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Incarvillea delavayi

Incarvillea delavayi - 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 UUID6440273922884295768008
Scientific name Incarvillea delavayi
Authority Bureau & Franch.
First published in J. Bot. (Morot) 5: 138 (1891)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Finnish isoinkarvillea
Norwegian Bokmål rosebasunblomst
Chinese 红波罗花
Chinese 鸡肉参
Chinese 土地黄
Chinese 波罗花
Chinese 红花角蒿

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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

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Database ID/link to page
World Flora Online wfo-0000778657
USDA Plants INDE2
Tropicos 3701348
KEW urn:lsid:ipni.org:names:109739-1
The Plant List kew-317213
Missouri Botanical Garden 277912
PFAF Incarvillea delavayi
Open Tree Of Life 1066484
NCBI Taxonomy 291324
IPNI 109739-1
iNaturalist 486410
GBIF 4091345
EPPO INVDE
Elurikkus 5234
USDA GRIN 19873
Wikipedia Incarvillea_delavayi

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
The Role of STATs in Ovarian Cancer: Exploring Their Potential for Therapy Standing D, Feess E, Kodiyalam S, Kuehn M, Hamel Z, Johnson J, Thomas SM, Anant S Cancers (Basel) 26-Apr-2023
PMCID:PMC10177275
doi:10.3390/cancers15092485
PMID:37173951
Novel STAT3 Inhibitors Targeting STAT3 Dimerization by Binding to the STAT3 SH2 Domain Hua Y, Yuan X, Shen YH, Wang J, Azeem W, Yang S, Gade A, Lellahi SM, Øyan AM, Ke X, Zhang WD, Kalland KH Front Pharmacol 27-May-2022
PMCID:PMC9196127
doi:10.3389/fphar.2022.836724
PMID:35712699
Two Alkaloids From Delphinium brunonianum Royle, Their Anti-inflammatory and Anti-oxidative Stress Activity via NF-κB Signaling Pathway Tang Q, Chen S, Rizvi SA, Qu J, Wang L, Wang S, Ma C, Liu L, Kang W Front Nutr 20-Jan-2022
PMCID:PMC8812339
doi:10.3389/fnut.2021.826957
PMID:35127798
Natural product anticipation through synthesis Hetzler BE, Trauner D, Lawrence AL Nat Rev Chem 14-Jan-2022
PMCID:PMC9899497
doi:10.1038/s41570-021-00345-7
PMID:36747591
Biologically Active Isoquinoline Alkaloids covering 2014-2018 Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH Med Res Rev 29-Jul-2020
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
From Pd(OAc)2 to Chiral Catalysts: The Discovery and Development of Bifunctional Mono-N-Protected Amino Acid Ligands for Diverse C–H Functionalization Reactions Shao Q, Wu K, Zhuang Z, Qian S, Yu JQ Acc Chem Res 31-Mar-2020
PMCID:PMC7738004
doi:10.1021/acs.accounts.9b00621
PMID:32227915
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
Natural Products Research in China From 2015 to 2016 Liu H, Zhu G, Fan Y, Du Y, Lan M, Xu Y, Zhu W Front Chem 20-Mar-2018
PMCID:PMC5869933
doi:10.3389/fchem.2018.00045
PMID:29616210
Brønsted Acid-Mediated Domino One-Pot Dual C–C Bond Formation: Chemoselective Synthesis of Fused Tricyclic Ketones Niharika P, Ramulu BV, Satyanarayana G ACS Omega 09-Jan-2018
PMCID:PMC6641420
doi:10.1021/acsomega.7b01553
PMID:31457889
The Use of Bio-Guided Fractionation to Explore the Use of Leftover Biomass in Dutch Flower Bulb Production as Allelochemicals against Weeds Wahyuni DS, van der Kooy F, Klinkhamer PG, Verpoorte R, Leiss K Molecules 17-Apr-2013
PMCID:PMC6269756
doi:10.3390/molecules18044510
PMID:23595089
Delavayol, a novel sesquiterpene from Incarvillea delavayi Bureau et Franchet. Chen YQ, Zhang WD, Kong LY, Lu T, Shen YH Nat Prod Res 01-Jun-2010
doi:10.1080/14786410802421026
PMID:20496228
Chemical constituents from Incarvillea delavayi Yun-Heng Shen, Tao Lu, Jian Tang, Run-Hui Liu, Hui-Liang Li, Wei-Dong Zhang Springer Science and Business Media LLC 24-May-2010
doi:10.1007/S10600-010-9598-1
Incarviditone: a novel cytotoxic benzofuranone dimer from Incarvillea delavayi Bureau et Franchet. Chen YQ, Shen YH, Su YQ, Kong LY, Zhang WD Chem Biodivers 01-May-2009
doi:10.1002/CBDV.200800084
PMID:19479844
Three New Compounds from <i>Incarvillea delavayi</i> Tao Lu, Yun‐Heng Shen, Min Lu, Jian Tang, Lei Shan, Run‐Hui Liu, Hui‐Liang Li, Wei‐Dong Zhang Wiley 07-Apr-2009
doi:10.1002/HLCA.200800394
Anther Appendages of Incarvillea Trigger a Pollen-dispensing Mechanism Han Y, Dai C, Yang CF, Wang QF, Motley TJ Ann Bot 20-Jun-2008
PMCID:PMC2701800
doi:10.1093/aob/mcn102
PMID:18567596

