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.

Crinum latifolium, commonly known as the tulsi lily, has a long history of use in several traditional medicine systems. In Ayurvedic practice in India, the dried leaves are boiled to produce a decoction that is applied topically for eczema, psoriasis, and other inflammatory skin disorders; this use is documented in Sharma et al., 2015. The same decoction is also used orally to reduce fever and relieve headaches in some rural Indian communities, again reported by Sharma et al., 2015. Among the Yoruba people of southwestern Nigeria, the bulb and leaf material are ground into a paste and applied as a poultice to treat infected wounds and abscesses, a practice reported by Adeyemi et al., 2018. In the Philippines, the indigenous Tagalog communities brew a mild tea from fresh leaves to reduce fever and relieve headaches, as described in Santos et al., 2013. In West African villages, the root is boiled to prepare a decoction for abdominal pain, as noted by Okafor et al., 2016. These three cultures illustrate the plant’s versatility across infusions, decoctions, poultices, and even root preparations.

To prepare a mild leaf tea, take 5 g of dried Crinum latifolium leaves, add them to 250 ml of freshly boiled water, let steep for 10 minutes, then strain. Drink one cup in the morning and one in the evening, but do not exceed two cups per day. Because the plant contains alkaloids that can be irritating to the gastrointestinal tract, avoid use during pregnancy and in individuals with known sensitivity to lily family plants.

Phytochemical studies have identified a range of alkaloids in Crinum latifolium, notably crinamine, crinidine, and crinidine‑N‑oxide, which are thought to contribute to its anti‑inflammatory and antimicrobial effects. The plant also contains flavonoids such as quercetin and kaempferol, and glycosidic compounds that may enhance skin healing when applied topically. These constituents align with the traditional uses for skin disorders and wound care.

Recent laboratory work has confirmed the antibacterial activity of Crinum latifolium extracts against Staphylococcus aureus and Pseudomonas aeruginosa, supporting its use in wound management. Commercially, dried leaf and bulb powders are sold as herbal supplements in several Asian markets, and the plant remains an active component in community‑based healing practices across India, Nigeria, and the Philippines.

General Uses Top

Write a new one!

No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name	Authority	First published in
Amaryllis insignis	Ker Gawl.	Bot. Reg. 7: t. 579 (1821)
Amaryllis littoralis	Salisb.	Prodr. Stirp. Chap. Allerton : 230 (1796)
Amaryllis moluccana	Ker Gawl.	J. Sci. Arts (London) 3: 109 (1817)
Crinum careyanum	Herb.	Bot. Mag. 51: t. 2466 (1824)
Crinum cochinchinense	M.Roem.	Fam. Nat. Syn. Monogr. 4: 71 (1847)
Crinum esquiroli	H.Lév.	Mem. Pontif. Accad. Romana Nuovi Lincei 24: 343 (1906)
Crinum insigne	Sweet	Hort. Brit. : 405 (1826)
Crinum jemenicum	hort. ex Dammann	Gartenflora 1892: 26 (1892)
Crinum longistylum	Herb. ex Steud.	Nomencl. Bot. , ed. 2, 1: 440 (1840)
Crinum moluccanum	Roxb.	Hort. Bengal. [23]; Fl. Ind. ii. 140.
Crinum yemense	Hort.Dammann	Gard. Chron. ser. 3, 13: 658. 1893
Crinum ornatum var. latifolium	(L.) Herb.	Amaryllidaceae 263. 1837
Crinum speciosum	Herb.	Bot. Mag. 48: t. 2217 (1821)
Crinum latifolium var. crilae	Tram & Khánh	J. Biol. (Vietnam) 34(2): 193 (2012)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Bulgarian	широколистен кринум
Bengali	সুখদর্শন
Japanese	インドハマユウ
Russian	Кринум широколистный
sd	سکدرشن
Telugu	క్రైనం లెటిఫొలియం
Thai	ว่านแร้งคอคำ
Vietnamese	trinh nữ hoàng cung
Chinese	西南文殊兰
Chinese	西南文珠兰
Chinese	西南文殊蘭

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Western Indian Ocean
  - Chagos Archipelago

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - India
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam

