Dracaena cinnabari

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Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID644025eb7af38729216072
Scientific name	Dracaena cinnabari
Authority	Balf.f.
First published in	Trans. & Proc. Bot. Soc. Edinburgh 30: 623 (1882)

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Synonyms Top

Scientific name	Authority	First published in
Draco cinnabari	(Balf.f.) Kuntze	Revis. Gen. Pl. 2: 710 (1891)

Common names Top

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Language	Common/alternative name
English	socotra dragontree
English	dragon's blood tree
Arabic	شجرة دم الأخوين
Arabic	شجرة دم الاخوين
Arabic	دم الأخوين
Azerbaijani	Əjdaha qanı ağacı
Bulgarian	драконово дърво
Czech	dračinec rumělkový
Esperanto	sokotora draceno
Esperanto	sokotra draceno
Persian	درخت خون اژدها
Finnish	sokotrantraakkipuu
French	dragonnier de socotra
Italian	albero del drago di socotra
Japanese	ベニイロリュウケツジュ
Lithuanian	raudonoji dracena
Lithuanian	drakono kraujamedis
Macedonian	Змејско крваво дрво
Russian	Драцена киноварно-красная
Russian	Сокотрово драконово дерево
szy	dika a kilang
Tamil	சுகுத்திரா டிராகன் மரம்
Ukrainian	Сокотрійське драконове дерево
Chinese	索科特拉龍血樹
Chinese	索科特拉龙血树

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Northeast Tropical Africa
  - Socotra

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000765713
USDA Plants	DRCI3
Tropicos	50328247
KEW	urn:lsid:ipni.org:names:534145-1
The Plant List	kew-304609
Open Tree Of Life	129243
Observations.org	284078
NCBI Taxonomy	1142948
IUCN Red List	30428
IPNI	534145-1
iNaturalist	124825
GBIF	5304574
Freebase	/m/05f98bk
EOL	1087616
Elurikkus	509398
USDA GRIN	14631
Wikipedia	Dracaena_cinnabari

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

Synthesis and Pharmacological Activities of Chalcone and Its Derivatives Bearing N-Heterocyclic Scaffolds: A Review

Mezgebe K, Melaku Y, Mulugeta E

ACS Omega

22-May-2023

PMCID:	PMC10249103
doi:	10.1021/acsomega.3c01035
PMID:	37305270

A Review of the In Vitro Inhibition of α-Amylase and α-Glucosidase by Chalcone Derivatives

Tran TD, Tu VL, Hoang TM, Dat TV, Tam DN, Phat NT, Hung DT, Huynh HH, Do TC, Le HH, Minh LH

Cureus

07-Apr-2023

PMCID:	PMC10164439
doi:	10.7759/cureus.37267
PMID:	37162770

Ten Plastomes of Crassula (Crassulaceae) and Phylogenetic Implications

Ding H, Han S, Ye Y, Bi D, Zhang S, Yi R, Gao J, Yang J, Wu L, Kan X

Biology (Basel)

07-Dec-2022

PMCID:	PMC9775174
doi:	10.3390/biology11121779
PMID:	36552287

Complete chloroplast genome sequencing and comparative analysis of threatened dragon trees Dracaena serrulata and Dracaena cinnabari

Ahmad W, Asaf S, Khan A, Al-Harrasi A, Al-Okaishi A, Khan AL

Sci Rep

06-Oct-2022

PMCID:	PMC9537188
doi:	10.1038/s41598-022-20304-6
PMID:	36202844

Bio-Guided Isolation of SARS-CoV-2 Main Protease Inhibitors from Medicinal Plants: In Vitro Assay and Molecular Dynamics

Abdallah HM, El-Halawany AM, Darwish KM, Algandaby MM, Mohamed GA, Ibrahim SR, Koshak AE, Elhady SS, Fadil SA, Alqarni AA, Abdel-Naim AB, Elfaky MA

Plants (Basel)

24-Jul-2022

PMCID:	PMC9332707
doi:	10.3390/plants11151914
PMID:	35893619

Seed Viability and Potential Germination Rate of Nine Endemic Boswellia Taxa (Burseraceae) from Socotra Island (Yemen)

Hamdiah S, Karas L, Houšková K, Van Damme K, Attorre F, Vahalík P, Habrová H, Lvončík S, Eler K, Maděra P

Plants (Basel)

