Scientific name	Authority	First published in
Rauvolfia canescens	L.	Sp. Pl. ed. 2 : 303 (1762)
Rauvolfia heterophylla	Willd. ex Roem. & Schult.	Syst. Veg., ed. 15 bis 4: 805 (1819)
Rauvolfia hirsuta	Jacq.	Enum. Syst. Pl. : 14 (1760)
Rauvolfia odontophora	Van Heurck & Müll.Arg.	Observ. Bot. Descript. Pl. Nov. Herb. Van Heurckiani 2: 150 (1871)
Rauvolfia subpubescens	L.	Mant. Pl. 2: 345 (1771)
Rauvolfia tomentosa	Jacq.	Enum. Syst. Pl. : 14 (1760)
Rauvolfia canescens var. glabra	Müll.Arg.	Linnaea 30: 395 (1860)
Rauvolfia canescens var. intermedia	Markgr.	Repert. Spec. Nov. Regni Veg. 20: 115 (1924)
Rauvolfia canescens var. tomentosa	Müll.Arg.	Linnaea 30: 395 (1860)
Rauvolfia heterophylla var. puberula	A.Gray	Proc. Amer. Acad. Arts 5: 187. 1861
Rauvolfia hirsuta var. glabra	(Müll.Arg.) Woodson	Ann. Missouri Bot. Gard. 26: 299 (1939)
Rauvolfia latifolia var. minor	Müll.Arg.	Linnaea 30: 396 (1860)
Rauvolfia canescens var. typica	Markgr.	Repert. Spec. Nov. Regni Veg. 20: 115 (1924)

Common names Top

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Filter by language:

Language	Common/alternative name
English	be still tree
Spanish	amatillo
Spanish	cabamuc
Spanish	curarina
Spanish	matacoyote
Spanish	viborilla
Persian	راولفیا تترافولا
Malayalam	പാമ്പുംകൊല്ലി
Thai	ระย่อมพินเก้
Chinese	四叶萝芙木
Chinese	四葉蘿芙木
Chinese	异叶萝芙木

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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
  - Nepal
- Indo-China
  - Andaman Islands
  - Vietnam

Australasia click to expand
- Australia
  - Queensland

Northern America click to expand
- Mexico
  - Mexico Central
  - Mexico Gulf
  - Mexico Northeast
  - Mexico Northwest
  - Mexico Southeast
  - Mexico Southwest

Southern America click to expand
- Caribbean
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Trinidad-Tobago
  - Venezuelan Antilles
  - Windward Islands
- Central America
  - Belize
  - Costa Rica
  - El Salvador
  - Guatemala
  - Honduras
  - Nicaragua
  - Panamá
- Northern South America
  - French Guiana
  - Venezuela
- Western South America
  - Bolivia
  - Colombia
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000295195
Florida Plant Atlas	1863
USDA Plants	RATE8
Tropicos	1800040
INPN	630534
KEW	urn:lsid:ipni.org:names:81663-1
The Plant List	kew-176987
Open Tree Of Life	927719
NCBI Taxonomy	545371
Nature Serve	2.131369
IUCN Red List	205547543
IPNI	81663-1
iNaturalist	167766
GBIF	3169782
Freebase	/m/0glpnt_
EPPO	RAUTE
EOL	400903
USDA GRIN	30896
Wikipedia	Rauvolfia_tetraphylla
CMAUP	NPO10353

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_030512225.1	ASM3051222v1	Contig	Refactoring Monoterpenoid Indole Alkaloid Biosynthesis in Microbial Cell Factories	2023-07-20	39.0x	348.04 Mb

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

Evolution and diversification of carboxylesterase-like [4+2] cyclases in aspidosperma and iboga alkaloid biosynthesis

DeMars MD II, O’Connor SE

Proc Natl Acad Sci U S A

06-Feb-2024

PMCID:	PMC10873640
doi:	10.1073/pnas.2318586121
PMID:	38319969

De novo biosynthesis of antiarrhythmic alkaloid ajmaline

Guo J, Gao D, Lian J, Qu Y

Nat Commun

11-Jan-2024

PMCID:	PMC10784492
doi:	10.1038/s41467-024-44797-z
PMID:	38212296

A chromosome-scale genome assembly of Rauvolfia tetraphylla facilitates identification of the complete ajmaline biosynthetic pathway

