Общепринятые (несистематические) названия жирных кислот

Common (non-systematic) Names for Fatty Acids

(Внимание! Авторством на эту таблицу владеют ее создатели!)
Источник — AOCS
© R. O. Adlof и F. D. Gunstone

Common name (acid) Structure Source
Acetic 2:0 Platelet activating factor
Acrylic 2e-3:1 Nnc
Adipic 6:0 di-acid Nnc
Adrenic 7c10c13c16c-22:4 Adrenal lipids
Agonandoic (aka. ximenynic) 9a,11t-18:2 Santalum acuminatum
Alchornoic cis-14,15-ep 11c-20:1 Alchornia cordifolia
Alepramic 3-Cp 3:0 Flacourtiaceae seed oils
Aleprestic 5-Cp 5:0 Flacourtiaceae seed oils
Alepric 9-Cp 9:0 Flacourtiaceae seed oils
Aleprolic 1-Cp 1:0 Flacourtiaceae seed oils
Aleprylic 7-Cp 7:0 Flacourtiaceae seed oils
Aleuritic 9,10,16-triOH 16:0 Shellac
Ambrettolic 16-OH 7c-16:1 Musk mellon seed oil
Angelic 2Me 2c-4:1 Angelica archangelica
Anteisoheptadecanoic 14Me 16:0 Animal fats
Anteisononadecanoic 16Me 18:0 Animal fats
Anteisopentadecanoic 12Me 14:0 Animal fats
Anteisotridecanoic 10Me 12:0 Animal fats
Arachidic 20:0 Groundnut (peanut) oil
Arachidonic 5c8c11c14c-20:4 Animal phospholipids
Argenonic 6-OH, 6-Me, 9-oxo-28:0 Papaveraceae
Artemesic See Coriolic
Asclepic 11c-18:1 Asclepia oils
Ascorbic Vitamin C
Auricolic 14-OH 11c17c-20:2 Lesquerella auriculata
Avenoleic 15(R)-OH 9c12c-18:2
Axillarenic 11,13-di OH, 9c-24:1 Euphorbiaeceae
Azelaic 9:0 di-acid Nnc
Behenic 22:0 Lophira alata
Behenolic 13a-22:0 Nnc
Bishomopinolenic 7c,11c,14c-20:3
Bolekic 9a11a13c-18:3 Isano oil
Bosseopentaenoic 5c8c10t12t14c-20:5 Bossiella orbigniana
Brassidic 13t-22:1 Trans form of erucic acid
Brassylic 13:0 di-acid Nnc
Buiolic (jalapinolic) 11-OH 16:0
Butolic 6-OH 14:0 Shellac
Butyric 4:0 Milk fats
Calendic ( α ) 8t10t12c-18:3 Calendula officinalis
Calendic ( β ) 8t10t12t-18:3 Trans form of α-calendic acid
Capric 10:0 Lauric oils
Caproic 6:0 Milk fats
Caproleic 9c-10:1 Milk fats
Caprylic 8:0 Lauric oils
Carboceric 27:0
Catalpic 9t11t13c-18:3 Catalpa ovata
Cerebronic 2-OH 24:0 Cerebrosides
Cerinic See Cerotic
Ceromelissic 33:0 (see psyllic)
Ceroplastic 35:0 Nnc
Cerotic 26:0 Waxes
Cervonic DHA
Cetelaidic 11t-20:1 Hydrogenated fish oils
Cetoleic 11c-22:1 Fish oils
Chaulmoogric 13-Cp 13:0 Flacourtiaceae seed oils
Chrysobalanic 4-oxo 9c11t13t15c-18:4 Chyrsobalanus icaco
Civetic 8t-17:1 di-acid
CLA Conjugated 18:2 isomers Ruminant fats
Clupadonic 7c10c13c16c19c-22:5 Fish oils
Colneleic 9-oxa-8t10t12c-18:3 Enzymic oxidation of linoleic acid
Colnelenic 9-oxa-8t10t12c15c-18:4 Enzymic oxidation of linolenic acid
Columbinic 5t9c12c-18:3 Aquilegia vulgaris
Coniferonic 5c,9c,12c,15c-18:4 Conifer
Convolvulinolic 11-OH 14:0 Ipomea oils
Coriolic 13-OH 9c11t-18:2 Xeranthemum annuum
Coronaric Cis-9,10-ep 12c-18:1 Chrysanthemum coronarium
Couepic See Licanic
Couepinic (licanic?) 4-keto 9c11c13c-18:3
Crepenynic 9c12a-18:2 Crepis and Afzelia oils
Daturic See Margaric Animal fats
Dehydrocrepenyic 9c12a14c-18:3
Demospongic C24-C34 5c9c-diene acids Sponges
Densipolic 12(R)-OH 9c15c-18:2 Lesquerella densipila
DHA 4c7c10c13c16c19c-22:6 Fish oils
*Dicramin 9c12c15c6a-18:4 Dicramium scoparium
Dihomolinoleic 11c14c-20:2
Dihomolinolenic 8c11c14c-20:3 Animal fats
Dihomo Mead's acid 7c10c13c-22:3
Dihomopinolenic 7c11c14c-20:3 Pinacae family
Dihomotaxoleic 7c11c-20:2 Taxus spp.
Dihydroxystearic 9,10-diOH 18:0
