Scientific name	Authority	First published in
Mirtana loureiroi	Pierre	Bull. Soc. Bot. France 52: 490 (1905)
Menispermum flavescens	Lam.	Encycl. 4: 98 (1797)
Tinospora havilandii	Diels	Pflanzenr. , IV, 94: 138 (1910)
Anamirta flavescens	Miq.	Fl. Ned. Ind. 1(2): 79 (1858)
Anamirta florescens	Müll.Berol.	Ann. Bot. Syst. 7: 63 (1868)
Anamirta luctuosa	Miers	Contr. Bot. 3: 55 (1871)
Anamirta lemniscata	Miers	Contr. Bot. 3: 54 (1871)
Anamirta lourieri	Pierre	Fl. Forest. Cochinch. t. 110.
Arcangelisia inclyta	Becc.	Malesia 1: 147 (1877)
Arcangelisia lemniscata	Becc.	Malesia 1: 147 (1877)
Arcangelisia loureiroi	Diels	Pflanzenr. , IV, 94: 104 (1910)
Cocculus flavescens	DC.	Syst. Nat. 1: 520 (1817)
Menispermum flavum	L.	Herb. Amboin. (Linn.) 18. 1754 [11 May 1754]

Common names Top

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Filter by language:

Language	Common/alternative name
Thai	ขมิ้นเครือ
Chinese	黄连藤
Chinese	黄古山龙
Chinese	黄古山龍

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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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 click to expand
- China
  - Hainan

Asia-tropical click to expand
- Indo-China
  - Laos
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000543220
Tropicos	50311085
KEW	urn:lsid:ipni.org:names:580199-1
The Plant List	kew-2646763
Open Tree Of Life	698903
NCBI Taxonomy	461553
IPNI	580199-1
GBIF	3830318
EOL	5517211
USDA GRIN	403218

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 Use of Natural Bioactive Nutraceuticals in the Management of Tick-Borne Illnesses

Shor SM, Schweig SK

Microorganisms

05-Jul-2023

PMCID:	PMC10384908
doi:	10.3390/microorganisms11071759
PMID:	37512931

Babesiosis: Current status and future perspectives in Pakistan and chemotherapy used in livestock and pet animals

Azhar M, Gadahi JA, Bhutto B, Tunio S, Vistro WA, Tunio H, Bhutto S, Ram T

Heliyon

18-Jun-2023

PMCID:	PMC10333442
doi:	10.1016/j.heliyon.2023.e17172
PMID:	37441378

Analytical determination, antioxidant and anti-inflammatory activities of Bhamrung-Lohit a traditional Thai medicine

Panchakul C, Thongdeeying P, Itharat A, Pipatrattanaseree W, Kongkwamcharoen C, Davies NM

Res Pharm Sci

01-Jun-2023

PMCID:	PMC10443669
doi:	10.4103/1735-5362.378091
PMID:	37614616

A Review of Medicinal Plants with Renoprotective Activity in Diabetic Nephropathy Animal Models

Putra IM, Fakhrudin N, Nurrochmad A, Wahyuono S

Life (Basel)

16-Feb-2023

PMCID:	PMC9963806
doi:	10.3390/life13020560
PMID:	36836916

A Review of Fibraurea tinctoria and Its Component, Berberine, as an Antidiabetic and Antioxidant

Purwaningsih I, Maksum IP, Sumiarsa D, Sriwidodo S

Molecules

29-Jan-2023

PMCID:	PMC9919506
doi:	10.3390/molecules28031294
PMID:	36770960

13-Butoxyberberine Bromide Inhibits Migration and Invasion in Skin Cancer A431 Cells

Laomethakorn P, Tayeh M, Samosorn S, Tananyuthawongse C, Watanapokasin R

Molecules

19-Jan-2023

PMCID:	PMC9921070
doi:	10.3390/molecules28030991
PMID:	36770659

Potential Antimicrobe Producer of Endophytic Bacteria from Yellow Root Plant (Arcangelisia flava (L.)) Originated from Enggano Island