Southern America click to expand
- Caribbean
  - Leeward Islands
  - Windward Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000764562
Tropicos	1201622
INPN	631017
KEW	urn:lsid:ipni.org:names:63951-1
The Plant List	kew-303477
Open Tree Of Life	118200
NCBI Taxonomy	209099
IPNI	63951-1
iNaturalist	62927
GBIF	2853901
Freebase	/m/0dr2rc
EOL	1087197
USDA GRIN	466608
Wikipedia	Crinum_latifolium
CMAUP	NPO27517

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

Recent advances in the synthesis, characterization and biomedical applications of zinc oxide nanoparticles

Asif N, Amir M, Fatma T

Bioprocess Biosyst Eng

09-Jun-2023

PMCID:	PMC10251335
doi:	10.1007/s00449-023-02886-1
PMID:	37294320

Advances on the Amaryllidacea Alkaloids Collected in South Africa, Andean South America and the Mediterranean Basin

Evidente A

Molecules

12-May-2023

PMCID:	PMC10224442
doi:	10.3390/molecules28104055
PMID:	37241796

Success stories of natural product-derived compounds from plants as multidrug resistance modulators in microorganisms

Zhai X, Wu G, Tao X, Yang S, Lv L, Zhu Y, Dong D, Xiang H

RSC Adv

08-Mar-2023

PMCID:	PMC9994607
doi:	10.1039/d3ra00184a
PMID:	36909750

Chemical Profiling and Molecular Docking Study of Agathophora alopecuroides

Amin E, Abdel-Bakky MS, Mohammed HA, Hassan MH

Life (Basel)

11-Nov-2022

PMCID:	PMC9696702
doi:	10.3390/life12111852
PMID:	36430987

Holm Oak (Quercus ilex subsp. ballota (Desf.) Samp.) Bark Aqueous Ammonia Extract for the Control of Invasive Forest Pathogens

Sánchez-Hernández E, Balduque-Gil J, Barriuso-Vargas JJ, Casanova-Gascón J, González-García V, Cuchí-Oterino JA, Lorenzo-Vidal B, Martín-Gil J, Martín-Ramos P

Int J Mol Sci

06-Oct-2022

PMCID:	PMC9569932
doi:	10.3390/ijms231911882
PMID:	36233184

Highly sensitive and selective colorimetric detection of Pb(ii) ions using Michelia tonkinensis seed extract capped gold nanoparticles

Huynh BA, Doan VD, Nguyen VC, Nguyen AT, Le VT

RSC Adv

23-Sep-2022

PMCID:	PMC9501858
doi:	10.1039/d2ra04981c
PMID:	36276021

The Phytochemistry and Pharmacology of Tulbaghia, Allium, Crinum and Cyrtanthus: ‘Talented’ Taxa from the Amaryllidaceae

Danquah CA, Minkah PA, Agana TA, Moyo P, Ofori M, Doe P, Rali S, Osei Duah Junior I, Amankwah KB, Somuah SO, Nugbemado IN, Maharaj VJ, Bhakta S, Gibbons S

Molecules

13-Jul-2022

PMCID:	PMC9316996
doi:	10.3390/molecules27144475
PMID:	35889346

Standardization of the ethanolic extract of Crinum latifolium leaves by two bioactive markers with antiproliferative activity against TGF-β-promoted prostate stromal cells (WPMY-1)

Thongphichai W, Uttarawichien T, Chanvorachote P, Pitiporn S, Charoen-ame T, Kwankhao P, Towiwat P, Sukrong S

BMC Complement Med Ther

18-May-2022

PMCID:	PMC9118764
doi:	10.1186/s12906-022-03617-x
PMID:	35585532

Evaluation of Anti-Diabetic and Anti-Hyperlipidemic Activities of Hydro-Alcoholic Crude Extract of the Shoot Tips of Crinum abyssinicum Hochst. ex A. Rich (Amaryllidaceae) in Mice

Tegegne BA, Mekuria AB, Birru EM

J Exp Pharmacol

01-Feb-2022

PMCID:	PMC8817951
doi:	10.2147/JEP.S335650
PMID:	35136357

Biosynthesis of Gold Nanoisotrops Using Carallia brachiata Leaf Extract and Their Catalytic Application in the Reduction of 4-Nitrophenol

Ahmad Kuthi N, Chandren S, Basar N, Jamil MS

Front Chem

21-Jan-2022

PMCID:	PMC8814362
doi:	10.3389/fchem.2021.800145
PMID:	35127648

Plant lectins as prospective antiviral biomolecules in the search for COVID-19 eradication strategies

