Incarvillea diffusa - Unknown
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Internal ID UUID644027393b026631915018
Scientific name Incarvillea diffusa
Authority Royle
First published in Ill. Bot. Himal. Mts. : t. 72 (1835)

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Synonyms Top

Scientific name Authority First published in
Incarvillea arguta var. longipedicellata Q.S.Zhao J. Sichuan Univ., Nat. Sci. Ed. 4: 93. 1983
Incarvillea arguta var. daochengensis Q.S.Zhao J. Sichuan Univ., Nat. Sci. Ed. 4: 94. 1983
Amphicome diffusa (Royle) Sprague Bull. Misc. Inform. Kew 1933: 386 (1933)
Amphicome arguta Royle ex G.Don Gen. Hist. 4: 665 (1838)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Qinghai
      • Tibet

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000778658
Tropicos 50043268
KEW urn:lsid:ipni.org:names:109740-1
The Plant List kew-317214
IPNI 109740-1
iNaturalist 866380
GBIF 4091340
USDA GRIN 461415

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 the Chemical Constituents of Turpinia arguta Seem Hongtao Li, Xiangming Wu, Fengxiang Lin, Yongming Luo Atlantis Press 10-Aug-2015
doi:10.2991/ICIMM-15.2015.46
A New Cyclooxygenase Inhibitor from Incarvillea arguta Qin-Gang Tan, Xiang-Hai Cai, Zhi-Zhi Du, Tao Feng, Xiao-Dong Luo Walter de Gruyter GmbH 04-Feb-2015
doi:10.1515/ZNB-2009-0414
Sesquiterpenoids from Incarvillea arguta: absolute configuration and biological evaluation. Yan YM, Wu GS, Dong XP, Shen L, Li Y, Su J, Luo HR, Zhu HJ, Cheng YX J Nat Prod 22-Jun-2012
doi:10.1021/NP200912P
PMID:22620677
Two new monoterpene alkaloid derivatives from the roots of Incarvillea arguta. Fu JJ, Qin JJ, Zeng Q, Huang Y, Zhang WD, Jin HZ Arch Pharm Res 01-Feb-2011
doi:10.1007/S12272-011-0203-3
PMID:21380801
Four new sesquiterpenoids from the roots of Incarvillea arguta and their inhibitory activities against lipopolysaccharide-induced nitric oxide production. Fu JJ, Qin JJ, Zeng Q, Huang Y, Jin HZ, Zhang WD Chem Pharm Bull (Tokyo) 01-Sep-2010
doi:10.1248/CPB.58.1263
PMID:20823614
Two Novel Monoterpene Alkaloid Dimers from <i>Incarvillea arguta</i> Jian‐Jun Fu, Hui‐Zi Jin, Yun‐Heng Shen, Wei‐Dong Zhang, Wen‐Zheng Xu, Qi Zeng, Shi‐Kai Yan Wiley 16-Nov-2007
doi:10.1002/HLCA.200790221

