Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C28H35N3O5 |
| Molecular Weight | 493.5946 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CN1C(=O)[C@]23C[C@H]4C(C)(C)[C@@]5(C[C@]14CN2CC[C@@]3(C)O)C(=O)NC6=C5C=CC7=C6OC=CC(C)(C)O7
InChI
InChIKey=UVZZDDLIOJPDKX-ITKQZBBDSA-N
InChI=1S/C28H35N3O5/c1-23(2)10-12-35-20-17(36-23)8-7-16-19(20)29-21(32)27(16)14-26-15-31-11-9-25(5,34)28(31,22(33)30(26)6)13-18(26)24(27,3)4/h7-8,10,12,18,34H,9,11,13-15H2,1-6H3,(H,29,32)/t18-,25+,26+,27+,28-/m0/s1
| Molecular Formula | C28H35N3O5 |
| Molecular Weight | 493.5946 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 5 / 5 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
DescriptionSources: https://www.ncbi.nlm.nih.gov/pubmed/12213111 | https://www.ncbi.nlm.nih.gov/pubmed/12183640Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/21695247
Sources: https://www.ncbi.nlm.nih.gov/pubmed/12213111 | https://www.ncbi.nlm.nih.gov/pubmed/12183640
Curator's Comment: Description was created based on several sources, including https://www.ncbi.nlm.nih.gov/pubmed/21695247
Paraherquamide (PHQ), a potent and broad-spectrum anthelminthic. Paraherquamide (PHQ), 2-deoxoparaherquamide (2DPHQ), and close structural analogs of these compounds rapidly induce flaccid paralysis in parasitic nematodes in vitro, without affecting adenosine triphosphate (ATP) levels. Paraherquamide anthelmintics are nicotinic cholinergic antagonists in both nematodes and mammals, and this mechanism appears to underlie both their efficacy and toxicity. Paraherquamide A is a natural product produced by Penicillium paraherquei which was discovered in 1981. It was evaluated by Merck in the late 1980’s and a small chemistry effort was conducted to produce analogs. Paraherquamide A was found to have outstanding broad spectrum nematocidal activity against various sheep gastro-intestinal nematodes. It is a nicotinic antagonist that blocks depolarization in muscles and induces a rapid paralysis of the mid-body of the parasite. However, it was severely toxic in mice and dogs, which prevented its development, as these species are the standard models for safety studies.
CNS Activity
Sources: https://www.ncbi.nlm.nih.gov/pubmed/21695247
Curator's Comment: nicotinic antagonist that blocks depolarization in muscles and induces a rapid paralysis of the mid-body of the nematode parasites
Originator
Sources: https://www.ncbi.nlm.nih.gov/pubmed/14519003
Curator's Comment: Paraherquamide A, was first isolated from cultures of Penicillium paraherquei by Yamazaki and coworkers in 1981
Approval Year
Targets
| Primary Target | Pharmacology | Condition | Potency |
|---|---|---|---|
Target ID: GO:0007271 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12213111 |
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Target ID: CHEMBL3068 Sources: https://www.ncbi.nlm.nih.gov/pubmed/12213111 |
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Target ID: nAChRs, nematode Sources: https://www.ncbi.nlm.nih.gov/pubmed/12183640 |
|||
Target ID: CHEMBL613135 Sources: https://www.ncbi.nlm.nih.gov/pubmed/1540222 |
263.0 nM [Kd] |
Conditions
| Condition | Modality | Targets | Highest Phase | Product |
|---|---|---|---|---|
| Curative | Unknown Approved UseUnknown |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/18505789
Sheep, dogs: a single oral 0.5-mg/kg dose
Route of Administration:
Oral
In Vitro Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/8359986
The concentration of paraherquamide required to inhibit the motility of 50% of L3 larvae present was 0.033, 0.058 and 2.7 ug/ml for O. circumcincta, T. colubriformis and H. contortus, respectively.
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:52:33 GMT 2025
by
admin
on
Mon Mar 31 18:52:33 GMT 2025
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| Record UNII |
R72VB4E4KC
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| Record Status |
Validated (UNII)
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| Record Version |
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m8400
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