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.

Orthosiphon aristatus, commonly called Java tea or cat’s whiskers, has a long history of use as an infusion and decoction in tropical Asia. Among the Javanese of Indonesia, the leaves are steeped in hot water to produce a mild diuretic tea that is traditionally taken to relieve kidney stones and urinary tract infections (Kumar et al., 2019). In Tamil Nadu, India, a decoction of fresh leaves and stems is brewed for its cooling effect and used to treat fevers, sore throats, and skin rashes; the same preparation is also applied as a poultice for bruises and swelling (Singh et al., 2015). Malay communities in Malaysia prepare a tincture by macerating dried leaves in 70 % ethanol for 48 h, which is then diluted for use as a topical wash to soothe eczema and dermatitis (B. R. Singh et al., 2017). These documented uses all involve infusions, decoctions, tinctures, or poultices and rely primarily on the aerial parts—leaves, stems, and occasionally roots.

A simple, safe tea can be made at home by taking 5 g of dried leaves (or 10 g of fresh leaves) and adding them to 250 ml of boiling water. Let the mixture steep for 5–10 minutes, strain, and sip warm. For a stronger effect, simmer the leaves for 15 minutes and reduce the liquid by half. This preparation is generally well tolerated, but because the plant has diuretic properties, it is advisable to limit intake to 2 cups per day, especially for pregnant women or individuals with kidney disease. If you experience excessive urination or dizziness, discontinue use and consult a healthcare professional.

The therapeutic actions of Orthosiphon aristatus are supported by several well‑established phytochemicals. The leaves contain the flavonoid sinensetin, which has been shown to inhibit inflammatory mediators, and rosmarinic acid, a potent antioxidant that protects renal tissue. Diterpenoids such as sinapic acid and the essential oil constituents (e.g., 1,8‑cineole, linalool) contribute to the plant’s cooling sensation and antimicrobial activity. These compounds collectively explain the traditional diuretic, anti‑inflammatory, and skin‑soothing effects reported by the Javanese, Tamil, and Malay users.

Modern research continues to validate these ethnobotanical claims. Recent in‑vitro and animal studies confirm the plant’s diuretic and anti‑inflammatory properties, and several commercial herbal tea blends now feature Orthosiphon aristatus as a key ingredient. The continued use of this plant in traditional medicine, coupled with growing scientific interest, underscores its relevance as a natural remedy for urinary and skin ailments.

General Uses Top

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Common products:
Orthosiphon aristatus is processed as a dried or semi-fermented herbal tea, frequently labeled “Java tea,” and also used to flavor non-alcoholic beverages. Primary processed forms include bulk dried leaf, cut-and-sift (teabag) material, and instant tea powders. Essential oil is a minor co-product obtained from steam distillation of fresh leaf.

Food and beverages (non-medicinal):
The dried leaf is infused in hot water to produce a beverage known as Orthosiphon tea or Misai kucing in Southeast Asia; it is traded internationally as a food ingredient or tea beverage. Food products are sold as ready-to-brew bagged tea, loose-leaf tea, or instant formulations, with production records from producing countries such as Indonesia. Commercial fragrance uses are confined to the essential oil, which finds limited application as a flavor/fragrance ingredient due to a fresh-herbaceous odor.

Colorants and tanning:
No documented commercial use as a natural dye, ink, or tanning agent has been found.

Wood and fiber:
No documented commercial timber, fiber, or paper applications are established.

Fragrance and cosmetics:
The essential oil, typically obtained in low yield, is the only product fraction applied in fragrance and flavor compositions. Cosmetic use is limited to fragrance function; specific cosmetic standards referencing Orthosiphon aristatus are not cited.

Properties relevant to use:
The beverage application is enabled by the leaves’ moderate tannin content and extractable soluble solids, which yield a characteristic aroma when infused. The leaf essential oil contains sesquiterpenes (e.g., β-caryophyllene) and other terpenes responsible for the herbaceous odor. The minor biochemicals such as sinensetin and eustifolin-D contribute to sensory attributes of infusions but have no specific standard designation in product specifications. The herb is notable for low caffeine.

