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Haplophyllum griffithianum

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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
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Details Top

Internal ID UUID64401fb80b2b8045995373
Scientific name Haplophyllum griffithianum
Authority Boiss.
First published in Diagn. Pl. Orient. , ser. 2, 1: 115 (1854)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ruta griffithiana (Boiss.) M.Hiroe Forest Pl. Hist. Jap. Islands 1: 196 (1974)
Haplophyllum leptomerum Lincz. & Vved. Fl. URSS 14: 731 (1949)
Haplophyllum tenuisectum Lincz. & Vved. Fl. URSS 14: 732 (1949)

Common names Top

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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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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
  • Asia-temperate
    • Middle Asia
      • Tadzhikistan
      • Uzbekistan
    • Western Asia
      • Afghanistan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000715537
Tropicos 28101522
KEW urn:lsid:ipni.org:names:771290-1
Open Tree Of Life 520170
Observations.org 127228
NCBI Taxonomy 1006075
IPNI 771290-1
GBIF 8196174
Elurikkus 649092

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties Szewczyk A, Pęczek F Int J Mol Sci 15-Aug-2023
PMCID:PMC10454094
doi:10.3390/ijms241612811
PMID:37628986
Alkaloids from Haplophyllum leptomerum V. I. Akhmedzhanova, L. Angenot, R. Sh. Shakirov Springer Science and Business Media LLC 08-Jul-2010
doi:10.1007/S10600-010-9661-Y
New alkaloids fromHaplophyllum V. I. Akhmedzhanova Springer Science and Business Media LLC 11-Feb-2006
doi:10.1007/BF02323293
Folipidine, a New Type Quinoline Alkaloid from Plants of the Haplophyllum Genus V. I. Akhmedzhanova, Kh. A. Rasulova, I. A. Bessonova, A. S. Shashkov, N. D. Abdullaev, L. Angenot Springer Science and Business Media LLC 10-Jun-2005
doi:10.1007/S10600-005-0075-1
Obtusifolin ? A new coumarin from roots of Haplophyllum obtusifolium I. A. Bessonova, �. Kh. Batirov, M. R. Yagudaev Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00596740
7-Isopentenyloxy-γ-fagarine from Haplophyllum perforatum I. A. Bessonova, V. I. Akhmedzhanova, S. Yu. Yunusov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00567894
Haplodimerine — A new type of dimeric quinoline alkaloids B. Tashkhodzhaev, S. V. Lindeman, I. A. Bessonova, D. M. Razakova, E. N. Tsapkina, Yu. T. Struchkov Springer Science and Business Media LLC 24-Nov-2004
doi:10.1007/BF00598191
Alkaloids ofHaplophyllum foliosum. III. Structure of folidine V. I. Akhmedzhanova, I. A. Bessonova, S. Yu. Yunusov Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00576220
Alkaloids of Haplophyllum leptomerum. I. The structure of leptomerine V. I. Akhmedzhanova, I. A. Bessonova, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00574586
Alkaloids of Haplophyllum acutifolium D. M. Gulyamova, I. A. Bessonova, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567972
Structure of foliminine I. A. Bessonova, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00568220
The structure of folimidine D. M. Razzakova, I. A. Bessonova, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564598
Alkaloids ofHaplophyllum foliosum V. I. Akhmedzhanova, I. A. Bessonova, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00564862
An investigation of the alkaloids of the fruit ofHaplophyllum foliosum D. Kurbanov, I. A. Bessonova, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567776
Alkaloids ofHaplophyllum foliosum. II. V. I. Akhmedzhanova, I. A. Bessonova Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565160