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(4R,4aR,7R,7aR)-2,2,4-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-2-ium-7-yl]methyl benzoate 101250592 Click to see CC1C[N+](CC2C1CCC2COC(=O)C3=CC=CC=C3)(C)C 302.40 unknown https://doi.org/10.1016/S0031-9422(99)00536-1
https://doi.org/10.1248/CPB.48.1826
[(4S,4aS,7S,7aR)-2,2,4-trimethyl-1,3,4,4a,5,6,7,7a-octahydrocyclopenta[c]pyridin-2-ium-7-yl]methyl benzoate 163189330 Click to see CC1C[N+](CC2C1CCC2COC(=O)C3=CC=CC=C3)(C)C 302.40 unknown https://doi.org/10.1016/S0031-9422(99)00536-1
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxy-3-methylbenzoic acid 68138 Click to see CC1=C(C=CC(=C1)C(=O)O)O 152.15 unknown https://doi.org/10.1007/S10600-010-9598-1
> Benzenoids / Indanes
(1S)-6-hydroxy-1-methyl-2,3-dihydro-1H-indene-4-carbaldehyde 162938157 Click to see CC1CCC2=C(C=C(C=C12)O)C=O 176.21 unknown https://doi.org/10.1002/HLCA.200800394
6-hydroxy-1-methyl-2,3-dihydro-1H-indene-4-carbaldehyde 102480556 Click to see CC1CCC2=C(C=C(C=C12)O)C=O 176.21 unknown https://doi.org/10.1002/HLCA.200800394
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Hexacosanoic acid 10469 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O 396.70 unknown https://doi.org/10.1007/S10600-010-9598-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(2s,6r)-2,6-Dimethyl-1,8-octanediol 10965032 Click to see CC(CCCC(C)CO)CCO 174.28 unknown https://doi.org/10.1007/S10600-010-9598-1
2,6-Dimethyloctane-1,8-diol 13498517 Click to see CC(CCCC(C)CO)CCO 174.28 unknown https://doi.org/10.1007/S10600-010-9598-1
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(1R,4aS,5R,7R,7aR)-1-ethoxy-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbaldehyde 102480555 Click to see CCOC1C2C(CC(C2C(=CO1)C=O)O)C 226.27 unknown https://doi.org/10.1002/HLCA.200800394
1-Ethoxy-5-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carbaldehyde 162991144 Click to see CCOC1C2C(CC(C2C(=CO1)C=O)O)C 226.27 unknown https://doi.org/10.1002/HLCA.200800394
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(1R,2S,3S,4aS,5R)-3-[(2R)-1,2-dihydroxypropan-2-yl]-4a,5-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene-1,2-diol 162968991 Click to see CC1CCC=C2C1(CC(C(C2O)O)C(C)(CO)O)C 270.36 unknown https://doi.org/10.1080/14786410802421026
3-(1,2-dihydroxypropan-2-yl)-4a,5-dimethyl-2,3,4,5,6,7-hexahydro-1H-naphthalene-1,2-diol 162968990 Click to see CC1CCC=C2C1(CC(C(C2O)O)C(C)(CO)O)C 270.36 unknown https://doi.org/10.1080/14786410802421026
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epideoxyloganic acid 443332 Click to see CC1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 360.36 unknown https://doi.org/10.1016/S0031-9422(99)00536-1
Deoxyloganic acid 4490284 Click to see CC1CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O 360.36 unknown https://doi.org/10.1016/S0031-9422(99)00536-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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/10.1080/14786410802421026
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1007/S10600-010-9598-1
https://doi.org/10.1080/14786410802421026
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/10.1007/S10600-010-9598-1
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/10.1080/14786410802421026
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1080/14786410802421026
https://doi.org/10.1007/S10600-010-9598-1
