Titanotrichum oldhamii - Unknown
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Internal ID UUID644046953c884826420169
Scientific name Titanotrichum oldhamii
Authority (Hemsl.) Soler.
First published in Ber. Deutsch. Bot. Ges. 27: 400 (1909)

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Synonyms Top

Scientific name Authority First published in
Rehmannia oldhamii Hemsl. J. Linn. Soc., Bot. 26: 194 (1890)
Matsumuria oldhamii Hemsl. Bull. Misc. Inform. Kew 1909: 361 (1909)

Common names Top

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Language Common/alternative name
Japanese マツムラソウ
Chinese 俄氏草
Chinese 台閩苣苔
Chinese 鱼鳞甲
Chinese 台闽苣苔

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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-temperate
    • China
      • China Southeast
    • Eastern Asia
      • Nansei-shoto
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001065118
Tropicos 14002202
KEW urn:lsid:ipni.org:names:383081-1
The Plant List tro-14002202
Open Tree Of Life 520383
NCBI Taxonomy 49121
IPNI 383081-1
iNaturalist 544510
GBIF 5830514
EPPO TTTOL
CMAUP NPO21689

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
Complete chloroplast genome of Petrocosmea qinlingensis (Gesneriaceae), a protected wild plant in the Qinling mountains Li CQ, Mu Q, Li Y, Kan SL, Liu GX Mitochondrial DNA B Resour 24-Jan-2024
PMCID:PMC10810633
doi:10.1080/23802359.2024.2306206
PMID:38274855
Langbiangia, a new genus of Gesneriaceae endemic to Langbiang Plateau, southern Vietnam and a taxonomic endeavor to achieve key targets of the post-2020 global biodiversity framework Luu HT, Hsieh CL, Chuang CR, Chen CW, Tran NT, Vu NL, Chung KF PLoS One 17-May-2023
PMCID:PMC10191291
doi:10.1371/journal.pone.0284650
PMID:37195912
Full-length transcriptome-referenced analysis reveals crucial roles of hormone and wounding during induction of aerial bulbils in lily Li J, Sun M, Li H, Ling Z, Wang D, Zhang J, Shi L BMC Plant Biol 27-Aug-2022
PMCID:PMC9419401
doi:10.1186/s12870-022-03801-8
PMID:36030206
WUSCHEL-related homeobox genes cooperate with cytokinin to promote bulbil formation in Lilium lancifolium He G, Cao Y, Wang J, Song M, Bi M, Tang Y, Xu L, Ming J, Yang P Plant Physiol 07-Jun-2022
PMCID:PMC9773970
doi:10.1093/plphys/kiac259
PMID:35670734
Cytokinin Type-B Response Regulators Promote Bulbil Initiation in Lilium lancifolium He G, Yang P, Cao Y, Tang Y, Wang L, Song M, Wang J, Xu L, Ming J Int J Mol Sci 24-Mar-2021
PMCID:PMC8037933
doi:10.3390/ijms22073320
PMID:33805045
Floral Color Diversity: How Are Signals Shaped by Elevational Gradient on the Tropical–Subtropical Mountainous Island of Taiwan? Tai KC, Shrestha M, Dyer AG, Yang EC, Wang CN Front Plant Sci 17-Dec-2020
PMCID:PMC7773721
doi:10.3389/fpls.2020.582784
PMID:33391297
Chemical Basis of Floral Color Signals in Gesneriaceae: The Effect of Alternative Anthocyanin Pathways Ogutcen E, Durand K, Wolowski M, Clavijo L, Graham C, Glauser G, Perret M Front Plant Sci 14-Dec-2020
PMCID:PMC7767864
doi:10.3389/fpls.2020.604389
PMID:33381138
Morphological and stage-specific transcriptome analyses reveal distinct regulatory programs underlying yam (Dioscorea alata L.) bulbil growth Wu ZG, Jiang W, Tao ZM, Pan XJ, Yu WH, Huang HL J Exp Bot 13-Dec-2019
PMCID:PMC7242083
doi:10.1093/jxb/erz552
PMID:31832647
Histological and Transcriptomic Analysis during Bulbil Formation in Lilium lancifolium Yang P, Xu L, Xu H, Tang Y, He G, Cao Y, Feng Y, Yuan S, Ming J Front Plant Sci 30-Aug-2017
PMCID:PMC5582597
doi:10.3389/fpls.2017.01508
PMID:28912794
Functionally different PIN proteins control auxin flux during bulbil development in Agave tequilana Abraham Juárez MJ, Hernández Cárdenas R, Santoyo Villa JN, O’Connor D, Sluis A, Hake S, Ordaz-Ortiz J, Terry L, Simpson J J Exp Bot 23-Apr-2015
PMCID:PMC4473989
doi:10.1093/jxb/erv191
PMID:25911746
Meristem identity and phyllotaxis in inflorescence development Bartlett ME, Thompson B Front Plant Sci 14-Oct-2014
PMCID:PMC4196479
doi:10.3389/fpls.2014.00508
PMID:25352850
High Efficiency Direct Shoot Organogenesis from Leaf Segments of Aerva lanata (L.) Juss. Ex Schult by Using Thidiazuron Varutharaju K, Soundar Raju C, Thilip C, Aslam A, Shajahan A ScientificWorldJournal 04-Feb-2014
PMCID:PMC3932266
doi:10.1155/2014/652919
PMID:24672349
Shoot Organogenesis and Plant Regeneration from Leaf Explants of Lysionotus serratus D. Don Li Q, Deng M, Zhang J, Zhao W, Song Y, Li Q, Huang Q ScientificWorldJournal 01-Aug-2013
PMCID:PMC3747412
doi:10.1155/2013/280384
PMID:23983626
Understanding the germination of bulbils from an ecological perspective: a case study on Chinese yam (Dioscorea polystachya) Walck JL, Cofer MS, Hidayati SN Ann Bot 29-Sep-2010
PMCID:PMC2990661
doi:10.1093/aob/mcq189
PMID:20880931
Expressions of ECE-CYC2 clade genes relating to abortion of both dorsal and ventral stamens in Opithandra (Gesneriaceae) Song CF, Lin QB, Liang RH, Wang YZ BMC Evol Biol 07-Oct-2009
PMCID:PMC2763874
doi:10.1186/1471-2148-9-244
PMID:19811633