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17S)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122411793 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00574586
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00574586
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00574586
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
(2R)-2-[(2R)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-2-yl]propane-1,2-diol 673466 Click to see CC(CO)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O 275.30 unknown https://doi.org/10.1007/BF00564475
(2S,3S)-2-(2-hydroxypropan-2-yl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-3-ol 163024601 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3N=C2O1)OC)O)O 275.30 unknown https://doi.org/10.1007/BF00565160
(2S)-2-[(2S)-1,2-dihydroxypropan-2-yl]-9-methyl-2,3-dihydrofuro[2,3-b]quinolin-4-one 928436 Click to see CC(CO)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O 275.30 unknown https://doi.org/10.1007/BF00567972
2-(1,2-Dihydroxypropan-2-yl)-9-methyl-2,3-dihydrofuro[2,3-b]quinolin-4-one 4835779 Click to see CC(CO)(C1CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O 275.30 unknown https://doi.org/10.1007/BF00567972
2-(2-Hydroxypropan-2-yl)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-3-ol 21769979 Click to see CC(C)(C1C(C2=C(C3=CC=CC=C3N=C2O1)OC)O)O 275.30 unknown https://doi.org/10.1007/BF00565160
2-(4-Methoxy-2,3-dihydrofuro[2,3-b]quinolin-2-yl)propan-2-ol 12314372 Click to see CC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O 259.30 unknown https://doi.org/10.1007/BF00565160
2-[(2S)-4-methoxy-2,3-dihydrofuro[2,3-b]quinolin-2-yl]propan-2-ol 12314371 Click to see CC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O 259.30 unknown https://doi.org/10.1007/BF00565160
Dubinidine 442897 Click to see CC(CO)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O 275.30 unknown https://doi.org/10.1007/BF00565160
https://doi.org/10.1007/S10600-005-0075-1
https://doi.org/10.1007/BF00564862
https://doi.org/10.1007/BF00564475
Lopac-D-7814 673467 Click to see CC(CO)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O 275.30 unknown https://doi.org/10.1007/S10600-005-0075-1
Platydesmine 6451457 Click to see CC(C)(C1CC2=C(C3=CC=CC=C3N=C2O1)OC)O 259.30 unknown https://doi.org/10.1007/BF00565160
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see COC1=C2C=COC2=NC3=CC=CC=C31 199.20 unknown https://doi.org/10.1007/S10600-010-9661-Y
Gamma-Fagarine 107936 Click to see COC1=CC=CC2=C1N=C3C(=C2OC)C=CO3 229.23 unknown https://doi.org/10.1007/S10600-010-9661-Y
https://doi.org/10.1007/BF00574586
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1007/BF00565160
https://doi.org/10.1007/S10600-005-0075-1
https://doi.org/10.1007/S10600-010-9661-Y
https://doi.org/10.1007/BF00564862
https://doi.org/10.1007/BF00598191
https://doi.org/10.1007/BF00574586
> Organoheterocyclic compounds / Quinolines and derivatives / Phenylquinolines
1-Methyl-2-phenyl-4(1H)-quinolinone 776143 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC=CC=C3 235.28 unknown https://doi.org/10.1007/BF00574586
https://doi.org/10.1007/S10600-010-9661-Y
https://doi.org/10.1007/BF00567776
2-(4'-Hydroxy-3'-methoxyphenyl)-1-methylquinolin-4-one 71437555 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC(=C(C=C3)O)OC 281.30 unknown https://doi.org/10.1007/BF00564598
> Organoheterocyclic compounds / Quinolines and derivatives / Pyrroloquinolines
(1S,2S,3R)-1-(4-methyl-1-phenylpyrrolo[3,4-b]quinolin-3-yl)butane-1,2,3,4-tetrol 163046787 Click to see CN1C2=CC=CC=C2C=C3C1=C(N=C3C4=CC=CC=C4)C(C(C(CO)O)O)O 378.40 unknown https://doi.org/10.1007/S10600-005-0075-1
1-(4-Methyl-1-phenylpyrrolo[3,4-b]quinolin-3-yl)butane-1,2,3,4-tetrol 11545338 Click to see CN1C2=CC=CC=C2C=C3C1=C(N=C3C4=CC=CC=C4)C(C(C(CO)O)O)O 378.40 unknown https://doi.org/10.1007/S10600-005-0075-1
