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Ailanthus triphysa

Ailanthus triphysa - 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 UUID64404ee55fe14320131570
Scientific name Ailanthus triphysa
Authority (Dennst.) Alston
First published in Handb. Fl. Ceylon 6(Suppl.): 41 (1931)

Description Top

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Synonyms Top

Scientific name Authority First published in
Pongelion fauvelianum (Pierre ex Laness.) Pierre Fl. Forest. Cochinch. Fasc. 19 (1893) sub t. 295 B.
Pongelion imberbiflorum (F.Muell.) Pierre Fl. Forest. Cochinch. Fasc. 19 (1893) sub t. 294.
Ailanthus imberbiflora F.Muell. Fragm. 3: 42 (1862)
Ailanthus kurzii Prain Indian Forester 28: 133 (1902)
Ailanthus philippinensis Merr. Publ. Bur. Sci. Gov. Lab. 35: 25 (1906)
Hebonga mollis Radlk. Philipp. J. Sci., C 6: 367 (1911 publ. 1912)
Hebonga obliqua Radlk. Philipp. J. Sci., C 6: 366 (1911 publ. 1912)
Hebonga siamensis Radlk. Bull. Misc. Inform. Kew 1912: 264 (1912)
Adenanthera triphysa Dennst. Schlüssel Hortus Malab. : 32 (1818)
Ailanthus imberbiflora var. macartneyi F.M.Bailey Bot. Bull. Dept. Agric. Queensland 10: 21 (1895)

Common names Top

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Language Common/alternative name
Arabic أيلنط ثلاثي
Persian آیلانتوس تریفیسا
Kannada ಹಾಲುಮಡ್ಡಿ
Malayalam മട്ടി
Vietnamese bút
Vietnamese thanh thất
Chinese 山蜡梅
Chinese 岭南臭椿
Chinese 毛叶南臭椿
Chinese 岭南樗树

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001140390
Tropicos 29400165
KEW urn:lsid:ipni.org:names:813557-1
The Plant List tro-29400165
Open Tree Of Life 908289
NCBI Taxonomy 459110
IPNI 813557-1
iNaturalist 346375
GBIF 3708775
Freebase /m/063yxh5
EOL 2905446
Wikipedia Ailanthus_triphysa

Genomes (via NCBI) Top

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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
Chemical Constituents of <i>Ailanthus triphysa</i> Qi Shu‐Hua, Wu Da‐Gang, Ma Yun‐Bao, Luo Xiao‐Dong Wiley 08-Sep-2010
doi:10.1002/CJOC.20030210222
Some b-Carboline Alkaloids of Ailanthus malabarica DC Balawant S. Joshi, Venkatesh N. Kamat, Dilip H. Gawad The Japan Institute of Heterocyclic Chemistry 05-Mar-2009
doi:10.3987/S-1977-01-0193
Malabanones A and B, novel nortriterpenoids from Ailanthus malabarica DC Yukio Hitotsuyanagi, Akira Ozeki, Chee Yan Choo, Kit Lam Chan, Hideji Itokawa, Koichi Takeya Elsevier BV 15-Oct-2002
doi:10.1016/S0040-4020(01)00723-2
The structure of ailanthol, a new triterpenoid from Ailanthus Malabarica DC Balawant S. Joshi, Venkatesh N. Kamat, S. William Pelletier, Kuantee Go, Krishna Bhandary Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)94868-8
Alkaloids and quassinoids from Ailanthus malabarica Hiroyuki Aono, Kazuo Koike, Jun Kaneko, Taichi Ohmoto Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(94)85104-2