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
> Benzenoids / Phenol ethers / Anisoles
Estragole 8815 Click to see COC1=CC=C(C=C1)CC=C 148.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(+)-Nortrachelogenin 479756 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
3-Hydroxy-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 321311 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
Nortrachelogenin 394846 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O 374.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carboxylic acid 92166187 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Dextropimarinal 12304198 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C=O)C)C=C 286.50 unknown via CMAUP database
Isopimara-7,15-dienal 12311183 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C=O)C)C1)C=C 286.50 unknown via CMAUP database
Isopimaric acid 442048 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C 302.50 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C 302.50 unknown via CMAUP database
Palustric acid 443613 Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C 302.50 unknown via CMAUP database
Pimaric acid 220338 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown via CMAUP database
Retene 10222 Click to see CC1=C2C=CC3=C(C2=CC=C1)C=CC(=C3)C(C)C 234.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Fenchol 439711 Click to see CC1(C2CCC(C2)(C1O)C)C 154.25 unknown via CMAUP database
Borneol 6552009 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
5beta,6beta-Dihydroxyboschnaloside 21609758 Click to see CC1CC(C2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown via CMAUP database
6beta-Hydroxyboschnaloside 101923515 Click to see CC1CC(C2C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown via CMAUP database
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown via CMAUP database
Euphroside 14589173 Click to see CC1(CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O)O 376.36 unknown via CMAUP database
Geniposidic acid 443354 Click to see C1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 374.34 unknown via CMAUP database
Plantarenaloside 155882 Click to see CC1CCC2(C1C(OC=C2C=O)OC3C(C(C(C(O3)CO)O)O)O)O 360.36 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid 8742 Click to see C1C(C(C(C=C1C(=O)O)O)O)O 174.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,2'R,4beta)-3,3',4,4'-Tetrahydro-2alpha,2'alpha-bis(3,4-dihydroxyphenyl)-4'beta-(benzylthio)-4,8'-bi(2H-1-benzopyran)-3alpha,3'alpha,5,5',7,7'-hexol 10372558 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=C(C(=CC(=C23)O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O 700.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(4S)-Epicatechin benzylthioether 10645351 Click to see C1=CC=C(C=C1)CSC2C(C(OC3=CC(=CC(=C23)O)O)C4=CC(=C(C=C4)O)O)O 412.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin 73202 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene 5316874 Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC 240.30 unknown via CMAUP database
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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