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Details

Stereochemistry ABSOLUTE
Molecular Formula C17H30O2
Molecular Weight 266.4189
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 2
Charge 0

SHOW SMILES / InChI
Structure of S-HYDROPRENE

SMILES

CCOC(=O)\C=C(C)\C=C\C[C@@H](C)CCCC(C)C

InChI

InChIKey=FYQGBXGJFWXIPP-OJROSNHMSA-N
InChI=1S/C17H30O2/c1-6-19-17(18)13-16(5)12-8-11-15(4)10-7-9-14(2)3/h8,12-15H,6-7,9-11H2,1-5H3/b12-8+,16-13+/t15-/m0/s1

HIDE SMILES / InChI

Molecular Formula C17H30O2
Molecular Weight 266.4189
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 2
Optical Activity UNSPECIFIED

Description
Curator's Comment: description was created based on several sources, including https://web.archive.org/web/20090624071746/http://www.epa.gov:80/oppbppd1/biopesticides/ingredients/factsheets/factsheet_igr.htm

S-Hydroprene is an insecticide used against cockroaches, beetles, and moths. S- Hydroprene belongs to the class of insecticides known as insect growth regulators. S-Hydroprene disrupts normal development and molting of insects by mimicking hormones produced by immature insects. S-Hydroprene causes different effects on different insects. It may cause adult sterility, physical body changes, water loss, and premature death. S-hydroprene is currently used indoors, and therefore are not expected to pose a risk to the environment.

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: Insect juvenile hormones
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Curative
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
Patents

Patents

Sample Use Guides

S-hydroprene diluted in distilled water to label concentration 0.12-0.6%
Route of Administration: Topical
Sections of blotter paper containing ten bed bug eggs (NY-1 colony) were directly sprayed with one of five treatments [(S)- methoprene (1x or 2x), (S)-hydroprene (2x or 3x) or control]. Eggs had been deposited 0–24 h or 48–72 h earlier. Each group of treated eggs was immediately transferred to an individual well of a 24-well cell culture plate. Egg hatch was observed daily for 8 days, at which point all eggs had either hatched or collapsed.
Substance Class Chemical
Created
by admin
on Sat Dec 16 04:54:31 GMT 2023
Edited
by admin
on Sat Dec 16 04:54:31 GMT 2023
Record UNII
ZPY1YX719Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
S-HYDROPRENE
JAN  
Common Name English
2,4-DODECADIENOIC ACID, 3,7,11-TRIMETHYL-, ETHYL ESTER, (S-(E,E))-
Common Name English
S-HYDROPRENE [JAN]
Common Name English
(7S)-HYDROPRENE
Common Name English
HYDROPRENE, (+)-
Common Name English
2,4-DODECADIENOIC ACID, 3,7,11-TRIMETHYL-, ETHYL ESTER, (2E,4E,7S)-
Common Name English
HYDROPRENE (S)-FORM [MI]
Common Name English
(S)-(+)-HYDROPRENE
Common Name English
HYDROPRENE, (S)-
Common Name English
ZR-2006
Code English
Classification Tree Code System Code
EPA PESTICIDE CODE 128966
Created by admin on Sat Dec 16 04:54:31 GMT 2023 , Edited by admin on Sat Dec 16 04:54:31 GMT 2023
Code System Code Type Description
EPA CompTox
DTXSID6035784
Created by admin on Sat Dec 16 04:54:31 GMT 2023 , Edited by admin on Sat Dec 16 04:54:31 GMT 2023
PRIMARY
MERCK INDEX
m6112
Created by admin on Sat Dec 16 04:54:31 GMT 2023 , Edited by admin on Sat Dec 16 04:54:31 GMT 2023
PRIMARY Merck Index
HSDB
8317
Created by admin on Sat Dec 16 04:54:31 GMT 2023 , Edited by admin on Sat Dec 16 04:54:31 GMT 2023
PRIMARY
PUBCHEM
5282198
Created by admin on Sat Dec 16 04:54:31 GMT 2023 , Edited by admin on Sat Dec 16 04:54:31 GMT 2023
PRIMARY
FDA UNII
ZPY1YX719Z
Created by admin on Sat Dec 16 04:54:31 GMT 2023 , Edited by admin on Sat Dec 16 04:54:31 GMT 2023
PRIMARY
CHEBI
32110
Created by admin on Sat Dec 16 04:54:31 GMT 2023 , Edited by admin on Sat Dec 16 04:54:31 GMT 2023
PRIMARY
CAS
65733-18-8
Created by admin on Sat Dec 16 04:54:31 GMT 2023 , Edited by admin on Sat Dec 16 04:54:31 GMT 2023
PRIMARY