26-May-2022

PMCID:	PMC9182641
doi:	10.3390/plants11111418
PMID:	35684190

Isolation and Characterization of Two Chalcone Derivatives with Anti-Hepatitis B Virus Activity from the Endemic Socotraen Dracaena cinnabari (Dragon’s Blood Tree)

Mothana RA, Arbab AH, ElGamal AA, Parvez MK, Al-Dosari MS

Molecules

30-Jan-2022

PMCID:	PMC8838591
doi:	10.3390/molecules27030952
PMID:	35164217

Plant Natural Products as Antimicrobials for Control of Streptomyces scabies: A Causative Agent of the Common Scab Disease

Gutierrez J, Bakke A, Vatta M, Merrill AR

Front Microbiol

27-Jan-2022

PMCID:	PMC8828645
doi:	10.3389/fmicb.2021.833233
PMID:	35154047

East Asian Herbal Medicine to Reduce Primary Pain and Adverse Events in Cancer Patients : A Systematic Review and Meta-Analysis With Association Rule Mining to Identify Core Herb Combination

Jo HG, Seo J, Choi S, Lee D

Front Pharmacol

17-Jan-2022

PMCID:	PMC8802093
doi:	10.3389/fphar.2021.800571
PMID:	35111066

Inhibitory mechanism of two homoisoflavonoids from Ophiopogon japonicus on tyrosinase activity: insight from spectroscopic analysis and molecular docking

Wang L, Qin Y, Wang Y, Zhou Y, Liu B, Bai M, Tong X, Fang R, Huang X

RSC Adv

22-Oct-2021

PMCID:	PMC9042378
doi:	10.1039/d1ra06091k
PMID:	35497266

Occurrence and Health Risk Assessment of Aflatoxins through Intake of Eastern Herbal Medicines Collected from Four Districts of Southern Punjab—Pakistan

Javed A, Naeem I, Benkerroum N, Riaz M, Akhtar S, Ismail A, Sajid M, Tayyab Khan M, Ismail Z

Int J Environ Res Public Health

10-Sep-2021

PMCID:	PMC8466447
doi:	10.3390/ijerph18189531
PMID:	34574455

Plant-Based Antioxidant Extracts and Compounds in the Management of Oral Cancer

Prakash S, Radha, Kumar M, Kumari N, Thakur M, Rathour S, Pundir A, Sharma AK, Bangar SP, Dhumal S, Singh S, Thiyagarajan A, Sharma A, Sharma M, Changan S, Sasi M, Senapathy M, Pradhan PC, Garg NK, Ilakiya T, Nitin M, Abdel-Daim MM, Puri S, Natta S, Dey A, Amarowicz R, Mekhemar M

Antioxidants (Basel)

26-Aug-2021

PMCID:	PMC8466097
doi:	10.3390/antiox10091358
PMID:	34572990

Phytochemistry and Pharmacological Activities of Dracaena cinnabari Resin

Al-Awthan YS, Bahattab OS

Biomed Res Int

22-Jul-2021

PMCID:	PMC8324360
doi:	10.1155/2021/8561696
PMID:	34337055

Dracorhodin perchlorate enhances wound healing via β-catenin, ERK/p38, and AKT signaling in human HaCaT keratinocytes

Lu CC, Yang JS, Chiu YJ, Tsai FJ, Hsu YM, Yin MC, Juan YN, Ho TJ, Chen HP

Exp Ther Med

02-Jun-2021

PMCID:	PMC8193218
doi:	10.3892/etm.2021.10254
PMID:	34131445

Exploring the historical distribution of Dracaena cinnabari using ethnobotanical knowledge on Socotra Island, Yemen