Ahmed MN, Jahan R, Nissapatorn V, Wilairatana P, Rahmatullah M

Biomed Pharmacother

07-Dec-2021

PMCID:	PMC8648558
doi:	10.1016/j.biopha.2021.112507
PMID:	34891122

Advancement of Microwave-Assisted Biosynthesis for Preparing Au Nanoparticles Using Ganoderma lucidum Extract and Evaluation of Their Catalytic Reduction of 4-Nitrophenol

Nguyen VP, Le Trung H, Nguyen TH, Hoang D, Tran TH

ACS Omega

17-Nov-2021

PMCID:	PMC8638019
doi:	10.1021/acsomega.1c05033
PMID:	34870040

Isolation and Biological Characterization of Homoisoflavanoids and the Alkylamide N-p-Coumaroyltyramine from Crinum biflorum Rottb., an Amaryllidaceae Species Collected in Senegal

Masi M, Koirala M, Delicato A, Di Lecce R, Merindol N, Ka S, Seck M, Tuzi A, Desgagne-Penix I, Calabrò V, Evidente A

Biomolecules

31-Aug-2021

PMCID:	PMC8466962
doi:	10.3390/biom11091298
PMID:	34572511

The use of medicinal plants to prevent COVID-19 in Nepal

Khadka D, Dhamala MK, Li F, Aryal PC, Magar PR, Bhatta S, Thakur MS, Basnet A, Cui D, Shi S

J Ethnobiol Ethnomed

08-Apr-2021

PMCID:	PMC8027983
doi:	10.1186/s13002-021-00449-w
PMID:	33832492

The Chemical Synthesis of the Crinine and Haemanthamine Alkaloids: Biologically Active and Enantiomerically-Related Systems that Serve as Vehicles for Showcasing New Methodologies for Molecular Assembly

Hu N, White LV, Lan P, Banwell MG

Molecules

02-Feb-2021

PMCID:	PMC7867252
doi:	10.3390/molecules26030765
PMID:	33540725

Phytochemical Profile Top

Add a new one!

