 15:56:03 GMT 2023
|
PRIMARY |
SUBSTANCE RECORD