Al-Okaishi A

J Ethnobiol Ethnomed

01-Apr-2021

PMCID:	PMC8017851
doi:	10.1186/s13002-021-00452-1
PMID:	33794944

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Hydroxy-2-methoxydihydrochalcone	129684399	Click to see COC1C=C(C=CC1C=CC(=O)C2=CC=CC=C2)O	256.30	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
3,6,19-Trimethyl-9-prop-1-en-2-yl-16-oxapentacyclo[12.5.1.03,11.06,10.017,20]icos-13-en-17-ol	78412746	Click to see CC1CC2(C3C1CC4(CCC5(CCC(C5C4CC=C3CO2)C(=C)C)C)C)O	370.60	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,5S,8R,9S,10S,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	13988616	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)OC(=O)C)C)C)C(C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Lanost-7-en-3-ol, acetate, (3beta)-	523664	Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C	470.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Lanost-7-en-3beta-ol, acetate	22211814	Click to see CC(C)CCCC(C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C	470.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Lup-20(29)-en-3beta-ol, acetate	323074	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
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/10.1016/0031-9422(94)00743-D
Lupeol acetate	92157	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C	468.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids
[(3S,4S,5R,10S,13R,14R,17R)-4,10,13,14-tetramethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate	163028211	Click to see CC1C2CCC3=C(C2(CCC1OC(=O)C)C)CCC4(C3(CCC4C(C)CCCC(C)C)C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
[4,10,13,14-Tetramethyl-17-(6-methylheptan-2-yl)-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate	86183575	Click to see CC1C2CCC3=C(C2(CCC1OC(=O)C)C)CCC4(C3(CCC4C(C)CCCC(C)C)C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
[(3S,4S,5R,9R,10S,13R,14R,17R)-4,10,13-trimethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	163034383	Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)OC(=O)C	442.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
[4,10,13-trimethyl-17-(6-methylheptan-2-yl)-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	85948745	Click to see CC1C(CCC2(C1CC=C3C2CCC4(C3CCC4C(C)CCCC(C)C)C)C)OC(=O)C	442.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
10,13-Dimethyl-17-(6-methylheptan-2-yl)-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	440	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C	384.60	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
2,15-Dimethyl-14-(6-methylheptan-2-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol	304	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Cholest-4-en-3-one	91477	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C	384.60	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Cholesterol	5997	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cucurbitacins
(3S,8R,9S,13R)-9-ethyl-4,4,13,14-tetramethyl-17-(6-methylheptan-2-yl)-2,3,5,6,7,8,10,11,12,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	5316233	Click to see CCC12CCC3(C(CCC3(C1CCC4C2CCC(C4(C)C)O)C)C(C)CCCC(C)C)C	444.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
[(1S,3R,6S,7S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(2R)-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate	14312806	Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1OC(=O)C)C)C(C)CCCC(C)C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
[(1S,3R,6S,8R,11S,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylheptan-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate	14060398	Click to see CC(C)CCCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C	470.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
[7,12,16-Trimethyl-15-(6-methylheptan-2-yl)-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate	14312805	Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1OC(=O)C)C)C(C)CCCC(C)C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
24-Methylene-cycloartanol	9547213	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
24-Methylenecycloartanol	94204	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
24-Methylenecycloartanol acetate	13151740	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C	482.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
29-Nor-cycloartanol	44423588	Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCCC(C)C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
9,19-Cyclolanostan-3-ol, 24-methylene-, 3-acetate, (3beta)-	550623	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C	482.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
