geosmin

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kemia kombinaĵo

Eksteraj rimedoj

registra numero laŭ Kemia Resumo-Servo
numero en Microsoft Academic
PubChem CID
UniChem compound ID
identigilo laŭ Kiota Enciklopedio de Genoj kaj Genaroj
OpenAlex ID
ChEMBL ID
Nikkaji ID
InChIKey
identigilo laŭ ChEBI
46702[8][10]

speco de bildiga rilato: ekzakta ekvivalento

identigilo de Römpp
SureChEMBL ID
AICS Chemical ID (BEING DELETED)
KNApSAcK ID
ECHA Substance Infocard ID
numero en ChemSpider
numero de kemiaĵo laŭ la Eŭropa Komunumo
243-239-8[1]
identigilo de substanco en DSSTOX
identigilo de Freebase
numero en registro de Reaxys
4656415[6]
2410491[6]
NALT ID
Internacia Kemia Identigilo
UNII

estas

speco de kemiaĵo

subaro de

noreudesmane

kemia strukturo

maso

182,167 daltono[15]

stereoizomero de

(+)-geosmin[16]

kemia formulo

C₁₂H₂₂O[3]

ĉefforma SMILES

CC1CCCC2(C1(CCCC2)O)C[3]

izomera SMILES

C[C@H]1CCC[C@@]2([C@@]1(CCCC2)O)C[3]

en taksono

Chaetomium globosum[19][20]
Cortinarius herculeus[24]
Cystoderma amianthinum[24]
Cystoderma carcharias[24]
Oscillatoria brevis[25]
Fazeolo[26]
Symphyogyna brongniartii[27]
Physarum polycephalum[28]
Streptomyces tendae[29][30]
Streptomyces coelicolor[31][32][33][34][35]
Streptomyces thermocarboxydus[36]
Streptomyces collinus[37]
Streptomyces griseus[38]
Streptomyces alboflavus[39]
Streptomyces halstedii[40]
Streptomyces avermitilis[41][42]
Streptomyces nodosus[43][44]
Streptomyces violaceusniger[45]
Streptomyces albidoflavus[35][34][31][32][33][46]
Streptomyces[47]