Standards and regulation:
In the United States, dried Orthosiphon aristatus is regulated as a dietary ingredient under the Dietary Supplement Health and Education Act (DSHEA) when presented as a supplement, while tea preparations are generally recognized as foods; the European Union and other major markets do not list Orthosiphon in positive lists for novel foods or botanicals, implying use as a traditional tea ingredient rather than a regulated novel food. Food labeling in Indonesia, Malaysia, and Singapore recognizes Orthosiphon tea as a non-alcoholic beverage under national food standards.

Sustainability and sourcing:
Commercial supply depends on cultivated crops and smallholder harvesting in Southeast Asia, especially Indonesia and Malaysia, with documented domestication and agronomic studies guiding agronomic practices. No major certification frameworks specifically address Orthosiphon production; sustainability thus hinges on general best-practice cultivation and post-harvest handling to maintain leaf quality.

Synonyms Top

Scientific name	Authority	First published in
Ocimum aristatum	Blume	Bijdr. Fl. Ned. Ind. : 833 (1826)
Ocimum grandiflorum	Blume	Bijdr. Fl. Ned. Ind. : 835 (1826)
Orthosiphon grandiflorus	(Blume) Bold.	Zakfl. Java : 110 (1916)
Orthosiphon spicatus	(Thunb.) Backer, Bakh.f. & Steenis	Blumea 6: 359 (1950)
Orthosiphon velterii	Doan	Fl. Indo-Chine 4: 936 (1936)

Common names Top

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Filter by language:

Language	Common/alternative name
English	java tea
English	cat's whiskers
Persian	ارتسیفن اریستاتوس
Indonesian	kumis kucing
Italian	tè di giava
Japanese	ネコノヒゲ
jv	bréngos kucing
jv	brengos kucing
Malayalam	പൂച്ചമീശ
su	kumis ucing
Tamil	பூனை மீசை செடி
Thai	หญ้าหนวดแมว
Tonga	kavaʻipusi
Vietnamese	râu mèo
Vietnamese	cỏ râu mèo
Chinese	化石草
Chinese	猫须草
Chinese	肾茶
Chinese	貓鬚草
Chinese	腎草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Orthosiphon aristatus var. aristatus		Unknown
Orthosiphon aristatus var. velteri	Suddee & A.J.Paton	Kew Bull. 60: 23 (2005)

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
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Taiwan

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

Australasia click to expand
- Australia
  - Queensland

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
- Southwestern Pacific
  - Fiji
  - Niue

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000261111
Tropicos	17608145
INPN	448539
KEW	urn:lsid:ipni.org:names:453446-1
The Plant List	kew-144294
Open Tree Of Life	1070846
NCBI Taxonomy	204151
IPNI	453446-1
iNaturalist	185264
GBIF	7308026
Freebase	/m/026m6cl
EOL	2868497
USDA GRIN	411815
Wikipedia	Orthosiphon_aristatus
CMAUP	NPO14797
CMAUP	NPO9091

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

Sinensetin protects against periodontitis through binding to Bach1 enhancing its ubiquitination degradation and improving oxidative stress

Yuan Z, Li J, Xiao F, Wu Y, Zhang Z, Shi J, Qian J, Wu X, Yan F

Int J Oral Sci

11-May-2024

PMCID:	PMC11088688
doi:	10.1038/s41368-024-00305-z
PMID:	38734708

A Study of Metabolites from Basidiomycota and Their Activities against Pseudomonas aeruginosa

Clericuzio M, Novello G, Bivona M, Gamalero E, Bona E, Caramaschi A, Massa N, Asteggiano A, Medana C

Antibiotics (Basel)

03-Apr-2024

PMCID:	PMC11047493
doi:	10.3390/antibiotics13040326
PMID:	38667002

Little Ironweed and Java Tea in Herbal Toothpaste Reduced Dentine Permeability: An In Vitro Study

Vajrabhaya LO, Korsuwannawong S, Harnirattisai C, Teanchai C, Salee W

J Int Soc Prev Community Dent

27-Feb-2024

PMCID:	PMC10980310
doi:	10.4103/jispcd.jispcd_67_23
PMID:	38559639

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

Isolation and identification of allelochemicals and their activities and functions

Kato-Noguchi H

J Pestic Sci

20-Feb-2024

PMCID:	PMC10912975
doi:	10.1584/jpestics.D23-052
PMID:	38450087

Isolation, structure modification, and anti-rheumatoid arthritis activity of isopimarane-type diterpenoids from Orthosiphon aristatus

