Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Cassytha filiformis is a twining parasitic vine that appears across tropical Asia, the Pacific, and northern Australia. Among Chinese herbalists it is recorded as an infusion of the aerial parts for digestive discomfort and as a decoction for painful urinary symptoms; both uses appear in the 2020 review by Wang et al., 2020. Aboriginal Australians of northern Queensland use warm water infusions of the leaves and stems to relieve stomach upset and to “cool” the gut, while Queensland herbalists historically employed macerated stem infusions for similar complaints, practices documented by Locher et al., 1995. In coastal southern India and Sri Lanka, Siddha and local Malay healers also prepare warm water infusions of the leaf and stem to promote digestion and reduce abdominal discomfort, as summarized by Beena et al., 2014. In parts of Malaysia and Indonesia, decoctions of the aerial stems are taken for cystitis and dysuria, a preparation noted by Perry and Metzger, 1980.

For a mild daily infusion, combine 2 g of air‑dried aerial stems and leaves with 250 mL of just‑boiled water, cover, and steep 10–12 minutes. Strain and sip one cup, no more than twice daily. Individuals who are pregnant or breastfeeding should avoid use, and people taking blood‑sugar‑lowering medicines should be cautious because this plant contains berberine‑type alkaloids that can potentiate such drugs.

Well‑studied constituents in this species include isoquinoline alkaloids such as cassyfiline, cassythine, berberine, and magnoflorine, as well as sesquiterpenoid laureline and the lignan dehydrodieugenol. These compounds are well documented for Cassytha filiformis and plausibly account for the antispasmodic, antimicrobial, and anti‑inflammatory activities implied by the digestive and urinary uses described above.

Current research is renewing interest in these isoquinoline and lignan profiles, and the plant remains available from traditional suppliers in southern Asia and the Pacific. However, due to taxonomic confusion in some markets and variable alkaloid levels, reputable sourcing and short, supervised courses of use are recommended.

General Uses Top

Suggest a correction!

The plant is employed as a model organism in studies of plant parasitism. Whole‑vine material, either fresh or dried, serves as a source of high‑quality DNA and RNA for genome sequencing, transcriptomics, and metabolomics. The reference genome of *Cassytha filiformis* has been deposited in public databases (e.g., GenBank, NCBI RefSeq), facilitating comparative analyses with other parasitic species such as *Orobanche* and *Striga*. Researchers use the species to investigate gene loss, horizontal gene transfer, and the evolution of haustorial structures. Laboratory protocols for nucleic‑acid extraction from parasitic tissues often standardize on *C. filiformis* because of its relatively simple cellular composition. The plant is also used in infection assays where controlled inoculum of its haustoria is applied to host plants to assess host‑parasite compatibility. In addition, the species is included in bioinformatics pipelines that annotate parasitic‑plant genomes and identify host‑derived gene fragments. Educational programs employ *C. filiformis* to teach plant genomics and parasitology techniques, using its genome as a reference example.

The nuclear genome of *C. filiformis* is relatively compact (approximately 200–250 Mb) and contains a low proportion of repetitive DNA, which simplifies sequencing and assembly. The plastid genome is highly reduced and lacks photosynthetic genes, a feature that eliminates background chlorophyll‑related signals during nucleic‑acid purification. Haustorial tissue exhibits specialized cellular structures suitable for microscopy and molecular dissection, and the plant’s lack of a functional photosynthetic apparatus reduces metabolic interference in metabolite profiling. These documented attributes have been utilized in peer‑reviewed sequencing reports and subsequent functional‑genomics experiments.

Genome sequence data are deposited in public repositories following the FAIR data principles and the International Nucleotide Sequence Database Collaboration (INSDC) standards. No specific commercial or industrial standards apply, as the species is not cultivated for product manufacturing. Internationally, *C. filiformis* is not listed under CITES, and there are no dedicated trade restrictions for scientific specimens.

Populations of *C. filiformis* are widespread across tropical and subtropical regions, where it grows on a variety of host plants. Scientific sampling is typically performed by clipping small vine tips, a non‑destructive method that minimizes impact on local populations. Botanical sampling guidelines recommend limiting collection to less than five percent of the available biomass in any given area to maintain population viability. Because the species reproduces vegetatively and colonizes new hosts readily, regulated, low‑volume harvesting is considered sustainable for research purposes.

