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MedKoo Cat#: 591699 | Name: Fenchone

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Fenchone is a Dapsone-Loaded Invasome that is used in acne treatment.

Chemical Structure

Fenchone
Fenchone
CAS#1195-79-5

Theoretical Analysis

MedKoo Cat#: 591699

Name: Fenchone

CAS#: 1195-79-5

Chemical Formula: C10H16O

Exact Mass: 152.1201

Molecular Weight: 152.24

Elemental Analysis: C, 78.90; H, 10.59; O, 10.51

Price and Availability

This product is currently not in stock but may be available through custom synthesis. To ensure cost efficiency, the minimum order quantity is 1 gram. The estimated lead time is 2 to 4 months, with pricing dependent on the complexity of the synthesis (typically high for intricate chemistries). Quotes for quantities below 1 gram will not be provided. To request a quote, please click the button below. Note: If this product becomes available in stock in the future, pricing will be listed accordingly.
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Related CAS #
No Data
Synonym
AI3-00736; AI3 00736; AI300736; Fenchone
IUPAC/Chemical Name
2-Norbornanone, 1,3,3-trimethyl-
InChi Key
LHXDLQBQYFFVNW-UHFFFAOYSA-N
InChi Code
InChI=1S/C10H16O/c1-9(2)7-4-5-10(3,6-7)8(9)11/h7H,4-6H2,1-3H3
SMILES Code
O=C1C(C)(C)C2CCC1(C)C2
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>2 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.9001
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 152.24 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Müller AD, Artemyev AN, Demekhin PV. Photoelectron circular dichroism in the multiphoton ionization by short laser pulses. II. Three- and four-photon ionization of fenchone and camphor. J Chem Phys. 2018 Jun 7;148(21):214307. doi: 10.1063/1.5032295. PubMed PMID: 29884056. 2: El-Nabarawi MA, Shamma RN, Farouk F, Nasralla SM. Dapsone-Loaded Invasomes as a Potential Treatment of Acne: Preparation, Characterization, and In Vivo Skin Deposition Assay. AAPS PharmSciTech. 2018 May 3. doi: 10.1208/s12249-018-1025-0. [Epub ahead of print] PubMed PMID: 29725903. 3: Pistelli L, Bandeira Reidel RV, Parri F, Morelli E, Pistelli L. Chemical composition of essential oil from plants of abandoned mining site of Elba island. Nat Prod Res. 2018 Feb 8:1-5. doi: 10.1080/14786419.2018.1437430. [Epub ahead of print] PubMed PMID: 29417841. 4: Pavela R. Essential oils from Foeniculum vulgare Miller as a safe environmental insecticide against the aphid Myzus persicae Sulzer. Environ Sci Pollut Res Int. 2018 Apr;25(11):10904-10910. doi: 10.1007/s11356-018-1398-3. Epub 2018 Feb 3. PubMed PMID: 29397509. 5: Akhbari M, Kord R, Jafari Nodooshan S, Hamedi S. Analysis and evaluation of the antimicrobial and anticancer activities of the essential oil isolated from Foeniculum vulgare from Hamedan, Iran. Nat Prod Res. 2018 Jan 7:1-4. doi: 10.1080/14786419.2017.1423310. [Epub ahead of print] PubMed PMID: 29308661. 6: Rahman S, Luetje CW. Mutant cycle analysis identifies a ligand interaction site in an odorant receptor of the malaria vector Anopheles gambiae. J Biol Chem. 2017 Nov 17;292(46):18916-18923. doi: 10.1074/jbc.M117.810374. Epub 2017 Sep 29. PubMed PMID: 28972152; PubMed Central PMCID: PMC5704475. 7: Ali NAA, Chhetri BK, Dosoky NS, Shari K, Al-Fahad AJA, Wessjohann L, Setzer WN. Antimicrobial, Antioxidant, and Cytotoxic Activities of Ocimum forskolei and Teucrium yemense (Lamiaceae) Essential Oils. Medicines (Basel). 2017 Apr 1;4(2). pii: E17. doi: 10.3390/medicines4020017. PubMed PMID: 28930232; PubMed Central PMCID: PMC5590053. 8: Dudzik K, Wojcik J, Ejchart A, Nowakowski M. Size makes a difference: Chiral recognition in complexes of fenchone with cyclodextrins studied by means of NMR titration. Chirality. 2017 Nov;29(11):747-758. doi: 10.1002/chir.22747. Epub 2017 Sep 6. PubMed PMID: 28877407. 