Luo YX, Gong X, Su ZC, Mo JF, Li DL, Wu RH, Jin JW, Lang M, Wang JP, Xu XT, Gan LS

J Enzyme Inhib Med Chem

17-Jan-2024

PMCID:	PMC10798283
doi:	10.1080/14756366.2023.2296355
PMID:	38234133

The complete chloroplast genome of Orthosiphon aristatus (Blume) Miq. (Lamiaceae)

Su Y, Li B, Liang W, Wen H, Wei W

Mitochondrial DNA B Resour

11-Jan-2024

PMCID:	PMC10786424
doi:	10.1080/23802359.2023.2301012
PMID:	38222982

Accumulation of Polyphenols and Associated Gene Expression in Hairy Roots of Salvia viridis Exposed to Methyl Jasmonate

Grzegorczyk-Karolak I, Krzemińska M, Grąbkowska R, Gomulski J, Żekanowski C, Gaweda-Walerych K

Int J Mol Sci

07-Jan-2024

PMCID:	PMC10815010
doi:	10.3390/ijms25020764
PMID:	38255839

Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Pharm Biol

22-Dec-2023

PMCID:	PMC10763916
doi:	10.1080/13880209.2023.2292261
PMID:	38131672

Anti-inflammatory activity of verbascoside- and isoverbascoside-rich Lamiales medicinal plants

Pongkitwitoon B, Putalun W, Triwitayakorn K, Kitisripanya T, Kanchanapoom T, Boonsnongcheep P

Heliyon

13-Dec-2023

PMCID:	PMC10770615
doi:	10.1016/j.heliyon.2023.e23644
PMID:	38187323

Risk assessment of aflatoxin B1 in herbal medicines and plant food supplements marketed in Malaysia using margin of exposure and RISK21 approaches

Ab Dullah SS, Sabran MR, Hasiah AH, Abdullah R

Genes Environ

23-Nov-2023

PMCID:	PMC10666461
doi:	10.1186/s41021-023-00286-1
PMID:	37993956

The immunomodulatory activity of Orthosiphon aristatus against atopic dermatitis: Evidence-based on network pharmacology and molecular simulations

Pandaleke TA, Handono K, Widasmara D, Susianti H

J Taibah Univ Med Sci

04-Nov-2023

PMCID:	PMC10692725
doi:	10.1016/j.jtumed.2023.10.005
PMID:	38047238

The role of sound stimulation in production of plant secondary metabolites

Wu L, Yang N, Guo M, Zhang D, Ghiladi RA, Bayram H, Wang J

Nat Prod Bioprospect

17-Oct-2023

PMCID:	PMC10581969
doi:	10.1007/s13659-023-00409-9
PMID:	37847483

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Essential Oils of Artemisia frigida Plants (Asteraceae): Conservatism and Lability of the Composition

Zhigzhitzhapova SV, Dylenova EP, Zhigzhitzhapov BV, Goncharova DB, Tykheev ZA, Taraskin VV, Anenkhonov OA

Plants (Basel)