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
Argutin A 50906934 Click to see CCCCCC=CC=CC(=O)OC1CC2C(C(CC(C23C(OC(C3=C1)OC(=O)C)OC(=O)C)O)C)(C)CC=C(C)C=C 584.70 unknown https://doi.org/10.2991/ICIMM-15.2015.46
Argutin B 50906935 Click to see CCCCCC=CC=CC(=O)OC1CC(C(C2C13C(OC(C3=CC(C2)O)OC(=O)C)OC(=O)C)(C)CC=C(C)C=C)C 584.70 unknown https://doi.org/10.2991/ICIMM-15.2015.46
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3R,5S,6R,8S)-8-hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]dec-9-ene-10-carbaldehyde 42638391 Click to see CC1CC(C=C(C12CCC(C2)C(=C)C)C=O)O 234.33 unknown https://doi.org/10.1515/ZNB-2009-0414
8-Hydroxy-6-methyl-3-prop-1-en-2-ylspiro[4.5]dec-9-ene-10-carbaldehyde 74833587 Click to see CC1CC(C=C(C12CCC(C2)C(=C)C)C=O)O 234.33 unknown https://doi.org/10.1515/ZNB-2009-0414
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3S,4aS,5R)-3-(3-hydroxyprop-1-en-2-yl)-4a,5-dimethyl-2,3,4,5,6,7-hexahydronaphthalen-1-one 46930872 Click to see CC1CCC=C2C1(CC(CC2=O)C(=C)CO)C 234.33 unknown https://doi.org/10.1248/CPB.58.1263
Argutosine B 46930873 Click to see CC1CCC=C2C1(CC(CC2=O)C(=C)CO)C 234.33 unknown https://doi.org/10.1021/NP200912P
Diincarvilone A 60155322 Click to see CC1CCC=C2C1(CC(=CC2=O)C3(CCC(C4=C3C(=O)C5=CCCC(C5(C4)C)C)(CO)O)CO)C 480.60 unknown https://doi.org/10.1021/NP200912P
Diincarvilone B 60155233 Click to see CC1CCC=C2C1(CC(=CC2=O)C3(CCC(C4=C3C(=O)C5=CCCC(C5(C4)C)C)(CO)O)CO)C 480.60 unknown https://doi.org/10.1021/NP200912P
Diincarvilone C 70696899 Click to see CC1CCC=C2C1(CC(=CC2=O)C3(CCC(C4=C3C(=O)C5=CCCC(C5(C4)C)C)CO)CO)C 464.60 unknown https://doi.org/10.1021/NP200912P
Diincarvilone D 60155324 Click to see CC1CCC=C2C1(CC(=CC2=O)C3(CCC(=O)C4=C3C(=O)C5=CCCC(C5(C4)C)C)CO)C 448.60 unknown https://doi.org/10.1021/NP200912P
Incarvilone A 70686503 Click to see CC1CCC=C2C1(CC(=CC2=O)C(C)CO)C 234.33 unknown https://doi.org/10.1021/NP200912P
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Cyclopenta(c)pyran-4-carboxaldehyde, 1-(beta-D-glucopyranosyloxy)-1,4a,5,6,7,7a-hexahydro-4a-hydroxy-7-methyl-, (1S,4aR,7S,7aR)- 157557 Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown https://doi.org/10.1515/ZNB-2009-0414
Yuheinoside 13890717 Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown https://doi.org/10.1515/ZNB-2009-0414
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aR,6aS,6bR,8aR,10R,12aR,14bS)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 476601 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1515/ZNB-2009-0414
(1S,2R,4aS,6aS,6bR,10S,12aR,12bR,14bS)-10-Hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,12b,13,14b-icosahydropicene-4a-carbaldehyde 14423519 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O 440.70 unknown https://doi.org/10.1515/ZNB-2009-0414
23-Hydroxytormenticacid 14055735 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown https://doi.org/10.1515/ZNB-2009-0414
3-Hydroxy-11-ursen-28,13-olide 21606663 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C 454.70 unknown https://doi.org/10.1515/ZNB-2009-0414
3-Oxo-12-ursen-28-oic acid 13893949 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O 454.70 unknown https://doi.org/10.1515/ZNB-2009-0414
3-Oxopomolic acid 12314450 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1(C)O)C)C(=O)O 470.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Acetylursolic acid 619164 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1515/ZNB-2009-0414
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1515/ZNB-2009-0414
CID 3838010 3838010 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown https://doi.org/10.1515/ZNB-2009-0414
CID 4450096 4450096 Click to see CC1CCC23CCC4(C5(CCC6C(C(CCC6(C5C=CC4(C2C1C)OC3=O)C)O)(C)C)C)C 454.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Euscaphic acid 471426 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Jacarandic acid 13653335 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O 488.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Myrianthic acid 182497 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O 504.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Pomonic acid 12314449 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1(C)O)C)C(=O)O 470.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Ursolic aldehyde 14423521 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C=O 440.70 unknown https://doi.org/10.1515/ZNB-2009-0414
Ursonic acid 9890209 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O 454.70 unknown https://doi.org/10.1515/ZNB-2009-0414
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
4-Hydroxy-4-(2-hydroxyethyl)cyclohexan-1-one 184824 Click to see C1CC(CCC1=O)(CCO)O 158.19 unknown https://doi.org/10.1515/ZNB-2009-0414
> Organoheterocyclic compounds / Benzofurans
(+)-Rengyolone 10725564 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown https://doi.org/10.1515/ZNB-2009-0414
Halleridone 146831 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown https://doi.org/10.1515/ZNB-2009-0414
> Organoheterocyclic compounds / Pyridines and derivatives
(E)-4-[(7R)-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridin-4-yl]but-3-en-2-one 5319968 Click to see CC1CCC2=C1C=NC=C2C=CC(=O)C 201.26 unknown https://doi.org/10.1007/S12272-011-0203-3
4-(7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridin-4-yl)but-3-en-2-one 78385340 Click to see CC1CCC2=C1C=NC=C2C=CC(=O)C 201.26 unknown https://doi.org/10.1007/S12272-011-0203-3
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridine carboxaldehydes
(5R,7R)-5-[(S)-hydroxy-[(7R)-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridin-4-yl]methyl]-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridine-4-carbaldehyde 162870490 Click to see CC1CCC2=C(C=NC=C12)C(C3CC(C4=C3C(=CN=C4)C=O)C)O 322.40 unknown https://doi.org/10.1002/HLCA.200790221
(5S,7S)-5-[(S)-hydroxy-[(7S)-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridin-4-yl]methyl]-7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridine-4-carbaldehyde 162870489 Click to see CC1CCC2=C(C=NC=C12)C(C3CC(C4=C3C(=CN=C4)C=O)C)O 322.40 unknown https://doi.org/10.1002/HLCA.200790221
(R)-Boschniakine 3530565 Click to see CC1CCC2=C1C=NC=C2C=O 161.20 unknown https://doi.org/10.1002/HLCA.200790221
Boschniakine 442507 Click to see CC1CCC2=C1C=NC=C2C=O 161.20 unknown https://doi.org/10.1002/HLCA.200790221
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
(7R)-6,7-Dihydro-7-methyl-5H-cyclopenta[c]pyridine-4-carboxylic acid 12300212 Click to see CC1CCC2=C(C=NC=C12)C(=O)O 177.20 unknown https://doi.org/10.2991/ICIMM-15.2015.46
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Acteoside;Kusaginin;TJC160 354009 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1515/ZNB-2009-0414
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1515/ZNB-2009-0414

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