USPP12401P2 - Hop plant named “YCR Accession No. 7” - Google Patents
Hop plant named “YCR Accession No. 7” Download PDFInfo
- Publication number
- USPP12401P2 USPP12401P2 US09/287,404 US28740499V USPP12401P2 US PP12401 P2 USPP12401 P2 US PP12401P2 US 28740499 V US28740499 V US 28740499V US PP12401 P2 USPP12401 P2 US PP12401P2
- Authority
- US
- United States
- Prior art keywords
- variety
- new
- hop
- galena
- hop plant
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 244000025221 Humulus lupulus Species 0.000 title description 17
- 241000218228 Humulus Species 0.000 claims abstract 3
- 229910052949 galena Inorganic materials 0.000 abstract description 7
- XCAUINMIESBTBL-UHFFFAOYSA-N lead(ii) sulfide Chemical compound [Pb]=S XCAUINMIESBTBL-UHFFFAOYSA-N 0.000 abstract description 7
- 241000221785 Erysiphales Species 0.000 abstract description 4
- 238000003306 harvesting Methods 0.000 abstract description 3
- 241000579741 Sphaerotheca <fungi> Species 0.000 abstract description 2
- 125000003118 aryl group Chemical group 0.000 abstract description 2
- IJXHLVMUNBOGRR-UHFFFAOYSA-N methyl nonanoate Chemical compound CCCCCCCCC(=O)OC IJXHLVMUNBOGRR-UHFFFAOYSA-N 0.000 description 6
- LSKONYYRONEBKA-UHFFFAOYSA-N 2-Dodecanone Chemical compound CCCCCCCCCCC(C)=O LSKONYYRONEBKA-UHFFFAOYSA-N 0.000 description 4
- GLZPCOQZEFWAFX-UHFFFAOYSA-N Geraniol Chemical compound CC(C)=CCCC(C)=CCO GLZPCOQZEFWAFX-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- ZAJNGDIORYACQU-UHFFFAOYSA-N decan-2-one Chemical compound CCCCCCCCC(C)=O ZAJNGDIORYACQU-UHFFFAOYSA-N 0.000 description 4
- YRHYCMZPEVDGFQ-UHFFFAOYSA-N methyl decanoate Chemical compound CCCCCCCCCC(=O)OC YRHYCMZPEVDGFQ-UHFFFAOYSA-N 0.000 description 4
- XPQPWPZFBULGKT-UHFFFAOYSA-N methyl undecanoate Chemical compound CCCCCCCCCCC(=O)OC XPQPWPZFBULGKT-UHFFFAOYSA-N 0.000 description 4
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 4
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 4
- 229930004725 sesquiterpene Natural products 0.000 description 4
- 150000004354 sesquiterpene derivatives Chemical class 0.000 description 4
- CYIFVRUOHKNECG-UHFFFAOYSA-N tridecan-2-one Chemical compound CCCCCCCCCCCC(C)=O CYIFVRUOHKNECG-UHFFFAOYSA-N 0.000 description 4
- KYWIYKKSMDLRDC-UHFFFAOYSA-N undecan-2-one Chemical compound CCCCCCCCCC(C)=O KYWIYKKSMDLRDC-UHFFFAOYSA-N 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 235000008694 Humulus lupulus Nutrition 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- FAMPSKZZVDUYOS-UHFFFAOYSA-N alpha-Caryophyllene Natural products CC1=CCC(C)(C)C=CCC(C)=CCC1 FAMPSKZZVDUYOS-UHFFFAOYSA-N 0.000 description 3
- QMAYBMKBYCGXDH-UHFFFAOYSA-N alpha-amorphene Natural products C1CC(C)=CC2C(C(C)C)CC=C(C)C21 QMAYBMKBYCGXDH-UHFFFAOYSA-N 0.000 description 3
- VEGYMPQCXPVQJY-UHFFFAOYSA-N (10ξ)-eudesma-4,6-diene Chemical compound C1CCC2(C)CCC(C(C)C)=CC2=C1C VEGYMPQCXPVQJY-UHFFFAOYSA-N 0.000 description 2
- RKQDKXOBRXTSFS-PIHCAMFYSA-N (4e,7e)-3,3,7,11-tetramethyl-12-oxabicyclo[9.1.0]dodeca-4,7-diene Chemical compound C1C(C)(C)\C=C\CC(/C)=C/CCC2(C)OC21 RKQDKXOBRXTSFS-PIHCAMFYSA-N 0.000 description 2
- GYSCBCSGKXNZRH-UHFFFAOYSA-N 1-benzothiophene-2-carboxamide Chemical compound C1=CC=C2SC(C(=O)N)=CC2=C1 GYSCBCSGKXNZRH-UHFFFAOYSA-N 0.000 description 2
- PVYFCGRBIREQLL-UHFFFAOYSA-N 2-Methylbutyl 2-methylbutanoate Chemical compound CCC(C)COC(=O)C(C)CC PVYFCGRBIREQLL-UHFFFAOYSA-N 0.000 description 2
- DUAXUBMIVRZGCO-UHFFFAOYSA-N 2-Methylbutyl 2-methylpropanoate Chemical compound CCC(C)COC(=O)C(C)C DUAXUBMIVRZGCO-UHFFFAOYSA-N 0.000 description 2
- RXGUIWHIADMCFC-UHFFFAOYSA-N 2-Methylpropyl 2-methylpropionate Chemical compound CC(C)COC(=O)C(C)C RXGUIWHIADMCFC-UHFFFAOYSA-N 0.000 description 2
- POQLVOYRGNFGRM-UHFFFAOYSA-N 2-Tetradecanone Chemical compound CCCCCCCCCCCCC(C)=O POQLVOYRGNFGRM-UHFFFAOYSA-N 0.000 description 2
- SEPQTYODOKLVSB-UHFFFAOYSA-N 3-methylbut-2-enal Chemical compound CC(C)=CC=O SEPQTYODOKLVSB-UHFFFAOYSA-N 0.000 description 2
- XKWSWANXMRXDES-UHFFFAOYSA-N 3-methylbutyl octanoate Chemical compound CCCCCCCC(=O)OCCC(C)C XKWSWANXMRXDES-UHFFFAOYSA-N 0.000 description 2
- NVEQFIOZRFFVFW-UHFFFAOYSA-N 9-epi-beta-caryophyllene oxide Natural products C=C1CCC2OC2(C)CCC2C(C)(C)CC21 NVEQFIOZRFFVFW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- ISOIDIYKQYJGMC-UHFFFAOYSA-N D-delta-Cadinol Natural products C1CC(C)(O)CC2C(C(C)C)CC=C(C)C21 ISOIDIYKQYJGMC-UHFFFAOYSA-N 0.000 description 2
- GHVNFZFCNZKVNT-UHFFFAOYSA-N Decanoic acid Natural products CCCCCCCCCC(O)=O GHVNFZFCNZKVNT-UHFFFAOYSA-N 0.000 description 2
- YWHLKYXPLRWGSE-UHFFFAOYSA-N Dimethyl trisulfide Chemical compound CSSSC YWHLKYXPLRWGSE-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- CYHBDKTZDLSRMY-UHFFFAOYSA-N Hexyl 2-methylpropanoate Chemical compound CCCCCCOC(=O)C(C)C CYHBDKTZDLSRMY-UHFFFAOYSA-N 0.000 description 2
- RKQDKXOBRXTSFS-FTFIOASISA-N Humulene epoxide Natural products C[C@]12O[C@@H]1CC(C)(C)/C=C/C/C(/C)=C\CC2 RKQDKXOBRXTSFS-FTFIOASISA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- STRABSCAWZINIF-UHFFFAOYSA-N Juniper camphor Chemical compound C1CCC(C)(O)C2CC(=C(C)C)CCC21C STRABSCAWZINIF-UHFFFAOYSA-N 0.000 description 2
