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Incarvillea mairei

Incarvillea mairei - 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 UUID64402739ea652708633574
Scientific name Incarvillea mairei
Authority (H.Lév.) Grierson
First published in Notes Roy. Bot. Gard. Edinburgh 23: 341 (1961)

Description Top

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Synonyms Top

Scientific name Authority First published in
Incarvillea mairei var. multifoliolata (C.Y.Wu & W.C.Yin) C.Y.Wu & W.Q.Yin Fl. Reipubl. Popularis Sin. 69: 45 (1990)
Incarvillea mairei f. multifoliolata C.Y.Wu & W.C.Yin Fl. Yunnan. 2: 721. 1979
Tecoma mairei H.Lév. Cat. Pl. Yun-Nan : 20 (1915)
Incarvillea racemosa Q.S.Zhao J. Sichuan Univ., Nat. Sci. Ed. 4: 92. 1983 (1983)
Incarvillea mairei var. grandiflora (Wernham) Grierson Notes Roy. Bot. Gard. Edinburgh 23: 344 1961
Incarvillea grandiflora var. brevipes Sprague Bull. Misc. Inform. Kew 1909: 263.
Incarvillea compacta var. grandiflora Wernham Die Garten-Stauden 2: 947. 1931
Incarvillea compacta var. brevipes (Sprague) Wernham Die Garten-Stauden 2: 947 1931

Common names Top

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Language Common/alternative name
Chinese 鸡肉参
Chinese 山羊参

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000778671
Tropicos 3702073
KEW urn:lsid:ipni.org:names:109752-1
The Plant List kew-317227
Open Tree Of Life 591877
NCBI Taxonomy 291319
IPNI 109752-1
iNaturalist 506463
GBIF 7298303
EOL 2895115
USDA GRIN 401302

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
Community-wide patterns in pollen and ovule production, their ratio (P/O), and other floral traits along an elevation gradient in southwestern China Nepal S, Trunschke J, Ren ZX, Burgess KS, Wang H BMC Plant Biol 14-Sep-2023
PMCID:PMC10500814
doi:10.1186/s12870-023-04433-2
PMID:37710175
Genomic and Metabolomic Analysis of the Potato Common Scab Pathogen Streptomyces scabiei Liu J, Nothias LF, Dorrestein PC, Tahlan K, Bignell DR ACS Omega 20-Apr-2021
PMCID:PMC8153979
doi:10.1021/acsomega.1c00526
PMID:34056303
Research Progress of Therapeutic Enzymes and Their Derivatives: Based on Herbal Medicinal Products in Rheumatoid Arthritis Cai M, Ni WJ, Han L, Chen WD, Peng DY Front Pharmacol 16-Mar-2021
PMCID:PMC8008143
doi:10.3389/fphar.2021.626342
PMID:33796022
Synthesis of the Hexahydropyrrolo-[3,2-c]-quinoline Core Structure and Strategies for Further Elaboration to Martinelline, Martinellic Acid, Incargranine B, and Seneciobipyrrolidine Haarr MB, Sydnes MO Molecules 11-Jan-2021
PMCID:PMC7827258
doi:10.3390/molecules26020341
PMID:33440776
Do annual and perennial populations of an insect-pollinated plant species differ in mating system? Ma Y, Barrett SC, Wang FY, Deng JC, Bai WN Ann Bot 09-Oct-2020
PMCID:PMC8225283
doi:10.1093/aob/mcaa178
PMID:33035305
Phytochemical Analysis, Antioxidant and Analgesic Activities of Incarvillea compacta Maxim from the Tibetan Plateau Guo J, Zhang D, Yu C, Yao L, Chen Z, Tao Y, Cao W Molecules 30-Apr-2019
PMCID:PMC6539126
doi:10.3390/molecules24091692
PMID:31052248
LOX inhibitor HOEC interfered arachidonic acid metabolic flux in collagen-induced arthritis rats Yang W, Wang X, Xu L, Li H, Wang R Am J Transl Res 15-Aug-2018
PMCID:PMC6129533
PMID:30210691
Discovery of Natural Products as Novel and Potent FXR Antagonists by Virtual Screening Diao Y, Jiang J, Zhang S, Li S, Shan L, Huang J, Zhang W, Li H Front Chem 30-Apr-2018
PMCID:PMC5936786
doi:10.3389/fchem.2018.00140
PMID:29761098
Synthesis of New Indolizidine Derivatives from 1-(2-Quinolyl)-2-propen-1-ol Giomi D, Ceccarelli J, Brandi A ACS Omega 15-Mar-2018
PMCID:PMC6641500
doi:10.1021/acsomega.8b00167
PMID:31458576
Seasonal variation in the mating system of a selfing annual with large floral displays Yin G, Barrett SC, Luo YB, Bai WN Ann Bot 31-Dec-2015
PMCID:PMC4765542
doi:10.1093/aob/mcv186
PMID:26721904
(+)-2-(1-Hydroxyl-4-oxocyclohexyl) ethyl caffeate suppresses solar UV-induced skin carcinogenesis by targeting PI3-K, ERK1/2 and p38 Lim DY, Lee MH, Shin SH, Chen H, Ryu J, Shan L, Li H, Bode AM, Zhang WD, Dong Z Cancer Prev Res (Phila) 20-May-2014
PMCID:PMC4125463
doi:10.1158/1940-6207.CAPR-13-0286
PMID:24845061
The reproductive strategy of a pollinator-limited Himalayan plant, Incarvillea mairei (Bignoniaceae) Ai H, Zhou W, Xu K, Wang H, Li D BMC Plant Biol 01-Dec-2013
PMCID:PMC4219382
doi:10.1186/1471-2229-13-195
PMID:24289097
A Unique Indolo‐[1,7]naphthyridine Alkaloid from <i>Incarvillea mairei</i> var. <i>grandiflora</i> (<scp>Wehrh.</scp>) <scp>Grierson</scp> Yun‐Heng Shen, Yong‐Qing Su, Jun‐Mian Tian, Sheng Lin, Hui‐Liang Li, Jian Tang, Wei‐Dong Zhang Wiley 15-Dec-2010
doi:10.1002/HLCA.201000092
Three New Monoterpene Alkaloids and a New Caffeic Acid Ester from <i>Incarvillea mairei</i> var. <i>multifoliolata</i> Ai‐Ting Xing, Jun‐Mian Tian, Chun‐Mei Liu, Hui‐Liang Li, Wei‐Dong Zhang, Lei Shan Wiley 15-Apr-2010
doi:10.1002/HLCA.200900284
Chemical constituents of Incarvillea mairei var. grandiflora Yong-Qing Su, Yun-Heng Shen, Jian Tang, Wei-Dong Zhang Springer Science and Business Media LLC 22-Mar-2010
doi:10.1007/S10600-010-9540-6