28-Sep-2023

PMCID:	PMC10574723
doi:	10.3390/plants12193422
PMID:	37836162

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
N-Formyl-4-hydroxybenzamide	71370414	Click to see C1=CC(=CC=C1C(=O)NC=O)O	165.15	unknown	via CMAUP database
N-Formylbenzamide	151196	Click to see	149.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
4-Hydroxybenzamide	65052	Click to see	137.14	unknown	via CMAUP database
Benzamide, N-[(2S)-2-hydroxy-2-phenylethyl]-	6542363	Click to see	241.28	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(cyanomethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid	15548729	Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC#N)C(C)(C)C(=O)O	525.60	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
(6,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,7,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate	53247090	Click to see	692.70	unknown	https://doi.org/10.1248/CPB.48.433 https://doi.org/10.1248/CPB.47.911
(7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate	85098422	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	692.70	unknown	https://doi.org/10.1248/CPB.48.433 https://doi.org/10.1248/CPB.47.911
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-3-ethenyl-2,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	11802781	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(C(C(C3=O)(C)O)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C	692.70	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-3-ethenyl-2,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10032594	Click to see	692.70	unknown	https://doi.org/10.1248/CPB.48.433 https://doi.org/10.1248/CPB.47.911
Neoorthosiphol A	10055454	Click to see	692.70	unknown	https://doi.org/10.1248/CPB.48.433 https://doi.org/10.1248/CPB.47.911
Staminol C	11490943	Click to see	692.70	unknown	via CMAUP database
Staminol D	11455867	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C)(C)C	568.60	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Cyclobutane lignans
[(1R,2R,3S,4S)-2-(2,4-dihydroxybenzoyl)-3,4-diphenylcyclobutyl]-(2,4-dihydroxyphenyl)methanone	102228233	Click to see	480.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(10-acetyloxy-5-benzoyloxy-2-ethenyl-6,7,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate	85105215	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C	634.70	unknown	https://doi.org/10.1021/NP030471+
(2,9-Diacetyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl) benzoate	162842454	Click to see	570.60	unknown	https://doi.org/10.1021/NP030471+
(3-Acetyloxy-4-benzoyloxy-7-ethenyl-8a,9-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl) benzoate	162849973	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5	632.70	unknown	https://doi.org/10.1021/NP030471+ https://doi.org/10.1021/NP000607T
(3-Acetyloxy-7-ethenyl-2,8a,9-trihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl) benzoate	162875931	Click to see	528.60	unknown	https://doi.org/10.1021/NP030471+
(3,9-diacetyloxy-4-benzoyloxy-7-ethenyl-5,8a-dihydroxy-1,1,4a,7-tetramethyl-8-oxo-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-yl) benzoate	85098364	Click to see	676.70	unknown	https://doi.org/10.1021/NP030471+
(3,9-Diacetyloxy-4-benzoyloxy-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl) benzoate	74124567	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C	674.70	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1021/NP030471+ https://doi.org/10.1248/CPB.48.433
(3,9-Diacetyloxy-7-ethenyl-2,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl) benzoate	85097732	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C	570.60	unknown	https://doi.org/10.1021/NP030471+ https://doi.org/10.1021/NP000607T
(6,10-Diacetyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1,7-dioxo-3,4,4a,8a,9,10-hexahydrophenanthren-4-yl) benzoate	75051747	Click to see	552.60	unknown	https://doi.org/10.1021/NP030471+
(6,10-Diacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1,7-dioxo-3,4,4a,5,6,8a,9,10-octahydrophenanthren-4-yl) benzoate	85105430	Click to see CC(=O)OC1CC2C(C(=O)C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)(C)C	674.70	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1248/CPB.48.433
(6,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,7,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate	163031916	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C	692.70	unknown	https://doi.org/10.1021/NP000607T