- JZIARAQCPRDGAC-UHFFFAOYSA-N Linalyl isobutyrate Chemical compound CC(C)C(=O)OC(C)(C=C)CCC=C(C)C JZIARAQCPRDGAC-UHFFFAOYSA-N 0.000 description 2
- YWSDDOFJTUOVMX-VAWYXSNFSA-N Methyl (E)-2-dodecenoate Chemical compound CCCCCCCCC\C=C\C(=O)OC YWSDDOFJTUOVMX-VAWYXSNFSA-N 0.000 description 2
- CRZQGDNQQAALAY-UHFFFAOYSA-N Methyl benzeneacetate Chemical compound COC(=O)CC1=CC=CC=C1 CRZQGDNQQAALAY-UHFFFAOYSA-N 0.000 description 2
- 239000005640 Methyl decanoate Substances 0.000 description 2
- MOYAFQVGZZPNRA-UHFFFAOYSA-N Terpinolene Chemical compound CC(C)=C1CCC(C)=CC1 MOYAFQVGZZPNRA-UHFFFAOYSA-N 0.000 description 2
- KGEKLUUHTZCSIP-HOSYDEDBSA-N [(1s,4s,6r)-1,7,7-trimethyl-6-bicyclo[2.2.1]heptanyl] acetate Chemical compound C1C[C@]2(C)[C@H](OC(=O)C)C[C@H]1C2(C)C KGEKLUUHTZCSIP-HOSYDEDBSA-N 0.000 description 2
- XUEHVOLRMXNRKQ-KHMAMNHCSA-N alpha-cubebene Chemical compound CC(C)[C@@H]([C@H]12)CC[C@@H](C)[C@]32[C@@H]1C(C)=CC3 XUEHVOLRMXNRKQ-KHMAMNHCSA-N 0.000 description 2
- OBETXYAYXDNJHR-UHFFFAOYSA-N alpha-ethylcaproic acid Natural products CCCCC(CC)C(O)=O OBETXYAYXDNJHR-UHFFFAOYSA-N 0.000 description 2
- OZQAPQSEYFAMCY-UHFFFAOYSA-N alpha-selinene Natural products C1CC=C(C)C2CC(C(=C)C)CCC21C OZQAPQSEYFAMCY-UHFFFAOYSA-N 0.000 description 2
- UAHWPYUMFXYFJY-UHFFFAOYSA-N beta-myrcene Chemical compound CC(C)=CCCC(=C)C=C UAHWPYUMFXYFJY-UHFFFAOYSA-N 0.000 description 2
- NVEQFIOZRFFVFW-RGCMKSIDSA-N caryophyllene oxide Chemical compound C=C1CC[C@H]2O[C@]2(C)CC[C@H]2C(C)(C)C[C@@H]21 NVEQFIOZRFFVFW-RGCMKSIDSA-N 0.000 description 2
- MNWFXJYAOYHMED-UHFFFAOYSA-N heptanoic acid Chemical compound CCCCCCC(O)=O MNWFXJYAOYHMED-UHFFFAOYSA-N 0.000 description 2
- JARKCYVAAOWBJS-UHFFFAOYSA-N hexanal Chemical compound CCCCCC=O JARKCYVAAOWBJS-UHFFFAOYSA-N 0.000 description 2
- QTGAEXCCAPTGLB-UHFFFAOYSA-N humulene epoxide II Natural products C1CC(C)=CCC(C)(C)C=CCC2(C)OC21 QTGAEXCCAPTGLB-UHFFFAOYSA-N 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- FGKJLKRYENPLQH-UHFFFAOYSA-N isocaproic acid Chemical compound CC(C)CCC(O)=O FGKJLKRYENPLQH-UHFFFAOYSA-N 0.000 description 2
- GWYFCOCPABKNJV-UHFFFAOYSA-N isovaleric acid Chemical compound CC(C)CC(O)=O GWYFCOCPABKNJV-UHFFFAOYSA-N 0.000 description 2
- XMGQYMWWDOXHJM-UHFFFAOYSA-N limonene Chemical compound CC(=C)C1CCC(C)=CC1 XMGQYMWWDOXHJM-UHFFFAOYSA-N 0.000 description 2
- CDOSHBSSFJOMGT-UHFFFAOYSA-N linalool Chemical compound CC(C)=CCCC(C)(O)C=C CDOSHBSSFJOMGT-UHFFFAOYSA-N 0.000 description 2
- QIYDQYBDGDYJKD-UHFFFAOYSA-N methyl 6-methylheptanoate Chemical compound COC(=O)CCCCC(C)C QIYDQYBDGDYJKD-UHFFFAOYSA-N 0.000 description 2
- NUKZAGXMHTUAFE-UHFFFAOYSA-N methyl hexanoate Chemical compound CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 2
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 description 2
- JGHZJRVDZXSNKQ-UHFFFAOYSA-N methyl octanoate Chemical compound CCCCCCCC(=O)OC JGHZJRVDZXSNKQ-UHFFFAOYSA-N 0.000 description 2
- GYHFUZHODSMOHU-UHFFFAOYSA-N nonanal Chemical compound CCCCCCCCC=O GYHFUZHODSMOHU-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- 229940023569 palmate Drugs 0.000 description 2
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N pentanal Chemical compound CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 2
- USDOQCCMRDNVAH-UHFFFAOYSA-N sigma-cadinene Natural products C1C=C(C)CC2C(C(C)C)CC=C(C)C21 USDOQCCMRDNVAH-UHFFFAOYSA-N 0.000 description 2
- 238000002798 spectrophotometry method Methods 0.000 description 2
- LHYHMMRYTDARSZ-YJNKXOJESA-N t-cadinol Natural products C1CC(C)=C[C@@H]2[C@H](C(C)C)CC[C@](C)(O)[C@@H]21 LHYHMMRYTDARSZ-YJNKXOJESA-N 0.000 description 2
- IIYFAKIEWZDVMP-UHFFFAOYSA-N tridecane Chemical compound CCCCCCCCCCCCC IIYFAKIEWZDVMP-UHFFFAOYSA-N 0.000 description 2
- XMUJIPOFTAHSOK-UHFFFAOYSA-N undecan-2-ol Chemical compound CCCCCCCCCC(C)O XMUJIPOFTAHSOK-UHFFFAOYSA-N 0.000 description 2
- 239000000341 volatile oil Substances 0.000 description 2
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
- OZQAPQSEYFAMCY-QLFBSQMISA-N α-selinene Chemical compound C1CC=C(C)[C@@H]2C[C@H](C(=C)C)CC[C@]21C OZQAPQSEYFAMCY-QLFBSQMISA-N 0.000 description 2
- NPNUFJAVOOONJE-ZIAGYGMSSA-N β-(E)-Caryophyllene Chemical compound C1CC(C)=CCCC(=C)[C@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-ZIAGYGMSSA-N 0.000 description 2
- USDOQCCMRDNVAH-KKUMJFAQSA-N β-cadinene Chemical compound C1C=C(C)C[C@H]2[C@H](C(C)C)CC=C(C)[C@@H]21 USDOQCCMRDNVAH-KKUMJFAQSA-N 0.000 description 2
- YOVSPTNQHMDJAG-QLFBSQMISA-N β-eudesmene Chemical compound C1CCC(=C)[C@@H]2C[C@H](C(=C)C)CC[C@]21C YOVSPTNQHMDJAG-QLFBSQMISA-N 0.000 description 2
- YKFLAYDHMOASIY-UHFFFAOYSA-N γ-terpinene Chemical compound CC(C)C1=CCC(C)=CC1 YKFLAYDHMOASIY-UHFFFAOYSA-N 0.000 description 2
- LFJQCDVYDGGFCH-JTQLQIEISA-N (+)-β-phellandrene Chemical compound CC(C)[C@@H]1CCC(=C)C=C1 LFJQCDVYDGGFCH-JTQLQIEISA-N 0.000 description 1
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
- FUCYIEXQVQJBKY-ZFWWWQNUSA-N (+)-δ-Cadinene Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CCC(C)=C21 FUCYIEXQVQJBKY-ZFWWWQNUSA-N 0.000 description 1
- LFJQCDVYDGGFCH-SNVBAGLBSA-N (+/-)-beta-Phellandrene Natural products CC(C)[C@H]1CCC(=C)C=C1 LFJQCDVYDGGFCH-SNVBAGLBSA-N 0.000 description 1