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 / Fatty Acyls / Fatty acid esters
Methyl 2-ethylheptanoate 522757 Click to see CCCCCC(CC)C(=O)OC 172.26 unknown https://doi.org/10.1002/HLCA.200900284
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aR,6aR,6bS,8aR,12aS,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 12358398 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/10.1007/S10600-010-9540-6
Olean-12-en-3beta-ol 225689 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/10.1007/S10600-010-9540-6
> Lipids and lipid-like molecules / Sphingolipids / Glycosphingolipids
(2R)-N-[(E,2S,3S,4R)-3,4-dihydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-11-en-2-yl]-2-hydroxyhexadecanamide 162858782 Click to see CCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCCCCC=CCCCCCC)O)O)O 732.00 unknown https://doi.org/10.1007/S10600-010-9540-6
> 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/10.1007/S10600-010-9540-6
> Organoheterocyclic compounds / Benzofurans
(+)-Rengyolone 10725564 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown https://doi.org/10.1007/S10600-010-9540-6
(3aR,7aS)-Hexahydro-3a-hydroxy-6(2H)-benzofuranone 11412510 Click to see C1CC2(CCOC2CC1=O)O 156.18 unknown https://doi.org/10.1007/S10600-010-9540-6
Cleroindicin C 10975728 Click to see C1CC2(CCOC2CC1=O)O 156.18 unknown https://doi.org/10.1007/S10600-010-9540-6
Halleridone 146831 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown https://doi.org/10.1007/S10600-010-9540-6
> Organoheterocyclic compounds / Piperidines
(4R,4aR,6S,7R,7aS)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-ol 130944510 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1002/HLCA.200800237
[(4S,4aR,7S,7aS)-2,4-dimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-7-yl]methanol 101505038 Click to see CC1CN(CC2C1CCC2CO)C 183.29 unknown https://doi.org/10.1002/HLCA.200900284
1H-2-Pyrindine, octahydro-2,4,7-trimethyl- 547509 Click to see CC1CCC2C1CN(CC2C)C 167.29 unknown https://doi.org/10.1002/HLCA.200800237
1H-Cyclopenta(c)pyridin-6-ol, octahydro-2,4,7-trimethyl-, (4R,4aS,6R,7S,7aR)- 588297 Click to see CC1CN(CC2C1CC(C2C)O)C 183.29 unknown https://doi.org/10.1002/HLCA.200800237
beta-Skytanthine 442552 Click to see CC1CCC2C1CN(CC2C)C 167.29 unknown https://doi.org/10.1002/HLCA.200800237
Mairine B 130146657 Click to see CC1CN(CC2C1CCC2CO)C 183.29 unknown https://doi.org/10.1002/HLCA.200900284
> Organoheterocyclic compounds / Piperidines / Phenylpiperidines
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[2-[4-[(5S,9S,16S)-12-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-1,8-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-10(15),11,13-trien-8-yl]phenyl]ethoxy]oxane-3,4,5-triol 163085157 Click to see C1CC2CCN(C3C2N(C1)C4=C3C=C(C=C4)CCOC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)CCOC7C(C(C(C(O7)CO)O)O)O 702.80 unknown https://doi.org/10.1002/HLCA.201000092
2-(Hydroxymethyl)-6-[2-[4-[12-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-1,8-diazatetracyclo[7.6.1.05,16.010,15]hexadeca-10(15),11,13-trien-8-yl]phenyl]ethoxy]oxane-3,4,5-triol 163085156 Click to see C1CC2CCN(C3C2N(C1)C4=C3C=C(C=C4)CCOC5C(C(C(C(O5)CO)O)O)O)C6=CC=C(C=C6)CCOC7C(C(C(C(O7)CO)O)O)O 702.80 unknown https://doi.org/10.1002/HLCA.201000092
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
(1R,2R,6R,7S,8R,12R)-6-hydroxy-11-[4-(2-hydroxyethyl)phenyl]-3-oxa-11-azatetracyclo[5.5.2.02,6.08,12]tetradecan-13-one 162954227 Click to see C1CN(C2C1C3CC(=O)C2C4C3(CCO4)O)C5=CC=C(C=C5)CCO 343.40 unknown https://doi.org/10.1002/HLCA.200800237
