Scientific name	Authority	First published in
Haemanthus albomaculatus	Baker	Gard. Chron. , n.s., 9: 202 (1878)
Haemanthus intermedius	M.Roem.	Fam. Nat. Syn. Monogr. 4: 36 (1847)
Haemanthus leucanthus	Miq.	J. Bot. Néerl. 1: 33 (1861)
Haemanthus virescens	Herb.	Amaryllidaceae : 235 (1837)
Diacles ciliaris	(L.) Salisb.	Gen. Pl. : 130 (1866)
Diacles pubescens	Salisb.	Gen. Pl. [Salisbury] 130. 1866 [Apr-May 1866]
Haemanthus albiflos var. brachyphyllus	Baker	Fl. Cap. 6: 235. 1896
Haemanthus albiflos var. burchellii	Baker	Fl. Cap. 6: 235. 1896
Haemanthus virescens var. pubescens	Herb.	Amaryllidaceae 235 1837
Haemanthus albiflos var. pubescens	(Herb.) Baker	Fl. Cap. 3: 235 1896
Haemanthus virescens var. intermedius	Herb.	Amaryllidaceae 235. 1837

Common names Top

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Filter by language:

Language	Common/alternative name
Arabic	زهرة الدم بيضاء الأزهار
Czech	bělokvět bělokvětý
Esperanto	sangofloro
Esperanto	blankflora hemanto
Croatian	slonov jezik
Croatian	slonovo uho (zvanikovke)
li	poejerbustel
Polish	krasnokwiat białokwiatowy
Punjab	رنگوالا برش
Swedish	elefanttunga
Chinese	白花网球花
Chinese	虎耳兰
Chinese	虎耳蘭

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Southern Africa
  - Cape Provinces
  - Kwazulu-Natal

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000647035
Tropicos	1200114
KEW	urn:lsid:ipni.org:names:64682-1
The Plant List	kew-276772
Open Tree Of Life	612499
NCBI Taxonomy	240634
IPNI	64682-1
iNaturalist	431086
GBIF	2855156
Freebase	/m/02x4mz0
EPPO	HNUAL
EOL	992160
Elurikkus	317792
USDA GRIN	18148
Wikipedia	Haemanthus_albiflos
CMAUP	NPO17050

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

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

Stomata in Close Contact: The Case of Pancratium maritimum L. (Amaryllidaceae)

Saridis P, Georgiadou X, Shtein I, Pouris J, Panteris E, Rhizopoulou S, Constantinidis T, Giannoutsou E, Adamakis ID

Plants (Basel)

05-Dec-2022

PMCID:	PMC9740904
doi:	10.3390/plants11233377
PMID:	36501416

Carbon dioxide expanded liquid: an effective solvent for the extraction of quercetin from South African medicinal plants

Pilařová V, Kuda L, Vlčková HK, Nováková L, Gupta S, Kulkarni M, Švec F, Van Staden J, Doležal K

Plant Methods

23-Jun-2022

PMCID:	PMC9219150
doi:	10.1186/s13007-022-00919-6
PMID:	35739596

Ethnobotany and Toxicity Status of Medicinal Plants with Cosmeceutical Relevance from Eastern Cape, South Africa

Ndhlala AR, Thibane VS, Masehla CM, Mokwala PW

Plants (Basel)

30-May-2022

PMCID:	PMC9182599
doi:	10.3390/plants11111451
PMID:	35684224

Prophyll in Monocots: The Starting Point of Lateral Shoot Phyllotaxis

Choob V

Front Plant Sci

13-Apr-2022

PMCID:	PMC9044502
doi:	10.3389/fpls.2022.855146
PMID:	35498710

A dormant resource for genome size estimation in ferns: C‐value inference of the Ophioglossaceae using herbarium specimen spores

Kuo L, Tang SK, Kao T, Ebihara A, Fawcett S, Hsiao M, Shinohara W, Dauphin B

Appl Plant Sci

07-Dec-2021

PMCID:	PMC8664048
doi:	10.1002/aps3.11452
PMID:	34938613

Reference standards for flow cytometric estimation of absolute nuclear DNA content in plants

Temsch EM, Koutecký P, Urfus T, Šmarda P, Doležel J

Cytometry A

18-Aug-2021

PMCID:	PMC9545105
doi:	10.1002/cyto.a.24495
PMID:	34405937

Diversity of Plastid Types and Their Interconversions

Choi H, Yi T, Ha SH

Front Plant Sci

17-Jun-2021

PMCID:	PMC8248682
doi:	10.3389/fpls.2021.692024
PMID:	34220916

Antiviral Evaluation of Herbal Drugs

Mukherjee PK

Quality Control and Evaluation of Herbal Drugs

21-Jun-2019

PMCID:	PMC7149824
doi:	10.1016/B978-0-12-813374-3.00016-8

Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus

Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J

Int J Mol Sci

14-May-2018

PMCID:	PMC5983620
doi:	10.3390/ijms19051459
PMID:	29757986

Calreticulin localizes to plant intra/extracellular peripheries of highly specialized cells involved in pollen-pistil interactions