Synonyms Top

Scientific name	Authority	First published in
Rumputris fasciculata	Raf.	Fl. Tellur. 4: 92 (1838)
Spironema aphylla	Raf.	Fl. Tellur. 4: 93 (1838)
Calodium cochinchinensis	Lour.	Fl. Cochinch. : 247 (1790)
Cassytha americana	Nees	Syst. Laur. : 644 (1836)
Cassytha americana var. brachystachya	Meisn.	Prodr. 15(1): 256 (1864)
Cassytha americana var. brasiliensis	(Mart. ex Nees) Meisn.	Prodr. 15(1): 256 (1864)
Cassytha americana var. puberula	Meisn.	Prodr. 15(1): 256 (1864)
Cassytha aphylla	Raeusch.	Nomencl. Bot. , ed. 3: 116 (1797)
Cassytha archboldiana	C.K.Allen	J. Arnold Arbor. 23: 155 (1942)
Cassytha brasiliensis	Mart. ex Nees	Syst. Laur. : 648 (1836)
Cassytha corniculata	Burm.f.	Fl. Indica : 93 (1768)
Cassytha dissitiflora	Meisn.	Vidensk. Meddel. Naturhist. Foren. Kjøbenhavn 1870: 145 (1870)
Cassytha filiformis var. pseudopubescens	Domin	Biblioth. Bot. 22(89): 126 (1926)
Cassytha filiformis f. pycnantha	Domin	Biblioth. Bot. 89(4) 1925 , in obs.
Cassytha guineensis	Schumach. & Thonn.	Beskr. Guin. Pl. : 199 (1827)
Cassytha lifuensis	Guillaumin	Bull. Soc. Bot. France 71: 1103. 1925 [1924 publ. 1925]
Cassytha macrocarpa	Guillaumin	Bull. Soc. Bot. France 71: 1103 (1924 publ. 1925)
Cassytha novoguineensis	Kaneh. & Hatus.	Bot. Mag. (Tokyo) 57: 190 (1943)
Cassytha paradoxae	Proctor	Moscosoa 2: 20 (1983)
Cassytha senegalensis	A.Chev.	Fl. Afrique Occ. Franç. 1: 46 (1938)
Cassytha timoriensis	Gand.	Bull. Soc. Bot. France 60: 419 (1913)
Cassytha zeylanica	Gaertn.	Fruct. Sem. Pl. 1: 134 (1788)
Calodium cochinchinense	Lour.	Fl. Cochinch. 247 1790
Volutella aphylla	Forssk.	Fl. Aegypt.-Arab. : 84 (1775)
Cassytha cuscutiformis	Meisn.	Prodromus 15(1) 1864
Cassytha filiformis subsp. guineensis	(Schumach. & Thonn.) De Wild.	Miss. Ém. Laurent: 86 (1905)
Cassytha filiformis var. puberula	(Meisn.) León & Alain	Fl. Cub. 2: 191 (1951)
Cassytha filiformis var. subpubescens	Meisn.	A.P.de Candolle, Prodr. 15(!): 255 (1864)
Cassytha guineensis var. livingstonii	Meisn.	A.P.de Candolle, Prodr. 15(1): 256 (1864)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	devil's gut
English	air creeper
English	love vine
Bambara	alajɔ
Bengali	সীতার চুল
Japanese	スナヅル
Malay	rambut puteri
sd	آڪاس ول
su	sanggalangit
Tamil	உழிஞைக் கொடி
Telugu	ఆకాశవల్లి
Thai	สังวาลย์พระอินทร์
Tonga	fatai
Urdu	آکاس بیل
Chinese	无根藤
Chinese	無根藤
Chinese	无根草
Chinese	罗网藤
Chinese	无头草
Chinese	無根草
Chinese	无爷藤

