| 词条 | Incensole |
| 释义 |
| ImageFile = Incensole.svg | ImageSize = | ImageAlt = | IUPACName = (1R,2R,5E,9Z)-1,5,9-trimethyl-12-propan-2-yl-15-oxabicyclo[10.2.1]pentadeca-5,9-dien-2-ol | OtherNames = |Section1={{Chembox Identifiers | CASNo = 22419-74-5 | PubChem = 102004667 | ChemSpiderID = 57579845 | EC_number = | UNII = | InChI=1S/C20H34O2/c1-15(2)20-12-11-17(4)8-6-7-16(3)9-10-18(21)19(5,22-20)13-14-20/h7,11,15,18,21H,6,8-10,12-14H2,1-5H3/b16-7+,17-11-/t18-,19-,20?/m1/s1 | InChIKey = SSBZLMMXFQMHDP-AWBFOCMTSA-N | SMILES = CC1=CCCC(=CCC2(CCC(O2)(C(CC1)O)C)C(C)C)C }} |Section2={{Chembox Properties | C=20|H=34|O=2 | MolarMass = | Appearance = | Density = | MeltingPtC = | BoilingPt = | Solubility = }} |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} }}Insensole, an organic compound found as its acetate ester in some frankinsence. It is a diterpene alcohol.[1] The formula of insensole is C20H34O2[2] Incensole acetate [3] Its effects on animals have been studied.[4]References1. ^{{cite journal|url = http://www.sciencedirect.com/science/article/pii/S0040402001826016 | doi=10.1016/S0040-4020(01)82601-6 | volume=23 | issue=4 | title=The structure of incensole | year=1967 | journal=Tetrahedron | pages=1977–1984 | last1 = Corsano | first1 = S. | last2 = Nicoletti | first2 = R.}} {{chem-stub}}2. ^[https://pubchem.ncbi.nlm.nih.gov/compound/102004667 Insensole (at PubChem)] 3. ^Incensole acetate (@NIST) 4. ^{{cite journal |doi=10.1177/0269881112458729 |title=Incensole acetate reduces depressive-like behavior and modulates hippocampal BDNF and CRF expression of submissive animals |year=2012 |last1=Moussaieff |first1=A |last2=Gross |first2=M |last3=Nesher |first3=E |last4=Tikhonov |first4=T |last5=Yadid |first5=G |last6=Pinhasov |first6=A |journal=J. Psychopharmacol. |volume=26 |issue=12 |pmid=23015543 |pages=1584–93}} 5 : Diterpenes|Alcohols|Heterocyclic compounds (2 rings)|Oxygen heterocycles|Isopropyl compounds |
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