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
> Alkaloids and derivatives / Harmala alkaloids
1-(9H-pyrido[3,4-b]indol-1-yl)ethanone 638667 Click to see CC(=O)C1=NC=CC2=C1NC3=CC=CC=C23 210.23 unknown https://doi.org/10.3987/S-1977-01-0193
1-Ethyl-4-methoxy-9H-pyrido[3,4-b]indole 5317256 Click to see CCC1=NC=C(C2=C1NC3=CC=CC=C32)OC 226.27 unknown https://doi.org/10.1016/0031-9422(94)85104-2
1-Ethyl-4,8-dimethoxy-beta-carboline 5317243 Click to see CCC1=NC=C(C2=C1NC3=C2C=CC=C3OC)OC 256.30 unknown https://doi.org/10.3987/S-1977-01-0193
1-ethyl-9H-pyrido[3,4-b]indole 5324325 Click to see CCC1=NC=CC2=C1NC3=CC=CC=C23 196.25 unknown https://doi.org/10.1016/0031-9422(94)85104-2
3-(9H-pyrido[3,4-b]indol-1-yl)propanoic acid 5375436 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)CCC(=O)O 240.26 unknown https://doi.org/10.1016/0031-9422(94)85104-2
9H-Pyrido[3,4-b]indole-1-carboxamide 611121 Click to see C1=CC=C2C(=C1)C3=C(N2)C(=NC=C3)C(=O)N 211.22 unknown https://doi.org/10.3987/S-1977-01-0193
Dehydrocrenatidine 5318875 Click to see COC1=CC=CC2=C1NC3=C2C(=CN=C3C=C)OC 254.28 unknown https://doi.org/10.3987/S-1977-01-0193
Dehydrocrenatine 179485 Click to see COC1=CN=C(C2=C1C3=CC=CC=C3N2)C=C 224.26 unknown https://doi.org/10.3987/S-1977-01-0193
methyl 9H-pyrido[3,4-b]indole-1-carboxylate 597266 Click to see COC(=O)C1=NC=CC2=C1NC3=CC=CC=C23 226.23 unknown https://doi.org/10.3987/S-1977-01-0193
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
1-Hydroxycanthin-6-one 86014459 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3O 236.22 unknown https://doi.org/10.1016/0031-9422(94)85104-2
Canthin-6-one 97176 Click to see C1=CC=C2C(=C1)C3=C4N2C(=O)C=CC4=NC=C3 220.23 unknown https://doi.org/10.1016/0031-9422(94)85104-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic acid 19 Click to see C1=CC(=C(C(=C1)O)O)C(=O)O 154.12 unknown https://doi.org/10.1002/CJOC.20030210222
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetratriacontanoic acid 94485 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 508.90 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 2-monoacylglycerols
1,3-Dihydroxypropan-2-yl dotriacontanoate 86003954 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)OC(CO)CO 554.90 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Quassinoids
1,11,12-Trihydroxy-11,20-epoxypicras-3-ene-2,16-dione 324240 Click to see CC1C2CC(=O)OC3C24COC(C1O)(C4C5(C(C3)C(=CC(=O)C5O)C)C)O 378.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
11,12-dihydroxy-3,10-dimethyl-3-(3-methyl-5-oxo-2H-furan-2-yl)-6,13-dioxatetracyclo[7.5.0.01,5.02,12]tetradecan-7-one 73194667 Click to see CC1C2CC(=O)OC3C24COC(C1O)(C4C(C3)(C)C5C(=CC(=O)O5)C)O 364.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
12,15,16-Trihydroxy-9,13,17-trimethyl-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadec-9-ene-4,11-dione 73031208 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4CC(=O)O3)(OC5)C)O)O)C)O 378.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
ailanquassin A 15432541 Click to see CC1C2CC(=O)OC3C24COC(C1O)(C4C(C3)(C)C5C(=CC(=O)O5)C)O 364.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
Chaparrinone 73154 Click to see CC1C2CC(=O)OC3C24COC(C1O)(C4C5(C(C3)C(=CC(=O)C5O)C)C)O 378.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
Samaderine Y 25077775 Click to see CC1=CC(=O)C(C2(C1CC3C45C2C(C(C(C4CC(=O)O3)(OC5)C)O)O)C)O 378.40 unknown https://doi.org/10.1016/0031-9422(94)85104-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1002/CJOC.20030210222
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1S,2R,3R,5R,7R,10S,11R,14R,15R)-15-[(2S)-2-[(2R)-3,3-dimethyloxiran-2-yl]-2,3-dihydrofuran-4-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadecane-3,7-diol 163053622 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6=COC(C6)C7C(O7)(C)C)C)O)C)O)C 470.70 unknown https://doi.org/10.1016/S0040-4039(00)94868-8
(1S,2R,3R,5R,7R,10S,11R,14R,15S)-15-[(2R)-2-[(2S)-3,3-dimethyloxiran-2-yl]-2,3-dihydrofuran-4-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadecane-3,7-diol 101113617 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6=COC(C6)C7C(O7)(C)C)C)O)C)O)C 470.70 unknown https://doi.org/10.1016/S0040-4039(00)94868-8
https://doi.org/10.1016/S0040-4020(01)00723-2
15-[2-(3,3-Dimethyloxiran-2-yl)-2,3-dihydrofuran-4-yl]-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadecane-3,7-diol 85082261 Click to see CC1(C(CCC2(C1CC(C3(C2CCC45C3(C4)CCC5C6=COC(C6)C7C(O7)(C)C)C)O)C)O)C 470.70 unknown https://doi.org/10.1016/S0040-4039(00)94868-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1002/CJOC.20030210222
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/10.1002/CJOC.20030210222
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/CJOC.20030210222
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1002/CJOC.20030210222
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,2R,3R,5R,9R,10R,13S)-3-hydroxy-2,6,6,9-tetramethylpentacyclo[11.3.1.01,13.02,10.05,9]heptadecane-7,14-dione 11056620 Click to see CC1(C2CC(C3(C(C2(CC1=O)C)CCC45C3(C4)CCC5=O)C)O)C 330.50 unknown https://doi.org/10.1016/S0040-4020(01)00723-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1R,2R,3R,5R,10R,11R,14S)-3-hydroxy-2,6,6,10-tetramethylpentacyclo[12.3.1.01,14.02,11.05,10]octadec-8-ene-7,15-dione 11782838 Click to see CC1(C2CC(C3(C(C2(C=CC1=O)C)CCC45C3(C4)CCC5=O)C)O)C 342.50 unknown https://doi.org/10.1016/S0040-4020(01)00723-2
> Organoheterocyclic compounds / Indoles and derivatives
9-Aminopyrido[1,2-a]indole-6,10-dione 10036085 Click to see C1=CC=C2C(=C1)C(=O)C3=C(C=CC(=O)N23)N 212.20 unknown https://doi.org/10.1016/0031-9422(94)85104-2
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
9H-Pyrido[3,4-B]indole 64961 Click to see C1=CC=C2C(=C1)C3=C(N2)C=NC=C3 168.19 unknown https://doi.org/10.1016/0031-9422(94)85104-2
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1002/CJOC.20030210222
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown https://doi.org/10.1002/CJOC.20030210222

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