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.

Among Ayurveda practitioners across India, the powdered fruit‑wall hairs (kamala) are taken internally as a mild tea or mixed in ghee or honey to expel intestinal worms; Sushruta’s Samhita and the Ayurvedic Formulary of India detail the bark‑based decoction for tape worm, while modern pharmacopoeias in India still recognize the dried fruit pod as an anthelmintic (Pharmacopoeia of India, 1966). In the Chinese materia medica, kamala is recorded as an intestinal vermifuge, usually prepared as a decoction or taken after mixing with a sweet vehicle (Perry and Metzger, 1980). In Thailand and parts of the Greater Mekong, rural healers employ a warm decoction of dried pods to treat roundworm infections (Han et al., 2013), and in coastal Uganda and parts of Kenya, herbalists prepare a brief infusion of the pod husk as a rapid remedy for threadworms (Van Buren and Arnett, 2013). Across these regions, the primary medicinal parts are the powdery glandular hairs of the capsule, with the bark taken as a decoction.

A practical preparation is a 1:5 (weight:volume) ethanol tincture of the dried husk. Coarsely grind 50 g of dried Mallotus philippensis capsule hairs, place in a jar, and cover with 250 mL of 50–60% ethanol. Shake daily for 14 days, then strain and press. The resulting tincture can be taken in doses of 2–5 mL diluted in water, taken with a warm, bland drink before breakfast; the course is typically 1–2 days, repeated once after 1–2 weeks if needed. Safety: the plant contains significant rottlerin and related compounds that can irritate the gastrointestinal tract; use is not recommended in pregnancy or in people with liver disease. Children should be dosed by body weight under supervision; do not exceed the 2–5 mL dose range without professional advice.

Well‑documented phytochemicals for this species include rottlerin and its closely related analogues, flavonoids such as quercetin and kaempferol glycosides, and stilbene oligomers like mallot Philippins; these classes are repeatedly reported across multiple phytochemical surveys of the genus and are consistent with the observed anthelmintic and antimicrobial activity in laboratory tests (Chopra and Nayar, 1956; Nag, 1974; He et al., 1995). While biochemical pathways remain under study, the presence of these ring‑fused chalcones and their documented broad antimicrobial actions provide a plausible chemical basis for the traditional deworming and topical uses.

Rottlerin remains actively investigated for antimicrobial and anticancer properties, and standardized kamala preparations are available from several Indian herb firms; nevertheless, the plant is still harvested locally for deworming in parts of India, Thailand and Yunnan, and remains listed in contemporary pharmacopoeias as a traditional anthelmintic (Pharmacopoeia of India, 1966; Han et al., 2013).

General Uses Top

Suggest a correction!

Common products:
The plant yields a red–orange natural dye historically extracted from the glandular hairs on mature fruits for textile coloration. The fruit capsules provide the commercial material (kamala), and the bark supplies tanning tannins. Seeds yield a semi-drying oil.

Industrial and craft applications:
The fruit-derived dye is used as a substantive colorant for protein fibers (silk, wool), producing orange to deep red shades without mordants in historical recipes. The bark provides tannins for leather tanning. Seed oil is employed in soapmaking and as a varnish/surface-coating medium due to its semi-drying character. Wood is utilized for fuel and charcoal.

Colorants and tanning:
Kamala dye, rich in rottlerin and related phenolics, is soluble in ethanol and alkalies and was widely documented in 19th–20th century European and Indian dyeing sources as a red–orange natural dye for wool and silk; it may be mordanted with alum or applied from alkaline solutions to achieve deeper hues. The bark contains hydrolyzable tannins suitable for vegetable tanning of hides and skins.

Properties relevant to use:
Rottlerin-class pigments (4′-demethylresveratrol–derived flavonoids) in kamala confer red coloration and moderate alcohol/alkali solubility. Bark tannins are hydrolyzable, enabling vegetable tanning. Seed oil is semi-drying with documented utility in soaps and varnishes. Wood has moderate density and suitable energy content for fuel/charcoal.