Lezin E, Carqueijeiro I, Cuello C, Durand M, Jansen HJ, Vergès V, Birer Williams C, Oudin A, Dugé de Bernonville T, Petrignet J, Celton N, St-Pierre B, Papon N, Sun C, Dirks RP, O’Connor SE, Jensen MK, Besseau S, Courdavault V

Plant Commun

28-Dec-2023

PMCID:	PMC11009098
doi:	10.1016/j.xplc.2023.100784
PMID:	38155576

The Rauvolfia tetraphylla genome suggests multiple distinct biosynthetic routes for yohimbane monoterpene indole alkaloids

Stander EA, Lehka B, Carqueijeiro I, Cuello C, Hansson FG, Jansen HJ, Dugé De Bernonville T, Birer Williams C, Vergès V, Lezin E, Lorensen MD, Dang TT, Oudin A, Lanoue A, Durand M, Giglioli-Guivarc’h N, Janfelt C, Papon N, Dirks RP, O’connor SE, Jensen MK, Besseau S, Courdavault V

Commun Biol

24-Nov-2023

PMCID:	PMC10673892
doi:	10.1038/s42003-023-05574-8
PMID:	38001233

Dandelion flower-fabricated Ag nanoparticles versus synthetic ones with characterization and determination of photocatalytic, antioxidant, antibacterial, and α-glucosidase inhibitory activities

Yousefzadeh-Valendeh S, Fattahi M, Asghari B, Alizadeh Z

Sci Rep

18-Sep-2023

PMCID:	PMC10507034
doi:	10.1038/s41598-023-42756-0
PMID:	37723218

Plant Extracts from the Yucatan Peninsula in the In Vitro Control of Curvularia lunata and Antifungal Effect of Mosannona depressa and Piper neesianum Extracts on Postharvest Fruits of Habanero Pepper

Cruz-Cerino P, Cristóbal-Alejo J, Ruiz-Carrera V, Gamboa-Angulo M

Plants (Basel)

09-Aug-2023

PMCID:	PMC10459550
doi:	10.3390/plants12162908
PMID:	37631120

From Nature to Lab: A Review of Secondary Metabolite Biosynthetic Pathways, Environmental Influences, and In Vitro Approaches

Reshi ZA, Ahmad W, Lukatkin AS, Javed SB

Metabolites

28-Jul-2023

PMCID:	PMC10456650
doi:	10.3390/metabo13080895
PMID:	37623839

Towards further understanding the applications of endophytes: enriched source of bioactive compounds and bio factories for nanoparticles

Choudhary N, Dhingra N, Gacem A, Yadav VK, Verma RK, Choudhary M, Bhardwaj U, Chundawat RS, Alqahtani MS, Gaur RK, Eltayeb LB, Al Abdulmonem W, Jeon BH

Front Plant Sci

10-Jul-2023

PMCID:	PMC10364642
doi:	10.3389/fpls.2023.1193573
PMID:	37492778

Posters

N/A

FEBS Open Bio

28-Jun-2023

PMCID:	PMC10300527
doi:	10.1002/2211-5463.13646

An assessment of the physicochemical characteristics and essential oil composition of Mentha longifolia (L.) Huds. exposed to different salt stress conditions

Singh R, Ahmed S, Luxmi S, Rai G, Gupta AP, Bhanwaria R, Gandhi SG

Front Plant Sci

18-Apr-2023

PMCID:	PMC10151762
doi:	10.3389/fpls.2023.1165687
PMID:	37143871

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

An insight into endophytic antimicrobial compounds: an updated analysis

Digra S, Nonzom S

Plant Biotechnol Rep

14-Mar-2023

PMCID:	PMC10013304
doi:	10.1007/s11816-023-00824-x
PMID:	37359493

In-vitro anticancer activity of Rauvolfia tetraphylla extract on mcf-7 breast cancer cell lines

Sabu A, J S, R G, E D

Bioinformation

31-Jan-2023

PMCID:	PMC10504496
doi:	10.6026/97320630019043
PMID:	37720282

A mass spectrometry imaging approach on spatiotemporal distribution of multiple alkaloids in Gelsemium elegans