(6,10-diacetyloxy-5-benzoyloxy-2-ethenyl-7,10a-dihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate	73193598	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C	676.70	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1021/NP030471+ https://doi.org/10.1016/0031-9422(93)85530-5 https://doi.org/10.1016/S0040-4020(01)89868-9 https://doi.org/10.1248/CPB.48.433 https://doi.org/10.1021/NP000607T
(7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-6,10a-dihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl) benzoate	73091933	Click to see	676.70	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1021/NP030471+ https://doi.org/10.1016/0031-9422(93)85530-5 https://doi.org/10.1016/S0040-4020(01)89868-9 https://doi.org/10.1248/CPB.48.433 https://doi.org/10.1021/NP000607T
(9-Acetyloxy-7-ethenyl-2,4,8a-trihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-3-yl) benzoate	72758950	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C	528.60	unknown	https://doi.org/10.1021/NP030471+
[(2R,4R,4aS,4bS,5R,6R,8aR,10R,10aR)-6,10-diacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1,7-dioxo-3,4,4a,5,6,8a,9,10-octahydrophenanthren-4-yl] benzoate	10055285	Click to see	674.70	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1248/CPB.48.433
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7,10-triacetyloxy-5-benzoyloxy-2-ethenyl-10a-hydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	9987409	Click to see	718.80	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7-acetyloxy-5-benzoyloxy-2-ethenyl-6,10,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10919284	Click to see CC(=O)OC1C(C(C2(C(C1(C)C)CC(C3(C2C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C)OC(=O)C5=CC=CC=C5)O	634.70	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-2,9-diacetyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate	101228590	Click to see	570.60	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-3-acetyloxy-7-ethenyl-2,8a,9-trihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-4-yl] benzoate	101228589	Click to see	528.60	unknown	via CMAUP database
[(2S,3S,4R,4aS,4bR,7R,8aR,9R,10aS)-9-acetyloxy-4-benzoyloxy-7-ethenyl-3,8a-dihydroxy-1,1,4a,7-tetramethyl-5,8-dioxo-2,3,4,4b,6,9,10,10a-octahydrophenanthren-2-yl] benzoate	10258500	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C5=CC=CC=C5)(C)C	632.70	unknown	via CMAUP database
Orthosiphol A	15385858	Click to see	676.70	unknown	https://doi.org/10.1016/S0040-4020(01)89868-9 https://doi.org/10.1021/NP030471+ https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1021/NP000607T https://doi.org/10.1248/CPB.48.433 https://doi.org/10.1016/0031-9422(93)85530-5
orthosiphol B	15385859	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	676.70	unknown	https://doi.org/10.1016/S0040-4020(01)89868-9 https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1248/CPB.48.433
Orthosiphol D	44583689	Click to see	552.60	unknown	https://doi.org/10.1021/NP030471+
Orthosiphol F	10327179	Click to see	676.70	unknown	via CMAUP database
Orthosiphol G	10076785	Click to see	572.60	unknown	via CMAUP database
Orthosiphol J	10438744	Click to see	612.70	unknown	via CMAUP database
Orthosiphol K	10054824	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)O)(C)C	634.70	unknown	https://doi.org/10.1021/NP000607T
Orthosiphol L	10101176	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C	692.70	unknown	via CMAUP database
Orthosiphol M	10030927	Click to see	570.60	unknown	https://doi.org/10.1021/NP030471+ https://doi.org/10.1021/NP000607T
Orthosiphol N	10258499	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(=O)CC(C3=O)(C)C=C)O)O)(C)C)OC(=O)C5=CC=CC=C5	632.70	unknown	https://doi.org/10.1021/NP030471+ https://doi.org/10.1021/NP000607T
Orthosiphol O	10032464	Click to see	676.70	unknown	https://doi.org/10.1021/NP030471+
Orthosiphol R	44583688	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)O)(C)C=C)O)C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)(C)C	692.70	unknown	via CMAUP database
Orthosiphol T	11082749	Click to see	634.70	unknown	via CMAUP database
Orthosiphol U	637182	Click to see	614.70	unknown	via CMAUP database
Orthosiphol V	10951947	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)O)OC(=O)C)(C)C	572.60	unknown	via CMAUP database
Orthosiphol W	11071897	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)O)(C)C	572.60	unknown	via CMAUP database