- STRABSCAWZINIF-RBSFLKMASA-N (-)-Eudesm-7(11)-en-4alpha-ol Natural products C1CC[C@@](C)(O)[C@@H]2CC(=C(C)C)CC[C@]21C STRABSCAWZINIF-RBSFLKMASA-N 0.000 description 1
- AYXPYQRXGNDJFU-QTPLKFIXSA-N (-)-Globulol Chemical compound [C@H]1([C@](CC[C@@H]2[C@H]3C2(C)C)(C)O)[C@H]3[C@H](C)CC1 AYXPYQRXGNDJFU-QTPLKFIXSA-N 0.000 description 1
- AYXPYQRXGNDJFU-QUMMREBQSA-N (-)-Globulol Natural products O[C@@]1(C)[C@H]2[C@H]([C@H](C)CC2)[C@@H]2C(C)(C)[C@@H]2CC1 AYXPYQRXGNDJFU-QUMMREBQSA-N 0.000 description 1
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
- LHYHMMRYTDARSZ-ZQDZILKHSA-N (-)-delta-cadinol Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CC[C@@](C)(O)[C@H]21 LHYHMMRYTDARSZ-ZQDZILKHSA-N 0.000 description 1
- LHYHMMRYTDARSZ-VXGQWTEUSA-N (1r,4s)-1,6-dimethyl-4-propan-2-yl-3,4,4a,7,8,8a-hexahydro-2h-naphthalen-1-ol Chemical compound C1CC(C)=CC2[C@H](C(C)C)CC[C@@](C)(O)C21 LHYHMMRYTDARSZ-VXGQWTEUSA-N 0.000 description 1
- 239000001490 (3R)-3,7-dimethylocta-1,6-dien-3-ol Substances 0.000 description 1
- SWCOCRTVQQHGKB-YSSOQSIOSA-N (8ar)-4,8a-dimethyl-6-propan-2-yl-2,4a,5,8-tetrahydro-1h-naphthalene Chemical compound C1CC=C(C)C2CC(C(C)C)=CC[C@]21C SWCOCRTVQQHGKB-YSSOQSIOSA-N 0.000 description 1
- IHPKGUQCSIINRJ-CSKARUKUSA-N (E)-beta-ocimene Chemical compound CC(C)=CC\C=C(/C)C=C IHPKGUQCSIINRJ-CSKARUKUSA-N 0.000 description 1
- HQTKNGJJNNTBLG-UHFFFAOYSA-N (E)-form-2,6-Dimethyl-2,4-heptadiene Natural products CC(C)C=CC=C(C)C HQTKNGJJNNTBLG-UHFFFAOYSA-N 0.000 description 1
- CDOSHBSSFJOMGT-JTQLQIEISA-N (R)-linalool Natural products CC(C)=CCC[C@@](C)(O)C=C CDOSHBSSFJOMGT-JTQLQIEISA-N 0.000 description 1
- LEAQUNCACNBDEV-KHPPLWFESA-N (Z)-undec-1-en-1-ol Chemical compound CCCCCCCCC\C=C/O LEAQUNCACNBDEV-KHPPLWFESA-N 0.000 description 1
- FAHUKNBUIVOJJR-UHFFFAOYSA-N 1-(4-fluorophenyl)-1,2,3,4-tetrahydropyrrolo[1,2-a]pyrazine Chemical compound C1=CC(F)=CC=C1C1C2=CC=CN2CCN1 FAHUKNBUIVOJJR-UHFFFAOYSA-N 0.000 description 1
- DOJDQRFOTHOBEK-UHFFFAOYSA-N 1-Octen-3-yl acetate Chemical compound CCCCCC(C=C)OC(C)=O DOJDQRFOTHOBEK-UHFFFAOYSA-N 0.000 description 1
- BQSLMQNYHVFRDT-UHFFFAOYSA-N 1-ethenyl-1-methyl-4-propan-2-ylidene-2-prop-1-en-2-ylcyclohexane Chemical compound CC(C)=C1CCC(C)(C=C)C(C(C)=C)C1 BQSLMQNYHVFRDT-UHFFFAOYSA-N 0.000 description 1
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 1
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
- HQTKNGJJNNTBLG-AATRIKPKSA-N 2,6-Dimethyl-2,4-heptadiene Chemical compound CC(C)\C=C\C=C(C)C HQTKNGJJNNTBLG-AATRIKPKSA-N 0.000 description 1
- 239000001278 2-(5-ethenyl-5-methyloxolan-2-yl)propan-2-ol Substances 0.000 description 1
- NVGOATMUHKIQQG-UHFFFAOYSA-N 2-Methyl-3-buten-1-ol Chemical compound OCC(C)C=C NVGOATMUHKIQQG-UHFFFAOYSA-N 0.000 description 1
- NWZQCEQAPBRMFX-UHFFFAOYSA-N 2-Methylpropyl 2-methylbutanoate Chemical compound CCC(C)C(=O)OCC(C)C NWZQCEQAPBRMFX-UHFFFAOYSA-N 0.000 description 1
- MVJLYXCJBPXRCY-UHFFFAOYSA-N 2-methylbutyl propanoate Chemical compound CCC(C)COC(=O)CC MVJLYXCJBPXRCY-UHFFFAOYSA-N 0.000 description 1
- WLAMNBDJUVNPJU-UHFFFAOYSA-N 2-methylbutyric acid Chemical compound CCC(C)C(O)=O WLAMNBDJUVNPJU-UHFFFAOYSA-N 0.000 description 1
- USOFNPBSEVMXHD-UHFFFAOYSA-N 2-methylheptyl propanoate Chemical compound CCCCCC(C)COC(=O)CC USOFNPBSEVMXHD-UHFFFAOYSA-N 0.000 description 1
- CPWJZWLDRWODFP-UHFFFAOYSA-N 2-methylnon-2-enoic acid Chemical compound CCCCCCC=C(C)C(O)=O CPWJZWLDRWODFP-UHFFFAOYSA-N 0.000 description 1
- PFCHFHIRKBAQGU-UHFFFAOYSA-N 3-hexanone Chemical compound CCCC(=O)CC PFCHFHIRKBAQGU-UHFFFAOYSA-N 0.000 description 1
- WJBLCSOLILMHEZ-UHFFFAOYSA-N 4,8-dimethylnona-1,7-diene Chemical compound C=CCC(C)CCC=C(C)C WJBLCSOLILMHEZ-UHFFFAOYSA-N 0.000 description 1
- YNKQMZRTPPVLLL-UHFFFAOYSA-N 5,5-Dimethyl-2(5H)-furanone Chemical compound CC1(C)OC(=O)C=C1 YNKQMZRTPPVLLL-UHFFFAOYSA-N 0.000 description 1
- DNHVYDQYTKODMM-UHFFFAOYSA-N 5,5-Dimethyl-2(5H)-furanone Natural products CC(C)(O)C=C=C=O DNHVYDQYTKODMM-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- PGTJIOWQJWHTJJ-CHWSQXEVSA-N Calamenene Chemical compound C1=C(C)C=C2[C@@H](C(C)C)CC[C@@H](C)C2=C1 PGTJIOWQJWHTJJ-CHWSQXEVSA-N 0.000 description 1
- DRSITEVYZGOOQG-UHFFFAOYSA-N Cohumulone Chemical compound CC(C)C(=O)C1=C(O)C(CC=C(C)C)=C(O)C(O)(CC=C(C)C)C1=O DRSITEVYZGOOQG-UHFFFAOYSA-N 0.000 description 1
- DRSITEVYZGOOQG-HXUWFJFHSA-N Cohumulone Natural products CC(C)C(=O)C1=C(O)C(CC=C(C)C)=C(O)[C@](O)(CC=C(C)C)C1=O DRSITEVYZGOOQG-HXUWFJFHSA-N 0.000 description 1
- VLXDPFLIRFYIME-GZBLMMOJSA-N Copaene Natural products C1C=C(C)[C@H]2[C@]3(C)CC[C@H](C(C)C)[C@H]2[C@@H]31 VLXDPFLIRFYIME-GZBLMMOJSA-N 0.000 description 1
- COGPRPSWSKLKTF-UHFFFAOYSA-N Cubenol Natural products C1CC(C)=CC2C(C(C)C)CCC(C)C21O COGPRPSWSKLKTF-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 239000005792 Geraniol Substances 0.000 description 1
- GLZPCOQZEFWAFX-YFHOEESVSA-N Geraniol Natural products CC(C)=CCC\C(C)=C/CO GLZPCOQZEFWAFX-YFHOEESVSA-N 0.000 description 1
- OGJYXQFXLSCKTP-LCYFTJDESA-N Geranyl 2-methylpropanoate Chemical compound CC(C)C(=O)OC\C=C(\C)CCC=C(C)C OGJYXQFXLSCKTP-LCYFTJDESA-N 0.000 description 1