*Dimorphecolic 9-OH,10t,12t-18:2 Dimorphecolic pluvialis
DPA 7c10c13c16c19c-22:5 Fish oils
Elaidic 9t-18:1 Trans isomer of oleic acid
Elaidolinolenic See Linolenelaidic
EPA 5c8c11c14c17c-20:5 Fish oils
Eleostearic ( α ) 9c11t13t-18:3 Tung oil
Eleostearic ( α ) 9c11t13t-18:3 Momordica charantia **
Eleostearic ( β ) 9t11t13t-18:3 All-trans α-eleostearic acid
Enanthic 7:0 Nnc
Ephedrenic 5c,11c-18:2 Ephedra
Erucic 13c-22:1 Cruciferae seed oils
Erythrogenic See Isanic
Exocarpic 9a11a13t-18:3 Isano oil
Gadelaidic 9t-20:1 Trans form of gadoleic acid
Gadoleic 9c-20:1 Fish oils
Gaidic 2t-16:1
Geddic 34:0
Gheddic 34:0
GLA 6c9c12c-18:3 Evening primrose, borage, etc
Glutaric 5:0 di-acid Nnc
Gondoic 11c-20:1 Fish oils
*Gondoleic 9c-20:1
Gorlic 13-Cp 6c-13:1 Flacourticeae oils
Helenynolic 9-OH 10t12a-18:2 Helychrysum bracteatum
*Hiragonic 7c10c13c-16:3 Fish oils
Hormelic 15-Cp 15:0 Flacourticeae oils
Hydnocarpic 11-Cp 11:0 Flacourticeae oils
*Hydrosorbic 3e-16:1 di-acid
Hydroxycerebronic 2-hydroxycerebronic Sphingolipids
Hydroxynervonic 2-hydroxynervonic Sphingolipids
Ipurolic 3,11-diOH 14:0 Ipomoca oils
Isanic 9a11a17e-18:3 Isano oil
Isanolic 8-OH 9a11a17e-18:3 Isano oil
Isoarachidic 18-Me 19:0
Isobutyric 2-Me 3:0
Isocaproic 4-Me 5:0
Isocerotic 24-Me 25:0
Isoheptadecanoic 15-Me-16:0
Isolauric 10-Me-11:0
Isomargaric 15-Me 16:0
Isomontanic 26-Me-27:0
*Isomycomycin 3c5c7a9a11a-13:5
Isomyristic 12-Me 13:0
Isononadecanoic 17-Me 18:0
Isopalmitic 14-Me 15:0
Isopentadecanoic 13-Me 14:0
Isoricinoleic 9-OH,12c-18:1 Strophanthus
Isostearic 16-Me-17:0
Isotridecanoic 11-Me 12:0
*Isovaleric 3-Me 4:0 Porpoise, dolphin
Jacaric 8c10t12c-18:3 Jacaranda mimosifolia
Jalapinolic 11-OH 16:0 Jalap resin
Japanic 21:0 di-acid
Jasmonic C12 cyclopentane acid Linoleic acid metabolite
Juniperic 16-OH 16:0 Conifer waxes
Juniperinic 16-OH 16:0 Conifer waxes
Juniperonic 5c11c14c17c-20:4 Conifer waxes
Kamlolenic ( α ) 18-OH 9c11t13t-18:3 Kamala oil
*Kamlolenic ( β ) 18-OH 9t11t13t-18:3 Kamala oil
*Kerrolic 4-OH-16:0 Shellac
Keteleeronic 5c11c-20:2 Gymnosperm sp
Labellenic 5,6-18:2 (R)-form Leonotis seed oil
Lacceric 32:0 Stick lac wax
Lacceroic See lacceric Stick lac wax
Lactarinic 6-oxo 18:0 Lactarius rufus
Lanoceric di-OH 30:0
Lamenallenic 5,6,16t-18:3 Laminium purpureum
Lactobacillic 11,12-Mt 18:0 Micro-organisms
Lauric 12:0 Lauric oils
Lauroleic 9c-12:1
Lesquerolic 14-OH 11c-20:1 Lesquerella spp
Levulinic (aka levulic) 4-oxo-5:0
Licanic ( α ) 4-oxo 9c11t13t-18:3 Licania rigida
Licanic ( β ) 4-oxo 9t11t13t-18:3 Trans-form of α-licanic acid
Lignoceric 24:0 Waxes
Linelaidic 9t12t-18:2 All-trans form of linoleic acid
Linderic 4c-12:1 Lindera obtusiloba
Linoleic 9c12c-18:2 All seed oils
Linolenelaidic 9t12t15t-18:3 All-trans form of linolenic acid
Linolenic 9c12c15c-18:3 Linseed
Lumequic 21c-30:1 Ximenia spp
Linusic 9,10,12,13,15,16-OH 18:0 From linolenic acid
Malonic 3:0 di-acid
Malvalic 8,9-Mt 8c-17:1 Cottonseed oil
Manaoic 11-Cp 6c-11:0 Flacourtiaceae seed oils
Mangold's acid 9t11t-18:2
Margaric 17:0 Animal fats
Margarolic ? 9c-17:1
Mead's acid 5c8c11c-20:3 Metabolite of oleic acid
Megatomic 3t5c-14:2 Black carpet beetle pheromone
Melissic 30:0 Bayberry
Mikusch's acid 10t12t-18:2
Montanic 28:0 Waxes (ie. carnuba)
Moroctic See stearidonic
Morotic See stearidonic