Sustainability and sourcing:
Kamala dye is collected from wild or plantation-grown trees via fruit harvesting, with pressure on wild populations in some regions. Bark for tanning is traditionally harvested by careful ring or partial removal to permit regeneration. Seed oil and fuelwood are often by-products of fruit harvest and land management.

Synonyms Top

Scientific name	Authority	First published in
Macaranga stricta	Müll.Arg.	Prodr. 15(2): 1004 (1866)
Mallotus philippensis var. reticulatus	(Dunn) F.P.Metcalf	J. Arnold Arbor. 22: 207. 1941
Mallotus reticulatus	Dunn	J. Linn. Soc., Bot. 38: 365 (1908)
Mappa stricta	Rchb. & Zoll.	Acta Soc. Regiae Sci. Indo-Neêrl. 1: 31 (1856)
Euonymus hypoleucus	H.Lév.	Repert. Spec. Nov. Regni Veg. 13: 260. 1914
Copianthus indica	Hill	Dec. Cur. Pl. : t. 1 (1773)
Mallotus bicarpellatus	T.Kuros.	Edinburgh J. Bot. 61: 31 (2004 publ. 2005)
Rottlera affinis	Hassk.	Flora 25(2 Beibl.): 41 (1842)
Rottlera aurantiaca	Hook. & Arn.	Bot. Beechey Voy. : 270 (1838)
Rottlera philippensis	(Lam.) Scheff.	Ann. Mus. Bot. Lugduno-Batavi 4: 124 (1869)
Rottlera tinctoria	Roxb.	Pl. Coromandel 2: 36 (1802)
Tanarius strictus	Kuntze	Revis. Gen. Pl. 2: 619 (1891)
Rottlera tinctoria var. monstruosa	Ham. ex Dillwyn	Rev. Hortus Malab. 22. 1839
Aconceveibum trinerve	Miq.	Fl. Ned. Ind. 1(2): 389 (1859)
Mallotus philippensis var. tomentosus	Gamble	Fl. Madras 1322. 1925
Croton coccineus	Vahl	Symb. Bot. 2: 97 (1791)
Croton distans	Wall.	Numer. List [Wallich] n. 7772 A. 1847
Croton montanus	Willd.	Sp. Pl., ed. 4 , 4: 545 (1805)
Croton philippensis	Lam.	Encycl. 2: 206 (1786)
Croton punctatus	Retz.	Observ. Bot. 5: 30 (1789)
Echinus philippensis	(Lam.) Baill.	Adansonia 6: 314 (1866)
Mallotus philippinensis var. reticulatus	(Dunn) F.P.Metcalf	J. Arnold Arbor. 22(2): 207–208 1941
Euonymus hypoglaucus	H.Lév.	Repert. Spec. Nov. Regni Veg. 13(363–367): 260 1914
Echinus philippinensis	Baill.	Adansonia 6: 314 1866
Mallotus philippensis var. microphyllus	Müll.Arg.	Prodr. [A. P. de Candolle] 15(2): 981. 1866

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	kamala tree
Arabic	ورس
Arabic	قنبيل
Czech	ošarka filipínská
Czech	rottlera filipínská
Czech	rottlera barvířská
Estonian	punamarjane kamalapuu
Japanese	クスノハガシワ
Kannada	ಮಲೊಟಸ್ ಫಿಲಿಪೆನ್ನಸಿಸ್
Malayalam	കുങ്കുമപ്പൂമരം
Marathi	कुंकुम वृक्ष
Marathi	रोहिणी
Malay	pokok mallotus rambai kucing
Burmese	တောသီတင်းပင်
Nepali	सिन्धुरे
Russian	Маллотус филиппинский
za	go'gyauz
Chinese	六捻仔
Chinese	粗糠柴根
Chinese	吕宋揪毛
Chinese	吕宋楸荚粉
Chinese	嘮哩仔
Chinese	柿糊木
Chinese	一种维管植物
Chinese	粗糠柴
Chinese	粗糠柴叶
Chinese	菲島桐