9,19-Cyclolanostan-3-ol, acetate, (3beta)-	537304	Click to see CC(C)CCCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C)C)C	470.80	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Cycloartanol	12760132	Click to see CC(C)CCCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	428.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	134766514	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
5-Cholestene-3-ol, 24-methyl-	312822	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Campesterol	173183	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,5S,9S,10S,13R,17R)-17-[(2R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol	91746710	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C	416.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
(3S,6R)-6-[(8R,9S,10S,13R,14S,17R)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl]-3-propan-2-ylheptan-1-ol	56924079	Click to see CC(C)C(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCCC4)C)C)CCO	416.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol	6743	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C	416.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
17-(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	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Stigmastanol	241572	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C	416.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(94)00743-D
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E,19Z,21E)-2,10,18-tris(4-hydroxyphenyl)-6,14,22-trimethoxytetracyclo[17.5.1.13,7.111,15]heptacosa-1(25),3,5,7(27),11,13,15(26),19,21-nonaene-4,12,20-triol	101219349	Click to see COC1=CC(=C2C=C(CC1)C(C3=C(C=C(C(=C3)CCC(C4=C(C=C(C(=C4)CCC2C5=CC=C(C=C5)O)OC)O)C6=CC=C(C=C6)O)OC)O)C7=CC=C(C=C7)O)O	768.90	unknown	https://doi.org/10.1016/S0031-9422(02)00354-0
(2S)-2-(5-hydroxy-2-methoxyphenyl)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3,4-dihydro-2H-chromen-7-ol	162968011	Click to see COC1=C(C=C(C=C1)O)C2CCC3=CC(=C(C=C3O2)O)C(CCC4=C(C=C(C=C4)O)OC)C5=CC=C(C=C5)O	528.60	unknown	https://doi.org/10.1055/S-2006-958096
(2S)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol	163045623	Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C4C(=C3)CCC(O4)C5=CC=C(C=C5)O)O	498.60	unknown	https://doi.org/10.1055/S-2006-958096
(2S)-6-[(1R)-3-[2-hydroxy-5-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propyl]-2-phenyl-3,4-dihydro-2H-chromen-7-ol	163090087	Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C(C(=C3)CCC(C4=CC=C(C=C4)O)C5=C(C=C6C(=C5)CCC(O6)C7=CC=CC=C7)O)O)OC	738.90	unknown	https://doi.org/10.1016/0031-9422(95)00044-8
(3R)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol	163011609	Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C4C(=C3)CC(CO4)CC5=CC=C(C=C5)O)O	512.60	unknown	https://doi.org/10.1055/S-2006-958096
(4R,12R,20R)-4,12,20-tris(4-hydroxyphenyl)-8,16,24-trimethoxytetracyclo[19.3.1.15,9.113,17]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-6,14,22-triol	162974230	Click to see COC1=CC(=C2C=C1CCC(C3=C(C=C(C(=C3)CCC(C4=C(C=C(C(=C4)CCC2C5=CC=C(C=C5)O)OC)O)C6=CC=C(C=C6)O)OC)O)C7=CC=C(C=C7)O)O	768.90	unknown	https://doi.org/10.1016/S0031-9422(02)00354-0
(4S,12R,20R)-4,12,20-tris(4-hydroxyphenyl)-8,16,24-trimethoxytetracyclo[19.3.1.15,9.113,17]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-6,14,22-triol	162974229	Click to see COC1=CC(=C2C=C1CCC(C3=C(C=C(C(=C3)CCC(C4=C(C=C(C(=C4)CCC2C5=CC=C(C=C5)O)OC)O)C6=CC=C(C=C6)O)OC)O)C7=CC=C(C=C7)O)O	768.90	unknown	https://doi.org/10.1016/S0031-9422(02)00354-0
2-(5-hydroxy-2-methoxyphenyl)-6-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3,4-dihydro-2H-chromen-7-ol	101687707	Click to see COC1=C(C=C(C=C1)O)C2CCC3=CC(=C(C=C3O2)O)C(CCC4=C(C=C(C=C4)O)OC)C5=CC=C(C=C5)O	528.60	unknown	https://doi.org/10.1055/S-2006-958096
3-[2-hydroxy-5-[(1R)-3-(2-hydroxy-4-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propan-1-one	162950359	Click to see COC1=CC(=C(C=C1)CCC(C2=CC=C(C=C2)O)C3=C(C=C(C(=C3)CCC(=O)C4=CC=C(C=C4)O)O)OC)O	528.60	unknown	https://doi.org/10.1016/0031-9422(94)00718-9
3-[2-hydroxy-5-[(1S)-3-(2-hydroxy-4-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propan-1-one	162950358	Click to see COC1=CC(=C(C=C1)CCC(C2=CC=C(C=C2)O)C3=C(C=C(C(=C3)CCC(=O)C4=CC=C(C=C4)O)O)OC)O	528.60	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
3-[2-Hydroxy-5-[3-(2-hydroxy-4-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propan-1-one	15230226	Click to see COC1=CC(=C(C=C1)CCC(C2=CC=C(C=C2)O)C3=C(C=C(C(=C3)CCC(=O)C4=CC=C(C=C4)O)O)OC)O	528.60	unknown	https://doi.org/10.1016/0031-9422(94)00718-9