Sipriyadi, Masrukhin, Wibowo RH, Darwis W, Yudha S, Purnaningsih I, Siboro R

Int J Microbiol

16-Nov-2022

PMCID:	PMC10270767
doi:	10.1155/2022/6435202
PMID:	37332491

Development of a DNA barcode library of plants in the Thai Herbal Pharmacopoeia and Monographs for authentication of herbal products

Urumarudappa SK, Tungphatthong C, Jaipaew J, Pornputtapong N, Pakdeesattayapong D, Vimolmangkang S, Sukrong S

Sci Rep

10-Jun-2022

PMCID:	PMC9187672
doi:	10.1038/s41598-022-13287-x
PMID:	35688884

Plants with Therapeutic Potential for Ischemic Acute Kidney Injury: A Systematic Review

Ali A, Lima Sampaio T, Khan H, Jeandet P, Küpeli Akkol E, Bahadar H, Costa Martins AM

Evid Based Complement Alternat Med

23-May-2022

PMCID:	PMC9152371
doi:	10.1155/2022/6807700
PMID:	35656467

Ethnomedicinal Plants in Herbal Remedies Used for Treatment of Skin Diseases by Traditional Healers in Songkhla Province, Thailand

Saising J, Maneenoon K, Sakulkeo O, Limsuwan S, Götz F, Voravuthikunchai SP

Plants (Basel)

25-Mar-2022

PMCID:	PMC9003147
doi:	10.3390/plants11070880
PMID:	35406860

Apoptosis Induction, a Sharp Edge of Berberine to Exert Anti-Cancer Effects, Focus on Breast, Lung, and Liver Cancer

Zhu Y, Xie N, Chai Y, Nie Y, Liu K, Liu Y, Yang Y, Su J, Zhang C

Front Pharmacol

27-Jan-2022

PMCID:	PMC8830521
doi:	10.3389/fphar.2022.803717
PMID:	35153781

Drug-Herb Interactions among Thai Herbs and Anticancer Drugs: A Scoping Review

Jiso A, Khemawoot P, Techapichetvanich P, Soopairin S, Phoemsap K, Damrongsakul P, Wongwiwatthananukit S, Vivithanaporn P

Pharmaceuticals (Basel)

26-Jan-2022

PMCID:	PMC8880589
doi:	10.3390/ph15020146
PMID:	35215264

Comparative toxicity, phytochemistry, and use of 53 Philippine medicinal plants

Clemen-Pascual LM, Macahig RA, Rojas NR

Toxicol Rep

10-Dec-2021

PMCID:	PMC8685920
doi:	10.1016/j.toxrep.2021.12.002
PMID:	34976744

Current Status, Distribution, and Future Directions of Natural Products against Colorectal Cancer in Indonesia: A Systematic Review

Illian DN, Hafiz I, Meila O, Utomo AR, Nuryawan A, Siregar GA, Basyuni M

Molecules

17-Aug-2021

PMCID:	PMC8398396
doi:	10.3390/molecules26164984
PMID:	34443572

The use of antimalarial plants as traditional treatment in Papua Island, Indonesia

Budiarti M, Maruzy A, Mujahid R, Sari AN, Jokopriyambodo W, Widayat T, Wahyono S

Heliyon

14-Dec-2020

PMCID:	PMC7736719
doi:	10.1016/j.heliyon.2020.e05562
PMID:	33344788

Phytochemical Profile Top

Add a new one!