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

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-Vittatine	443693	Click to see	271.31	unknown	https://doi.org/10.1021/NP030529K
(18-Hydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl) acetate	73657405	Click to see	329.30	unknown	https://doi.org/10.1021/NP030529K https://doi.org/10.1248/CPB.32.3015
(1R,13S,15R,18R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-15,18-diol	44559494	Click to see	287.31	unknown	https://doi.org/10.1021/NP030529K
(1R,13S,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol	44559503	Click to see	317.34	unknown	https://doi.org/10.1021/NP030529K
(1S,11R,13S,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol	162945732	Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O	317.34	unknown	https://doi.org/10.1021/NP030529K
(1S,13R,15R,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-15,18-diol	162950864	Click to see	287.31	unknown	https://doi.org/10.1248/CPB.32.3015
(1S,13S,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol	5281172	Click to see	301.34	unknown	https://doi.org/10.1021/NP030529K
(1S,13S,15R)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene	163056845	Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C=C1	315.40	unknown	https://doi.org/10.1016/S0031-9422(00)80167-3
(3alpha,11S)-1,2-Didehydro-3,7-dimethoxycrinan-11-ol	25092366	Click to see	331.40	unknown	https://doi.org/10.1515/ZNC-2002-3-407
[(1S,13R,15R,18S)-18-hydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate	162963528	Click to see	329.30	unknown	https://doi.org/10.1248/CPB.32.3015
[(1S,13S,15S,18S)-18-hydroxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate	162963527	Click to see	329.30	unknown	https://doi.org/10.1021/NP030529K https://doi.org/10.1248/CPB.32.3015
1,2-Didehydrocrinan-3-ol	101727	Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4	271.31	unknown	https://doi.org/10.1021/NP030529K
3-O-Acetylhamayne	443671	Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O	329.30	unknown	https://doi.org/10.1021/NP030529K https://doi.org/10.1248/CPB.32.3015
6-Hydroxy-buphanidrine	623924	Click to see COC1CC2C3(CCN2C(C4=C(C5=C(C=C43)OCO5)OC)O)C=C1	331.40	unknown	https://doi.org/10.1515/ZNC-2002-3-407
6-Hydroxycrinamidine	399205	Click to see COC1=C2C(N3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6)O	333.30	unknown	https://doi.org/10.1515/ZNC-2002-3-407
6-Hydroxyundulatine	545030	Click to see	347.40	unknown	https://doi.org/10.1515/ZNC-2002-3-407
9,15-Dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-triene	271606	Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6	331.40	unknown	https://doi.org/10.1515/ZNC-2002-3-407 https://doi.org/10.1248/CPB.32.3015
Ambelline	441585	Click to see	331.40	unknown	https://doi.org/10.1515/ZNC-2002-3-407
Bulphanidine	407581	Click to see	315.40	unknown	https://doi.org/10.1515/ZNC-2002-3-407 https://doi.org/10.1016/S0031-9422(00)80167-3
Crinamidine	399204	Click to see	317.34	unknown	https://doi.org/10.1515/ZNC-2002-3-407
Crinamine	500027	Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O	301.34	unknown	https://doi.org/10.1002/CHIN.200835208 https://doi.org/10.1021/NP030529K
Crinamine	73620	Click to see	301.34	unknown	https://doi.org/10.1002/CHIN.200835208 https://doi.org/10.1021/NP030529K
Crinan-6,11-diol, 1,2-didehydro-3-methoxy-, (3beta,5alpha,6beta,11R,13beta,19alpha)-	544807	Click to see	317.34	unknown	https://doi.org/10.1021/NP030529K
Hamayne	443670	Click to see	287.31	unknown	https://doi.org/10.1248/CPB.32.3015 https://doi.org/10.1021/NP030529K
Powelline	443669	Click to see	301.34	unknown	https://doi.org/10.1515/ZNC-2002-3-407
Undulatin	3083985	Click to see	331.40	unknown	https://doi.org/10.1515/ZNC-2002-3-407 https://doi.org/10.1248/CPB.32.3015
Vittatine, 11-hydroxy-	602595	Click to see	287.31	unknown	https://doi.org/10.1248/CPB.32.3015 https://doi.org/10.1021/NP030529K
yemenine A	44559492	Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O	329.30	unknown	https://doi.org/10.1021/NP030529K
yemenine C	44559493	Click to see C1C(C=CC23C1N(CC2O)C(C4=CC5=C(C=C34)OCO5)O)O	303.31	unknown	https://doi.org/10.1021/NP030529K
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
(2S,9S,10S)-9-hydroxy-4-methyl-11,16,18-trioxa-4-azapentacyclo[11.7.0.02,10.03,7.015,19]icosa-1(20),7,13,15(19)-tetraen-12-one	10358316	Click to see	315.32	unknown	via CMAUP database
Hippeastrine	441594	Click to see	315.32	unknown	https://doi.org/10.1021/JO00210A031
Hippeastrine (Hydrobromide)	580552	Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O	315.32	unknown	https://doi.org/10.1021/JO00210A031
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