Komuneja kategorio

Geosmin

Referenco

  1. 1,0 1,1 1,2 Global Substance Registration System, 20 nov. 2016, angla lingvo, geosmin, MYW912WXJ4
  2. CAS Common Chemistry, 10 apr. 2021, JLPUXFOGCDVKGO-TUAOUCFPSA-N, https://commonchemistry.cas.org/detail?cas_rn=19700-21-1
  3. 3,0 3,1 3,2 3,3 3,4 3,5 PubChem, 20 nov. 2016, angla lingvo, 29746, GEOSMIN
  4. 4,0 4,1 4,2 4,3 JLPUXFOGCDVKGO-TUAOUCFPSA-N, InChIKey
  5. UniChem
  6. 6,0 6,1 6,2 6,3 Kemiaj Entoj de Biologia Intereso, 6 okt. 2016, angla lingvo, (-)-geosmin, 46702
  7. OpenAlex, 26 jan. 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  8. 8,0 8,1 ChEMBL, 20 nov. 2016, angla lingvo, CHEMBL2374043, CHEMBL2374043
  9. ChEBI release 2020-09-01
  10. Internacia Kemia Identigilo, InChI=1S/C12H22O/c1-10-6-5-8-11(2)7-3-4-9-12(10,11)13/h10,13H,3-9H2,1-2H3/t10-,11+,12-/m0/s1
  11. inferred from InChIKey
  12. ECHA Substance Infocard database, 27 dec. 2018, 100.039.294, [4S-(4α,4aα,8aβ)]-octahydro-4,8a-dimethyl-4a(2H)-naphthol, CAS no.: 19700-21-1
  13. ChemSpider, 6 okt. 2016, angla lingvo, 27642, geosmin
  14. Freebase Data Dumps, 28 okt. 2013
  15. PubChem, 6 okt. 2016, angla lingvo, 29746, GEOSMIN
  16. inferred from InChI
  17. Volatiles of corn kernels and husks: possible corn ear worm attractants
  18. Volatile components of corn silk (Zea mays L.): possible Heliothis zea (Boddie) attractants
  19. Odorous metabolites of fungi, Chaetomium globosum Kinze ex Fr. and Botrytis cinerea Pers. ex Fr., and a blue-green alga, Phormidium tenue (Meneghini) Gomont.
  20. Odorous metabolites of a fungus, Chaetomium globosum Kinze ex Fr. Identification of geosmin, a musty-smelling compound.
  21. Volatile flavor components of malabar-nightshade (Basella rubra L.)
  22. Geosmin, the earthy component of table beet odor
  23. Characterisation of the aroma of green Mexican coffee and identification of mouldy/earthy defect
  24. 24,0 24,1 24,2 Geosmin, a Sesquiterpenoid Compound Responsible for the Musty-Earthy Odor of Cortinarius herculeus, Cystoderma amianthinum, and Cy. carcharias
  25. Geosmin production in the cyanobacterium Oscillatoria brevis
  26. Geosmin, a musty off-flavor of dry beans
  27. Occurrence of (-)-Geosm in and Other Terpenoids in an Axenic Culture of the Liverwort Symphyogyna brongniartii
  28. Odorous metabolites of an acellular slime mold, Physarum polycephalum Schw., and a basidiomycete, Phallus impudicus Pers.
  29. Spore and geosmin production by Streptomyces tendae on several media
  30. Effects of farnesol and the off-flavor derivative geosmin on Streptomyces tendae
  31. 31,0 31,1 Biosynthesis of the earthy odorant geosmin by a bifunctional Streptomyces coelicolor enzyme
  32. 32,0 32,1 Geosmin biosynthesis. Streptomyces coelicolor germacradienol/germacrene D synthase converts farnesyl diphosphate to geosmin
  33. 33,0 33,1 Transcriptomic analysis of Streptomyces coelicolor differentiation in solid sporulating cultures: first compartmentalized and second multinucleated mycelia have different and distinctive transcriptomes
  34. 34,0 34,1 Exploitation of the Streptomyces coelicolor A3(2) genome sequence for discovery of new natural products and biosynthetic pathways
  35. 35,0 35,1 Streptomyces coelicolor as an expression host for heterologous gene clusters.
  36. Production of distinct labdane-type diterpenoids using a novel cryptic labdane-like cluster from Streptomyces thermocarboxydus K155
  37. Identification and activation of novel biosynthetic gene clusters by genome mining in the kirromycin producer Streptomyces collinus Tü 365.
  38. The effect of disinfectants on a geosmin-producing strain of Streptomyces griseus
  39. Antifungal activity of volatile organic compounds from Streptomyces alboflavus TD-1.
  40. Effects of carbon source, phosphorus concentration, and several micronutrients on biomass and geosmin production by Streptomyces halstedii
  41. Relationship between volatile odorous substances and production of avermectins by Streptomyces avermitilis.
  42. Geosmin biosynthesis in Streptomyces avermitilis. Molecular cloning, expression, and mechanistic study of the germacradienol/geosmin synthase
  43. Exploiting the genome sequence of Streptomyces nodosus for enhanced antibiotic production.
  44. Feeding of [5,5-2H(2)]-1-desoxy-D-xylulose and [4,4,6,6,6-2H(5)]-mevalolactone to a geosmin-producing Streptomyces sp. and Fossombronia pusilla
  45. Identification of isoafricanol and its terpene cyclase in Streptomyces violaceusniger using CLSA-NMR
  46. Albaflavenone, a sesquiterpene ketone with a zizaene skeleton produced by a streptomycete with a new rope morphology
  47. Generation of a cluster-free Streptomyces albus chassis strains for improved heterologous expression of secondary metabolite clusters