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
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-17-olate	10426199	Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)[O-]	321.30	unknown	https://doi.org/10.1021/NP50023A011
Berberine	2353	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC	336.40	unknown	https://doi.org/10.1021/NP50023A011
Columbamine	72310	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC	338.40	unknown	https://doi.org/10.1021/NP50023A011
Dehydrocorydaline	34781	Click to see CC1=C2C=CC(=C(C2=C[N+]3=C1C4=CC(=C(C=C4CC3)OC)OC)OC)OC	366.40	unknown	https://doi.org/10.1021/NP50023A011
Dehydrocorydalmine	3083983	Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)OC	338.40	unknown	https://doi.org/10.1021/NP50023A011
Palmatine	19009	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC	352.40	unknown	https://doi.org/10.1021/NP50023A011
Thalifendine	3084288	Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O	322.30	unknown	https://doi.org/10.1021/NP50023A011
> Benzenoids / Phenols / Methoxyphenols
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1016/J.PHYTOL.2011.07.002
> Lignans, neolignans and related compounds
Limacine	7656034	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC	608.70	unknown	https://doi.org/10.1021/NP50023A011
Thalrugosine	100257	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC	608.70	unknown	https://doi.org/10.1021/NP50023A011
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,2R,4R,10S,11R,12S,14S)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.02,7.012,14]pentadec-7-en-6-one	162923295	Click to see CC12CC=C3C(=O)OC(CC3(C1CC4C(C2(C(=C)OC)O)O4)C)C5=COC=C5	386.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.07.002
(1R,2R,4R,7R,10S,11R,12S,14S)-4-(furan-3-yl)-11-hydroxy-11-(1-methoxyethenyl)-2,10-dimethyl-5,13-dioxatetracyclo[8.5.0.02,7.012,14]pentadecan-6-one	162938141	Click to see CC12CCC3C(=O)OC(CC3(C1CC4C(C2(C(=C)OC)O)O4)C)C5=COC=C5	388.50	unknown	https://doi.org/10.1016/J.PHYTOL.2011.07.002
methyl (2R,4aS,6aR,9S,10aS,10bS)-2-(furan-3-yl)-9-hydroxy-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate	162947949	Click to see CC12CCC3C(=O)OC(CC3(C1CC(C=C2C(=O)OC)O)C)C4=COC=C4	374.40	unknown	https://doi.org/10.1248/CPB.33.479
Tinophyllol	101607221	Click to see CC12CCC3C(=O)OC(CC3(C1CC(C=C2C(=O)OC)O)C)C4=COC=C4	374.40	unknown	https://doi.org/10.1248/CPB.35.4839 https://doi.org/10.1248/CPB.33.479
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	https://doi.org/10.1016/J.PHYTOL.2011.07.002
> Organoheterocyclic compounds / Dihydroisoquinolines
Pycnarrhine	20056242	Click to see C[N+]1=CC2=CC(=C(C=C2CC1)OC)O	192.23	unknown	https://doi.org/10.1021/NP50023A011
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one	10065647	Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC	337.40	unknown	https://doi.org/10.1021/NP50023A011
> Organoheterocyclic compounds / Naphthopyrans
(1R,2S,3R,5R,10R,11S,12R,13R,15R)-5-(furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione	163030293	Click to see CC12CC(OC(=O)C1=CC(C3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6	388.40	unknown	https://doi.org/10.1248/CPB.33.479
(1R,2S,3R,5R,11S,12R,13R,15R)-5-(furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione	162924412	Click to see CC12CC=C3C(=O)OC(CC3(C1C4C5C(C2(C(=O)O4)O)O5)C)C6=COC=C6	372.40	unknown	https://doi.org/10.1248/CPB.33.479
(1R,2S,3S,5R,8S,10S,11S,12R)-5-(furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione	162961158	Click to see CC12CC(OC(=O)C1CC(C3(C2C4C=CC3(C(=O)O4)O)C)O)C5=COC=C5	374.40	unknown	https://doi.org/10.1248/CPB.35.4839
(1R,2S,5R,8R,10R,11R,13R,16S)-8-(furan-3-yl)-1,16-dihydroxy-2,10-dimethyl-15-methylidene-7,14-dioxatetracyclo[11.2.1.02,11.05,10]hexadecan-6-one	162866617	Click to see CC12CCC3C(=O)OC(CC3(C1CC4C(C2(C(=C)O4)O)O)C)C5=COC=C5	374.40	unknown	https://doi.org/10.1016/J.PHYTOL.2011.07.002