Orthosiphol X	10054823	Click to see	634.70	unknown	via CMAUP database
Orthosiphol Y	11144807	Click to see	448.50	unknown	via CMAUP database
Orthosiphol Z	11090752	Click to see CC(=O)OC1=CC2(C(CC(C3(C2C(=O)CC(C3=O)(C)C=C)O)O)C(C1=O)(C)C)C	404.50	unknown	via CMAUP database
orthosiphonone A	10439492	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C4=CC=CC=C4)OC(=O)C)OC(=O)C5=CC=CC=C5)(C)C	674.70	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1021/NP030471+ https://doi.org/10.1248/CPB.48.433
Orthosiphonone C	11226314	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)O)OC(=O)C4=CC=CC=C4)O)(C)C	528.60	unknown	https://doi.org/10.1021/NP030471+
Siphonol A	10952715	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	734.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[8-(2-acetylbuta-1,3-dienyl)-2,6-diacetyloxy-3-hydroxy-4,4,8a-trimethyl-7-oxo-2,3,4a,5,6,8-hexahydro-1H-naphthalen-1-yl] benzoate	85136532	Click to see	540.60	unknown	https://doi.org/10.1021/NP000607T
Norstaminone A	10414921	Click to see	540.60	unknown	https://doi.org/10.1021/NP000607T
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-ene-11,22-diol	44253988	Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6O)C)C)C)C)(C)CO)O	472.70	unknown	via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R,22R)-10-(hydroxymethyl)-22-methoxy-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-ol	44253989	Click to see	486.70	unknown	via CMAUP database
(1R,2R,5S,6R,9R,10S,11S,14R,15R,19S,21R)-11-hydroxy-10-(hydroxymethyl)-2,5,6,10,14,21-hexamethyl-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-22-one	102482971	Click to see CC12CCC(C(C1CCC3(C2CC=C4C3(CCC5(C4CC6(CC5OC6=O)C)C)C)C)(C)CO)O	470.70	unknown	via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,10S,12aR,14bR)-10-hydroxy-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-2-carboxylic acid	21594159	Click to see CC12CCC(CC1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)CO)O)C)(C)C(=O)O	472.70	unknown	via CMAUP database
(2R,4aS,6aR,6aS,6bR,8aR,9S,12aR,14bR)-9-(hydroxymethyl)-2,4a,6a,6b,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-2-carboxylic acid	44253990	Click to see CC12CCC(CC1C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)CO)C)(C)C(=O)O	470.70	unknown	via CMAUP database
(3S,4S,4aR,6aR,6bS,8aR,9R,11R,12aS,14aR,14bR)-4,11-bis(hydroxymethyl)-4,6a,6b,8a,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-3,9-diol	14335966	Click to see	474.70	unknown	via CMAUP database
24-Hydroxy-beta-amyrin	14167253	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C)C	442.70	unknown	via CMAUP database
Melilotigenin B	91895471	Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)C)C	454.70	unknown	via CMAUP database
Melilotigenin C	10551785	Click to see CC1(CC2C3=CCC4C5(CCC(=O)C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)C)C	456.70	unknown	via CMAUP database
Soyasapogenol B	115012	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1)O)C)C)C)(C)CO)O)C)C	458.70	unknown	via CMAUP database
Soyasapogenol E	13632872	Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C1)C)C)C)(C)CO)O)C)C	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E	10963687	Click to see	736.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(3,8-diacetyloxy-7-ethenyl-5,8a-dihydroxy-1,1,4a,7-tetramethyl-2-oxo-5,6,8,9,10,10a-hexahydro-4bH-phenanthren-9-yl) acetate	72981100	Click to see	492.60	unknown	https://doi.org/10.1021/NP030471+
14-deoxo-14-O-acetylorthosiphol Y	21578028	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(C(CC3O)(C)C=C)OC(=O)C)O)C)OC(=O)C)(C)C	492.60	unknown	https://doi.org/10.1021/NP030471+
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Staminol A	10628761	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(C(C3OC(=O)C4=CC=CC=C4)C=C)(C)O)O)C)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	734.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
Secoorthosiphol B	15548728	Click to see	558.60	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Benzofuranones
2-[(1S,2'S)-4-hydroxy-6-methoxy-2'-methyl-3,5'-dioxospiro[2-benzofuran-1,3'-oxolane]-2'-yl]acetic acid	102434056	Click to see	322.27	unknown	https://doi.org/10.1021/NP030471+
> Organoheterocyclic compounds / Benzopyrans
Oxytropisoflavan B	46918734	Click to see COC1=C(C(=C(C=C1)C2CC3(CCC(=O)C=C3OC2)O)O)OC	320.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(1R)-1-(7,8-dimethoxy-2,2-dimethylchromen-6-yl)ethanol	100945948	Click to see	264.32	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1248/CPB.48.433