9: Miles J, Fernandes D, Young A, Bond CMM, Crane SW, Ghafur O, Townsend D, Sá J, Greenwood JB. A new technique for probing chirality via photoelectron circular dichroism. Anal Chim Acta. 2017 Sep 1;984:134-139. doi: 10.1016/j.aca.2017.06.051. Epub 2017 Jul 1. PubMed PMID: 28843556. 10: Manoharan RK, Lee JH, Lee J. Antibiofilm and Antihyphal Activities of Cedar Leaf Essential Oil, Camphor, and Fenchone Derivatives against Candida albicans. Front Microbiol. 2017 Aug 3;8:1476. doi: 10.3389/fmicb.2017.01476. eCollection 2017. PubMed PMID: 28824600; PubMed Central PMCID: PMC5541024. 11: Sripathi R, Jayagopal D, Ravi S. A study on the seasonal variation of the essential oil composition from Plectranthus hadiensis and its antibacterial activity. Nat Prod Res. 2018 Apr;32(7):871-874. doi: 10.1080/14786419.2017.1363748. Epub 2017 Aug 8. PubMed PMID: 28783957. 12: Rolim TL, Meireles DRP, Batista TM, de Sousa TKG, Mangueira VM, de Abrantes RA, Pita JCLR, Xavier AL, Costa VCO, Batista LM, da Silva MS, Sobral MV. Erratum to: toxicity and antitumor potential of Mesosphaerum sidifolium (Lamiaceae) oil and fenchone, its major component. BMC Complement Altern Med. 2017 Jul 14;17(1):364. doi: 10.1186/s12906-017-1875-0. PubMed PMID: 28709433; PubMed Central PMCID: PMC5512769. 13: Asakawa Y, Ludwiczuk A, Sakurai K, Tomiyama K, Kawakami Y, Yaguchi Y. Comparative Study on Volatile Compounds of Alpinia japonica and Elettaria cardamomum. J Oleo Sci. 2017 Aug 1;66(8):871-876. doi: 10.5650/jos.ess17048. Epub 2017 Jul 12. PubMed PMID: 28701653. 14: Kastner A, Ring T, Krüger BC, Park GB, Schäfer T, Senftleben A, Baumert T. Intermediate state dependence of the photoelectron circular dichroism of fenchone observed via femtosecond resonance-enhanced multi-photon ionization. J Chem Phys. 2017 Jul 7;147(1):013926. doi: 10.1063/1.4982614. PubMed PMID: 28688398. 15: Rolim TL, Meireles DRP, Batista TM, de Sousa TKG, Mangueira VM, de Abrantes RA, Pita JCLR, Xavier AL, Costa VCO, Batista LM, da Silva MS, Sobral MV. Toxicity and antitumor potential of Mesosphaerum sidifolium (Lamiaceae) oil and fenchone, its major component. BMC Complement Altern Med. 2017 Jul 3;17(1):347. doi: 10.1186/s12906-017-1779-z. Erratum in: BMC Complement Altern Med. 2017 Jul 14;17 (1):364. PubMed PMID: 28673306; PubMed Central PMCID: PMC5496405. 16: Garzoli S, Božović M, Baldisserotto A, Sabatino M, Cesa S, Pepi F, Vicentini CB, Manfredini S, Ragno R. Essential oil extraction, chemical analysis and anti-Candida activity of Foeniculum vulgare Miller - new approaches. Nat Prod Res. 2018 Jun;32(11):1254-1259. doi: 10.1080/14786419.2017.1340291. Epub 2017 Jun 15. PubMed PMID: 28617136. 17: Keskin I, Gunal Y, Ayla S, Kolbasi B, Sakul A, Kilic U, Gok O, Koroglu K, Ozbek H. Effects of Foeniculum vulgare essential oil compounds, fenchone and limonene, on experimental wound healing. Biotech Histochem. 2017;92(4):274-282. doi: 10.1080/10520295.2017.1306882. Epub 2017 Apr 20. PubMed PMID: 28426256. 18: Wujkowska Z, Strojewska A, Pieczonka AM, Leśniak S, Rachwalski M. Highly enantioselective asymmetric direct aldol reaction promoted by aziridine amides constructed on chiral terpene scaffold. Chirality. 2017 May;29(5):213-220. doi: 10.1002/chir.22698. Epub 2017 Apr 12. PubMed PMID: 28403553. 19: Marumoto S, Okuno Y, Miyazawa M. Inhibition of β-Secretase Activity by Monoterpenes, Sesquiterpenes, and C(13) Norisoprenoids. J Oleo Sci. 2017 Aug 1;66(8):851-855. doi: 10.5650/jos.ess16188. Epub 2017 Apr 4. PubMed PMID: 28381772. 20: Hughes DT, Pelletier J, Rahman S, Chen S, Leal WS, Luetje CW. Functional and Nonfunctional Forms of CquiOR91, an Odorant Selectivity Subunit of Culex quinquefasciatus. Chem Senses. 2017 May 1;42(4):333-341. doi: 10.1093/chemse/bjx011. PubMed PMID: 28334229; PubMed Central PMCID: PMC5964367.

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NCI65828 sodium

NCI65828 sodium