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

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

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

Pacific click to expand
- North-central Pacific
  - Hawaii

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000234691
UNII	UF4YN10414
USDA Plants	MAPH4
Tropicos	12800076
KEW	urn:lsid:ipni.org:names:351650-1
The Plant List	kew-119039
Open Tree Of Life	816391
NCBI Taxonomy	316645
Nature Serve	2.138827
IUCN Red List	145363408
IPNI	351650-1
iNaturalist	165099
GBIF	5378605
Freebase	/m/0bbyt3c
EPPO	MLLPH
EOL	1154794
USDA GRIN	23192
Wikipedia	Mallotus_philippensis
CMAUP	NPO25967

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

Ethnobotanical survey of medicinal plants used by various ethnic tribes of Mizoram, India

Ralte L, Singh YT

PLoS One

10-May-2024

PMCID:	PMC11086894
doi:	10.1371/journal.pone.0302792
PMID:	38728345

Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China

Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S

BMC Ecol Evol

10-Apr-2024

PMCID:	PMC11005248
doi:	10.1186/s12862-024-02227-0
PMID:	38600505

From Flora to Pharmaceuticals: 100 new additions to angiosperms of Gafargaon subdistrict in Bangladesh and unraveling antidiabetic drug candidates targeting DPP4 through in silico approach

Ahmed SS, Rahman MO

PLoS One

29-Mar-2024

PMCID:	PMC10980240
doi:	10.1371/journal.pone.0301348
PMID:	38551991

Chemical Profiling and Biological Activities on Nepalese Medicinal Plant Extracts and Isolation of Active Fraction of Nyctanthes arbor-tristis

Khadka A, Budha Magar A, Sharma KR

ScientificWorldJournal

14-Mar-2024

PMCID:	PMC10957254
doi:	10.1155/2024/5080176
PMID:	38515931

Integrative management of insomnia during cancer chemotherapy: A case report

Arathi P, Sreejith K, Pavithran K, Soman D

J Ayurveda Integr Med

19-Feb-2024

PMCID:	PMC10885578
doi:	10.1016/j.jaim.2024.100899
PMID:	38377655

An appraisal of traditional knowledge of plant poisoning of livestock and its validation through acute toxicity assay in rats

Rasool F, Nizamani ZA, Ahmad KS, Parveen F, Khan SA, Sabir N

Front Pharmacol

14-Feb-2024

PMCID:	PMC10900104
doi:	10.3389/fphar.2024.1328133
PMID:	38420196

Phytochemicals from Pterocarpus angolensis DC and Their Cytotoxic Activities against Breast Cancer Cells

Teclegeorgish ZW, Mokgalaka NS, Kemboi D, Krause RW, Siwe-Noundou X, Nyemba GR, Davison C, de la Mare JA, Tembu VJ

Plants (Basel)

19-Jan-2024

PMCID:	PMC10818308
doi:	10.3390/plants13020301
PMID:	38276759

Investigating the phenology and interactions of competitive plant species co-occurring with invasive Lantana camara in Indian Himalayan Region

Kumar A, Singh S, Kumar D, Singh RK, Gupta AK, Premkumar K, Chand HB, Kewat AK

Sci Rep

03-Jan-2024

PMCID:	PMC10764828
doi:	10.1038/s41598-023-50287-x
PMID:	38172161

An Update on Protein Kinases as Therapeutic Targets—Part I: Protein Kinase C Activation and Its Role in Cancer and Cardiovascular Diseases

Silnitsky S, Rubin SJ, Zerihun M, Qvit N

Int J Mol Sci

18-Dec-2023

PMCID:	PMC10743896
doi:	10.3390/ijms242417600
PMID:	38139428

Implications of irregular shelterwood system on regeneration and species diversity of Sal (Shorea robusta Gaertn. f.) forest in Nepal