- WVRPFQGZHKZCEB-UHFFFAOYSA-N Isopropyl 2-methylpropanoate Chemical compound CC(C)OC(=O)C(C)C WVRPFQGZHKZCEB-UHFFFAOYSA-N 0.000 description 1
- CKZXONNJVHXSQM-UHFFFAOYSA-N Ledol Natural products CC(C)C1CCC(C)(O)C2C3CC(C)CC123 CKZXONNJVHXSQM-UHFFFAOYSA-N 0.000 description 1
- BRHDDEIRQPDPMG-UHFFFAOYSA-N Linalyl oxide Chemical compound CC(C)(O)C1CCC(C)(C=C)O1 BRHDDEIRQPDPMG-UHFFFAOYSA-N 0.000 description 1
- VVBWOSGRZNCEBX-MDZDMXLPSA-N Methyl 2-decenoate Chemical class CCCCCCC\C=C\C(=O)OC VVBWOSGRZNCEBX-MDZDMXLPSA-N 0.000 description 1
- ZWNPUELCBZVMDA-CMDGGOBGSA-N Methyl 2-nonenoate Chemical compound CCCCCC\C=C\C(=O)OC ZWNPUELCBZVMDA-CMDGGOBGSA-N 0.000 description 1
- ACOBBFVLNKYODD-CSKARUKUSA-N Methyl geranate Chemical compound COC(=O)\C=C(/C)CCC=C(C)C ACOBBFVLNKYODD-CSKARUKUSA-N 0.000 description 1
- 239000005641 Methyl octanoate Substances 0.000 description 1
- GLZPCOQZEFWAFX-JXMROGBWSA-N Nerol Natural products CC(C)=CCC\C(C)=C\CO GLZPCOQZEFWAFX-JXMROGBWSA-N 0.000 description 1
- CEQGYPPMTKWBIU-UHFFFAOYSA-N Octyl propanoate Chemical compound CCCCCCCCOC(=O)CC CEQGYPPMTKWBIU-UHFFFAOYSA-N 0.000 description 1
- QURFFFCYNQXLCU-UHFFFAOYSA-N Pentyl 3-methylbutanoate Chemical compound CCCCCOC(=O)CC(C)C QURFFFCYNQXLCU-UHFFFAOYSA-N 0.000 description 1
- AZFUASHXSOTBNU-UHFFFAOYSA-N Propyl 2-methylpropanoate Chemical compound CCCOC(=O)C(C)C AZFUASHXSOTBNU-UHFFFAOYSA-N 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
- XYONNSVDNIRXKZ-UHFFFAOYSA-N S-methyl methanethiosulfonate Chemical compound CSS(C)(=O)=O XYONNSVDNIRXKZ-UHFFFAOYSA-N 0.000 description 1
- ACWQBUSCFPJUPN-UHFFFAOYSA-N Tiglaldehyde Natural products CC=C(C)C=O ACWQBUSCFPJUPN-UHFFFAOYSA-N 0.000 description 1
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 description 1
- 239000002156 adsorbate Substances 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- NBZANZVJRKXVBH-GYDPHNCVSA-N alpha-Cryptoxanthin Natural products O[C@H]1CC(C)(C)C(/C=C/C(=C\C=C\C(=C/C=C/C=C(\C=C\C=C(/C=C/[C@H]2C(C)=CCCC2(C)C)\C)/C)\C)/C)=C(C)C1 NBZANZVJRKXVBH-GYDPHNCVSA-N 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- QMAYBMKBYCGXDH-RRFJBIMHSA-N alpha-Muurolene Natural products C1CC(C)=C[C@@H]2[C@H](C(C)C)CC=C(C)[C@H]21 QMAYBMKBYCGXDH-RRFJBIMHSA-N 0.000 description 1
- VLXDPFLIRFYIME-MWHZVNNOSA-N alpha-Ylangene Chemical compound C1C=C(C)C2[C@@]3(C)CCC(C(C)C)C2C31 VLXDPFLIRFYIME-MWHZVNNOSA-N 0.000 description 1
- PFXFABJPDNHACA-UHFFFAOYSA-N alpha-copaene Natural products CC(C)C1C2CC(=CCC2C3(C)CC13)C PFXFABJPDNHACA-UHFFFAOYSA-N 0.000 description 1
- IPZIYGAXCZTOMH-UHFFFAOYSA-N alpha-eudesmol Natural products CC1=CCCC2CCC(CC12)C(C)(C)O IPZIYGAXCZTOMH-UHFFFAOYSA-N 0.000 description 1
- QMAYBMKBYCGXDH-ZNMIVQPWSA-N alpha-muurolene Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CC=C(C)[C@H]21 QMAYBMKBYCGXDH-ZNMIVQPWSA-N 0.000 description 1
- VYBREYKSZAROCT-UHFFFAOYSA-N alpha-myrcene Natural products CC(=C)CCCC(=C)C=C VYBREYKSZAROCT-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- VLXDPFLIRFYIME-QRTUWBSPSA-N alpha-ylangene Natural products C1C=C(C)[C@@H]2[C@@]3(C)CC[C@@H](C(C)C)[C@@H]2[C@H]31 VLXDPFLIRFYIME-QRTUWBSPSA-N 0.000 description 1
- 230000011681 asexual reproduction Effects 0.000 description 1
- 238000013465 asexual reproduction Methods 0.000 description 1
- FSRZGYRCMPZNJF-UHFFFAOYSA-N beta-Cubebene Natural products C12C(C(C)C)CCC(C)C32C1C(=C)CC3 FSRZGYRCMPZNJF-UHFFFAOYSA-N 0.000 description 1
- NPNUFJAVOOONJE-UHFFFAOYSA-N beta-cariophyllene Natural products C1CC(C)=CCCC(=C)C2CC(C)(C)C21 NPNUFJAVOOONJE-UHFFFAOYSA-N 0.000 description 1
- FSRZGYRCMPZNJF-KHMAMNHCSA-N beta-cubebene Chemical compound CC(C)[C@@H]([C@H]12)CC[C@@H](C)[C@]32[C@@H]1C(=C)CC3 FSRZGYRCMPZNJF-KHMAMNHCSA-N 0.000 description 1
- YOVSPTNQHMDJAG-UHFFFAOYSA-N beta-helmiscapene Natural products C1CCC(=C)C2CC(C(=C)C)CCC21C YOVSPTNQHMDJAG-UHFFFAOYSA-N 0.000 description 1
- LFJQCDVYDGGFCH-UHFFFAOYSA-N beta-phellandrene Natural products CC(C)C1CCC(=C)C=C1 LFJQCDVYDGGFCH-UHFFFAOYSA-N 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
- 229940115397 bornyl acetate Drugs 0.000 description 1
- RDWUNORUTVEHJF-UHFFFAOYSA-N bornyl formate Chemical compound C1CC2(C)C(OC=O)CC1C2(C)C RDWUNORUTVEHJF-UHFFFAOYSA-N 0.000 description 1
- 230000001488 breeding effect Effects 0.000 description 1
- 229930002314 cadinol Natural products 0.000 description 1
- CINDRKBXFXDHMX-UHFFFAOYSA-N calamendiol Natural products CC(C)C1(O)CCC(C)(O)C2CCC(=C)CC12 CINDRKBXFXDHMX-UHFFFAOYSA-N 0.000 description 1
- PAYPBTPGBHRBLY-UHFFFAOYSA-N calamenene Natural products C1=CC(C)=CC2C(C(C)C)CCC(C)C21 PAYPBTPGBHRBLY-UHFFFAOYSA-N 0.000 description 1
- NPNUFJAVOOONJE-UONOGXRCSA-N caryophyllene Natural products C1CC(C)=CCCC(=C)[C@@H]2CC(C)(C)[C@@H]21 NPNUFJAVOOONJE-UONOGXRCSA-N 0.000 description 1
- 229940117948 caryophyllene Drugs 0.000 description 1
- RSYBQKUNBFFNDO-UHFFFAOYSA-N caryophyllene oxide Natural products CC1(C)CC2C(=C)CCC3OC3(C)CCC12C RSYBQKUNBFFNDO-UHFFFAOYSA-N 0.000 description 1