Mycoceranic 2,4,6-triMe 26:0 Tubercle bacilli
Mycocerosic See mycoceranic
Mycolic RCHOHCH(R')COOH Mycobacteria
Mycolipenic 2,4,6-tri-Me-2t-24:1 Tuburele bacilli
Mycomycin 3t5c7,8,10a12a-13:6
Myristelaidic 9t-14:1 Trans form of myristoleic acid
Myristic 14:0 Lauric oils
Myristoleic 9c-14:1
Nemotinic 4e6a8a10a-11:4
*Nemotinic 4-OH, 5,6,8a,10a-11:4 Basidomycetis moulds
Nervonic 15c-24:1 Honesty seed oil, nerve tissue
Nisinic 6c9c12c15c18c21c-24:6 Fish oils
Obtusilic 4c-14:1 Lindera obtisiloba
Oleic 9c-18:1 All oils and fats
Oncobic 15-Cp 8c-15:0 Flacourtiaceae seed oils
Osbond's acid See DPA
Oxalic 2:0 di-acid
Palmitelaidic 9t-16:1 Trans form of palmitoleic acid
Palmitic 16:0 All oils and fats
Palmitoleic 9c-16:1 Fish oils, macadamia oil
Parinaric ( α ) 9c11t13t15c-18:4 Parinarium laurinum
Parinaric ( β ) 9t11t13t15c-18:4 Trans-form of α-parinaric acid
Pelargonic 9:0
Petroselaidic 6t-18:1 Trans form of petroselinic acid
Petroselinic 6c-18:1 Umbelliferae oils
Phellonic 22-OH 22:0 Cork
Phloionolic 9S10S18S-triOH 18:0 Cork
Phlomic 7,8-20:2
*Phthioic 3,13,19-triMe 23:0
Phrenosic See cerebronic
Phrenosinic See cerebronic
Phthianoic See mycoceranic
Phthioic Polybranched acids Micro-organisms
Physeteric 5c-14:1 Whale oil
Physetoleic See Palmitoleic
Phytanic 3,7,11,15-tetraMe 16:0 Marine animal fats
*Phytenic See Phytenoic
Phytenoic 3,7,11,15-tetraMe 2e-16:1 Marine animal fats
Phytomonic See Lactobacillic
Pimelic 7:0 di-acid
Pinolenic 5c9c12c-18:3 Toucrium depressum
Podocarpic 5c11c14c-20:3 Podocarpus nagera
Pristanic 2,6,10,14-tetraMe 15:0 Marine animal fats
Pseudoeleostearic 10t12t14t-18:3 Isomerized linolenic acid
Psyllic 33:0
Punicic 9c11t13c-18:3 Punica granatum
Punicic 9c11t13c-18:3 Trichosanthes anguina*
Pyrulic 8a10t-17:2 Pyrularia pubera
Ricinelaidic 12-OH 9t-18:1 Trans form of ricinoleic acid
Ricinoleic 12-OH 9c-18:1 Castor oil
Rosilic 10-OH 18:0 Leaf waxes
Rumenic 9c11t-18:2 Ruminant fats
Sabinic 12-OH 12:0 Juniperus oxycedrus leaves
Santalbic See ximenynic
Sativic 9,10,12,13-tetraOH 18:0 From oxidation of linoleic acid
Sciadonic 5c11c14c-20:3 Pinus species
*Scoliodonic 24:5
Sebacic 10:0 di-acid
Selacholeic 15c-24:1 (see nervonic) Shark liver oils
Shibic 26:5 Fish oils
*Sorbic 2t4t-6:2 di-acid
Stearic 18:0 Animal fats, cocoa butter
Stearidonic 6c9c12c15c-18:4 Echium oils, fish oils
Stearolic 9a-18:1 Santalaceae
Sterculic 9,10-Mt 9c-18:1 Cottonseed oil
Sterculynic 9,10-Mt 9c17a-18:2 Sterculia alata
Stillingic 2c4t-10:2 Sapium sebiferum
Strophanthus 9-OH,12c-18:1 Apocyanaceae
Suberic 8:0 di-acid
Succinic 4:0 di-acid
Tariric 6a-18:1 Picramnia spp
Taxoleic 5c9c-18:2 Gymnospermae seed lipids
Thapsic (or thaspic) 16:0 di-acid Waxes
Thynnic 26:6 (probably n-3) Fish oils
Timnodonic (see EPA) 4c8c12c15c18c-20:5c**
Traumatic 2t-20:1 di-acid
Trichosanic See punicic
Tsuduic 4-14:1 Lindera obtisiloba
Tsuzuic 4-14:1 Lindera obtisiloba
Tuberculostearic 10-Me 18:0 Tubercle bacilli
Undecylenic 10e-11:1 Castor oil
Ustilic 15,16-diOH 16:0 Ustilagic acid (antibiotic)
Vaccenic 11t-18:1 Ruminant fats
Valeric 5:0
Vernolic 12,13-ep, 9c-18:1 Vernonia oils
Wyerone acid? 2c,(3,4-F*),5a7c-10:3 Exocarpus cupressiformis
Ximenic 17c-26:1 Ximenia americana
Ximenynic 9a11t-18:2 Santalum acuminatum
Ximenynolic 8-OH, 9a11t-18:2
Zoomaric See palmitoleic