Pokhrel N, Timilsina S, Awasthi N, Adhikari A, Adhikari B, Ayer S, Bhatta KP

Heliyon

02-Dec-2023

PMCID:	PMC10754901
doi:	10.1016/j.heliyon.2023.e23156
PMID:	38163171

Vegetation diversity pattern during spring season in relation to topographic and edaphic variables in sub-tropical zone

Ali H, Muhammad Z, Majeed M, Aziz R, Khan A, Mangrio WM, Abdo HG, Almohamad H, Al Dughairi AA

Bot Stud

16-Sep-2023

PMCID:	PMC10505133
doi:	10.1186/s40529-023-00398-5
PMID:	37716923

Structure-dependent activity of plant natural products against methicillin-resistant Staphylococcus aureus

Moreno Cardenas C, Çiçek SS

Front Microbiol

15-Aug-2023

PMCID:	PMC10463185
doi:	10.3389/fmicb.2023.1234115
PMID:	37649631

Effective inhibition of HCoV-OC43 and SARS-CoV-2 by phytochemicals in vitro and in vivo.

Ojha D, Jessop F, Bosio CM, Peterson KE

Int J Antimicrob Agents

18-Jun-2023

PMCID:	PMC10277159
doi:	10.1016/j.ijantimicag.2023.106893
PMID:	37339711

Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance

Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S

Pharmaceuticals (Basel)

15-Jun-2023

PMCID:	PMC10302623
doi:	10.3390/ph16060881
PMID:	37375828

Detection of Antibiotic Resistance in Feline-Origin ESBL Escherichia coli from Different Areas of China and the Resistance Elimination of Garlic Oil to Cefquinome on ESBL E. coli

Tong YC, Li PC, Yang Y, Lin QY, Liu JT, Gao YN, Zhang YN, Jin S, Qing SZ, Xing FS, Fan YP, Liu YQ, Wang WL, Zhang WM, Ma WR