- ACOBBFVLNKYODD-UHFFFAOYSA-N cis-geranic acid methyl ester Natural products COC(=O)C=C(C)CCC=C(C)C ACOBBFVLNKYODD-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- VLXDPFLIRFYIME-BTFPBAQTSA-N copaene Chemical compound C1C=C(C)[C@H]2[C@]3(C)CC[C@@H](C(C)C)[C@H]2[C@@H]31 VLXDPFLIRFYIME-BTFPBAQTSA-N 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- OYKYYOKNASFMLL-UHFFFAOYSA-N delta-Cadinol Natural products CC(C)C1CCC(=C2CCC(C)(O)CC12)C OYKYYOKNASFMLL-UHFFFAOYSA-N 0.000 description 1
- YOCDGWMCBBMMGJ-UHFFFAOYSA-N delta-cadinene Natural products C1C=C(C)CC2C(C(C)C)CCC(=C)C21 YOCDGWMCBBMMGJ-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 1
- IEICDHBPEPUHOB-UHFFFAOYSA-N ent-beta-selinene Natural products C1CCC(=C)C2CC(C(C)C)CCC21C IEICDHBPEPUHOB-UHFFFAOYSA-N 0.000 description 1
- WRHGORWNJGOVQY-RRFJBIMHSA-N gamma-Muurolene Natural products C1CC(C)=C[C@@H]2[C@H](C(C)C)CCC(=C)[C@H]21 WRHGORWNJGOVQY-RRFJBIMHSA-N 0.000 description 1
- JBHJOURGKXURIW-UHFFFAOYSA-N gamma-cadinene Natural products CC(C)C1CCC(=C2CCC(=C)CC12)C JBHJOURGKXURIW-UHFFFAOYSA-N 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- RVOXATXFYDNXRE-UHFFFAOYSA-N gamma-elemene Natural products CC(=C1CCC(C)(C(C1)C(=C)C)C(=C)C)C RVOXATXFYDNXRE-UHFFFAOYSA-N 0.000 description 1
- WWULHQLTPGKDAM-UHFFFAOYSA-N gamma-eudesmol Natural products CC(C)C1CC(O)C2(C)CCCC(=C2C1)C WWULHQLTPGKDAM-UHFFFAOYSA-N 0.000 description 1
- BXWQUXUDAGDUOS-UHFFFAOYSA-N gamma-humulene Natural products CC1=CCCC(C)(C)C=CC(=C)CCC1 BXWQUXUDAGDUOS-UHFFFAOYSA-N 0.000 description 1
- WRHGORWNJGOVQY-ZNMIVQPWSA-N gamma-muurolene Chemical compound C1CC(C)=C[C@H]2[C@H](C(C)C)CCC(=C)[C@H]21 WRHGORWNJGOVQY-ZNMIVQPWSA-N 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 description 1
- 229940113087 geraniol Drugs 0.000 description 1
- HIGQPQRQIQDZMP-DHZHZOJOSA-N geranyl acetate Chemical compound CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 description 1
- -1 geranyl ester Chemical class 0.000 description 1
- NKIWRYQBASKLRK-UHFFFAOYSA-N globulol Natural products CC1CCC2CC(C)(O)CC3C(C12)C3(C)C NKIWRYQBASKLRK-UHFFFAOYSA-N 0.000 description 1
- BGYICJVBGZQOCY-UHFFFAOYSA-N heptyl propanoate Chemical compound CCCCCCCOC(=O)CC BGYICJVBGZQOCY-UHFFFAOYSA-N 0.000 description 1
- QBNFBHXQESNSNP-UHFFFAOYSA-N humulene Natural products CC1=CC=CC(C)(C)CC=C(/C)CCC1 QBNFBHXQESNSNP-UHFFFAOYSA-N 0.000 description 1
- 230000010354 integration Effects 0.000 description 1
- VFTGLSWXJMRZNB-UHFFFAOYSA-N isoamyl isobutyrate Chemical compound CC(C)CCOC(=O)C(C)C VFTGLSWXJMRZNB-UHFFFAOYSA-N 0.000 description 1
- 229940024423 isopropyl isobutyrate Drugs 0.000 description 1
- 235000001510 limonene Nutrition 0.000 description 1
- 229940087305 limonene Drugs 0.000 description 1
- 229930007744 linalool Natural products 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- FDNCPIRKQFHDBX-ZHACJKMWSA-N methyl (e)-undec-2-enoate Chemical compound CCCCCCCC\C=C\C(=O)OC FDNCPIRKQFHDBX-ZHACJKMWSA-N 0.000 description 1
- CRHITZQXHNFRAZ-FPLPWBNLSA-N methyl (z)-dec-4-enoate Chemical compound CCCCC\C=C/CCC(=O)OC CRHITZQXHNFRAZ-FPLPWBNLSA-N 0.000 description 1
- VZZWXHWOLMCDOT-UHFFFAOYSA-N methyl 2,5-dimethylhexanoate Chemical compound COC(=O)C(C)CCC(C)C VZZWXHWOLMCDOT-UHFFFAOYSA-N 0.000 description 1
- SYGMGFWHASCAQF-UHFFFAOYSA-N methyl deca-3,6-dienoate Chemical compound CCCC=CCC=CCC(=O)OC SYGMGFWHASCAQF-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- YAHNYLGSSPTTAG-UHFFFAOYSA-N methyl n-(3,4-dichlorophenyl)carbamodithioate Chemical compound CSC(=S)NC1=CC=C(Cl)C(Cl)=C1 YAHNYLGSSPTTAG-UHFFFAOYSA-N 0.000 description 1
- MFRQOOPOGJBAPT-UHFFFAOYSA-N methyl trideca-2,4-dienoate Chemical compound CCCCCCCCC=CC=CC(=O)OC MFRQOOPOGJBAPT-UHFFFAOYSA-N 0.000 description 1
- USOOLPVJOOLOKK-UHFFFAOYSA-N methyl undeca-2,4-dienoate Chemical compound CCCCCCC=CC=CC(=O)OC USOOLPVJOOLOKK-UHFFFAOYSA-N 0.000 description 1
- KISVAASFGZJBCY-UHFFFAOYSA-N methyl undecenate Chemical compound COC(=O)CCCCCCCCC=C KISVAASFGZJBCY-UHFFFAOYSA-N 0.000 description 1
- DUWWHGPELOTTOE-UHFFFAOYSA-N n-(5-chloro-2,4-dimethoxyphenyl)-3-oxobutanamide Chemical compound COC1=CC(OC)=C(NC(=O)CC(C)=O)C=C1Cl DUWWHGPELOTTOE-UHFFFAOYSA-N 0.000 description 1
- OGJYXQFXLSCKTP-UHFFFAOYSA-N neryl isobutyrate Natural products CC(C)C(=O)OCC=C(C)CCC=C(C)C OGJYXQFXLSCKTP-UHFFFAOYSA-N 0.000 description 1
- PQCYCHFQWMNQRJ-UHFFFAOYSA-N octyl 2-methyl-propionyl Chemical compound CCCCCCCCOC(=O)C(C)C PQCYCHFQWMNQRJ-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- UYGGIIOLYXRSQY-UHFFFAOYSA-N pentyl 2-methylpropanoate Chemical compound CCCCCOC(=O)C(C)C UYGGIIOLYXRSQY-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 230000033458 reproduction Effects 0.000 description 1
- XBNCUVKYQNARCE-UHFFFAOYSA-N s-methyl heptanethioate Chemical compound CCCCCCC(=O)SC XBNCUVKYQNARCE-UHFFFAOYSA-N 0.000 description 1
- VPQBJIRQUUEAFC-UHFFFAOYSA-N selinene Natural products C1CC=C(C)C2CC(C(C)C)CCC21C VPQBJIRQUUEAFC-UHFFFAOYSA-N 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- UHEPJGULSIKKTP-UHFFFAOYSA-N sulcatone Chemical compound CC(C)=CCCC(C)=O UHEPJGULSIKKTP-UHFFFAOYSA-N 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- UAXOELSVPTZZQG-UHFFFAOYSA-N tiglic acid Natural products CC(C)=C(C)C(O)=O UAXOELSVPTZZQG-UHFFFAOYSA-N 0.000 description 1