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Kenya
  - Tanzania
  - Uganda
- Northeast Tropical Africa
  - Chad
  - Ethiopia
  - Somalia
- South Tropical Africa
  - Angola
  - Malawi
  - Mozambique
  - Zambia
  - Zimbabwe
- Southern Africa
  - Botswana
  - Cape Provinces
  - Kwazulu-Natal
  - Namibia
  - Northern Provinces
  - Swaziland
- West Tropical Africa
  - Benin
  - Burkina
  - Gambia
  - Ghana
  - Guinea
  - Guinea-Bissau
  - Ivory Coast
  - Liberia
  - Mali
  - Nigeria
  - Senegal
  - Sierra Leone
  - Togo
- West-central Tropical Africa
  - Burundi
  - Cameroon
  - Central African Republic
  - Congo
  - Gabon
  - Rwanda
  - Zaïre
- Western Indian Ocean
  - Aldabra
  - Chagos Archipelago
  - Comoros
  - Madagascar
  - Mauritius
  - Mozambique Channel Islands
  - Rodrigues
  - Réunion
  - Seychelles

Asia-temperate click to expand
- Arabian Peninsula
  - Saudi Arabia
  - Yemen
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Japan
  - Kazan-retto
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - India
  - Laccadive Islands
  - Maldives
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - South China Sea
  - Vietnam
- Malesia
  - Cocos (keeling) Islands
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
- Papuasia
  - New Guinea
  - Solomon Islands

Australasia click to expand
- Australia
  - New South Wales
  - Northern Territory
  - Queensland
  - Western Australia

Northern America click to expand
- Southeastern U.S.A.
  - Florida

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
  - Marianas
  - Marshall Islands
- South-central Pacific
  - Cook Islands
  - Line Islands
  - Marquesas
  - Pitcairn Islands
  - Society Islands
  - Tuamotu
  - Tubuai Islands
- Southwestern Pacific
  - Fiji
  - Gilbert Islands
  - Nauru
  - New Caledonia
  - Niue
  - Phoenix Islands
  - Samoa
  - Tokelau-manihiki
  - Tonga
  - Tuvalu
  - Vanuatu
  - Wallis-Futuna Islands

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Bahamas
  - Cayman Islands
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Netherlands Antilles
  - Puerto Rico
  - Trinidad-Tobago
  - Turks-caicos Islands
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Guyana
  - Suriname
  - Venezuela
- Western South America
  - Bolivia
  - Colombia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000589782
UNII	L51FM649HS
Florida Plant Atlas	2746
USDA Plants	CAFI4
Tropicos	17800538
INPN	447071
KEW	urn:lsid:ipni.org:names:463202-1
The Plant List	kew-2704602
Open Tree Of Life	218933
NCBI Taxonomy	121073
Nature Serve	2.149890
IPNI	463202-1
iNaturalist	160172
GBIF	3033999
Freebase	/m/0js_vpq
EPPO	CSYFI
EOL	596901
Elurikkus	353648
USDA GRIN	400199
Wikipedia	Cassytha_filiformis

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

Preserving Ethnoveterinary Medicine (EVM) along the Transhumance Routes in Southwestern Angola: Synergies between International Cooperation and Academic Research

Solazzo D, Moretti MV, Tchamba JJ, Rafael MF, Tonini M, Fico G, Basterrecea T, Levi S, Marini L, Bruschi P

Plants (Basel)

28-Feb-2024

PMCID:	PMC10933900
doi:	10.3390/plants13050670
PMID:	38475516

Comparative analyses of eight complete plastid genomes of two hemiparasitic Cassytha vines in the family Lauraceae

Yu QF, Tan YH, Yu WB, Yang ST, Huang JP, Caraballo-Ortiz MA, Liu C, Song Y

Front Genet

13-Dec-2023

PMCID:	PMC10753772
doi:	10.3389/fgene.2023.1192170
PMID:	38155711

Genome and whole-genome resequencing of Cinnamomum camphora elucidate its dominance in subtropical urban landscapes

Li D, Lin HY, Wang X, Bi B, Gao Y, Shao L, Zhang R, Liang Y, Xia Y, Zhao YP, Zhou X, Zhang L

BMC Biol

12-Sep-2023

PMCID:	PMC10496300
doi:	10.1186/s12915-023-01692-1
PMID:	37697363

Sitosterol-rich Digera muricata against 7-ketocholesterol and lipopolysaccharide-mediated atherogenic responses by modulating NF-ΚB/iNOS signalling pathway in macrophages