Wu ZH, Wang RZ, Sun ZL, Su Y, Xiao LT

Front Plant Sci

18-Nov-2022

PMCID:	PMC9718364
doi:	10.3389/fpls.2022.1051756
PMID:	36466241

A microbial supply chain for production of the anti-cancer drug vinblastine

Zhang J, Hansen LG, Gudich O, Viehrig K, Lassen LM, Schrübbers L, Adhikari KB, Rubaszka P, Carrasquer-Alvarez E, Chen L, D’Ambrosio V, Lehka B, Haidar AK, Nallapareddy S, Giannakou K, Laloux M, Arsovska D, Jørgensen MA, Chan LJ, Kristensen M, Christensen HB, Sudarsan S, Stander EA, Baidoo E, Petzold CJ, Wulff T, O’Connor SE, Courdavault V, Jensen MK, Keasling JD

Nature

31-Aug-2022

PMCID:	PMC9452304
doi:	10.1038/s41586-022-05157-3
PMID:	36045295

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Ajmaline-sarpagine alkaloids
Ajmaline	6100671	Click to see CCC1C2CC3C4C5(CC(C2C5O)N3C1O)C6=CC=CC=C6N4C	326.40	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Aritmina	2073	Click to see CCC1C2CC3C4C5(CC(C2C5O)N3C1O)C6=CC=CC=C6N4C	326.40	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
> Alkaloids and derivatives / Yohimbine alkaloids
19-epi-Ajmalicine	179460	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1007/S00425-012-1608-Z
Aricine	251575	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=C4C=C(C=C5)OC	382.50	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Corynanthine	92766	Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O	354.40	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Deserpidine	8550	Click to see COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=CC=CC=C45)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC	578.70	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Isoreserpiline	161345	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC	412.50	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Isoreserpine	5701996	Click to see COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)OC(=O)C6=CC(=C(C(=C6)OC)OC)OC	608.70	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Lamuran	251561	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC=CC=C45	352.40	unknown	https://doi.org/10.1007/S00425-012-1608-Z
methyl (1S,15S,19S,20S)-18-hydroxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate	120635	Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O	354.40	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Rauwolscine	643606	Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O	354.40	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Reserpiline	67228	Click to see CC1C2CN3CCC4=C(C3CC2C(=CO1)C(=O)OC)NC5=CC(=C(C=C45)OC)OC	412.50	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
Yohimbine	8969	Click to see COC(=O)C1C(CCC2C1CC3C4=C(CCN3C2)C5=CC=CC=C5N4)O	354.40	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
> 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
[(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 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	via CMAUP database
Neoorthosiphol A	10055454	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)O)(C)C	692.70	unknown	via CMAUP database
Staminol B	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
staminol C	11490943	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)C)O)OC(=O)C5=CC=CC=C5)(C)C	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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(13R)-1alpha-(Benzoyloxy)-2alpha-acetoxy-3alpha,7alpha,8-trihydroxypimara-15-ene-11,14-dione	101228589	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)O	528.60	unknown	via CMAUP database
(13R)-1alpha-(Benzoyloxy)-2alpha,8-dihydroxy-3alpha,7alpha-diacetoxypimara-15-ene-11,14-dione	101228590	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)C)(C)C	570.60	unknown	via CMAUP database
(13R)-1alpha,11alpha-Bis(benzoyloxy)-2alpha,6beta,8-trihydroxy-3alpha,7alpha-diacetoxypimara-15-ene-14-one	10930480	Click to see CC(=O)OC1C(C2C(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)O	692.70	unknown	via CMAUP database
(13R)-1alpha,11alpha-Bis(benzoyloxy)-2alpha,7alpha,8-trihydroxy-3alpha-acetoxypimara-15-ene-14-one	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
(13S)-1alpha,11alpha-Bis(benzoyloxy)-3alpha,7alpha-diacetoxy-2alpha,8beta,12alpha-trihydroxypimara-15-ene-14-one	10032595	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
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-6,7-diacetyloxy-5-benzoyloxy-2-ethenyl-10,10a-dihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10327179	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C	676.70	unknown	via CMAUP database
[(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 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)OC(=O)C)(C)C	718.80	unknown	via CMAUP database