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
(S)-Edulinine 356087 Click to see CC(C)(C(CC1=C(C2=CC=CC=C2N(C1=O)C)OC)O)O 291.34 unknown https://doi.org/10.1007/BF00565160
https://doi.org/10.1007/BF00564862
[(2R)-3-hydroxy-1-(4-methoxy-1-methyl-2-oxoquinolin-8-yl)oxy-3-methylbutan-2-yl] acetate 92139158 Click to see CC(=O)OC(COC1=CC=CC2=C1N(C(=O)C=C2OC)C)C(C)(C)O 349.40 unknown https://doi.org/10.1007/BF02323293
[(2S)-3-hydroxy-1-(4-methoxy-1-methyl-2-oxoquinolin-8-yl)oxy-3-methylbutan-2-yl] acetate 92139157 Click to see CC(=O)OC(COC1=CC=CC2=C1N(C(=O)C=C2OC)C)C(C)(C)O 349.40 unknown https://doi.org/10.1007/BF02323293
2-(1,3-Benzodioxol-5-yl)quinolin-4(1H)-one 10901503 Click to see C1OC2=C(O1)C=C(C=C2)C3=CC(=O)C4=CC=CC=C4N3 265.26 unknown https://doi.org/10.1007/BF00565160
2-(Hept-4-enyl)-1,4-dihydroquinolin-4-one 54120998 Click to see CCC=CCCCC1=CC(=O)C2=CC=CC=C2N1 241.33 unknown https://doi.org/10.1007/S10600-010-9661-Y
2-[(E)-hept-4-enyl]-1H-quinolin-4-one 19774525 Click to see CCC=CCCCC1=CC(=O)C2=CC=CC=C2N1 241.33 unknown https://doi.org/10.1007/S10600-010-9661-Y
2-heptylquinolin-4(1H)-one 164974 Click to see CCCCCCCC1=CC(=O)C2=CC=CC=C2N1 243.34 unknown https://doi.org/10.1007/S10600-010-9661-Y
4-Methoxy-1-methyl-8-(2'-oxo-3'-methylbutoxy)-2-quinolone 14167659 Click to see CC(C)C(=O)COC1=CC=CC2=C1N(C(=O)C=C2OC)C 289.33 unknown https://doi.org/10.1007/BF00576220
4,8-dimethoxy-3-methyl-1H-quinolin-2-one 10846522 Click to see CC1=C(C2=C(C(=CC=C2)OC)NC1=O)OC 219.24 unknown https://doi.org/10.1007/BF00565160
4,8-dimethoxy-N-methyl-2-quinolone 10680379 Click to see CN1C(=O)C=C(C2=C1C(=CC=C2)OC)OC 219.24 unknown https://doi.org/10.1007/BF00564475
Foliosidine 2837663 Click to see CC(C)(C(COC1=CC=CC2=C1N(C(=O)C=C2OC)C)O)O 307.34 unknown https://doi.org/10.1016/0031-9422(88)80170-5
https://doi.org/10.1007/BF00564862
https://doi.org/10.1007/BF00565160
Foliosidine acetate 4413625 Click to see CC(=O)OC(COC1=CC=CC2=C1N(C(=O)C=C2OC)C)C(C)(C)O 349.40 unknown https://doi.org/10.1016/0031-9422(88)80170-5
https://doi.org/10.1007/BF02323293
Graveoline 353825 Click to see CN1C2=CC=CC=C2C(=O)C=C1C3=CC4=C(C=C3)OCO4 279.29 unknown https://doi.org/10.1007/BF00565160
https://doi.org/10.1007/BF00564862
https://doi.org/10.1007/BF00564475
Leptomerine 10856530 Click to see CCCC1=CC(=O)C2=CC=CC=C2N1C 201.26 unknown https://doi.org/10.1007/BF00574586
https://doi.org/10.1007/S10600-010-9661-Y
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
(+)-(R)-Ribalinine 638264 Click to see CC1(C(CC2=C(O1)N(C3=CC=CC=C3C2=O)C)O)C 259.30 unknown https://doi.org/10.1007/BF00565160
(1R,2R,14S,15R)-4,8,9-trimethoxy-16,16-dimethyl-13,17-dioxa-11,25-diazaheptacyclo[13.12.0.02,14.03,12.05,10.018,27.019,24]heptacosa-3,5(10),6,8,11,18(27),19,21,23-nonaen-26-one 163195628 Click to see CC1(C2C(C3C2OC4=NC5=C(C=CC(=C5OC)OC)C(=C34)OC)C6=C(O1)C7=CC=CC=C7NC6=O)C 486.50 unknown https://doi.org/10.1007/BF00596740
11-Methoxy-4,4-dimethyl-3,15-dioxa-17-azatetracyclo[8.7.0.02,7.012,16]heptadeca-1(10),2(7),8,11,13,16-hexaene 23824780 Click to see CC1(CCC2=C(O1)C3=C(C=C2)C(=C4C=COC4=N3)OC)C 283.32 unknown https://doi.org/10.1007/BF00567894
https://doi.org/10.1007/BF00568220
4,8,9-Trimethoxy-16,16-dimethyl-13,17-dioxa-11,25-diazaheptacyclo[13.12.0.02,14.03,12.05,10.018,27.019,24]heptacosa-3,5(10),6,8,11,18(27),19,21,23-nonaen-26-one 4486112 Click to see CC1(C2C(C3C2OC4=NC5=C(C=CC(=C5OC)OC)C(=C34)OC)C6=C(O1)C7=CC=CC=C7NC6=O)C 486.50 unknown https://doi.org/10.1007/BF00596740
Haplodimerine 442909 Click to see CC1(C2C(C3C2OC4=NC5=C(C=CC(=C5OC)OC)C(=C34)OC)C6=C(O1)C7=CC=CC=C7NC6=O)C 486.50 unknown https://doi.org/10.1007/BF00598191
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/BF00564862
https://doi.org/10.1007/BF00565160

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