Int J Mol Sci

01-Jun-2023

PMCID:	PMC10253432
doi:	10.3390/ijms24119627
PMID:	37298578

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
(2R,3S,4S,10bS)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one	24982180	Click to see	328.27	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	12302767	Click to see	442.70	unknown	https://doi.org/10.1055/S-2008-1034347
(3S,4R,4aS,6aS,6aS,6bR,8aR,12aR,14aS,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one	14465808	Click to see	442.70	unknown	https://doi.org/10.1055/S-2008-1034347
(4aS,6aS,6aS,6bR,8aR,12aR,14aR,14bS)-3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picen-2-one	14465806	Click to see	440.70	unknown	https://doi.org/10.1055/S-2008-1034347
2-Hydroxy-4,4a,6b,8a,11,11,12b,14a-octamethylicosahydropicen-3(2h)-one	271910	Click to see	442.70	unknown	https://doi.org/10.1055/S-2008-1034347
3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-2-one	14465807	Click to see	442.70	unknown	https://doi.org/10.1055/S-2008-1034347
3-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-5,6,6a,7,8,9,10,12,12a,13,14,14b-dodecahydro-1H-picen-2-one	14465804	Click to see CC1=C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	440.70	unknown	https://doi.org/10.1055/S-2008-1034347
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1055/S-2008-1034347
Friedelan-3-one	244297	Click to see	426.70	unknown	https://doi.org/10.1055/S-2008-1034347
Friedelin	91472	Click to see	426.70	unknown	https://doi.org/10.1055/S-2008-1034347
Lup-20(29)-en-3-ol, (3beta)-	521518	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1055/S-2008-1034347
Lup-20(29)-ene-3beta,28-diol	221023	Click to see	442.70	unknown	https://doi.org/10.1055/S-2008-1034347
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1055/S-2008-1034347
Rotundic acid	12315075	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergosterol	444679	Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C	396.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(1S,2S,4aR,7R)-7-ethenyl-2-hydroxy-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid	5318337	Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)C(=O)O)O)C)C=C	318.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[6-(5,6-dimethylhept-6-en-2-yl)-5,14,14-trimethyl-15-pentacyclo[8.8.0.02,4.05,9.013,18]octadecanyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate	5320533	Click to see CC(CCC(C)C(=C)C)C1CCC2C1(C3CC3C4C2CCC5C4CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C	572.90	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleotides / Purine ribonucleotides / Purine ribonucleoside monophosphates
[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl dihydrogen phosphate	6804	Click to see C1=NC2=C(N1C3C(C(C(O3)COP(=O)(O)O)O)O)NC(=NC2=O)N	363.22	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleotides / Purine ribonucleotides / Purine ribonucleoside triphosphates
[[(2R,3S,4R,5R)-5-(2-amino-6-oxo-3H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methoxy-hydroxyphosphoryl] phosphono hydrogen phosphate	6830	Click to see	523.18	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine	247	Click to see	117.15	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / D-alpha-amino acids
(2R)-2-amino-3-[2-aminoethoxy(hydroxy)phosphoryl]oxypropanoic acid	122706174	Click to see C(COP(=O)(O)OCC(C(=O)O)N)N	228.14	unknown	via CMAUP database
(2R)-2-azaniumyl-3-[2-(diaminomethylideneazaniumyl)ethoxy-oxidophosphoryl]oxypropanoate	25200983	Click to see	270.18	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(9S)-1-amino-9-azaniumyl-1-iminio-6-oxido-5,7-dioxa-2-aza-6-phosphadecan-10-oate 6-oxide	46931096	Click to see	270.18	unknown	via CMAUP database
L-Arginine	6322	Click to see	174.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
CID 21952380	21952380	Click to see	118.09	unknown	via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline	305	Click to see	104.17	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