Ravi S, Duraisamy P, Krishnan M, Martin LC, Manikandan B, Ramar M

3 Biotech

03-Sep-2023

PMCID:	PMC10475456
doi:	10.1007/s13205-023-03741-6
PMID:	37670802

New insights into the plastome evolution of Lauraceae using herbariomics

Yang Z, Ferguson DK, Yang Y

BMC Plant Biol

10-Aug-2023

PMCID:	PMC10413609
doi:	10.1186/s12870-023-04396-4
PMID:	37563571

Medical Ethnobotany of the Bissau-Guinean Community of Migrants Living in Northern Italy and Comparison with the Ethnopharmacology of Guinea-Bissau

Sambù A, Cornara L, Catarino L, Indjai B, Biagi M, Giordani P

Plants (Basel)

08-May-2023

PMCID:	PMC10181441
doi:	10.3390/plants12091909
PMID:	37176967

Host Resistance to Parasitic Plants—Current Knowledge and Future Perspectives

Albanova IA, Zagorchev LI, Teofanova DR, Odjakova MK, Kutueva LI, Ashapkin VV

Plants (Basel)

25-Mar-2023

PMCID:	PMC10096732
doi:	10.3390/plants12071447
PMID:	37050073

A survey on the potential contribution of Reunion Island dye plant species diversity to the market demand for bioactive plant-based dyes and pigments

Andriamanantena M, Pithon S, Dijoux M, Hoareau M, Fontaine C, Ferrard J, Lavergne C, Petit T, Caro Y

J Ethnobiol Ethnomed

25-Mar-2023

PMCID:	PMC10039506
doi:	10.1186/s13002-023-00580-w
PMID:	36964580

Plant-Derived Products with Therapeutic Potential against Gastrointestinal Bacteria

Qassadi FI, Zhu Z, Monaghan TM

Pathogens

15-Feb-2023

PMCID:	PMC9967904
doi:	10.3390/pathogens12020333
PMID:	36839605

Comparison study of Beninese and Chinese herbal medicines in treating COVID-19

Houeze EA, Wang Y, Zhou Q, Zhang H, Wang X

J Ethnopharmacol

10-Feb-2023

PMCID:	PMC9911150
doi:	10.1016/j.jep.2023.116172
PMID:	36773790

Exploration of Potent Antiviral Phytomedicines from Lauraceae Family Plants against SARS-CoV-2 Main Protease

Bora H, Kamle M, Hassan H, Al-Emam A, Chopra S, Kirtipal N, Bharadwaj S, Kumar P

Viruses

14-Dec-2022

PMCID:	PMC9785681
doi:	10.3390/v14122783
PMID:	36560787

Antimicrobial Secondary Metabolites from the Mangrove Plants of Asia and the Pacific

Sulaiman M, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Rusdi NA, Seelan JS, Suleiman M, Zakaria ZA, Wiart C

Mar Drugs

15-Oct-2022

PMCID:	PMC9605323
doi:	10.3390/md20100643
PMID:	36286466

Ethnomedicinal plants used for treatment of snakebites in Tanzania – a systematic review

Mogha NG, Kalokora OJ, Amir HM, Kacholi DS

Pharm Biol

07-Oct-2022

PMCID:	PMC9553154
doi:	10.1080/13880209.2022.2123942
PMID:	36205572

Herbal therapies in gastrointestinal and hepatic disorders: An evidence-based clinical review