Wasąg P, Suwińska A, Zakrzewski P, Walczewski J, Lenartowski R, Lenartowska M

Protoplasma

15-Jun-2017

PMCID:	PMC5756280
doi:	10.1007/s00709-017-1134-8
PMID:	28620697

Traditional Medicines in the World: Where to Go Next?

Pan SY, Litscher G, Chan K, Yu ZL, Chen HQ, Ko KM

Evid Based Complement Alternat Med

29-Dec-2014

PMCID:	PMC4295149
doi:	10.1155/2014/739895
PMID:	25610481

Lipotubuloids in ovary epidermis of Ornithogalum umbellatum act as metabolons: suggestion of the name ‘lipotubuloid metabolon’

Kwiatkowska M, Polit JT, Stępiński D, Popłońska K, Wojtczak A, Domίnguez E, Heredia A

J Exp Bot

24-Dec-2014

PMCID:	PMC4438445
doi:	10.1093/jxb/eru469
PMID:	25540439

Homogalacturonan deesterification during pollen–ovule interaction in Larix decidua Mill.: an immunocytochemical study

Rafińska K, Świdziński M, Bednarska-Kozakiewicz E

Planta

04-May-2014

PMCID:	PMC4065381
doi:	10.1007/s00425-014-2074-6
PMID:	24793355

Phytotherapeutic Information on Plants Used for the Treatment of Tuberculosis in Eastern Cape Province, South Africa