4,12,20-Tris(4-hydroxyphenyl)-8,16,24-trimethoxytetracyclo[19.3.1.15,9.113,17]heptacosa-1(25),5,7,9(27),13,15,17(26),21,23-nonaene-6,14,22-triol	5322090	Click to see COC1=CC(=C2C=C1CCC(C3=C(C=C(C(=C3)CCC(C4=C(C=C(C(=C4)CCC2C5=CC=C(C=C5)O)OC)O)C6=CC=C(C=C6)O)OC)O)C7=CC=C(C=C7)O)O	768.90	unknown	https://doi.org/10.1016/S0031-9422(02)00354-0
6-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-7-ol	101687708	Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C4C(=C3)CCC(O4)C5=CC=C(C=C5)O)O	498.60	unknown	https://doi.org/10.1055/S-2006-958096
6-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol	101687709	Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C4C(=C3)CC(CO4)CC5=CC=C(C=C5)O)O	512.60	unknown	https://doi.org/10.1055/S-2006-958096
6-[3-[2-hydroxy-5-[3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-4-methoxyphenyl]-1-(4-hydroxyphenyl)propyl]-2-phenyl-3,4-dihydro-2H-chromen-7-ol	163090085	Click to see COC1=C(C=CC(=C1)O)CCC(C2=CC=C(C=C2)O)C3=C(C=C(C(=C3)CCC(C4=CC=C(C=C4)O)C5=C(C=C6C(=C5)CCC(O6)C7=CC=CC=C7)O)O)OC	738.90	unknown	https://doi.org/10.1016/0031-9422(95)00044-8
> 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	https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxyflavanone	1890	Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=CC=C3	240.25	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Flavonoids / Flavones
4',7-Dihydroxyflavone	5282073	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C=C3)O)O	254.24	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-Phenylchroman-7-ol	3512638	Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=CC=C3	226.27	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxyflavan	442413	Click to see C1CC2=C(C=C(C=C2)O)OC1C3=CC=CC=C3	226.27	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(4-hydroxy-3-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol	11277283	Click to see COC1=C(C=CC(=C1)C2CCC3=C(O2)C=C(C=C3)O)O	272.29	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
7,4'-Dihydroxy-3'-methoxyflavan	14157887	Click to see COC1=C(C=CC(=C1)C2CCC3=C(O2)C=C(C=C3)O)O	272.29	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
(S)-2-(3-Hydroxy-4-methoxyphenyl)chroman-7-ol	44257179	Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O	272.29	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
2-(3-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-chromen-7-ol	11196546	Click to see COC1=C(C=C(C=C1)C2CCC3=C(O2)C=C(C=C3)O)O	272.29	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans
(3S)-3-[(3-hydroxy-4-methoxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol	163009232	Click to see COC1=C(C=C(C=C1)CC2CC3=C(C=C(C=C3)O)OC2)O	286.32	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
(3S)-3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol	124350722	Click to see C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O	256.30	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
(3S)-3-[(4-hydroxyphenyl)methyl]-8-methoxy-3,4-dihydro-2H-chromen-7-ol	162989465	Click to see COC1=C(C=CC2=C1OCC(C2)CC3=CC=C(C=C3)O)O	286.32	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
3-(4-Hydroxybenzyl)-7,8-methylenedioxychroman	90971271	Click to see C1C(COC2=C1C=CC3=C2OCO3)CC4=CC=C(C=C4)O	284.31	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
4-[[(7S)-7,8-dihydro-6H-[1,3]dioxolo[4,5-h]chromen-7-yl]methyl]phenol	162984897	Click to see C1C(COC2=C1C=CC3=C2OCO3)CC4=CC=C(C=C4)O	284.31	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxy-3-(3-hydroxy-4-methoxybenzyl)chroman	14331400	Click to see COC1=C(C=C(C=C1)CC2CC3=C(C=C(C=C3)O)OC2)O	286.32	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxy-3-(4-hydroxybenzyl)-8-methoxychroman	44445077	Click to see COC1=C(C=CC2=C1OCC(C2)CC3=CC=C(C=C3)O)O	286.32	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
7-Hydroxy-3-(4-hydroxybenzyl)chroman	11708657	Click to see C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O	256.30	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
2-Methoxy-4-hydroxydihydrochalcone	42607734	Click to see COC1=C(C=CC(=C1)O)CCC(=O)C2=CC=CC=C2	256.30	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
Loureirin C	14157896	Click to see COC1=C(C=CC(=C1)O)CCC(=O)C2=CC=C(C=C2)O	272.29	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
1-(4-Hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one	25201046	Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=C(C=C2)O	270.28	unknown	https://doi.org/10.1016/0031-9422(94)00738-F
2'-O-Methylisoliquiritigenin	5319688	Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=C(C=C2)O	270.28	unknown	https://doi.org/10.1016/0031-9422(94)00738-F

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Dracaena cinnabari

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