Mine sisu juurde

chavicol

Lehekülje sisu ei toetata teistes keeltes.

keemiline ühend

Välised allikad

Freebase
Reaxys registry number
2039682[2]
PubChem CID
DSSTOX compound identifier
UniChem compound ID
KEGG ID
NSC number
ChEMBL ID
InChIKey
Human Metabolome Database ID
ChEBI ID
50158[2][9]

mapping relation type: täpne vaste

SureChEMBL ID
AICS Chemical ID (BEING DELETED)
KNApSAcK ID
ECHA Substance Infocard ID
ChemSpider ID
EC number
207-929-2[12]
NMRShiftDB structure ID
CAS Registry Number
DSSTox substance ID
FL number
04.058[15]
Microsoft Academic ID
JECFA number
1527[16]
InChI
UNII

üksikjuht nähtusest

type of chemical entity

mille alamklass

keemiline struktuur

mass/kaal

134,073 aatommassiühik[3]

chemical formula

C₉H₁₀O[3]

canonical SMILES

C=CCC1=CC=C(C=C1)O[3]

found in taxon

Cinnamomum sieboldii[17]
Osmorhiza aristata[18]
Alpinia conchigera[19][20]
läikiv peiulill[21]
Nicotiana bonariensis[22]
Agastache rugosa[24]
Alpinia galanga[25]
Mandragora autumnalis[26]
Magnolia garrettii[27]
Ocimum kenyense[28]
Pimenta racemosa[29][30][31]
Viburnum furcatum[32][32]
Viburnum japonicum[33]
Illicium difengpi[35]
Alnus pendula[36]
Cyperus conglomeratus[37]
Magnolia obovata[38][39][40]
Solidago odora[42]
Viburnum mathewsii[32]
Magnolia officinalis[44]
Achillea crithmifolia[46]
Clausena anisata[47]

koosseisu osa

Commonsi kategooria

Chavicol

Viited

  1. Freebase Data Dumps, 28. oktoober 2013
  2. 2,0 2,1 2,2 2,3 ChEBI, 6. oktoober 2016, inglise keel, chavicol, 50158
  3. 3,0 3,1 3,2 3,3 3,4 3,5 PubChem, 6. oktoober 2016, inglise keel, 68148, Chavicol
  4. 4,0 4,1 4,2 4,3 4,4 4,5 4,6 RGIBXDHONMXTLI-UHFFFAOYSA-N, InChIKey
  5. UniChem
  6. ChEMBL, 6. oktoober 2016, inglise keel, CHAVICOL, CHEMBL108862
  7. ChEBI release 2020-09-01
  8. 8,0 8,1 8,2 inferred from InChIKey
  9. International Chemical Identifier, InChI=1S/C9H10O/c1-2-3-8-4-6-9(10)7-5-8/h2,4-7,10H,1,3H2
  10. ECHA Substance Infocard database, 27. detsember 2018, 100.007.209, p-allylphenol, CAS no.: 501-92-8
  11. ChemSpider, 6. oktoober 2016, inglise keel, 21105856, chavicol
  12. 12,0 12,1 Global Substance Registration System, 6. oktoober 2016, inglise keel, CHAVICOL, Q5ER4K6969
  13. CAS Common Chemistry, 9. aprill 2021, RGIBXDHONMXTLI-UHFFFAOYSA-N, https://commonchemistry.cas.org/detail?cas_rn=501-92-8
  14. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  15. EFSA database, 23. jaanuar 2021, CAS no.: 501-92-8, 04.058
  16. Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 13. mai 2021
  17. Miscellaneous contributions to the essential oils of plants from various territories. XLVII. On the components of essential oils of Cinnamomum sieboldii Meisn
  18. Studies on the Constituents of Osmorhiza aristata (THUNB.) MAKINO et YABE
  19. A 17-Diarylheptanoid from Alpinia conchigera
  20. Chemical Composition of the Rhizome Oil ofAlpinia conchigeraGriff from Malaysia
  21. Constituents ofTagetes lucida Cav. ssp.lucida Essential Oil
  22. Phylogenetic fragrance patterns in Nicotiana sections Alatae and Suaveolentes
  23. 23,0 23,1 Identification of fungicidal and nematocidal components in the leaves of Piper betle (Piperaceae)
  24. Volatile Constituents ofAgastache rugosa
  25. The essential oil of greater galanga (Alpinia galanga) from Malaysia
  26. 26,0 26,1 Composition of the Essential Oil and the Headspace Sample ofMandragora autumnalisBertol. Fruits
  27. Biphenyl Type Lignans and Costunolide from Manglietia garrettii
  28. Composition of the leaf essential oil of ocimum keniense ayobangira
  29. Chemical composition of the essential oils of chemotypes ofPimenta racemosa var.racemosa (P. Miller) J. W. Moore (Bois d'Inde) of Guadeloupe (F.W.I.)
  30. Volatile Leaf Oils of Caribbean Myrtaceae. I. Three Varieties ofPimenta racemosa(Miller) J. Moore of the Dominican Republic and the Commercial Bay Oil
  31. Chemical Compositon of the Leaf Oil ofPimenta racemosa(Mill.) J. Moore from Western Cuba
  32. 32,0 32,1 32,2 Three iridoid glycosides from Viburnum furcatum
  33. Chavicol, as a larva-growth inhibitor, from Viburnum japonicum spreng.
  34. Contact and fumigant toxicity of hexane flower bud extract of Syzygium aromaticum and its compounds against Pediculus humanus capitis (Phthiraptera: Pediculidae).
  35. Toxicity of the essential oil of Illicium difengpi stem bark and its constituent compounds towards two grain storage insects
  36. Chemical Constituents of the Male Flower ofAlnus pendula(BETULACEAE)
  37. ChemInform Abstract: Two Novel Flavans from Cyperus conglomeratus.
  38. Studies on the Components of Magnolia obovata THUNB. IV. Components of Leaves. (1)
  39. Studies on the components of Magnolia obovata Thunb. IV. Components of leaves. (1) (author's transl)
  40. Composition of the Bark Oil of Magnolia obovata Thunb.
  41. Glycosides from Pinus contorta needles
  42. Sesquiterpene and diterpene derivatives from Solidago species
  43. Biosynthesis of methyleugenol and methylisoeugenol in Daucus carota leaves: Characterization of eugenol/isoeugenol synthase and O-Methyltransferase
  44. Comparison of the volatile constituents of different parts of Cortex magnolia officinalis by GC-MS combined with chemometric resolution method.
  45. Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity
  46. Volatile Constituents of Achillea crithmifolia Flowers from Greece
  47. Constituents of the Essential Oil of Clausena anisata Leaves.