(1S)-1-(7,8-dimethoxy-2,2-dimethylchromen-6-yl)ethanol	100945949	Click to see	264.32	unknown	https://doi.org/10.1248/CPB.48.433
1-(7,8-Dimethoxy-2,2-dimethyl-2H-1-benzopyran-6-yl)ethanone	177148	Click to see	262.30	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1248/CPB.48.433
1-(8-Methoxy-2,2-dimethyl-2H-1-benzopyran-6-yl)ethan-1-one	10466473	Click to see	232.27	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1248/CPB.48.433
6-(1-Hydroxyethyl)-7,8-dimethoxy-2,2-dimethyl-2h-1-benzopyran	10706737	Click to see	264.32	unknown	https://doi.org/10.1248/CPB.47.695 https://doi.org/10.1248/CPB.48.433
6,7,8-Trimethoxy-2,2-dimethylchromene	441969	Click to see	250.29	unknown	https://doi.org/10.1248/CPB.48.433
> Organoheterocyclic compounds / Indoles and derivatives / Benzoylindoles
(3-Hydroxyindol-1-yl)-(3-hydroxyphenyl)methanone	46850207	Click to see	253.25	unknown	via CMAUP database
(3-Hydroxyindol-1-yl)-(4-hydroxyphenyl)methanone	46850031	Click to see	253.25	unknown	via CMAUP database
(3-Hydroxyindol-1-yl)-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]methanone	46850206	Click to see CC(=CCC1=C(C=CC(=C1)C(=O)N2C=C(C3=CC=CC=C32)O)O)C	321.40	unknown	via CMAUP database
(3-Hydroxyindol-1-yl)-phenylmethanone	46850030	Click to see C1=CC=C(C=C1)C(=O)N2C=C(C3=CC=CC=C32)O	237.25	unknown	via CMAUP database
(4-Hydroxy-3-methoxyindol-1-yl)-(4-hydroxyphenyl)methanone	46850205	Click to see	283.28	unknown	via CMAUP database
(4-Hydroxyphenyl)-(3-methoxyindol-1-yl)methanone	46850032	Click to see COC1=CN(C2=CC=CC=C21)C(=O)C3=CC=C(C=C3)O	267.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
[(1S,4aR,6R,6aR,8R,10R,10aS,10bS)-6-acetyloxy-8-ethenyl-1,6a-dihydroxy-4,4,8,10b-tetramethyl-3,7-dioxo-4a,5,6,9,10,10a-hexahydro-1H-benzo[h]isochromen-10-yl] benzoate	163081099	Click to see	514.60	unknown	https://doi.org/10.1021/NP030471+
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	https://doi.org/10.1016/0031-9422(91)83190-V
2-(3,4-Dihydroxyphenyl)ethenyl 3-(3,4-dihydroxyphenyl)prop-2-enoate	78384837	Click to see C1=CC(=C(C=C1C=CC(=O)OC=CC2=CC(=C(C=C2)O)O)O)O	314.29	unknown	https://doi.org/10.1016/0031-9422(91)83190-V
3-(3,4-Dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]propanoic acid	5099	Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	360.30	unknown	https://doi.org/10.1016/0031-9422(91)83190-V
3,4-Dihydroxycinnamoyl-(Z)-2-(3,4-dihydroxyphenyl)ethenol	14353342	Click to see	314.29	unknown	https://doi.org/10.1016/0031-9422(91)83190-V
Caftaric Acid	6440397	Click to see	312.23	unknown	via CMAUP database
p-Hydroxyphenethyl trans-ferulate	637308	Click to see COC1=C(C=CC(=C1)C=CC(=O)OCCC2=CC=C(C=C2)O)O	314.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-7-hydroxyflavanone	688857	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3	240.25	unknown	via CMAUP database
Liquiritigenin	114829	Click to see	256.25	unknown	via CMAUP database
Pinocembrin	68071	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
Chrysin	5281607	Click to see	254.24	unknown	via CMAUP database
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin	5281654	Click to see	316.26	unknown	via CMAUP database
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Myricetin	5281672	Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	318.23	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one	60200223	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)O)O)O)O	608.50	unknown	via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	21668680	Click to see	726.60	unknown	via CMAUP database
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	10865825	Click to see	872.80	unknown	via CMAUP database
Biorobin	15944778	Click to see	594.50	unknown	via CMAUP database
Mauritianin	10919701	Click to see	740.70	unknown	via CMAUP database
Oxytroflavoside A	60200065	Click to see	752.70	unknown	via CMAUP database
Oxytroflavoside B	60200066	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)OC)C5=CC=C(C=C5)O)CO)O)OC(=O)CC(C)(CC(=O)O)O)O)O)O	752.70	unknown	via CMAUP database
Oxytroflavoside C	60200220	Click to see	752.70	unknown	via CMAUP database
Oxytroflavoside D	60200221	Click to see	606.50	unknown	via CMAUP database
Oxytroflavoside E	60200222	Click to see	768.70	unknown	via CMAUP database
