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Ranunculus ternatus

Ranunculus ternatus - 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 UUID643fffae3c585416308150
Scientific name Ranunculus ternatus
Authority Thunb.
First published in Fl. Jap. (Thunberg) 241. 1784 [Aug 1784]

Description Top

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Synonyms Top

Scientific name Authority First published in
Ranunculus extorris Hance Ann. Sci. Nat., Bot. , sér. 5, 5: 204 (1866)
Ranunculus formosanus Masam. J. Soc. Trop. Agric. 2: 48 (1930)
Ranunculus leiocladus Hayata Icon. Pl. Formosan. 3: 7 (1913)
Ranunculus zuccarinii Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 5 (1867)
Ranunculus taquetii H.Lév. Repert. Spec. Nov. Regni Veg. 9: 449 (1911)
Ranunculus zuccarinii var. dissectissimus Migo J. Shanghai Sci. Inst. Sect. 3 , 3: 4 (1934)
Ranunculus dissectissimus (Migo) Luferov Novosti Sist. Vyssh. Rast. 45: 147 (2014)

Common names Top

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Language Common/alternative name
English catclaw buttercup
Japanese ヒキノカサ
Korean 개구리갓
Chinese 小毛茛
Chinese 小毛莨
Chinese 猫爪草
Chinese 貓爪草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Ranunculus ternatus var. dissectissimus (Migo) Hand.-Mazz. Acta Horti Gothob. 13: 167 1939

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000461999
Tropicos 27104957
KEW urn:lsid:ipni.org:names:713964-1
The Plant List kew-2525186
PFAF Ranunculus ternatus
Open Tree Of Life 685195
Observations.org 506006
NCBI Taxonomy 376254
IPNI 713964-1
iNaturalist 543459
GBIF 3923071
EPPO RANTE
Elurikkus 649129
CMAUP NPO1136

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
An exploration of the effect of Chinese herbal compound on the occurrence and development of large intestine cancer and intestinal flora Liu P, Ying J, Guo X, Tang X, Zou W, Wang T, Xu X, Zhao B, Song N, Cheng J Heliyon 10-Dec-2023
PMCID:PMC10761579
doi:10.1016/j.heliyon.2023.e23533
PMID:38173486
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
Yiqi Chutan Formula Reverses Cisplatin-Induced Apoptosis and Ferroptosis of Skeletal Muscle by Alleviating Oxidative Stress Wu Y, Pi D, Zhou S, Wang W, Ye H, Yi Z, Chen Y, Ouyang M Integr Cancer Ther 03-May-2023
PMCID:PMC10161340
doi:10.1177/15347354231172117
PMID:37132527
Chinese medicinal herbs for reducing endocrine therapy-induced side effects in patients with hormone receptor‐positive breast cancer: a systematic review and meta-analysis Chen S, Gao Y, Liu H, Jing J, Yang Z, Zhu H, Chen B, Wang Y, Zhang T, Wang S, Lin J Pharm Biol 25-Apr-2023
PMCID:PMC10132232
doi:10.1080/13880209.2023.2203193
PMID:37096936
Bio-Derived Furanic Compounds with Natural Metabolism: New Sustainable Possibilities for Selective Organic Synthesis Romashov LV, Kucherov FA, Kozlov KS, Ananikov VP Int J Mol Sci 16-Feb-2023
PMCID:PMC9966152
doi:10.3390/ijms24043997
PMID:36835429
Therapeutic Potential of Extracts from Macaranga tanarius (MTE) in Diabetic Nephropathy Hsu YC, Chang CC, Hsieh CC, Shih YH, Chang HC, Lin CL Plants (Basel) 02-Feb-2023
PMCID:PMC9920382
doi:10.3390/plants12030656
PMID:36771740
Bibliometric Analysis and Visualization of Research Progress in the Diabetic Nephropathy Field from 2001 to 2021 Shao Y, Shi X Oxid Med Cell Longev 21-Jan-2023
PMCID:PMC9884171
doi:10.1155/2023/4555609
PMID:36718276
Traditional Herbal Medicine: A Potential Therapeutic Approach for Adjuvant Treatment of Non-small Cell Lung Cancer in the Future Huang J, Li JX, Ma LR, Xu DH, Wang P, Li LQ, Yu LL, Li Y, Li RZ, Zhang H, Zheng YH, Tang L, Yan PY Integr Cancer Ther 25-Dec-2022
PMCID:PMC9806388
doi:10.1177/15347354221144312
PMID:36567455
Using omics approaches to dissect the therapeutic effects of Chinese herbal medicines on gastrointestinal cancers Li SY, Wang WJ, Li QY, Yang PH, Li XL, Yan Y, Yuan Y, Feng YB, Hong M Front Pharmacol 23-Sep-2022
PMCID:PMC9538923
doi:10.3389/fphar.2022.884822
PMID:36210831
Therapeutic Potential of Ranunculus Species (Ranunculaceae): A Literature Review on Traditional Medicinal Herbs Goo YK Plants (Basel) 17-Jun-2022
PMCID:PMC9227133
doi:10.3390/plants11121599
PMID:35736749
Deciphering the Effects and Mechanisms of Yi-Fei-San-Jie-pill on Non-Small Cell Lung Cancer With Integrating Network Target Analysis and Experimental Validation Yang H, Guo Q, Wu J, Zhong L, Sun L, Liu W, Wang J, Lin L Front Pharmacol 11-May-2022
PMCID:PMC9130494
doi:10.3389/fphar.2022.851554
PMID:35645820
New Therapeutic Horizon of Graves’ Hyperthyroidism: Treatment Regimens Based on Immunology and Ingredients From Traditional Chinese Medicine He Q, Dong H, Gong M, Guo Y, Xia Q, Gong J, Lu F Front Pharmacol 05-Apr-2022
PMCID:PMC9020194
doi:10.3389/fphar.2022.862831
PMID:35462920
Bushen Jianpi Formula Combined with Entecavir for the Treatment of HBeAg-Negative Chronic Hepatitis B: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial Zhang JH, Zhang X, Zhou ZH, Zhu XJ, Zheng C, Li M, Jin SG, Mao DW, Xue JD, Shi WB, Chi XL, Wang XB, Li XD, Li Y, Wang H, Li Q, Zhou DQ, Wang CB, Shi CH, Li CZ, Wu JH, Kong XN, Sun XH, Gao YQ Evid Based Complement Alternat Med 25-Mar-2022
PMCID:PMC8975667
doi:10.1155/2022/6097221
PMID:35368769
Ranunculus ternatus Thunb extract attenuates renal fibrosis of diabetic nephropathy via inhibiting SMYD2 Xu W, Peng R, Chen S, Wu C, Wang X, Yu T, Jian J, Zhang N, Zuo S, Chen M, Guo B, Liu L Pharm Biol 10-Feb-2022
PMCID:PMC8843125
doi:10.1080/13880209.2022.2030759
PMID:35142600
The TCM Prescription Yi-Fei-Jie-Du-Tang Inhibit Invasive Migration and EMT of Lung Cancer Cells by Activating Autophagy Wang S, Wang Z, Wu Y, Hou C, Dai X, Wang Q, Wu Y, Qian C, Zhang X Evid Based Complement Alternat Med 29-Jan-2022
PMCID:PMC8817838
doi:10.1155/2022/9160616
PMID:35132327