[(2R,4R,4aS,4bS,5R,6S,7S,8aS,9S,10R,10aR)-6,10-diacetyloxy-5-benzoyloxy-2-ethenyl-7,9,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	10101175	Click to see CC(=O)OC1C(C(C2C(C(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)OC(=O)C)O)(C)C)O	692.70	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
[(2S,3S,4R,4aS,4bS,5R,7R,8aR,9R,10aS)-2,3-diacetyloxy-7-ethenyl-5,8a,9-trihydroxy-1,1,4a,7-tetramethyl-8-oxo-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-4-yl] benzoate	10076785	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)O)O)O)(C)C)OC(=O)C	572.60	unknown	via CMAUP database
[(2S,3S,4S,4aS,4bS,5R,6S,7S,8aS,10R,10aR)-7,10-diacetyloxy-5-benzoyloxy-2-ethenyl-3,6,10a-trihydroxy-2,4b,8,8-tetramethyl-1-oxo-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-4-yl] benzoate	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
[(4aR,4bR,7R,8aR,9R,10aR)-3-acetyloxy-7-ethenyl-8a-hydroxy-1,1,4a,7-tetramethyl-2,5,8-trioxo-6,9,10,10a-tetrahydro-4bH-phenanthren-9-yl] acetate	10072248	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3=O)(C)C=C)O)C)OC(=O)C)(C)C	446.50	unknown	via CMAUP database
orthosiphol A	15385858	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	via CMAUP database
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	via CMAUP database
orthosiphol D	44583689	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=C)O)C)OC(=O)C)(C)C	552.60	unknown	via CMAUP database
orthosiphol I	10674582	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)C	570.60	unknown	via CMAUP database
orthosiphol J	10438744	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)C)(C)C	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	via CMAUP database
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 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	via CMAUP database
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	via CMAUP database
orthosiphol O	10032464	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)OC(=O)C5=CC=CC=C5)(C)C	676.70	unknown	via CMAUP database
Orthosiphol S	10099906	Click to see CC1(C2CC(C3(C(C2(C(C(=O)C1OC(=O)C4=CC=CC=C4)OC(=O)C5=CC=CC=C5)C)C(=O)CC(C3=O)(C)C=C)O)O)C	588.60	unknown	via CMAUP database
orthosiphol T	11082749	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)O	634.70	unknown	via CMAUP database
Orthosiphol U	637182	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)OC(=O)C)(C)C	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 CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)C)C(CC(C3=O)(C)C=C)O)O)O)(C)C)OC(=O)C5=CC=CC=C5	634.70	unknown	via CMAUP database
Orthosiphol Y	11144807	Click to see CC(=O)OC1CC2C(C(=O)C(=CC2(C3C1(C(=O)C(CC3O)(C)C=C)O)C)OC(=O)C)(C)C	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	via CMAUP database
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	via CMAUP database
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
Siphonol B	11017910	Click to see CC(=O)OC1C(C(C2CC(C3(C(C2(C1OC(=O)C4=CC=CC=C4)CO)C(CC(C3=O)(C)C=C)OC(=O)C5=CC=CC=C5)O)O)(C)C)OC(=O)C	692.70	unknown	via CMAUP database
Siphonol C	11115145	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)O)OC(=O)C)(C)C	692.70	unknown	via CMAUP database
SiphonolD	11828707	Click to see CC(=O)OCC12C(CC(C3(C1C(CC(C3=O)(C)C=C)OC(=O)C4=CC=CC=C4)O)O)C(C(C(C2OC(=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
Norstaminone A	10414921	Click to see CC(=O)C(=CC1C(=O)C(CC2C1(C(C(C(C2(C)C)O)OC(=O)C)OC(=O)C3=CC=CC=C3)C)OC(=O)C)C=C	540.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Vomifoliol	5280462	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(2R)-2-[[(1S,4aR,6S,8aR)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methyl]-3-methyl-2H-furan-5-one	162881984	Click to see CC1=CC(=O)OC1CC2C(=C)CCC3C2(CCC(C3(C)C)O)C	318.40	unknown	https://doi.org/10.3184/174751911X13220462651507
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,4S,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-4,9-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid	21604188	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C(=O)O	472.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	via CMAUP database
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/10.3184/174751911X13220462651507
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/10.3184/174751911X13220462651507
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
Ursolic Acid	64945	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