- PGTJIOWQJWHTJJ-UHFFFAOYSA-N trans-Calamenene Natural products C1=C(C)C=C2C(C(C)C)CCC(C)C2=C1 PGTJIOWQJWHTJJ-UHFFFAOYSA-N 0.000 description 1
- 210000003462 vein Anatomy 0.000 description 1
- IHPKGUQCSIINRJ-UHFFFAOYSA-N β-ocimene Natural products CC(C)=CCC=C(C)C=C IHPKGUQCSIINRJ-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01H—NEW PLANTS OR NON-TRANSGENIC PROCESSES FOR OBTAINING THEM; PLANT REPRODUCTION BY TISSUE CULTURE TECHNIQUES
- A01H6/00—Angiosperms, i.e. flowering plants, characterised by their botanic taxonomy
- A01H6/28—Cannabaceae, e.g. cannabis
Definitions
- This invention relates to a new and distinct variety of hop plant, and more particularly to a new hop plant variety of unknown parentage which was discovered among plants created as part of a controlled breeding program.
- the new variety has been stably reproduced over successive generations. Discovery of the new variety and initial reproduction by root cuttings was carried out in a research nursery in Prosser, Wash., U.S.A. Subsequent asexual reproduction took place in Granger, Wash., U.S.A.
- FIG. 1 shows a hop cone of the new hop plant variety
- FIG. 2 shows a cluster of hop cones of the new hop variety
- FIG. 3 shows a cluster of hop cones of the new hop variety
- FIG. 4 shows a blossom and leaf of the new hop plant variety
- FIG. 5 shows a bine of the new hop plant variety
- FIG. 6 shows a hop plant of the new variety.
- the new hop plant variety is a bittering-type cultivar of recent origin. Its bittering and aromatic properties are similar to the Galena (unpatented) hop variety. However, unlike Galena which is susceptible to powdery mildew, the new variety is moderately tolerant to powdery mildew. It is also tolerant to Sphaerotheca. The new variety produces a medium size cone with fair to good pickability (similar to Galena), and fair to good storageability (25% to 30% alpha loss after six months common storage). Harvest is medium-late (approximately September 5 in Granger Wash.), with a crop yield of 2450 to 2550 pounds per acre (2750 to 2860 kg/ha).
- Bract tip Yellow green (144A). Bract base: Yellow green (145D). Bracteole: Yellow green (145C).
- Bracteole tip shape Narrowly rounded tip.
- Beta acids 8.0%-9.0% of cone weight (ASBC Spectrophotometric method).
- Aroma. Mild, floral with spicy notes.
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Natural Medicines & Medicinal Plants (AREA)
- Physiology (AREA)
- Botany (AREA)
- Developmental Biology & Embryology (AREA)
- Environmental Sciences (AREA)
- Detergent Compositions (AREA)
- Breeding Of Plants And Reproduction By Means Of Culturing (AREA)
Abstract
The new hop plant variety is a bittering-type cultivar of recent origin. Its bittering and aromatic properties are similar to the Galena hop variety. However, unlike Galena which is susceptible to powdery mildew, the new variety is moderately tolerant to powdery mildew. It is also tolerant to Sphaerotheca. The new variety produces a medium size cone with fair to good pickability, and fair to good storageability. Harvest is medium-late, with a crop yield of 2450 to 2550 pounds per acre (2750 to 2860 kg/ha).
Description
This invention relates to a new and distinct variety of hop plant, and more particularly to a new hop plant variety of unknown parentage which was discovered among plants created as part of a controlled breeding program. The new variety has been stably reproduced over successive generations. Discovery of the new variety and initial reproduction by root cuttings was carried out in a research nursery in Prosser, Wash., U.S.A. Subsequent asexual reproduction took place in Granger, Wash., U.S.A.
FIG. 1 shows a hop cone of the new hop plant variety;
FIG. 2 shows a cluster of hop cones of the new hop variety;
FIG. 3 shows a cluster of hop cones of the new hop variety;
FIG. 4 shows a blossom and leaf of the new hop plant variety;
FIG. 5 shows a bine of the new hop plant variety; and
FIG. 6 shows a hop plant of the new variety.
The new hop plant variety is a bittering-type cultivar of recent origin. Its bittering and aromatic properties are similar to the Galena (unpatented) hop variety. However, unlike Galena which is susceptible to powdery mildew, the new variety is moderately tolerant to powdery mildew. It is also tolerant to Sphaerotheca. The new variety produces a medium size cone with fair to good pickability (similar to Galena), and fair to good storageability (25% to 30% alpha loss after six months common storage). Harvest is medium-late (approximately September 5 in Granger Wash.), with a crop yield of 2450 to 2550 pounds per acre (2750 to 2860 kg/ha).
The following is a detailed botanical description of the new and distinct variety of Humulus lupulus, based on observations of specimens grown in Grange, Wash. during the 1998 growing season. All colors are described according to The Royal Horticultural Society Colour Chart. It should be understood that the botanical and analytical chemical characteristics described will vary somewhat depending upon cultural practices and climatic conditions and can vary with location and season.
1. Bine:
Color.—Yellow green (146D).
