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Hydrangea febrifuga

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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 UUID64406264d7014717894426
Scientific name Hydrangea febrifuga
Authority (Lour.) Y.De Smet & C.Granados
First published in Taxon 64: 750 (2015)

Description Top

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Synonyms Top

Scientific name Authority First published in
Adamia chinensis Gardner & Champ. Hooker's J. Bot. Kew Gard. Misc. 1: 311 (1849)
Adamia cyanea Wall. Tent. Fl. Napal. : 46 (1826)
Adamia sylvatica Meisn. Repert. Bot. Syst. 2: 377 (1843)
Cyanitis chinensis Hook.f. & Thomson J. Proc. Linn. Soc., Bot. 2: 76 (1857)
Cyanitis versicolor Hook.f. & Thomson J. Proc. Linn. Soc., Bot. 2: 76 (1857)
Dichroa cyanea (Wall.) Schltr. Dict. Prat. Hort. 2: 202 (1893-1894)
Dichroa cyanitis Miq. Fl. Ned. Ind. 1(1): 721 (1856)
Dichroa henryi H.Lév. Sert. Yunnan. : 1 (1916)
Dichroa latifolia Miq. Fl. Ned. Ind. 1(1): 722 (1856)
Dichroa parviflora Schltr. Bot. Jahrb. Syst. 52: 121 (1914)
Dichroa pentandra Schltr. Bot. Jahrb. Syst. 52(1-2): 121. 1914 [24 Nov 1914]
Dichroa philippinensis Schltr. Bot. Jahrb. Syst. 52: 122 (1914)
Dichroa pubescens Miq. Fl. Ned. Ind. 1(1): 722 (1856)
Dichroa schumanniana Schltr. Bot. Jahrb. Syst. 52: 122 (1914)
Dichroa yunnanensis S.M.Hwang Acta Phytotax. Sin. 25: 387 (1987)
Hydrangea pubescens Zipp. ex Miq. Fl. Ned. Ind. 1(1): 722 (1856)
Dichroa febrifuga Lour. Fl. Cochinch. : 301 (1790)
Cianitis sylvatica Reinw. Syll. Pl. Nov. 2: 11. 1825
Dichroa febrifuga var. glabra S.Y.Hu J. Arnold Arbor. 61: 77 (1980)

Common names Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
    • Papuasia
      • New Guinea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001344651
KEW urn:lsid:ipni.org:names:77152127-1
Open Tree Of Life 221379
NCBI Taxonomy 152286
IPNI 77152127-1
GBIF 8682693

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
Halofuginone-guided nano-local therapy: Nano-thermosensitive hydrogels for postoperative metastatic canine mammary carcinoma with scar removal Zuo R, Kong L, Pang W, Jiang S Int J Pharm X 26-Mar-2024
PMCID:PMC10987322
doi:10.1016/j.ijpx.2024.100241
PMID:38572023
Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India Ralte L, Sailo H, Singh YT J Ethnobiol Ethnomed 03-Jan-2024
PMCID:PMC10765666
doi:10.1186/s13002-023-00642-z
PMID:38172927
Nrf2, A Target for Precision Oncology in Cancer Prognosis and Treatment Ngo HK, Le H, Surh YJ J Cancer Prev 30-Dec-2023
PMCID:PMC10774478
doi:10.15430/JCP.2023.28.4.131
PMID:38205365
Aminoacyl-tRNA synthetase interactions in SARS-CoV-2 infection Khan D, Fox PL Biochem Soc Trans 18-Dec-2023
PMCID:PMC10754286
doi:10.1042/BST20230527
PMID:38108455
Integrated Stress Response (ISR) Pathway: Unraveling Its Role in Cellular Senescence Kalinin A, Zubkova E, Menshikov M Int J Mol Sci 13-Dec-2023
PMCID:PMC10743681
doi:10.3390/ijms242417423
PMID:38139251
Two haplotype-resolved genomes reveal important flower traits in bigleaf hydrangea (Hydrangea macrophylla) and insights into Asterid evolution Wu X, Simpson SA, Youngblood RC, Liu XF, Scheffler BE, Rinehart TA, Alexander LW, Hulse-Kemp AM Hortic Res 09-Nov-2023
PMCID:PMC10734616
doi:10.1093/hr/uhad217
PMID:38130599
Extensive characterization of 28 complete chloroplast genomes of Hydrangea species: A perspective view of their organization and phylogenetic and evolutionary relationships Raman G, Choi KS, Lee EM, Morden CW, Shim H, Kang JS, Yang TJ, Park S Comput Struct Biotechnol J 10-Oct-2023
PMCID:PMC10589384
doi:10.1016/j.csbj.2023.10.010
PMID:37867966
Molecular Identification and Pathogenicity of Diaporthe eres and D. hongkongensis (Diaporthales, Ascomycota) Associated with Cherry Trunk Diseases in China Chen P, Abeywickrama PD, Ji S, Zhou Y, Li X, Zhang W, Yan J Microorganisms 26-Sep-2023
PMCID:PMC10609160
doi:10.3390/microorganisms11102400
PMID:37894058
Phytochemicals targeting glycolysis in colorectal cancer therapy: effects and mechanisms of action Zhan L, Su F, Li Q, Wen Y, Wei F, He Z, Chen X, Yin X, Wang J, Cai Y, Gong Y, Chen Y, Ma X, Zeng J Front Pharmacol 24-Aug-2023
PMCID:PMC10484417
doi:10.3389/fphar.2023.1257450
PMID:37693915
Analysis of the RNA Editing Sites and Orthologous Gene Function of Transcriptome and Chloroplast Genomes in the Evolution of Five Deutzia Species Cai H, Ren Y, Du J, Liu L, Long L, Yang M Int J Mol Sci 19-Aug-2023
PMCID:PMC10454583
doi:10.3390/ijms241612954
PMID:37629135
In silico identification of natural compounds against SARS-CoV-2 main protease from Chinese herbal medicines Kuang Y, Shen W, Ma X, Wang Z, Xu R, Rao Q, Yang S Future Sci OA 14-Jun-2023
PMCID:PMC10357396
doi:10.2144/fsoa-2023-0055
PMID:37485448
Plants, Cells, Algae, and Cyanobacteria In Vitro and Cryobank Collections at the Institute of Plant Physiology, Russian Academy of Sciences—A Platform for Research and Production Center Yuorieva N, Sinetova M, Messineva E, Kulichenko I, Fomenkov A, Vysotskaya O, Osipova E, Baikalova A, Prudnikova O, Titova M, Nosov AV, Popova E Biology (Basel) 09-Jun-2023
PMCID:PMC10295647
doi:10.3390/biology12060838
PMID:37372123
Natural Nrf2 Inhibitors: A Review of Their Potential for Cancer Treatment Zhang J, Xu HX, Zhu JQ, Dou YX, Xian YF, Lin ZX Int J Biol Sci 04-Jun-2023
PMCID:PMC10321279
doi:10.7150/ijbs.82401
PMID:37416770
Control of fibrosis with enhanced safety via asymmetric inhibition of prolyl‐tRNA synthetase 1 Yoon I, Kim S, Cho M, You KA, Son J, Lee C, Suh JH, Bae D, Kim JM, Oh S, Park S, Kim S, Cho SH, Park S, Bang K, Seo M, Kim JH, Lee B, Park JS, Hwang KY, Kim S EMBO Mol Med 22-May-2023
PMCID:PMC10331583
doi:10.15252/emmm.202216940
PMID:37212275
EPRS1 Controls the TGF-β Signaling Pathway via Interaction with TβRI in Hepatic Stellate Cell Yoon I, Song JA, Suh JH, Kim S, Son J, Kim JH, Jang SY, Hwang KY, Kim MH, Kim S Mol Cell Biol 08-May-2023
PMCID:PMC10184599
doi:10.1080/10985549.2023.2205344
PMID:37154023