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/10.1007/S10600-010-9598-1
> 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/10.1007/S10600-010-9598-1
Beta-Sitosterol 222284 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/S10600-010-9598-1
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/10.1007/S10600-010-9598-1
CID 13051622 13051622 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 815.30 unknown https://doi.org/10.1080/14786410802421026
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/10.1007/S10600-010-9598-1
Sitoindoside I 9832350 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 815.30 unknown https://doi.org/10.1080/14786410802421026
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Rengyol 363707 Click to see C1CC(CCC1O)(CCO)O 160.21 unknown https://doi.org/10.1007/S10600-010-9598-1
> 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/S10600-010-9598-1
> Organoheterocyclic compounds / Benzofurans
(+)-Rengyolone 10725564 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown https://doi.org/10.1002/CBDV.200800084
Halleridone 146831 Click to see C1COC2C1(C=CC(=O)C2)O 154.16 unknown https://doi.org/10.1002/CBDV.200800084
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
4-(Hydroxymethyl)-2-(3-methylbutyl)furan-3-carboxylic acid 101483166 Click to see CC(C)CCC1=C(C(=CO1)CO)C(=O)O 212.24 unknown https://doi.org/10.1002/HLCA.200800394
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
2-[(5,6-Dihydroxy-2-methyl-4,8,9-trioxobenzo[g]chromen-7-yl)methyl-methylamino]acetic acid 53483341 Click to see CC1=CC(=O)C2=C(O1)C=C3C(=C2O)C(=C(C(=O)C3=O)CN(C)CC(=O)O)O 373.30 unknown https://doi.org/10.1007/S10600-010-9598-1
> Organoheterocyclic compounds / Tetrahydrofurans
(1R,3S,4S,8R,11R,12S,16R)-4-hydroxy-2,7,17-trioxapentacyclo[10.7.0.01,16.03,11.04,8]nonadecane-10,14-dione 162885151 Click to see C1COC2C13C(CC(=O)C2)C4C(O3)C5(CCOC5CC4=O)O 308.33 unknown https://doi.org/10.1002/CBDV.200800084
4-Hydroxy-2,7,17-trioxapentacyclo[10.7.0.01,16.03,11.04,8]nonadecane-10,14-dione 74954680 Click to see C1COC2C13C(CC(=O)C2)C4C(O3)C5(CCOC5CC4=O)O 308.33 unknown https://doi.org/10.1002/CBDV.200800084
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(1,4-Dihydroxycyclohexyl)ethyl 3-(3,4-dihydroxyphenyl)prop-2-enoate 74974866 Click to see C1CC(CCC1O)(CCOC(=O)C=CC2=CC(=C(C=C2)O)O)O 322.40 unknown https://doi.org/10.1002/HLCA.200800394
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/S10600-010-9598-1
Ethyl caffeate 5317238 Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O 208.21 unknown https://doi.org/10.1007/S10600-010-9598-1
> 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/S10600-010-9598-1
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/S10600-010-9598-1
> 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/S10600-010-9598-1
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 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)O 448.40 unknown https://doi.org/10.1007/S10600-010-9598-1
Quercitrin 5280459 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)O 448.40 unknown https://doi.org/10.1007/S10600-010-9598-1
> Phenylpropanoids and polyketides / Phenylpropanoic acids
Delavayine B 10713200 Click to see CC1CCC2=C(C=[N+](C=C12)C(CC3=CC=CC=C3)C(=O)O)C(OC)OC 356.40 unknown https://doi.org/10.1248/CPB.48.1826

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