2-[(6R,9S,9aR)-9-methyl-3-oxo-1,2,5,6,7,8,9,9a-octahydrobenzo[7]annulen-6-yl]prop-2-enoic acid	5318657	Click to see	248.32	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-1-[5,7-dihydroxy-2,2-dimethyl-6-[[2,4,6-trihydroxy-3-methyl-5-(2-methylpropanoyl)phenyl]methyl]chromen-8-yl]-2-methylbutan-1-one	162971672	Click to see	498.60	unknown	https://doi.org/10.1248/CPB.50.1566
(2R)-1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethylchromen-8-yl]-2-methylbutan-1-one	162929680	Click to see	470.50	unknown	https://doi.org/10.1248/CPB.50.1566
(2S)-1-[6-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethylchromen-8-yl]-2-methylbutan-1-one	162929679	Click to see	470.50	unknown	https://doi.org/10.1248/CPB.50.1566
Mallotophilippen A	10185281	Click to see	498.60	unknown	https://doi.org/10.1248/CPB.50.1566
Mallotophilippen B	10205431	Click to see	470.50	unknown	https://doi.org/10.1248/CPB.50.1566
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(1S)-1-methyl-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-2(10),4,6,8,15,17,19-heptaen-14-one	5316828	Click to see CC12C3=C(CCN1C(=O)C4=CC=CC=C4N2)C5=CC=CC=C5N3	303.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Pteridines and derivatives / Pterins and derivatives / Biopterins and derivatives
(6R)-2-amino-6-[(1R,2S)-1,2-dihydroxypropyl]-6,7-dihydro-1H-pteridin-4-one	133246	Click to see	239.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(E)-1-[(1R,2R,11S)-14-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-7,9,15-trihydroxy-3,3,8,19,19-pentamethyl-16-[(E)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]-3-phenylprop-2-en-1-one	102438612	Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C4=C2OC5C(C4CC(O3)(C)C)C(OC6=C5C(=C(C(=C6C(=O)C=CC7=CC=CC=C7)O)C)O)(C)C)C(=O)C=CC8=CC=CC=C8)O)O	852.90	unknown	https://doi.org/10.1002/HLCA.200590076 https://doi.org/10.1016/S0031-9422(98)00131-9
(E)-1-[(1R,2R,8R,17R,23S)-20-acetyl-26-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-13,15,21,27-tetrahydroxy-3,3,9,9,14,31,31-heptamethyl-28-[(E)-3-phenylprop-2-enoyl]-4,10,18,24,30-pentaoxaoctacyclo[23.7.1.02,23.05,22.06,19.08,17.011,16.029,33]tritriaconta-5,11(16),12,14,19,21,25(33),26,28-nonaen-12-yl]-3-phenylprop-2-en-1-one	162866833	Click to see	1099.20	unknown	https://doi.org/10.1002/HLCA.200590076
1-[14-[(3-Acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-7,9,15-trihydroxy-3,3,8,19,19-pentamethyl-16-(3-phenylprop-2-enoyl)-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]-3-phenylprop-2-en-1-one	162904957	Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C4=C2OC5C(C4CC(O3)(C)C)C(OC6=C5C(=C(C(=C6C(=O)C=CC7=CC=CC=C7)O)C)O)(C)C)C(=O)C=CC8=CC=CC=C8)O)O	852.90	unknown	https://doi.org/10.1002/HLCA.200590076
1-[20-Acetyl-26-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-13,15,21,27-tetrahydroxy-3,3,9,9,14,31,31-heptamethyl-28-(3-phenylprop-2-enoyl)-4,10,18,24,30-pentaoxaoctacyclo[23.7.1.02,23.05,22.06,19.08,17.011,16.029,33]tritriaconta-5,11(16),12,14,19,21,25(33),26,28-nonaen-12-yl]-3-phenylprop-2-en-1-one	162866832	Click to see	1099.20	unknown	https://doi.org/10.1002/HLCA.200590076
1-[6-[(3-Acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-2,2-dimethyl-2H-1-benzopyran-8-yl]-3-phenyl-2-propen-1-one	5103	Click to see	516.50	unknown	https://doi.org/10.1002/HLCA.200590076 https://doi.org/10.1016/J.PHYMED.2013.03.012
3,4-Dihydroxyrottlerin	5316826	Click to see	548.50	unknown	via CMAUP database
Rottlerin	5281847	Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C=CC4=CC=CC=C4)O)O	516.50	unknown	https://doi.org/10.1016/J.PHYMED.2013.03.012 https://doi.org/10.1002/HLCA.200590076
Tocris-1610	6603986	Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C(C(=C3C(=C2O)C=CC(O3)(C)C)C(=O)C=CC4=CC=CC=C4)O)O	516.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
4-Hydroxyrottlerin	5318333	Click to see	532.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-8-methyl-6-(3-methyl-2-butenyl)-2-phenyl-, (S)-	179806	Click to see	338.40	unknown	https://doi.org/10.1002/HLCA.200590076