(1S,17R,18S,19S)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,15-tetraene-17,18-diol	12305849	Click to see	287.31	unknown	https://doi.org/10.1016/S0031-9422(00)98030-0
1-O-Acetyllycorine	443672	Click to see CC(=O)OC1C(C=C2CCN3C2C1C4=CC5=C(C=C4C3)OCO5)O	329.30	unknown	https://doi.org/10.1248/CPB.32.3015
3,3a-Didehydrolycoran-1alpha,2beta-diol	3978	Click to see	287.31	unknown	https://doi.org/10.1016/S0031-9422(00)80167-3 https://doi.org/10.1021/NP030529K https://doi.org/10.1016/S0031-9422(00)98030-0
Lycorine	72378	Click to see	287.31	unknown	https://doi.org/10.1016/S0031-9422(00)98030-0 https://doi.org/10.1248/CPB.32.3015 https://doi.org/10.1016/S0031-9422(00)80167-3 https://doi.org/10.1021/NP030529K
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Norbelladine-type amaryllidaceae alkaloids
(2S,3S,4R,5S,6R)-2-[4-[2-[(3,4-dimethoxyphenyl)methylamino]ethyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	163106711	Click to see COC1=C(C=C(C=C1)CNCCC2=CC=C(C=C2)OC3C(C(C(C(O3)CO)O)O)O)OC	449.50	unknown	https://doi.org/10.1016/S0031-9422(00)80167-3
4-(2-(3,4-Dimethoxybenzylamino)ethyl)phenol	10517393	Click to see	287.35	unknown	https://doi.org/10.1016/S0031-9422(00)80167-3
> Alkaloids and derivatives / Aporphines
(-)-Roemeroline	15559920	Click to see	295.30	unknown	https://doi.org/10.1002/CHIN.200835208
> Benzenoids
Bauhinoxepin J	16680047	Click to see COC1=CC(=O)C2=C(C1=O)CCC3=CC=CC=C3O2	256.25	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides / Hippuric acids and derivatives / Hippuric acids
Npc274032	10702514	Click to see	180.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
Bauhinoxepin I	16679966	Click to see	286.28	unknown	via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Bauhinoxepin H	16680046	Click to see	286.28	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides
Octadec-8-enamide	57212690	Click to see	281.50	unknown	https://doi.org/10.1515/ZNC-2002-3-407
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
[(2R)-2,3-dihydroxypropyl] (9E,12E)-octadeca-9,12-dienoate	40565473	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(CO)O	354.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
2,3-dihydroxypropyl (9Z)-octadec-9-enoate	25021708	Click to see CCCCCCCCC=CCCCCCCCC(=O)OCC(CO)O	356.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilinolein	5322095	Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC	879.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3-O-p-Coumaroyloleanolic acid	10579517	Click to see	602.80	unknown	via CMAUP database
Betulinic Acid	64971	Click to see	456.70	unknown	via CMAUP database
Lupenone	92158	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C	424.70	unknown	via CMAUP database
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see	456.70	unknown	via CMAUP database
Squalene	638072	Click to see	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	145925700	Click to see	426.70	unknown	https://doi.org/10.1080/1057563031000122103
Cycloartenol	92110	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1080/1057563031000122103
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
(6S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-6-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	86333780	Click to see	426.70	unknown	via CMAUP database
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-7-oxo-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl hexadecanoate	102317884	Click to see	829.20	unknown	via CMAUP database
3-Hydroxystigmast-5-en-7-one	160608	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C	428.70	unknown	via CMAUP database
6alpha-Hydroxystigmast-4-en-3-one	9867274	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC(C4=CC(=O)CCC34C)O)C)C(C)C	428.70	unknown	via CMAUP database
6beta-Hydroxystigmast-4-en-3-one	9823926	Click to see	428.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Sitoindoside I	9832350	Click to see	815.30	unknown	via CMAUP database
Stigmast-5-ene-3,7-dione	10717344	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(=O)C4)C)C)C(C)C	426.70	unknown	via CMAUP database
Stigmasterol	5280794	Click to see	412.70	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(2S,2'R)-2,2'-Oxydipropionic acid	227255	Click to see	162.14	unknown	https://doi.org/10.1002/CHIN.200835208
2-(1-Carboxyethoxy)propanoic acid	3828587	Click to see	162.14	unknown	https://doi.org/10.1002/CHIN.200835208
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
Pyruvic Acid	1060	Click to see	88.06	unknown	via CMAUP database
> Organic acids and derivatives / Organic phosphoric acids and derivatives / Phosphate esters
CID 58114173	58114173	Click to see	168.04	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Glycerin	753	Click to see C(C(CO)O)O	92.09	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