Stripe.—None.
Stipule color.—Yellow green (146D).
Stipule direction.—Down, forked.
Diameter.—1.05 cm (measurement taken at 2.75 m).
Shoot emergence.—Medium early to medium; similar to Galena.
2. Leaves:
Leaf arrangement.—Opposite.
Leaf shape.—Cordate to palmate.
Average length.—18.8 cm.
Average width.—19.7 cm.
Color — upper surface, mature.—Green (139A).
Color — lower surface, mature.—Green (137B).
Color — upper surface, immature.—Green (139A).
Color — lower surface, immature.—Green (137B).
Number of leaf lobes.—1-5.
Margin.—Serrate.
Serrations per inch.—5 min., 8 max.
Pose.—Downward.
Average petiole length.—8.9 cm.
Venation.—Palmate.
Vein color.—Yellow green (146D).
3. Cones:
Average length.—3.3 cm.
Average diameter.—1.7 cm.
Color.—Bract tip: Yellow green (144A). Bract base: Yellow green (145D). Bracteole: Yellow green (145C).
Shape.—Ovoid.
Bract shape.—Obovate.
Bract tip shape.—Mucronate.
Bract tip position.—Recurved.
Bracteole shape.—Oblanceolate.
Bracteole tip shape.—Narrowly rounded tip.
Shattering potential at harvest.—Similar to Galena.
% Alpha acids.—12.0%-14.0% of cone weight (ASBC Spectrophotometric method).
% Beta acids.—8.0%-9.0% of cone weight (ASBC Spectrophotometric method).
% Cohumulone.—32%-35% of alpha acids.
Total oils.—1.5-1.8 mL/100 g.
Aroma.—Mild, floral with spicy notes.
4. Technical data: Essential Oil Profile of YCR Accession No. 7: 103 mg of 10% Adsorbate/150C/5 Min. by DTD-GC-MS.
| MS | Area | ||
| Spec# | Integration | Peak Assignment | Area % |
| 76-212 | 18520 | acetone + isoprene | 0.297 |
| 235-256 | 8148 | 2-methyl-3-buten-1-ol | 0.131 |
| 274 | 412 | pentanal ? | 0.007 |
| 280 | 1051 | hexene | 0.017 |
| 287 | 412 | ? | 0.007 |
| 297 | 189 | ? | 0.003 |
| 302 | 145 | ? | 0.002 |
| 317 | 128 | ? | 0.002 |
| 350 | 2519 | acetic acid | 0.040 |
| 364 | 105 | methylpentanone | 0.002 |
| 371 | 1887 | ? m/z 56, 70 peaks | 0.030 |
| 387 | 166 | ? | 0.003 |
| 404 | 615 | 3-methyl-2-butenal | 0.010 |
| 415 | 466 | hexanal | 0.007 |
| 426 | 3539 | isobutyric acid | 0.057 |
| 432 | 3119 | n-octane | 0.050 |
| 460 | 284 | ? | 0.005 |
| 473 | 229 | isopropylisobutyrate | 0.004 |
| 482 | 7032 | 3-methylbutyric acid | 0.112 |
| 491 | 4103 | 2-methylbutyric acid | 0.066 |
| 505 | 221 | ? m/z 82/81/67 peaks | 0.004 |
| 508 | 877 | ? m/z 81 peak | 0.014 |
| 521 | 14624 | propanoic acid + propylisobutyrate | 0.234 |
| 528 | 1939 | 2,6-dimethyl-2,4-heptadiene | 0.031 |
| 537 | 2721 | 5,5-dimethyl-2(5H)-furanone | 0.044 |
| 546 | 1776 | alpha-pinene | 0.028 |
| 554 | 587 | isobutylisobutyrate | 0.009 |
| 557 | 704 | 4-methylpentanoic acid | 0.011 |
| 562 | 842 | dimethyltrisulfide | 0.013 |
| 569 | 30632 | 2-methylbutylpropanoate | 0.491 |
| 578 | 600 | 6-methyl-5-heptene-2-one | 0.010 |
| 582 | 43591 | beta-pinene + methyl-5- | 0.698 |
| methylhexanoate | |||
| 595 | 1589016 | myrcene | 25.451 |
| 600 | 2746 | isobutyl-2-methylbutyrate | 0.044 |
| 607 | 38160 | 3-methylbutylisobutyrate | 0.611 |
| 611 | 102594 | 2-methylbutylisobutyrate | 1.643 |
| 615 | 18027 | methylheptanoate | 0.289 |
| 621 | 1084 | ? sulfur-compd. possibly | 0.017 |
| S-methylmethanethiosulphonate | |||
| 629 | 12559 | limonene + beta-phellandrene | 0.201 |
| 634 | 2067 | ? terpene | 0.033 |
| 645 | 86156 | beta-ocimene + | 1.380 |
| pentyl-2-methylpropanoate | |||
| 654 | 400 | methyl-2,5-dimethylhexanoate | 0.006 |
| 656 | 665 | gamma-terpinene | 0.011 |
| 662 | 450 | isoctanol | 0.007 |
| 672 | 6486 | heptanoic acid | 0.104 |
| 676 | 51375 | methyl-6-methylheptanoate | 0.823 |
| 682 | 1875 | linalool oxide | 0.030 |
| 686 | 650 | terpinolene | 0.010 |
| 691 | 24253 | linalool + nonanal | 0.388 |
| 697 | 16354 | 2-methylbutyl-2-methylbutyrate | 0.262 |
| 700 | 10821 | pentyl-3-methylbutyrate | 0.173 |
| 704 | 661 | ? sulfur-compd. | 0.011 |
| 713 | 51579 | methyloctanoate | 0.826 |
| 718 | 888 | ? sulfur-compd. | 0.014 |
| 725 | 1636 | 2,3-dihydro-3,5-dihydroxy-6- | 0.026 |
| methyl-4(H)-pyran-4-one | |||
| 734 | 11124 | octanoic acid (branched isomer) | 0.178 |
| 740 | 12989 | hexylisobutyrate | 0.208 |
| 743 | 450 | cis-3-hexenylisobutyrate | 0.007 |
| 745 | 1999 | 2-decanone (branched isomer) | 0.032 |
| 752 | 458 | heptanethioic acid, S-methyl ester | 0.007 |
| 758 | 439 | methylphenylacetate | 0.007 |
| 771 | 22724 | ? m.w. branched alcohol m/z 59 base | 0.364 |
| peak + octanoic acid | |||
| 779 | 262 | 4,8-dimethylnona-1,7-diene | 0.004 |
| 783 | 16073 | methylnonanoate (branched isomer) | 0.257 |
| 789 | 11463 | methylnonanoate (branched isomer) | 0.184 |
| 795 | 165 | ? | 0.003 |
| 801 | 1728 | heptylpropanoate | 0.028 |
| 807 | 4605 | methylnonenoate | 0.074 |
| 818 | 541 | ? 164 m.w. w/149 base peak | 0.009 |
| (phenolic ?) | |||
| 824 | 26497 | methylnonanoate | 0.424 |
| 831 | 83 | nerol | 0.001 |
| 841 | 1433 | nonanoic acid (branched isomer) | 0.023 |
| 848 | 347 | ? | 0.006 |
| 853 | 4011 | 2-methylheptylpropanoate | 0.064 |
| 858 | 4500 | geraniol | 0.072 |
| 861 | 12462 | 2-undecanone (branched isomer) | 0.200 |
| 870 | 211 | methyl, 2-methylnonenoate | 0.003 |
| 873 | 222 | 2-undecanol | 0.004 |
| 882 | 11051 | undecenyl alcohol + nonanoic acid | 0.177 |
| 895 | 474 | octenyl acetate | 0.008 |
| 902 | 49630 | methyldecanoate (branched isomer) | 0.795 |
| 905 | 29807 | 2-undecanone | 0.477 |
| 910 | 511 | ? 180 m.w., 95 base peak, possibly | 0.008 |
| bornylformate | |||
| 921 | 2556 | octylpropanoate | 0.041 |
| 926 | 267900 | methyl-4-decenoate + methyl-4,8- | 4.291 |