6-C-Prenyl-8-C-methylpinocembrin	42607875	Click to see	338.40	unknown	https://doi.org/10.1002/HLCA.200590076
8-[(3-Acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2-phenyl-2,3-dihydrochromen-4-one	14188386	Click to see	518.60	unknown	https://doi.org/10.1002/HLCA.200590076
Mallotus B	73352327	Click to see	518.60	unknown	https://doi.org/10.1002/HLCA.200590076
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(8R)-10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one	162846241	Click to see	532.50	unknown	https://doi.org/10.1002/HLCA.200590076
(8R)-5-hydroxy-2,2,10-trimethyl-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one	163070967	Click to see	336.40	unknown	https://doi.org/10.1002/HLCA.200590076
(8S)-10-[(3-acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2,2-dimethyl-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one	163016703	Click to see CC1=C(C(=C(C(=C1O)C(=O)C)O)CC2=C3C(=C(C4=C2OC(CC4=O)C5=CC=CC=C5)O)C=CC(O3)(C)C)O	516.50	unknown	https://doi.org/10.1002/HLCA.200590076
10-[(3-Acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2,2-dimethyl-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one	12304392	Click to see	516.50	unknown	https://doi.org/10.1002/HLCA.200590076
10-[(3-Acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-8-(4-hydroxyphenyl)-2,2-dimethyl-7,8-dihydropyrano[3,2-g]chromen-6-one	101721038	Click to see	532.50	unknown	https://doi.org/10.1002/HLCA.200590076
5-Hydroxy-2,2,10-trimethyl-8-phenyl-7,8-dihydropyrano[3,2-g]chromen-6-one	101273418	Click to see	336.40	unknown	https://doi.org/10.1002/HLCA.200590076
6-[(3-Acetyl-2,4,6-trihydroxy-5-methylphenyl)methyl]-5-hydroxy-2,2-dimethyl-8-phenyl-8,9-dihydropyrano[2,3-f]chromen-10-one	5318656	Click to see	516.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(6aS,12aR)-9-acetyl-1,3,8,10-tetrahydroxy-2,6,6,11-tetramethyl-7,12a-dihydro-6aH-chromeno[3,2-c]chromen-4-yl]-3-phenylprop-2-en-1-one	101721039	Click to see	530.60	unknown	https://doi.org/10.1002/HLCA.200590076
(E)-3-phenyl-1-[(1R,2R,11S)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-[(E)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]prop-2-en-1-one	102438611	Click to see CC1=C(C2=C(C(=C1O)C(=O)C=CC3=CC=CC=C3)OC(C4C2OC5=C6C4CC(OC6=C(C(=C5C)O)C(=O)C=CC7=CC=CC=C7)(C)C)(C)C)O	672.80	unknown	https://doi.org/10.1016/S0031-9422(98)00131-9
(E)-3-phenyl-1-[(1S,2S,11R)-7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-[(E)-3-phenylprop-2-enoyl]-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]prop-2-en-1-one	163193329	Click to see CC1=C(C2=C(C(=C1O)C(=O)C=CC3=CC=CC=C3)OC(C4C2OC5=C6C4CC(OC6=C(C(=C5C)O)C(=O)C=CC7=CC=CC=C7)(C)C)(C)C)O	672.80	unknown	https://doi.org/10.1002/HLCA.200590076
1-(9-acetyl-1,3,8,10-tetrahydroxy-2,6,6,11-tetramethyl-7,12a-dihydro-6aH-chromeno[3,2-c]chromen-4-yl)-3-phenylprop-2-en-1-one	163071447	Click to see	530.60	unknown	https://doi.org/10.1002/HLCA.200590076
3-Phenyl-1-[7,9,15-trihydroxy-3,3,8,14,19,19-hexamethyl-16-(3-phenylprop-2-enoyl)-4,12,18-trioxapentacyclo[11.7.1.02,11.05,10.017,21]henicosa-5(10),6,8,13(21),14,16-hexaen-6-yl]prop-2-en-1-one	162851557	Click to see	672.80	unknown	https://doi.org/10.1016/S0031-9422(98)00131-9 https://doi.org/10.1002/HLCA.200590076
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Mallotophilippen C	10050581	Click to see CC(=CCCC(=CCC1=C(C(=C2C(=C1O)C=CC(O2)(C)C)C(=O)C=CC3=CC=C(C=C3)O)O)C)C	474.60	unknown	via CMAUP database
Mallotophilippen D	9983046	Click to see	490.60	unknown	via CMAUP database
rac-(2E)-1-[5,7-dihydroxy-2-methyl-6-(3-methylbut-2-en-1-yl)-2-(4-methylpent-3-en-1-yl)-2H-chromen-8-yl]-3-(3,4-dihydroxyphenyl)prop-2-en-1-one	10458296	Click to see CC(=CCCC1(C=CC2=C(C(=C(C(=C2O1)C(=O)C=CC3=CC(=C(C=C3)O)O)O)CC=C(C)C)O)C)C	490.60	unknown	via CMAUP database

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.

Mallotus philippensis

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