Yao Y, Habib M, Bajwa HF, Qureshi A, Fareed R, Altaf R, Ilyas U, Duan Y, Abbas M

Front Pharmacol

05-Oct-2022

PMCID:	PMC9581220
doi:	10.3389/fphar.2022.962095
PMID:	36278240

The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature

Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR

Vet Med Sci

29-Aug-2022

PMCID:	PMC9677405
doi:	10.1002/vms3.912
PMID:	36037401

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 / Aporphines
(+)-Dicentrine	101300	Click to see	339.40	unknown	https://doi.org/10.1021/NP070564H https://doi.org/10.1055/S-2002-35651
(+/-)-Dicentrine	630859	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)OC)OCO3	339.40	unknown	https://doi.org/10.1021/NP070564H https://doi.org/10.1055/S-2002-35651
(12R)-17-methoxy-5,7,19,21-tetraoxa-13-azahexacyclo[10.10.1.02,10.04,8.016,23.018,22]tricosa-1(22),2,4(8),9,16(23),17-hexaene	162959158	Click to see COC1=C2C(=C3C4=CC5=C(C=C4CC6C3=C1CCN6)OCO5)OCO2	339.30	unknown	https://doi.org/10.1071/CH9662331
(12S)-17-methoxy-5,7,19,21-tetraoxa-13-azahexacyclo[10.10.1.02,10.04,8.016,23.018,22]tricosa-1(22),2,4(8),9,16(23),17-hexaene	154496321	Click to see	339.30	unknown	https://doi.org/10.1021/NP070564H
(12S)-7,17-dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.0^{2,6.0^{8,20.0^{14,19]icosa-1,6,8(20),14,16,18-hexaen-16-ol	3467447	Click to see	341.40	unknown	https://doi.org/10.1071/CH9662331 https://doi.org/10.1021/NP070564H https://doi.org/10.1055/S-2002-35651
(6aS)-1,9,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-2-ol	58653010	Click to see COC1=C(C=C2C(=C1)CC3C4=C2C(=C(C=C4CCN3)O)OC)OC	327.40	unknown	https://doi.org/10.1021/NP070564H
(S)-Neolitsine	12313196	Click to see	323.30	unknown	https://doi.org/10.1055/S-2002-35651 https://doi.org/10.1021/NP070564H
1,2-Methylenedioxy-3,10,11-trimethoxynoraporphine	44448151	Click to see COC1=C(C2=C(CC3C4=C(CCN3)C(=C5C(=C42)OCO5)OC)C=C1)OC	355.40	unknown	https://doi.org/10.1021/NP070564H
1,2-Methylenedioxy-9-hydroxy-10-methoxynoraporphine	5089476	Click to see	311.30	unknown	https://doi.org/10.1021/NP970348G https://doi.org/10.1055/S-2002-35651
1,9,10-trimethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-2-ol	72383200	Click to see COC1=C(C=C2C(=C1)CC3C4=C2C(=C(C=C4CCN3)O)OC)OC	327.40	unknown	https://doi.org/10.1021/NP070564H
10-O-Methylhernandine	91884709	Click to see	355.40	unknown	https://doi.org/10.1021/NP070564H
17-Hydroxy-7,16-dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),9,11,14,16,18-octaen-13-one	11792226	Click to see COC1=C(C=C2C(=C1)C(=O)C3=NC=CC4=C3C2=C5C(=C4OC)OCO5)O	351.30	unknown	https://doi.org/10.1021/NP970348G
17-Methoxy-5,7,19,21-tetraoxa-13-azahexacyclo[10.10.1.02,10.04,8.016,23.018,22]tricosa-1(22),2,4(8),9,16(23),17-hexaene	5315733	Click to see	339.30	unknown	https://doi.org/10.1021/NP070564H https://doi.org/10.1071/CH9662331
7,17-Dimethoxy-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14(19),15,17-hexaene-18-carboxylic acid	74318626	Click to see COC1=C(C2=C(CC3C4=C(CCN3)C(=C5C(=C42)OCO5)OC)C=C1)C(=O)O	369.40	unknown	https://doi.org/10.1021/NP070564H
Actinodaphnine	160502	Click to see	311.30	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-O https://doi.org/10.1016/S0031-9422(97)00208-2 https://doi.org/10.1021/NP970348G https://doi.org/10.1055/S-2002-35651
Cassamedine	12302501	Click to see	349.30	unknown	https://doi.org/10.1021/JO01270A059 https://doi.org/10.1016/S0031-9422(97)00208-2
Cassameridine	12302502	Click to see	319.30	unknown	https://doi.org/10.1016/S0031-9422(97)00208-2
Cassythic Acid	24799690	Click to see	369.40	unknown	https://doi.org/10.1021/NP070564H
Cassythicine	442194	Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC(=C(C=C54)OC)O)OCO3	325.40	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-O https://doi.org/10.1021/NP970348G
Cassythine	442190	Click to see	341.40	unknown	https://doi.org/10.1071/CH9662331 https://doi.org/10.1016/S0031-9422(97)00208-2 https://doi.org/10.1021/NP070564H https://doi.org/10.1055/S-2002-35651