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 / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Protocatechuic acid, methyl ester 287064 Click to see COC(=O)C1=CC(=C(C=C1)O)O 168.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
4-Ethoxy-4-oxobutanoic acid 70610 Click to see CCOC(=O)CCC(=O)O 146.14 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Monomethyl succinate 77487 Click to see COC(=O)CCC(=O)O 132.11 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z)-9,10-dideuteriooctadec-9-enoic acid 13011408 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 284.50 unknown via CMAUP database
2-Dodecyl-3-methylbutanedioic acid 99891 Click to see CCCCCCCCCCCCC(C(C)C(=O)O)C(=O)O 300.40 unknown via CMAUP database
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Elaidic Acid 637517 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Azelaic Acid 2266 Click to see C(CCCC(=O)O)CCCC(=O)O 188.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Gamma-keto acids and derivatives
Levulinic acid 11579 Click to see CC(=O)CCC(=O)O 116.11 unknown via CMAUP database
Methyl 5-hydroxy-4-oxopentanoate 10464455 Click to see COC(=O)CCC(=O)CO 146.14 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
6-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4(9),5,7,15,17,19-octaen-14-one 163077522 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C5=C(N4)C6=NC7=CC=CC=C7C(=O)N6CC5)O)O)O)O)O)O 611.60 unknown https://doi.org/10.1248/CPB.55.1267
6-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4(9),5,7,15,17,19-octaen-14-one 73409886 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=C(N4)C=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O 465.50 unknown https://doi.org/10.1248/CPB.55.1267
6-[3,4,5-Trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4(9),5,7,15,17,19-octaen-14-one 73409887 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C5=C(N4)C6=NC7=CC=CC=C7C(=O)N6CC5)O)O)O)O)O)O 611.60 unknown https://doi.org/10.1248/CPB.55.1267
Ternatoside C 17757758 Click to see C1CN2C(=NC3=CC=CC=C3C2=O)C4=C1C5=C(N4)C=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O 465.50 unknown https://doi.org/10.1248/CPB.55.1267
Ternatoside D 17757759 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C5=C(N4)C6=NC7=CC=CC=C7C(=O)N6CC5)O)O)O)O)O)O 611.60 unknown https://doi.org/10.1248/CPB.55.1267
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Ternatusine A 71681275 Click to see C1C2=C(N(C=C2C3C(OC1(O3)CO)C(CO)O)CCCC(=O)O)C=O 355.34 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(r)-5-(Hydroxymethyl)dihydrofuran-2(3h)-one 6950353 Click to see C1CC(=O)OC1CO 116.11 unknown via CMAUP database
(S)-3-Hydroxy-4,4-dimethyldihydrofuran-2(3H)-one 736053 Click to see CC1(COC(=O)C1O)C 130.14 unknown via CMAUP database
(s)-5-(Hydroxymethyl)dihydrofuran-2(3h)-one 2733813 Click to see C1CC(=O)OC1CO 116.11 unknown via CMAUP database
5-(hydroxymethyl)dihydrofuran-2(3H)-one 98431 Click to see C1CC(=O)OC1CO 116.11 unknown via CMAUP database
DL-Pantolactone 989 Click to see CC1(COC(=O)C1O)C 130.14 unknown via CMAUP database
Pantolactone 439368 Click to see CC1(COC(=O)C1O)C 130.14 unknown via CMAUP database
> 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 via CMAUP database
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database

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