Nomenclature:
c = cis; t = trans; a = acetylene; e = ethylenic bond (stereochemistry not relevant or unknown); ep = epoxy; Me = methyl group; Mt = methano -CH2-; Cp = 2-cyclopentenyl (C5H7); P = cyclopropenyl; Nnc = not natural constituent of normal fats; F* = furanoid; * = Spelling or structure uncertain.

Examples:
14:2 = 14 carbon atoms, 2 sites of unsaturation; 9:0 di-acid = HOOC(CH2)7COOH.

References:

  1. C.Y. Hopkins (1972), Fatty Acids With Conjugated Unsaturation, in Topics in Lipid Chemistry (F. Gunstone, ed.), Elek Science, London, pp. 37-87.

  2. P.G. Robinson (1982), Common Names And Abbreviated Formula For Fatty Acids. J. Lip. Res. 23: pp.1251-1253.

  3. G.D. Fasman (1989), Practical Handbook of Biochemistry and Molecular Biology, CRC Press, Boca Raton, FL, pp. 514-522.

  4. F.D. Gunstone, J.L. Harwood and F.B. Padley, The Lipid Handbook (2nd Ed.), Chapman and Hall, London, 1992.

  5. F.D. Gunstone and B.G. Herslof, A Lipid Glossary, The Oily Press, Dundee, first edition 1992, second edition in press.

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