Siphonol E	10963687	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(C(=O)C(CC3OC(=O)C4=CC=CC=C4)(C)C=O)O)CO)OC(=O)C5=CC=CC=C5)OC(=O)C)OC(=O)C)(C)C	736.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
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	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide	10026486	Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3	444.50	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
Norstaminolactone A	11146922	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C14OC(=O)C(O4)(C(C3OC(=O)C5=CC=CC=C5)CNC)C)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C	707.80	unknown	via CMAUP database
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
Staminolactone A	10770905	Click to see CC(=O)OC1C(C(C2CC(C34C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C(C(O3)(C(=O)O4)C)C=C)OC(=O)C6=CC=CC=C6)O)(C)C)OC(=O)C	690.70	unknown	via CMAUP database
Staminolactone B	10676125	Click to see CC(=O)OC1C(C(C2CC(C34C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C(C(O3)(OC4=O)C)C=C)OC(=O)C6=CC=CC=C6)O)(C)C)OC(=O)C	690.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tetracarboxylic acids and derivatives
2-[(1S,2R,4R,4aR,6R,8R,8aS)-4-acetyloxy-8-benzoyloxy-1-(carboxymethyl)-6-ethenyl-4a-hydroxy-1,6-dimethyl-5-oxo-2,3,4,7,8,8a-hexahydronaphthalen-2-yl]-2-methylpropanoic acid	15548710	Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC(=O)O)C(C)(C)C(=O)O	544.60	unknown	via CMAUP database
secoorthosiphol B	15548728	Click to see CC(=O)OC1CC(C(C2C1(C(=O)C(CC2OC(=O)C3=CC=CC=C3)(C)C=C)O)(C)CC(=O)O)C(C)(C)C(=O)OC	558.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
L-Tartaric acid	444305	Click to see C(C(C(=O)O)O)(C(=O)O)O	150.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
13-Ethyl-9-methoxy-9-methyl-8,15-diazapentacyclo[9.7.1.02,7.08,19.012,17]nonadeca-2,4,6,12,14,16-hexaene	163192737	Click to see CCC1=C2C3CC(N4C3C(CC2=CN=C1)C5=CC=CC=C54)(C)OC	320.40	unknown	https://doi.org/10.1076/PHBI.39.3.239.5923
> Organoheterocyclic compounds / Naphthopyrans
[(1S,2S,3R,4S,5S,7S,9R,10R,12R,15S,16S,17S)-4,9-diacetyloxy-3-benzoyloxy-5,10,15-trihydroxy-2,6,6,12-tetramethyl-11,13-dioxatetracyclo[8.7.0.02,7.012,16]heptadecan-17-yl] benzoate	10963538	Click to see CC(=O)OC1CC2C(C(C(C(C2(C3C1(OC4(C(C3OC(=O)C5=CC=CC=C5)C(CO4)O)C)O)C)OC(=O)C6=CC=CC=C6)OC(=O)C)O)(C)C	696.70	unknown	via CMAUP database
Norstaminol A	11765116	Click to see CC(=O)OC1C(C(C2CC3C4(O3)C(C2(C1OC(=O)C5=CC=CC=C5)C)C(C6C(COC6(O4)C)O)OC(=O)C7=CC=CC=C7)(C)C)OC(=O)C	678.70	unknown	via CMAUP database
Norstaminol C	10951829	Click to see CC(=O)C1=CC2C3(C(CC(C24OCC1O4)OC(=O)C)C(C(C(C3OC(=O)C5=CC=CC=C5)OC(=O)C)O)(C)C)C	556.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid	639655	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	via CMAUP database
2-Propenoic acid, 3-(3,4-dihydroxyphenyl)-, ethyl ester	66883	Click to see CCOC(=O)C=CC1=CC(=C(C=C1)O)O	208.21	unknown	via CMAUP database
Methyl 3,4-dihydroxycinnamate	92202	Click to see COC(=O)C=CC1=CC(=C(C=C1)O)O	194.18	unknown	via CMAUP database
Methyl rosmarinate	6479915	Click to see COC(=O)C(CC1=CC(=C(C=C1)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O	374.30	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 / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid	2518	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
Caffeic Acid	689043	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3',4',6,7-tetramethoxyflavone	152430	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC	358.30	unknown	via CMAUP database
5-Hydroxy-3',4',7-trimethoxyflavone	5272653	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O)OC	328.30	unknown	via CMAUP database
6-Hydroxy-5,7-dimethoxy-2-(4-methoxyphenyl)-4H-chromen-4-one	243760	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)OC	328.30	unknown	via CMAUP database
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	via CMAUP database
Ladanein	3084066	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)O)O	314.29	unknown	via CMAUP database
Salvigenin	161271	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O	328.30	unknown	via CMAUP database
Sinensetin	145659	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC	372.40	unknown	via CMAUP database
Tetramethylscutellarein	96118	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)OC	342.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
2-(3,4-Dimethoxyphenyl)-6,7,8-trimethoxy-4H-1-benzopyran-4-one	44584772	Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=CC(=C(C(=C3O2)OC)OC)OC)OC	372.40	unknown	via CMAUP database

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Rauvolfia tetraphylla

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