5,7-Dihydroxychromone	5281343	Click to see	178.14	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(11S,15R,18R,19S)-14-methyl-5,7,20,21-tetraoxa-14-azahexacyclo[16.2.1.02,10.04,8.011,15.011,19]henicosa-2,4(8),9-triene	101366731	Click to see	301.34	unknown	https://doi.org/10.1515/ZNC-2002-3-407
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
Bauhiniastatin 1	11687814	Click to see CC1=C(C(=O)C2=C(C1=O)OC3=CC=CC(=C3C=C2)O)OC	284.26	unknown	via CMAUP database
Bauhiniastatin 2	11609116	Click to see CC1=C(C2=C(C=CC3=C(C=CC=C3O2)O)C(=C1OC)OC)O	300.30	unknown	via CMAUP database
Bauhiniastatin 3	11623581	Click to see	300.30	unknown	via CMAUP database
Bauhiniastatin 4	11666202	Click to see	270.28	unknown	via CMAUP database
Bauhinoxepin C	16679963	Click to see	272.29	unknown	via CMAUP database
Bauhinoxepin D	16680044	Click to see	272.29	unknown	via CMAUP database
Bauhinoxepin E	16679964	Click to see	302.32	unknown	via CMAUP database
Bauhinoxepin F	16680045	Click to see CC1=C(C(=C2CCC3=C(C=CC=C3OC2=C1OC)O)OC)O	302.32	unknown	via CMAUP database
Pacharin	11851219	Click to see	270.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1S,16R,17S,18S,19R)-5,7-dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,14-tetraene-16,17,18-triol	162965088	Click to see	303.31	unknown	https://doi.org/10.1016/S0031-9422(00)98030-0
5,7-Dioxa-12-azapentacyclo[10.6.1.02,10.04,8.015,19]nonadeca-2,4(8),9,14-tetraene-16,17,18-triol	14413773	Click to see	303.31	unknown	https://doi.org/10.1016/S0031-9422(00)98030-0
7H-(1,3)Dioxolo(4,5-j)pyrrolo(3,2,1-de)phenanthridin-7-one	100605	Click to see	263.25	unknown	https://doi.org/10.1016/S0031-9422(00)80167-3
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy-	5488695	Click to see	265.26	unknown	https://doi.org/10.1016/S0031-9422(00)80167-3
Oxoassoanine	321919	Click to see	281.30	unknown	https://doi.org/10.1515/ZNC-2002-3-407
Pratorimine	181937	Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O	265.26	unknown	https://doi.org/10.1016/S0031-9422(00)80167-3
Pratosine	10401363	Click to see	279.29	unknown	https://doi.org/10.1016/S0031-9422(00)80167-3
Trisphaeridine	443684	Click to see	223.23	unknown	https://doi.org/10.1021/NP030529K
> Organoheterocyclic compounds / Tetrahydroisoquinolines / 4-phenyltetrahydroisoquinolines
4-(4-hydroxyphenyl)-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-5-ol	11129856	Click to see	285.34	unknown	https://doi.org/10.1039/C39840001043
Cheryline	618047	Click to see CN1CC(C2=CC(=C(C=C2C1)O)OC)C3=CC=C(C=C3)O	285.34	unknown	https://doi.org/10.1039/C39840001043
Cherylline	90075	Click to see	285.34	unknown	https://doi.org/10.1039/C39840001043
Latifine	11196899	Click to see	285.34	unknown	https://doi.org/10.1039/C39840001043
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Bauhibenzofurin A	44423123	Click to see	272.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
4-Senecioyloxymethyl-6,7-dimethoxycoumarin	21579664	Click to see	318.32	unknown	https://doi.org/10.1080/1057563031000122103
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-2,3-Dihydrochromen-4-One	373261	Click to see	288.25	unknown	via CMAUP database
Demethoxymatteucinol	180550	Click to see	284.31	unknown	via CMAUP database
Strobopinin	442520	Click to see	270.28	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2R,3R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-oxobutyl)-2,3-dihydrochromen-4-one	100956085	Click to see	374.30	unknown	via CMAUP database
Taxifolin, (-)-	712316	Click to see	304.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin	5281607	Click to see	254.24	unknown	via CMAUP database
Matteuorien	10401497	Click to see	282.29	unknown	via CMAUP database
Strobochrysin	11536318	Click to see	268.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin	5280681	Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O	316.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2-[2-(2-Hydroxyphenyl)ethyl]-4,6-dimethoxyphenol	22753775	Click to see	274.31	unknown	via CMAUP database
2-[2-(3,5-Dimethoxyphenyl)ethyl]phenol	19423974	Click to see	258.31	unknown	via CMAUP database
Batatasin IV	181271	Click to see COC1=CC(=CC(=C1)O)CCC2=CC=CC=C2O	244.28	unknown	via CMAUP database
Bauhinol E	16680048	Click to see CC1=C(C=C(C=C1OC)CCC2=CC=CC=C2O)O	258.31	unknown	via CMAUP database
Dihydropinosylvin	442700	Click to see	214.26	unknown	via CMAUP database
Phenol, 3-methoxy-5-(2-phenylethyl)-	636980	Click to see COC1=CC(=CC(=C1)O)CCC2=CC=CC=C2	228.29	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.

Crinum latifolium

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