Lawal IO, Grierson DS, Afolayan AJ

Evid Based Complement Alternat Med

22-Apr-2014

PMCID:	PMC4016884
doi:	10.1155/2014/735423
PMID:	24864158

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
(1S,13R,14R,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-14,18-diol	162934987	Click to see COC1C=CC23C(CN(C2C1O)CC4=CC5=C(C=C34)OCO5)O	317.34	unknown	https://doi.org/10.3987/COM-93-6668
(1S,13R,15S,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	38988650	Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O	301.34	unknown	https://doi.org/10.3987/COM-93-6668
15-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-14,18-diol	162934986	Click to see COC1C=CC23C(CN(C2C1O)CC4=CC5=C(C=C34)OCO5)O	317.34	unknown	https://doi.org/10.3987/COM-93-6668
Crinamine	500027	Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O	301.34	unknown	https://doi.org/10.3987/COM-93-6668
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
Sekisanolin	5321780	Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O	331.40	unknown	https://doi.org/10.1002/CBER.19540871011 https://doi.org/10.1021/JA01610A045
Tazettine	271607	Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O	331.40	unknown	https://doi.org/10.1021/JA01610A045 https://doi.org/10.1002/CBER.19540871011
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-dimethoxybenzoate	370912	Click to see COC1=C(C(=CC=C1)OC)C(=O)OCC2=CC=CC=C2	272.29	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D	10905866	Click to see CC1=C2CC(C3(C(CCCC3(C2=CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5	418.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid	5192	Click to see C(CCCCC(=O)O)CCCC(=O)O	202.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10698321	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C	572.60	unknown	via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10531102	Click to see CC1C2C(CC3=C1C=CO3)C4(CC=CC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C	570.60	unknown	via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate	6479669	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C	464.60	unknown	via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate	10951647	Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)COC(=O)C6=CC=CC=C6	540.60	unknown	via CMAUP database
Isovouacapenol A	636673	Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C	420.50	unknown	via CMAUP database
Isovouacapenol B	11812203	Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3(C)O)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C	438.60	unknown	via CMAUP database
Isovouacapenol C	3009285	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C	438.60	unknown	via CMAUP database
Pulcharrin G	11750983	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)O)O)(C)C)C	438.60	unknown	via CMAUP database
Pulcherrimin F	11375664	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)C	510.60	unknown	via CMAUP database
Pulcherrin D	54597502	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(CC2OC(=O)C)O)(C)C)C	360.50	unknown	via CMAUP database
Pulcherrin E	54597503	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)O)O)(C)C)C	376.50	unknown	via CMAUP database
Pulcherrin F	54597504	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C)O)(C)C)C	376.50	unknown	via CMAUP database
Pulcherrin H	54597566	Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O	422.60	unknown	via CMAUP database
Pulcherrin I	54597567	Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5	422.60	unknown	via CMAUP database
Pulcherrin J	54597568	Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C=CC5=CC=CC=C5	448.60	unknown	via CMAUP database
Pulcherrin K	53388795	Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C=O)C	452.50	unknown	via CMAUP database
Pulcherrin L	53388797	Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O	438.60	unknown	via CMAUP database
Pulcherrin M	54597569	Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5	452.50	unknown	via CMAUP database
Pulcherrin O	53388938	Click to see CC(=O)OC1C(C2C(CC3=C(C2C(=O)OC)C=CO3)C4(C1(C(C(CC4)OC(=O)C5=CC=CC=C5)(C)C)O)C)O	540.60	unknown	via CMAUP database
Vouacapen-5alpha-ol	73354918	Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O	302.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(7S,11S)-3,7,11,15-Tetramethyl-2-hexadecene-1-ol	40467768	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C	296.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	42433495	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	7067459	Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C	220.35	unknown	via CMAUP database
7-Hydroxycadalene	608115	Click to see CC1=C2C=C(C(=CC2=C(C=C1)C(C)C)C)O	214.30	unknown	via CMAUP database
alpha-Cadinol	10398656	Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol	92231	Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol	16046185	Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	10627788	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)OC(=O)C)C	630.70	unknown	via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid	11157932	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)OC(=O)C6=CC=CC=C6)C	630.70	unknown	via CMAUP database
(8beta,10beta,14alpha)-6beta,7beta-Bis(benzoyloxy)-3beta,5alpha-dihydroxy-12,16-epoxycassa-12,15-dien-19-oic acid	10698605	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)O)C	588.60	unknown	via CMAUP database
Pulcherrin N	53388796	Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6	572.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
Pulcherrin P	53388939	Click to see CC(=O)OCC1(C(CCC2(C1(C(C(C3C2CC4=C(C3C(=O)OC)C=CO4)OC(=O)C)O)O)C)OC(=O)C5=CC=CC=C5)C	598.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	11870456	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
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 oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone	68262	Click to see COC1=CC(=O)C=C(C1=O)OC	168.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
Neocaesalpin E	11450901	Click to see CC1C2CCC3(C(CCCC3(C2CC4(C1=CC(=O)O4)OC)C)(C)C)O	348.50	unknown	via CMAUP database
Neocaesalpin F	11386164	Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C	484.60	unknown	via CMAUP database
Neocaesalpin G	11295185	Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C	510.60	unknown	via CMAUP database
Pulcherrin Q	53388940	Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C	436.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercimeritrin	5282160	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one	689011	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC	284.31	unknown	via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone	10336604	Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC4=C(C=C3)OCO4)C(=C1)OC	328.30	unknown	via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy-	11681403	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4	326.30	unknown	via CMAUP database
5,7-Dimethoxyflavone	88881	Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one	44260091	Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O	340.30	unknown	via CMAUP database
6-Methoxypulcherrimin	44260092	Click to see COC1=C(C(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O)OC	370.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-(2,4-Dimethoxybenzylidene)-7-hydroxychroman-4-one	101356812	Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC	312.30	unknown	via CMAUP database
(3E)-3-(4-Methoxybenzylidene)-7-methoxychroman-4-one	6507117	Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)OC	296.30	unknown	via CMAUP database
(3E)-3-[(3,4-dimethoxyphenyl)methylidene]-7-methoxychromen-4-one	5783568	Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC(=C(C=C3)OC)OC)CO2	326.30	unknown	via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one	16082056	Click to see COC1=CC(=CC(=C1OC)OC)C=C2COC3=C(C2=O)C=CC(=C3)O	342.30	unknown	via CMAUP database
3-(4-Hydroxybenzylidene)-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one	14079440	Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC=C(C=C3)O)CO2	282.29	unknown	via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one	18778791	Click to see C1C(=CC2=CC3=C(C=C2)OCO3)C(=O)C4=C(O1)C=C(C=C4)O	296.27	unknown	via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one	101489712	Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2	310.30	unknown	via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-6,7-dimethoxy-2,3-dihydro-4H-1-benzopyran-4-one	44475180	Click to see COC1=C(C=C(C=C1)C=C2COC3=CC(=C(C=C3C2=O)OC)OC)O	342.30	unknown	via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one	13846662	Click to see COC1=C(C=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)O	298.29	unknown	via CMAUP database
Bonducellin	14079439	Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O	282.29	unknown	via CMAUP database
Isobonducellin	10423880	Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O	282.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one	51533159	Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C=CC(=C3)O	284.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone	10337542	Click to see COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2OC)OC)O	344.40	unknown	via CMAUP database
4,2'-Dihydroxy-4'-methoxychalcone	6537040	Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O	270.28	unknown	via CMAUP database

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Haemanthus albiflos

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