Oxytroflavoside G	60200370	Click to see	754.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 3-O-(Alpha-L-Rhamnopyranosyl(1->2)-Beta-D-Galactopyranosyl)-7-O-Alpha-L-Rhamnopyranoside	57397583	Click to see	740.70	unknown	via CMAUP database
Robinin	5281693	Click to see	740.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(-)-Pinostrobin	73201	Click to see	270.28	unknown	via CMAUP database
(2S)-2-(4-hydroxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	14157884	Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=C(C=C3)O	270.28	unknown	via CMAUP database
(R,S)-7-Methoxy-2-phenyl-chroman-4-one	688883	Click to see COC1=CC2=C(C=C1)C(=O)CC(O2)C3=CC=CC=C3	254.28	unknown	via CMAUP database
5-Hydroxy-6,7,3',4'-Tetramethoxyflavone	152430	Click to see	358.30	unknown	https://doi.org/10.1248/CPB.48.433
5,6,7,4'-Tetramethoxyflavone	96118	Click to see	342.30	unknown	https://doi.org/10.1248/CPB.48.433
Eupatorin	97214	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O	344.30	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274529/ https://doi.org/10.1016/J.FITOTE.2012.06.002 https://doi.org/10.1248/CPB.48.433
Ladanein	3084066	Click to see	314.29	unknown	via CMAUP database
Sakuranetin	73571	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O	286.28	unknown	via CMAUP database
Sinensetin	145659	Click to see	372.40	unknown	https://doi.org/10.1248/CPB.48.433
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Demethoxynobiletin	44584772	Click to see	372.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-hydroxyphenyl)methyl]-2,3-dihydrochromen-4-one	26088035	Click to see	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain	91510	Click to see	284.26	unknown	via CMAUP database
(6Ar,11Ar)-3,8-Dihydroxy-9,10-Dimethoxypterocarpan	46918735	Click to see	316.30	unknown	via CMAUP database
(l)-Edunol	182148	Click to see	352.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Daidzein	5281708	Click to see	254.24	unknown	via CMAUP database
Pseudobaptigenin	5281805	Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O	282.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavanquinones
5-[(3R)-7-hydroxy-3,4-dihydro-2H-chromen-3-yl]-2,3-dimethoxycyclohexa-2,5-diene-1,4-dione	10403457	Click to see COC1=C(C(=O)C(=CC1=O)C2CC3=C(C=C(C=C3)O)OC2)OC	316.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Daidzein-4'-glucoside	49862229	Click to see	416.40	unknown	via CMAUP database
Sophoricoside	5321398	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-Methoxydaidzein	5319422	Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
Isomucronulatol, (-)-	10380176	Click to see	302.32	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
(3R)-2',3',7-trihydroxy-4'-methoxyisoflavan	15939757	Click to see COC1=C(C(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O)O	288.29	unknown	via CMAUP database
(R)-Mucronulatol	13873811	Click to see	302.32	unknown	via CMAUP database
Calycosin	5280448	Click to see	284.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2'-Hydroxybiochanin A	5282075	Click to see	300.26	unknown	via CMAUP database
Formononetin	5280378	Click to see	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids / 7-O-methylisoflavones
Isoformononetin	3764	Click to see	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
2',4'-Dihydroxydihydrochalcone	586491	Click to see	242.27	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One	425	Click to see	256.25	unknown	via CMAUP database
1-(2,4-Dihydroxyphenyl)-3-phenylprop-2-en-1-one	344530	Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2)O)O	240.25	unknown	via CMAUP database
2-Propen-1-one, 1-(2-hydroxy-4-methoxyphenyl)-3-(4-hydroxyphenyl)-	592216	Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O	270.28	unknown	via CMAUP database
2',4'-Dihydroxychalcone	5376979	Click to see	240.25	unknown	via CMAUP database
2a(2),4a(2)-Dihydroxy-4-methoxychalcone	166795	Click to see	270.28	unknown	via CMAUP database
4'-Methoxy-2'-hydroxy chalcone	265720	Click to see	254.28	unknown	via CMAUP database
Isoliquiritigenin	638278	Click to see	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4',4-Trihydroxy-3'-prenylchalcone	193568	Click to see	324.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-phenylprop-2-en-1-one	71442332	Click to see	254.28	unknown	via CMAUP database

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Orthosiphon aristatus

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Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

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