6-Hydroxy-11-[4-(2-hydroxyethyl)phenyl]-3-oxa-11-azatetracyclo[5.5.2.02,6.08,12]tetradecan-13-one 162954226 Click to see C1CN(C2C1C3CC(=O)C2C4C3(CCO4)O)C5=CC=C(C=C5)CCO 343.40 unknown https://doi.org/10.1002/HLCA.200800237
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(2,4,7-Trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-yl) 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 72757275 Click to see CC1CN(CC2C1CC(C2C)OC(=O)C=CC3=CC(=C(C=C3)O)OC)C 359.50 unknown https://doi.org/10.1002/HLCA.200800237
[(2R,3R,4S,5R,6R)-5-(3,4-dihydroxyphenyl)-6-ethoxy-3,5-dihydroxy-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 6438553 Click to see CCOC1C(C(C(C(O1)COC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC3C(C(C(C(O3)C)O)O)O)(C4=CC(=C(C=C4)O)O)O 624.60 unknown https://doi.org/10.1007/S10600-010-9540-6
[(4S,4aR,6S,7R,7aS)-2,4,7-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-6-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 10406174 Click to see CC1CN(CC2C1CC(C2C)OC(=O)C=CC3=CC(=C(C=C3)O)OC)C 359.50 unknown https://doi.org/10.1002/HLCA.200800237
[5-(3,4-Dihydroxyphenyl)-6-ethoxy-3,5-dihydroxy-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]methyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 57369781 Click to see CCOC1C(C(C(C(O1)COC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC3C(C(C(C(O3)C)O)O)O)(C4=CC(=C(C=C4)O)O)O 624.60 unknown https://doi.org/10.1007/S10600-010-9540-6
2-(1-Hydroxy-4,4-dimethoxycyclohexyl)ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 162858698 Click to see COC1(CCC(CC1)(CCOC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC 366.40 unknown https://doi.org/10.1002/HLCA.200900284
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester 66883 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown https://doi.org/10.1007/S10600-010-9540-6
Ethyl caffeate 5317238 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown https://doi.org/10.1007/S10600-010-9540-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/S10600-010-9540-6
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/S10600-010-9540-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 https://doi.org/10.1007/S10600-010-9540-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4S)-2-(3-hydroxy-4-methoxyphenyl)-3-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-chromene-4,5,7-triol 163103861 Click to see COC1=C(C=C(C=C1)C2C(C(C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 482.40 unknown https://doi.org/10.1007/S10600-010-9540-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
quercetin 7-O-alpha-D-rhamnopyranoside 72193676 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-010-9540-6
Quercetin 7-rhamnoside 14130919 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC(=C(C=C4)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-010-9540-6
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(E)-3-[4-[2-(4-hydroxyphenyl)ethyl]-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 163192871 Click to see C1=CC(=CC=C1CCC2=CC(=C(C=C2)C=CC(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 446.40 unknown https://doi.org/10.1007/S10600-010-9540-6
3-[4-[2-(4-Hydroxyphenyl)ethyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoic acid 162997799 Click to see C1=CC(=CC=C1CCC2=CC(=C(C=C2)C=CC(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 446.40 unknown https://doi.org/10.1007/S10600-010-9540-6
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Schisandrin 3001664 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC 432.50 unknown https://doi.org/10.1007/S10600-010-9540-6
Schizandrin 23915 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC 432.50 unknown https://doi.org/10.1007/S10600-010-9540-6

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