U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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
Structure of PARAHERQUAMIDE

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

HIDE SMILES / InChI

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

Description
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

Curator's Comment: nicotinic antagonist that blocks depolarization in muscles and induces a rapid paralysis of the mid-body of the nematode parasites

Originator

Curator's Comment: Paraherquamide A, was first isolated from cultures of Penicillium paraherquei by Yamazaki and coworkers in 1981

Approval Year

TargetsConditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Potential drug development candidates for human soil-transmitted helminthiases.
2011-06
Asymmetric, stereocontrolled total synthesis of paraherquamide A.
2003-10-08
Patents

Sample Use Guides

Sheep, dogs: a single oral 0.5-mg/kg dose
Route of Administration: Oral
In Vitro Use Guide
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 Mon Mar 31 18:52:33 GMT 2025
Edited
by admin
on Mon Mar 31 18:52:33 GMT 2025
Record UNII
R72VB4E4KC
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
(-)-PARAHERQUAMIDE
Preferred Name English
PARAHERQUAMIDE
MI  
Common Name English
PARAHERQUAMIDE [MI]
Common Name English
(1'R,5'AS,7'R,8'AS,9'AR)-2',3',8'A,9'-TETRAHYDRO-1'-HYDROXY-1',4,4,8',8',11'-HEXAMETHYLSPIRO(4H,8H-(1,4)DIOXEPINO(2,3-G)INDOLE-8,7'(8'H)-(5H,6H-5A,9A)(IMINOMETHANO)(1H)CYCLOPENT(F)INDOLIZINE)-9,10'(10H)-DIONE
Common Name English
Code System Code Type Description
PUBCHEM
156934
Created by admin on Mon Mar 31 18:52:33 GMT 2025 , Edited by admin on Mon Mar 31 18:52:33 GMT 2025
PRIMARY
CAS
77392-58-6
Created by admin on Mon Mar 31 18:52:33 GMT 2025 , Edited by admin on Mon Mar 31 18:52:33 GMT 2025
PRIMARY
MESH
C063985
Created by admin on Mon Mar 31 18:52:33 GMT 2025 , Edited by admin on Mon Mar 31 18:52:33 GMT 2025
PRIMARY
MERCK INDEX
m8400
Created by admin on Mon Mar 31 18:52:33 GMT 2025 , Edited by admin on Mon Mar 31 18:52:33 GMT 2025
PRIMARY Merck Index
FDA UNII
R72VB4E4KC
Created by admin on Mon Mar 31 18:52:33 GMT 2025 , Edited by admin on Mon Mar 31 18:52:33 GMT 2025
PRIMARY
EPA CompTox
DTXSID70998607
Created by admin on Mon Mar 31 18:52:33 GMT 2025 , Edited by admin on Mon Mar 31 18:52:33 GMT 2025
PRIMARY