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Lonicera morrowii

Lonicera morrowii - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64405ae58e9db490868822
Scientific name Lonicera morrowii
Authority A.Gray
First published in Narr. Exped. China Japan 2: 313 (1857)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lonicera insularis Nakai Bot. Mag. (Tokyo) 31: 30 (1917)
Caprifolium morrowii Kuntze Revis. Gen. Pl. 1: 274 (1891)
Xylosteon morrowii (A.Gray) Moldenke Phytologia 17: 114 (1968)
Lonicera tatarica var. morrowii (A.Gray) Q.E.Yang, Landrein, Borosova & Osborne Fl. China 19: 634 (2011)

Common names Top

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Language Common/alternative name
English morrow's honeysuckle
Armenian Ցախակեռաս Մորրովի
Icelandic vindtoppur
Japanese キンギンボク
Swedish spärrtry

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Ontario
      • Québec
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Minnesota
      • Missouri
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Wyoming
    • Southeastern U.S.A.
      • Arkansas
      • Delaware
      • District Of Columbia
      • Kentucky
      • Maryland
      • North Carolina
      • South Carolina
      • Tennessee
      • Virginia
    • Western Canada
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001290734
Flora of Alabama 3701
Canadensys 4220
USDA Plants LOMO2
UConn 264
Tropicos 6000314
KEW urn:lsid:ipni.org:names:148944-1
Missouri Botanical Garden 278976
NBN Atlas NBNSYS0200002559
Nature Serve 2.155789
IPNI 148944-1
iNaturalist 59773
GBIF 5334275
Freebase /m/01jtj7
WisFlora 4117
EPPO LONMO
Elurikkus 518923
USDA GRIN 22606
Wikipedia Lonicera_morrowii
CMAUP NPO14802.1

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Studies on Monoterpene Glucosides and Related Natural Products. LII. Mechanism for Iridane Skeleton Formation from Acyclic Monoterpenes in the Biosynthesis of Secoiridoid Glucosides and Indole Alkaloids SHINICHI UESATO, SATOKO MATSUDA, HIROYUKI INOUYE Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.104.12_1232
Mechanism for iridane skeleton formation from acyclic monoterpenes in the biosynthesis of secologanin and vindoline in Catharanthus roseus and Lonicera morrowii. Shinichi Uesato, Satoko Matsuda, Hiroyuki Inouye Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.32.1671
Studies on monoterpene glucosides and related natural products. XLII. On the possibility of the intermediacy of 10-hydroxyloganin in the biosynthesis of secologanin. KENICHIRO INOUE, YOSHIO TAKEDA, TAKAO TANAHASHI, HIROYUKI INOUYE Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.29.981
Radioimmunoassay for the determination of loganin and the biotransformation of loganin to secologanin by plant cell cultures Takao Tanahashi, Naotaka Nagakura, Hiroyuki Inouye, Meinhart H. Zenk Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84941-9
Structures of iridoids from lonicera morrowii A. Gray II I. Souzu, H. Mitsuhashi Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(01)97672-5
7-feruloylloganin: an iridoid glucoside from stems of Lonicera insularis. Lee JS, Kim HJ, Woo ER, Park YA, Lee YS, Park H Planta Med 01-Feb-2001
doi:10.1055/S-2001-10623
PMID:11270737
Iridoid Glucosides from the Fruits of Lonicera morrowii. Ikeshiro Y, Todo Y, Mase I, Tomita Y, Tanaka S, Herath WH Planta Med 01-Feb-1992
doi:10.1055/S-2006-961403
PMID:17226446
Structures of iridoids from Lonicera morrowii A. Gray. Souzu I, Mitsuhashi H Tetrahedron Lett 01-Jan-1970
doi:10.1016/S0040-4039(01)88253-8
PMID:5802381