(1R,3S,5R,11R,12R)-5-(furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione	134745274	Click to see CC12CC=C3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)O)C)C5=COC=C5	356.40	unknown	https://doi.org/10.1248/CPB.33.479
(1S,2R,3R,5R,8S,10S,11R,12S)-5-(furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione	162961159	Click to see CC12CC(OC(=O)C1CC(C3(C2C4C=CC3(C(=O)O4)O)C)O)C5=COC=C5	374.40	unknown	https://doi.org/10.1248/CPB.33.479
(1S,2R,3S,5R,8S,10S,11R,12S,13R,15R)-5-(furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadecane-7,17-dione	162963992	Click to see CC12CC(OC(=O)C1CC(C3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6	390.40	unknown	https://doi.org/10.1248/CPB.33.479
(1S,2S,3S,5R,10S,11S,12S,13S,15S)-5-(furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione	163030292	Click to see CC12CC(OC(=O)C1=CC(C3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6	388.40	unknown	https://doi.org/10.1248/CPB.35.4839
(1S,2S,3S,5R,11S,12S,13S,15S)-5-(furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione	21626390	Click to see CC12CC(OC(=O)C1=CC(C3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6	388.40	unknown	https://doi.org/10.1248/CPB.35.4839 https://doi.org/10.1248/CPB.33.479
(1S,2S,3S,5R,8S,10S,11S,12S,13S,15S)-5-(furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadecane-7,17-dione	162963993	Click to see CC12CC(OC(=O)C1CC(C3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6	390.40	unknown	https://doi.org/10.1248/CPB.35.4839
5-(Furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione	73813159	Click to see CC12CC(OC(=O)C1CC(C3(C2C4C=CC3(C(=O)O4)O)C)O)C5=COC=C5	374.40	unknown	https://doi.org/10.1248/CPB.35.4839 https://doi.org/10.1248/CPB.33.479
5-(Furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione	73813165	Click to see CC12CC(OC(=O)C1=CC(C3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6	388.40	unknown	https://doi.org/10.1248/CPB.33.479 https://doi.org/10.1248/CPB.35.4839
5-(Furan-3-yl)-10,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadecane-7,17-dione	14059405	Click to see CC12CC(OC(=O)C1CC(C3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6	390.40	unknown	https://doi.org/10.1248/CPB.33.479 https://doi.org/10.1248/CPB.35.4839
5-(Furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione	56678199	Click to see CC12CC=C3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)O)C)C5=COC=C5	356.40	unknown	https://doi.org/10.1248/CPB.35.4839
5-(Furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione	12309884	Click to see CC12CC=C3C(=O)OC(CC3(C1C4C5C(C2(C(=O)O4)O)O5)C)C6=COC=C6	372.40	unknown	https://doi.org/10.1248/CPB.35.4839 https://doi.org/10.1248/CPB.33.479 https://doi.org/10.1016/J.PHYTOL.2011.07.002
Fibleucin	44589004	Click to see CC12CC=C3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)O)C)C5=COC=C5	356.40	unknown	https://doi.org/10.1248/CPB.35.4839
Fibraurin	21626387	Click to see CC12CC=C3C(=O)OC(CC3(C1C4C5C(C2(C(=O)O4)O)O5)C)C6=COC=C6	372.40	unknown	https://doi.org/10.1248/CPB.33.479 https://doi.org/10.1248/CPB.35.4839 https://doi.org/10.1016/J.PHYTOL.2011.07.002
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Peganetin	5491743	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)OC3C(C(C(C(O3)COC(=O)C)O)O)O)OC4=CC(=C5C(=C4)OC(=CC5=O)C6=CC=C(C=C6)OC)O)COC7C(C(C(C(O7)CO)O)O)O)O)O)O	958.90	unknown	https://doi.org/10.1248/CPB.35.4839 https://doi.org/10.1248/CPB.33.479

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Arcangelisia flava

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

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