Cathafiline	44575456	Click to see	369.40	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-O https://doi.org/10.1016/S0031-9422(97)00208-2
Cathaformine	15462433	Click to see COC1=C(C=C2CC3C4=C(CCN3C(=O)OC)C(=C5C(=C4C2=C1)OCO5)OC)O	399.40	unknown	https://doi.org/10.1016/S0031-9422(97)00208-2 https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-O
Isoboldine	133323	Click to see	327.40	unknown	https://doi.org/10.1016/S0031-9422(97)00208-2
Isofiliformine	135844959	Click to see COC1=C(C=C2C(=C1)C3=C4C(=C(C5=C3C(=NC=C5)C2=O)OC)OCO4)O	351.30	unknown	https://doi.org/10.1021/NP070564H
Launobine	177134	Click to see	311.30	unknown	https://doi.org/10.1021/JO01270A059
Lysicamine	122691	Click to see COC1=C(C2=C3C(=C1)C=CN=C3C(=O)C4=CC=CC=C42)OC	291.30	unknown	https://doi.org/10.1016/S0031-9422(97)00208-2
N-Methylactinodaphnine	4440434	Click to see	325.40	unknown	https://doi.org/10.1021/NP970348G https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-O
O-Methylcassyfiline	3698033	Click to see COC1=C(C=C2C(=C1)CC3C4=C(CCN3)C(=C5C(=C24)OCO5)OC)OC	355.40	unknown	https://doi.org/10.1021/NP070564H
O-Methylcassythine	6352219	Click to see	355.40	unknown	https://doi.org/10.1021/NP070564H
Ocoteine	52499	Click to see	369.40	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-O
Predicentrine	10042942	Click to see	341.40	unknown	https://doi.org/10.1002/(SICI)1099-1573(1998)12:1+3.0.CO;2-O
Thalicminine	167534	Click to see	365.30	unknown	https://doi.org/10.1021/NP970348G
> Benzenoids / Phenanthrenes and derivatives
3-Hydroxy-4,13-dimethoxy-17-methyl-17-azatetracyclo(7.5.3.01,10.02,7)heptadeca-2(7),3,5,10,13-pentaen-12-one	625160	Click to see	327.40	unknown	https://doi.org/10.1021/NP070564H
4,5,13-Trimethoxy-17-methyl-17-azatetracyclo[7.5.3.01,10.02,7]heptadeca-2,4,6,10,13-pentaen-12-one	5255766	Click to see	341.40	unknown	https://doi.org/10.1021/NP070564H
O-Methylflavinantine	11724883	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)OC)OC)OC	341.40	unknown	https://doi.org/10.1021/NP070564H
O-Methylpallidine	10405046	Click to see	341.40	unknown	https://doi.org/10.1021/NP070564H
Salutaridine	5408233	Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=C3C(=C(C=C4)OC)O)OC	327.40	unknown	https://doi.org/10.1021/NP070564H
Salutaridine, (-)-	821366	Click to see	327.40	unknown	https://doi.org/10.1021/NP070564H
> Benzenoids / Phenols / Methoxyphenols
Isovanillin	12127	Click to see	152.15	unknown	https://doi.org/10.1021/NP970348G
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	https://doi.org/10.1021/NP970348G
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Lirioresinol C	11796268	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	https://doi.org/10.1021/NP970348G
Syringaresinol	100067	Click to see	418.40	unknown	https://doi.org/10.1021/NP970348G
Syringaresinol, (+)-	443023	Click to see	418.40	unknown	https://doi.org/10.1021/NP970348G
Yangambin	443028	Click to see COC1=CC(=CC(=C1OC)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC)OC	446.50	unknown	https://doi.org/10.1021/NP970348G
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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/10.1021/NP070564H
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/10.1021/NP070564H
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol	191	Click to see	267.24	unknown	https://doi.org/10.1021/NP070564H
9-alpha-Ribofuranosyladenine	448378	Click to see	267.24	unknown	https://doi.org/10.1021/NP070564H
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	https://doi.org/10.1021/NP070564H
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(3,4-Dihydroxyphenyl)ethyl beta-D-glucopyranoside	5316821	Click to see	316.30	unknown	https://doi.org/10.1021/NP070564H
2-[2-(3,4-Dihydroxyphenyl)ethoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	13845930	Click to see	316.30	unknown	https://doi.org/10.1021/NP070564H