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lignans, neolignans and related compounds
3-[4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3-methoxyphenyl]prop-2-enal 73805566 Click to see COC1=C(C=CC(=C1)C=CC=O)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 374.40 unknown https://doi.org/10.1055/S-2001-10623
threo-Guaiacylglycerol-beta-coniferyl aldehyde ether 21582570 Click to see COC1=C(C=CC(=C1)C=CC=O)OC(CO)C(C2=CC(=C(C=C2)O)OC)O 374.40 unknown https://doi.org/10.1055/S-2001-10623
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Pinoresinol 12309636 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1055/S-2001-10623
4-[6-(4-Hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 234817 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O 358.40 unknown https://doi.org/10.1055/S-2001-10623
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Kirenol 15736732 Click to see CC1(CCC2C(=C1)CCC3C2(CC(CC3(C)CO)O)C)C(CO)O 338.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-Isopropyl-5-methylanisole 14104 Click to see CC1=CC(=C(C=C1)C(C)C)OC 164.24 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
methyl (2R,3R,4S)-3-ethenyl-4-(2-oxoethyl)-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate 124351303 Click to see COC(=O)C1=COC(C(C1CC=O)C=C)OC2C(C(C(C(O2)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0040-4039(01)97672-5
Methyl 2-(hexopyranosyloxy)-4-(2-oxoethyl)-3-vinyl-3,4-dihydro-2H-pyran-5-carboxylate 369002 Click to see COC(=O)C1=COC(C(C1CC=O)C=C)OC2C(C(C(C(O2)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0040-4039(01)97672-5
Secologanin 161276 Click to see COC(=O)C1=COC(C(C1CC=O)C=C)OC2C(C(C(C(O2)CO)O)O)O 388.40 unknown https://doi.org/10.1248/CPB.29.981
https://doi.org/10.1248/YAKUSHI1947.104.12_1232
https://doi.org/10.1248/CPB.32.1671
Secoxyloganin 162868 Click to see COC(=O)C1=COC(C(C1CC(=O)O)C=C)OC2C(C(C(C(O2)CO)O)O)O 404.40 unknown https://doi.org/10.1055/S-2006-961403
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
7-Ketologanin 12311348 Click to see CC1C2C(CC1=O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 388.40 unknown https://doi.org/10.1055/S-2006-961403
Loganin 87691 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1055/S-2006-961403
https://doi.org/10.1016/S0031-9422(00)84941-9
methyl (1S,4aS,6S,7R,7aS)-6-[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101108233 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC 566.50 unknown https://doi.org/10.1055/S-2001-10623
methyl (1S,4aS,6S,7R,7aS)-6-[(Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163191390 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC 566.50 unknown https://doi.org/10.1055/S-2001-10623
Methyl 6-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 163003219 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC 566.50 unknown https://doi.org/10.1055/S-2001-10623
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(2Z)-6-methyl-2-[2-(5-methyl-2-oxochromen-4-yl)oxyethylidene]hept-5-enyl] acetate 23786283 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OCC=C(CCC=C(C)C)COC(=O)C 370.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Taraxasterol 115250 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)O)C 426.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(4aS,8S,8aS)-1-methyl-3-oxo-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,8,8a-tetrahydro-1H-pyrano[3,4-c]pyran-5-yl] acetate 6325484 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C 404.40 unknown https://doi.org/10.1055/S-2006-961403
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one 581257 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/S0040-4039(01)97672-5
CID 25178022 25178022 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown via CMAUP database
Kingiside 12304884 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 404.40 unknown https://doi.org/10.1055/S-2006-961403
methyl (1S,3S,4aS,8S,8aS)-3-hydroxy-1-methyl-8-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 163087459 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown https://doi.org/10.1016/S0040-4039(01)88253-8
methyl (4aS,8aS)-3-hydroxy-1-methyl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,4,4a,8,8a-hexahydropyrano[3,4-c]pyran-5-carboxylate 138107798 Click to see CC1C2C(CC(O1)O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC 406.40 unknown https://doi.org/10.1055/S-2006-961403
Sweroside 161036 Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O 358.34 unknown https://doi.org/10.1016/S0040-4039(01)97672-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+/-)-Balanophonin 72729357 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1055/S-2001-10623
(E)-3-[(2R,3S)-2-[4-[(1R,2S)-1,3-dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 163191434 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C=C4)O)OC)O)OC)C=CC=O 582.60 unknown https://doi.org/10.1055/S-2001-10623
3-[2-[4-[1,3-Dihydroxy-1-(4-hydroxy-3-methoxyphenyl)propan-2-yl]oxy-3,5-dimethoxyphenyl]-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal 75579704 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C=C4)O)OC)O)OC)C=CC=O 582.60 unknown https://doi.org/10.1055/S-2001-10623
Balanophonin 21582569 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)C=CC=O 356.40 unknown https://doi.org/10.1055/S-2001-10623
buddlenol A 50909267 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)OC(CO)C(C4=CC(=C(C=C4)O)OC)O)OC)C=CC=O 582.60 unknown https://doi.org/10.1055/S-2001-10623
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 4-hydroxycoumarins
4-Hydroxy-5-methylcoumarin 54688203 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2O 176.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Morusin 5281671 Click to see CC(=CCC1=C(OC2=C(C1=O)C(=CC3=C2C=CC(O3)(C)C)O)C4=C(C=C(C=C4)O)O)C 420.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
Rhamnazin 5320945 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)OC)O 330.29 unknown via CMAUP database

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