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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1248/YAKUSHI1947.111.6_299
> 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/10.1248/YAKUSHI1947.111.6_299
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/10.1248/YAKUSHI1947.111.6_299
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
Hydrangenol 119199 Click to see C1C(OC(=O)C2=C1C=CC=C2O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1248/YAKUSHI1947.111.6_299
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
(+)-Isofebrifugine 11208839 Click to see C1CC(C(NC1)CC(=O)CN2C=NC3=CC=CC=C3C2=O)O 301.34 unknown https://doi.org/10.1055/S-2006-960230
https://doi.org/10.1021/NP970433O
https://doi.org/10.1021/JM990131E
1H-quinazolin-4-one 63112 Click to see C1=CC=C2C(=C1)C(=O)N=CN2 146.15 unknown https://doi.org/10.1021/NP970433O
3-(3-(3-Hydroxypiperidin-2-yl)-2-oxopropyl)quinazolin-4(3H)-one 115723 Click to see C1CC(C(NC1)CC(=O)CN2C=NC3=CC=CC=C3C2=O)O 301.34 unknown https://doi.org/10.1021/JA01171A080
https://doi.org/10.1021/JA01185A028
https://doi.org/10.1021/JA01186A031
3-[[(2S,3aS,7aR)-2-hydroxy-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridin-2-yl]methyl]quinazolin-4-one 137795500 Click to see C1CC2C(CC(O2)(CN3C=NC4=CC=CC=C4C3=O)O)NC1 301.34 unknown https://doi.org/10.1021/JA01186A031
https://doi.org/10.1021/JA01185A028
https://doi.org/10.1021/JA01171A080
3-[[(3aS,7aS)-2-hydroxy-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridin-2-yl]methyl]quinazolin-4-one 431195 Click to see C1CC2C(CC(O2)(CN3C=NC4=CC=CC=C4C3=O)O)NC1 301.34 unknown https://doi.org/10.1021/JA01171A080
https://doi.org/10.1021/JA01185A028
https://doi.org/10.1021/JA01186A031
beta-Dichroine 63224 Click to see C1CC(C(NC1)CC(=O)CN2C=NC3=CC=CC=C3C2=O)O 301.34 unknown https://doi.org/10.1055/S-2006-960230
https://doi.org/10.1021/JA01186A031
https://doi.org/10.1021/NP970433O
https://doi.org/10.1021/JA01185A028
https://doi.org/10.1021/JM990131E
https://doi.org/10.1021/JA01171A080
Halofuginone 456390 Click to see C1CC(C(NC1)CC(=O)CN2C=NC3=CC(=C(C=C3C2=O)Cl)Br)O 414.70 unknown https://doi.org/10.1016/0304-4165(93)90123-P
Isofebrifugine 9851693 Click to see C1CC2C(CC(O2)(CN3C=NC4=CC=CC=C4C3=O)O)NC1 301.34 unknown https://doi.org/10.1021/JM990131E
https://doi.org/10.1021/NP970433O
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-8-methoxycoumarin 5316302 Click to see COC1=C(C=CC2=C1OC(=O)C=C2)O 192.17 unknown https://doi.org/10.1248/YAKUSHI1947.111.6_299
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1248/YAKUSHI1947.111.6_299

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