MedKoo Cat#: 584500 | Name: Longiborneol

Description:

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

Longiborneol is a sesquiterpene alcohol which has the same ring structure as culmorin.

Chemical Structure

Longiborneol
Longiborneol
CAS#465-24-7

Theoretical Analysis

MedKoo Cat#: 584500

Name: Longiborneol

CAS#: 465-24-7

Chemical Formula: C15H26O

Exact Mass: 222.1984

Molecular Weight: 222.37

Elemental Analysis: C, 81.02; H, 11.79; O, 7.19

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
Longiborneol
IUPAC/Chemical Name
1,4-Methanoazulen-9-ol, decahydro-1,5,5,8a-tetramethyl-, (1R,3aR,4S,8aS,9S)-
InChi Key
MNNFKQAYXGEKFA-MUGBGTHKSA-N
InChi Code
InChI=1S/C15H26O/c1-13(2)7-5-8-14(3)10-6-9-15(14,4)12(16)11(10)13/h10-12,16H,5-9H2,1-4H3/t10-,11-,12+,14+,15+/m1/s1
SMILES Code
O[C@@H]1[C@]2(C)CC[C@]3([H])[C@@]1([H])C(C)(C)CCC[C@]23C
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
>3 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
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 222.37 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: Schmidt R, Durling MB, de Jager V, Menezes RC, Nordkvist E, Svatoš A, Dubey M, Lauterbach L, Dickschat JS, Karlsson M, Garbeva P. Deciphering the genome and secondary metabolome of the plant pathogen Fusarium culmorum. FEMS Microbiol Ecol. 2018 Jun 1;94(6). doi: 10.1093/femsec/fiy078. PubMed PMID: 29718180. 2: Bresso E, Leroux V, Urban M, Hammond-Kosack KE, Maigret B, Martins NF. Structure-based virtual screening of hypothetical inhibitors of the enzyme longiborneol synthase-a potential target to reduce Fusarium head blight disease. J Mol Model. 2016 Jul;22(7):163. doi: 10.1007/s00894-016-3021-1. Epub 2016 Jun 21. PubMed PMID: 27324634. 3: Bahadoor A, Schneiderman D, Gemmill L, Bosnich W, Blackwell B, Melanson JE, McRae G, Harris LJ. Hydroxylation of Longiborneol by a Clm2-Encoded CYP450 Monooxygenase to Produce Culmorin in Fusarium graminearum. J Nat Prod. 2016 Jan 22;79(1):81-8. doi: 10.1021/acs.jnatprod.5b00676. Epub 2015 Dec 16. PubMed PMID: 26673640. 4: Sharma P, Shah GC. Composition and antioxidant activity of Senecio nudicaulis Wall. ex DC. (Asteraceae): a medicinal plant growing wild in Himachal Pradesh, India. Nat Prod Res. 2015;29(9):883-6. doi: 10.1080/14786419.2014.990904. Epub 2014 Dec 17. PubMed PMID: 25515495. 5: Gaviria M, Quijano C, Pino J, Madriñán S. Chemical composition and antibacterial activity of the essential oil of Drimys granadensis L.f. leaves from Colombia. Chem Biodivers. 2011 Mar;8(3):532-9. doi: 10.1002/cbdv.201000170. PubMed PMID: 21404436. 6: McCormick SP, Alexander NJ, Harris LJ. CLM1 of Fusarium graminearum encodes a longiborneol synthase required for culmorin production. Appl Environ Microbiol. 2010 Jan;76(1):136-41. doi: 10.1128/AEM.02017-09. Epub 2009 Oct 30. PubMed PMID: 19880637; PubMed Central PMCID: PMC2798659. 7: Ihara M. Syntheses of biologically active natural products and leading compounds for new pharmaceuticals employing effective construction of a polycyclic skeleton. Chem Pharm Bull (Tokyo). 2006 Jun;54(6):765-74. PubMed PMID: 16755041. 8: Takasu K. [Development of boomerang-type intramolecular cascade reactions and application to natural product synthesis]. Yakugaku Zasshi. 2001 Dec;121(12):887-98. Review. Japanese. PubMed PMID: 11766403. 9: Takasu K, Mizutani S, Noguchi M, Makita K, Ihara M. Total synthesis of (+/-)-culmorin and (+/-)-longiborneol: an efficient construction of Tricyclo[6.3.0.0(3,9)]undecan-10-one by intramolecular double Michael addition. J Org Chem. 2000 Jun 30;65(13):4112-9. PubMed PMID: 10866628. 10: Ihara M, Makita K, Fujiwara Y, Tokunaga Y, Fukumoto K. Stereoselective Construction of Copaborneol and Longiborneol Frameworks by Intramolecular Double Michael Reaction. J Org Chem. 1996 Sep 6;61(18):6416-6421. PubMed PMID: 11667485.