| decadienoate | |||
| 937 | 4377 | methyldecenoate isomer + tridecane | 0.070 |
| 940 | 4657 | methylgeranate | 0.075 |
| 947 | 91720 | methyldecanoate | 1.469 |
| 959 | 2258 | decanoic acid (branched isomer) | 0.036 |
| 976 | 7728 | octyl-2-methylpropanoate | 0.124 |
| 981 | 578 | ? unsaturated alcohol or aldehyde | 0.009 |
| 987 | 6658 | 2-dodecanone (branched isomer) | 0.107 |
| 993 | 15287 | methyl-2-undecenoate | 0.245 |
| 999 | 3411 | alpha-cubebene | 0.055 |
| 1007 | 8331 | decanoic acid | 0.133 |
| 1014 | 15024 | geranyl acetate | 0.241 |
| 1020 | 307 | ? acetate | 0.005 |
| 1024 | 769 | possibly bornylacetate | 0.012 |
| 1029 | 40607 | methylundecanoate (branched isomer) | 0.650 |
| 1034 | 15141 | alpha-ylangene + 2-dodecanone | 0.243 |
| 1038 | 2758 | 2-methydecanoic acid | 0.044 |
| 1048 | 2282 | alpha-copaene | 0.037 |
| 1055 | 2036 | methylundecadienoate | 0.033 |
| 1064 | 3883 | methyl-10-undecenoate | 0.062 |
| 1071 | 665 | ? sesquiterpene 206 m.w. 163 base peak | 0.011 |
| 1076 | 3061 | methylundecanoate | 0.049 |
| 1091 | 755736 | caryophyllene | 12.104 |
| 1100 | 18236 | beta-cubebene | 0.292 |
| 1106 | 718 | linalylisobutyrate | 0.011 |
| 1111 | 1009 | 3-methylbutyloctanoate | 0.016 |
| 1120 | 4584 | 2-tridecanone (branched isomer) | 0.073 |
| 1135 | 1466661 | humulene | 23.491 |
| 1140 | 2713 | ? 204 m.w. sesquiterpene 161 base peak | 0.043 |
| 1145 | 1812 | methyldodecenoate | 0.029 |
| 1156 | 48981 | gamma-muurolene + | 0.785 |
| methyldodecanoate | |||
| 1165 | 4436 | 2-tridecanone | 0.071 |
| 1170 | 739846 | beta-selinene | 11.850 |
| 1177 | 19970 | methyl-3,6-decadienoate | 0.320 |
| 1183 | 64588 | alpha-selinene | 1.034 |
| 1186 | 28882 | geranyl isobutyrate | 0.463 |
| 1192 | 4917 | methyldodecenoate + delta-cadinene | 0.079 |
| 1202 | 32080 | alpha-muurolene | 0.514 |
| 1206 | 2266 | calamenene | 0.036 |
| 1213 | 54844 | beta-cadinene | 0.878 |
| 1225 | 4495 | delta-selinene | 0.072 |
| 1232 | 10491 | sesquiterpene w/no common name | 0.168 |
| CAS#16728-99-7, cadinene-type | |||
| 1242 | 4032 | selina-3,7-diene (eudesma-3,7-diene) | 0.065 |
| 1250 | 201 | 2-tetradecanone (branched isomer) | 0.003 |
| 1258 | 6066 | elixene | 0.097 |
| 1264 | 284 | ? | 0.005 |
| 1268 | 139 | caryophyllyl alcohol | 0.002 |
| 1282 | 10530 | caryophyllene oxide | 0.169 |
| 1293 | 300 | methyltridecadienoate | 0.005 |
| 1299 | 1823 | humulene epoxide | 0.029 |
| 1304 | 307 | methyridecenoate | 0.005 |
| 1313 | 18259 | humulene epoxide | 0.292 |
| 1319 | 1141 | globulol | 0.018 |
| 1324 | 1521 | ? 222 m.w. sesquiterpene | 0.024 |
| 1339 | 6389 | delta-cadinol | 0.102 |
| 1351 | 8125 | cadinol | 0.130 |
| 1363 | 1200 | eudesmol | 0.019 |
| 1366 | 12410 | Juniper Camphor (eudesma-7-en-4-ol) | 0.199 |
| 1387 | 378 | geranyl ester ? | 0.006 |
| 1391 | 145 | ? | 0.002 |
| 1439 | 198 | ? | 0.003 |
| 1520 | 1897 | ? 250 m.w. w/115 base peak | 0.030 |
| 6243539 | Total Essential Oil Components | 100.000 | |
Claims (1)
1. A new variety of hop plant substantially as herein shown and
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/287,404 USPP12401P2 (en) | 1999-04-06 | 1999-04-06 | Hop plant named “YCR Accession No. 7” |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US09/287,404 USPP12401P2 (en) | 1999-04-06 | 1999-04-06 | Hop plant named “YCR Accession No. 7” |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USPP12401P2 true USPP12401P2 (en) | 2002-02-12 |
Family
ID=23102754
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US09/287,404 Expired - Lifetime USPP12401P2 (en) | 1999-04-06 | 1999-04-06 | Hop plant named “YCR Accession No. 7” |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USPP12401P2 (en) |
-
1999
- 1999-04-06 US US09/287,404 patent/USPP12401P2/en not_active Expired - Lifetime
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| USPP12213P2 (en) | Hop plant named ‘YCR Accession No. 14’ | |
| USPP12401P2 (en) | Hop plant named “YCR Accession No. 7” | |
| USPP12404P2 (en) | Hop plant named YCR Accession No. 5 | |
| USPP11037P (en) | Verbena plant named `Sunmariripi` | |
| USPP15663P2 (en) | Hop plant named ‘YCR Accession No. 4’ | |
| USPP35570P2 (en) | Hop plant named ‘YQH-1320 EXP’ | |
| USPP14127P2 (en) | Hop plant named “VGXP01” | |
| USPP35764P2 (en) | Physocarpus plant named ‘SueCKat’ | |
| USPP36905P2 (en) | Shrub rose plant named ‘ZLELisaAnnHansen’ | |
| USPP10325P (en) | Pear tree named `Biehn` | |
| USPP5008P (en) | Lily plant (Lilium Goldrush) | |
| USPP6038P (en) | Chrysanthemum plant named Rekel | |
| USPP4133P (en) | Chrysanthemum | |
| USPP10722P (en) | Argyranthemum frutescens cultivar named `Primrose Petite` | |
| USPP6090P (en) | Chrysanthemum named "Blue Refla" | |
| USPP18459P3 (en) | Avocado tree named ‘Wheeling’ | |
| USPP4969P (en) | Lily plant: Lilium Golddigger | |
| USPP12323P2 (en) | Apple tree named ‘Co-op 25’ | |
| USPP860P (en) | Rose plant | |
| USPP4137P (en) | Chrysanthemum named Imperial Yellow | |
| USPP6545P (en) | Chrysanthemum named "Repin" | |
| USPP16429P3 (en) | Artichoke plant named ‘BCV 8-11’ | |
| USPP5955P (en) | Chrysanthemum plant named Funny Redemine | |
| USPP5973P (en) | Chrysanthemum | |
| USPP10720P (en) | Argyranthemum frutescens cultivar named `Blanche` |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: YAKIMA CHIEF RANCHES, INC., WASHINGTON Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:ZIMMERMANN, CHARLES E.;REEL/FRAME:010065/0911 Effective date: 19990621 |