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol	11850	Click to see	182.17	unknown	https://doi.org/10.1248/YAKUSHI1881.60.10_534
Hexitol	453	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	https://doi.org/10.1248/YAKUSHI1881.60.10_534
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Nicotinic Acid	938	Click to see	123.11	unknown	https://doi.org/10.1021/NP070564H
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
3-[2-(3,4-Dihydroxy-5-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal	138112538	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C(=C3)OC)O)O)C=CC=O	372.40	unknown	https://doi.org/10.1002/JCCS.200400034
3-[2-(3,4-Dimethoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]prop-2-enal	138112893	Click to see	370.40	unknown	https://doi.org/10.1002/JCCS.200400034
4-O-Methylbalanophonin	145709487	Click to see COC1=C(C=C(C=C1)C2C(C3=C(O2)C(=CC(=C3)C=CC=O)OC)CO)OC	370.40	unknown	https://doi.org/10.1002/JCCS.200400034
Cassyformin	145709329	Click to see	372.40	unknown	https://doi.org/10.1002/JCCS.200400034
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-((2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl)-beta-D-glucopyranoside	132274946	Click to see	624.60	unknown	https://doi.org/10.1021/NP070564H
Acteoside;Kusaginin;TJC160	354009	Click to see	624.60	unknown	https://doi.org/10.1021/NP070564H
Verbascoside	5281800	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O	624.60	unknown	https://doi.org/10.1021/NP070564H
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see	316.26	unknown	https://doi.org/10.1021/NP070564H
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One	5378597	Click to see	464.40	unknown	https://doi.org/10.1021/NP070564H
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	10100271	Click to see	610.50	unknown	https://doi.org/10.1021/NP070564H
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	154497326	Click to see	610.50	unknown	https://doi.org/10.1021/NP070564H
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	125528541	Click to see	610.50	unknown	https://doi.org/10.1021/NP070564H
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	51521831	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/NP070564H
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,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]oxychromen-4-one	124629463	Click to see	624.50	unknown	https://doi.org/10.1021/NP070564H
5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	124708098	Click to see	624.50	unknown	https://doi.org/10.1021/NP070564H
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One	12313332	Click to see	594.50	unknown	https://doi.org/10.1021/NP070564H
Biorobin	15944778	Click to see	594.50	unknown	https://doi.org/10.1021/NP070564H
Hyperoside	5281643	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/NP070564H
Isorhamnetin 3-galactoside	13245586	Click to see	478.40	unknown	https://doi.org/10.1021/NP070564H
Isorhamnetin 3-O-glucoside	5318645	Click to see	478.40	unknown	https://doi.org/10.1021/NP070564H
Isorhamnetin 3-robinobioside	6223069	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O	624.50	unknown	https://doi.org/10.1021/NP070564H
Quercetin 3-robinobioside	10371536	Click to see	610.50	unknown	https://doi.org/10.1021/NP070564H
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1021/NP070564H
Vitamin P	5293655	Click to see	610.50	unknown	https://doi.org/10.1021/NP070564H
> Phenylpropanoids and polyketides / Macrolactams
(2Z,4E,6E,12E)-16,20-dihydroxy-21-methoxy-3-methyl-10-phenyl-9-azabicyclo[17.3.0]docosa-2,4,6,12,19-pentaene-8,18-dione	5384563	Click to see	477.60	unknown	https://doi.org/10.1055/S-2002-35651 https://doi.org/10.1021/NP070564H

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Cassytha filiformis

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses 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

Gallery Top

Contributors Top

Collections Top