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Details

Stereochemistry MIXED
Molecular Formula C10H20
Molecular Weight 140.2658
Optical Activity NONE
Additional Stereochemistry Yes
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0
Stereo Comments CIS/TRANS MIXTURE

SHOW SMILES / InChI
Structure of P-MENTHANE

SMILES

CC(C)C1CCC(C)CC1

InChI

InChIKey=CFJYNSNXFXLKNS-UHFFFAOYSA-N
InChI=1S/C10H20/c1-8(2)10-6-4-9(3)5-7-10/h8-10H,4-7H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C10H20
Molecular Weight 140.2658
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Description
Curator's Comment: description was created based on several sources, including http://www.ncbi.nlm.nih.gov/pubmed/2240626

Menfegol-coated condom represents a new birth control method in which the contraceptive efficacy of the condom is enhanced by the spermicidal activity of menfegol. Menfegol possesses in vitro activity against human immunodeficiency virus (HIV). A randomized placebo-controlled safety study covered the use of menfegol foaming tablets for 14 days at increasing frequencies of insertion by 125 prostitutes in Dakar, Senegal. The frequencies of colposcopically diagnosed genital lesions were 5.0%, 11.8%, 27.8%, 49.7%, and 29.4% among menfegol recipients when tablets were used once every other day or 1, 2, 4, or 8 times a day, respectively (P < .05). Among placebo recipients, frequencies were 11.1% and 23.5% when tablets were used < 8 times daily and 8 times daily, respectively. There was no association between subjective genital symptoms and the incidence of colposcopically detected lesions. The high incidence of genital lesions when menfegol foaming tablets were used more than once daily suggests that their frequent use should not be recommended to prevent HIV transmission. In use at low frequency, the tablets' toxicity might be balanced by anti-HIV properties. Safety studies on vaginal microbicides should use objective methods, such as colposcopy, to assess the incidence of lesions.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
Preventing
Unknown

Approved Use

Unknown
PubMed

PubMed

TitleDatePubMed
In vitro effect of menfegol on Neisseria gonorrhoeae.
1989 Oct
Frequent use of menfegol spermicidal vaginal foaming tablets associated with a high incidence of genital lesions.
1995 Jun
Patents

Patents

Sample Use Guides

In Vivo Use Guide
Curator's Comment: The frequencies of colposcopically diagnosed genital lesions were 5.0%, 11.8%, 27.8%, 49.7%, and 29.4% among menfegol recipients when tablets were used once every other day or 1, 2, 4, or 8 times a day, respectively (P < .05)
table once every day
Route of Administration: Vaginal
In Vitro Use Guide
The distribution of the MICs of N. gonorrhoeae to Menfegol consisted of 2 groups. Resistant strains showed the MICs of more than 3200 micrograms/ml while the MICs of sensitive strains were less than or equal to 200 micrograms/ml. When the resistant strains were suspended in several concentrations of Menfegol and were incubated at 35 degrees C, no concentrations inactivated gonococci completely. However, the number of organisms was remarkably decreased within 30 minutes.
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:41:40 GMT 2023
Edited
by admin
on Fri Dec 15 18:41:40 GMT 2023
Record UNII
CGW5GN8TXU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-MENTHANE
Systematic Name English
CYCLOHEXANE, 1-METHYL-4-(1-METHYLETHYL)-
Systematic Name English
1-METHYL-4-ISOPROPYLCYCLOHEXANE
Systematic Name English
1-ISOPROPYL-4-METHYLCYCLOHEXANE [HSDB]
Common Name English
WOODY RIVER 10
Brand Name English
4-METHYL-1-(1-METHYLETHYL)CYCLOHEXANE
Systematic Name English
Code System Code Type Description
WIKIPEDIA
p-Menthane
Created by admin on Fri Dec 15 18:41:40 GMT 2023 , Edited by admin on Fri Dec 15 18:41:40 GMT 2023
PRIMARY
CHEBI
25826
Created by admin on Fri Dec 15 18:41:40 GMT 2023 , Edited by admin on Fri Dec 15 18:41:40 GMT 2023
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HSDB
5328
Created by admin on Fri Dec 15 18:41:40 GMT 2023 , Edited by admin on Fri Dec 15 18:41:40 GMT 2023
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EPA CompTox
DTXSID9025530
Created by admin on Fri Dec 15 18:41:40 GMT 2023 , Edited by admin on Fri Dec 15 18:41:40 GMT 2023
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ECHA (EC/EINECS)
202-790-4
Created by admin on Fri Dec 15 18:41:40 GMT 2023 , Edited by admin on Fri Dec 15 18:41:40 GMT 2023
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PUBCHEM
7459
Created by admin on Fri Dec 15 18:41:40 GMT 2023 , Edited by admin on Fri Dec 15 18:41:40 GMT 2023
PRIMARY
CAS
99-82-1
Created by admin on Fri Dec 15 18:41:40 GMT 2023 , Edited by admin on Fri Dec 15 18:41:40 GMT 2023
PRIMARY
FDA UNII
CGW5GN8TXU
Created by admin on Fri Dec 15 18:41:40 GMT 2023 , Edited by admin on Fri Dec 15 18:41:40 GMT 2023
PRIMARY