Scientific name	Authority	First published in
Cephalotaxus mannii subsp. thailandensis	(Silba) Silba	J. Int. Conifer Preserv. Soc. 14(1): 13 (2007)
Cephalotaxus sinensis subsp. hainanensis	(H.L.Li) Silba	J. Int. Conifer Preserv. Soc. 14(1): 17 (2007)
Cephalotaxus harringtonii var. thailandensis	Silba	J. Int. Conifer Preserv. Soc. 7: 22 (2000)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	hainan plum yew
Arabic	طقسوس برقوقي هيناني
Chinese	海南粗榧
Chinese	红壳松
Chinese	薄叶篦子杉

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

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

Asia-tropical click to expand
- Indo-China
  - Myanmar
  - Thailand
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000594959
Tropicos	6900037
KEW	urn:lsid:ipni.org:names:828269-1
The Plant List	kew-2709750
Open Tree Of Life	828859
NCBI Taxonomy	191701
IUCN Red List	34065
IPNI	828269-1
iNaturalist	136155
GBIF	2685278
Freebase	/m/027zgs4
EPPO	CEXHS
EOL	128818
Wikipedia	Cephalotaxus_hainanensis
CMAUP	NPO15166

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

Genome-Wide Identification and Expression Profile Analysis of the Phenylalanine Ammonia-Lyase Gene Family in Hevea brasiliensis

Liu H, He Q, Hu Y, Lu R, Wu S, Feng C, Yuan K, Wang Z

Int J Mol Sci

06-May-2024

PMCID:	PMC11084274
doi:	10.3390/ijms25095052
PMID:	38732270

Natural products as potential drug treatments for acute promyelocytic leukemia

Chen J, Ding Z

Chin Med

03-Apr-2024

PMCID:	PMC10988969
doi:	10.1186/s13020-024-00928-8
PMID:	38566147

A review of natural products targeting tumor immune microenvironments for the treatment of lung cancer

Yao P, Liang S, Liu Z, Xu C

Front Immunol

01-Feb-2024

PMCID:	PMC10867126
doi:	10.3389/fimmu.2024.1343316
PMID:	38361933

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

ACC010, a novel BRD4 inhibitor, synergized with homoharringtonine in acute myeloid leukemia with FLT3 ‐ITD

Qian Y, Zhang X, Mao S, Wei W, Lin X, Ling Q, Ye W, Li F, Pan J, Zhou Y, Zhao Y, Huang X, Huang J, Tong H, Sun J, Jin J

Mol Oncol

21-Jan-2023

PMCID:	PMC10323884
doi:	10.1002/1878-0261.13368
PMID:	36567628

Dihydropyrimidinase‐like 2 can serve as a novel therapeutic target and prognostic biomarker in acute myeloid leukemia

Li F, Ling Q, Lian J, Chen Y, Hu C, Yang M, Zhang X, Li C, Mao S, Ye W, Li X, Lin X, Wei W, Huang X, Pan J, Qian Y, Wang J, Lu Y, Jin J

Cancer Med

09-Jan-2023

PMCID:	PMC10134331
doi:	10.1002/cam4.5531
PMID:	36621846

Elucidation of the 1-phenethylisoquinoline pathway from an endemic conifer Cephalotaxus hainanensis

Qiao F, He Y, Zhang Y, Jiang X, Cong H, Wang Z, Sun H, Xiao Y, Zhao Y, Nick P

Proc Natl Acad Sci U S A

28-Dec-2022

PMCID:	PMC9910586
doi:	10.1073/pnas.2209339120
PMID:	36577068

Antimicrobial potentials of natural products against multidrug resistance pathogens: a comprehensive review

Elmaidomy AH, Shady NH, Abdeljawad KM, Elzamkan MB, Helmy HH, Tarshan EA, Adly AN, Hussien YH, Sayed NG, Zayed A, Abdelmohsen UR

RSC Adv

13-Oct-2022

PMCID:	PMC9558262
doi:	10.1039/d2ra04884a
PMID:	36320761

Drugs That Changed Society: Microtubule-Targeting Agents Belonging to Taxanoids, Macrolides and Non-Ribosomal Peptides

Christensen SB

Molecules

01-Sep-2022

PMCID:	PMC9457747
doi:	10.3390/molecules27175648
PMID:	36080414

Characterization of the Newly Established Homoharringtonine- (HHT-) Resistant Cell Lines and Mechanisms of Resistance

Li F, Ling Q, Hu C, Wang H, Ye W, Li X, Zhang X, Lin X, Wei W, Huang X, Qian Y, Zhuang H, Jin J, Lu Y

J Oncol

30-Aug-2022

PMCID:	PMC9448541
doi:	10.1155/2022/2813938
PMID:	36081671

Homoharringtonine is synergistically lethal with BCL-2 inhibitor APG-2575 in acute myeloid leukemia

Wei W, Huang S, Ling Q, Mao S, Qian Y, Ye W, Li F, Pan J, Lin X, Huang J, Huang X, Zhai Y, Sun J, Jin J

J Transl Med

06-Jul-2022

PMCID:	PMC9258085
doi:	10.1186/s12967-022-03497-2
PMID:	35794605

Sulfur-Containing Compounds from Endophytic Fungi: Sources, Structures and Bioactivities

Fan Y, Ma Z, Zhang Y, Wang Y, Ding Y, Wang C, Cao S

J Fungi (Basel)

13-Jun-2022

PMCID:	PMC9224594
doi:	10.3390/jof8060628
PMID:	35736111

Metabolomics Analysis and Antioxidant Potential of Endophytic Diaporthe fraxini ED2 Grown in Different Culture Media

Tan WN, Nagarajan K, Lim V, Azizi J, Khaw KY, Tong WY, Leong CR, Chear NJ

J Fungi (Basel)

18-May-2022

PMCID:	PMC9144047
doi:	10.3390/jof8050519
PMID:	35628774

Translational Phytomedicines against Cancer: Promise and Hurdles

Devan AR, Nair B, Nath LR

Adv Pharm Bull

28-Apr-2022

PMCID:	PMC10278225
doi:	10.34172/apb.2023.023
PMID:	37342376

Targeting natural products against SARS-CoV-2

Al-Harrasi A, Behl T, Upadhyay T, Chigurupati S, Bhatt S, Sehgal A, Bhatia S, Singh S, Sharma N, Vijayabalan S, Palanimuthu VR, Das S, Kaur R, Aleya L, Bungau S

Environ Sci Pollut Res Int

01-Apr-2022

PMCID:	PMC8972763
doi:	10.1007/s11356-022-19770-2
PMID:	35362883

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 / Homolycorine-type amaryllidaceae alkaloids
Lycorenan-7-one,9,10-dimethoxy-1-methyl-	573128	Click to see CN1CCC2=CCC3C(C21)C4=CC(=C(C=C4C(=O)O3)OC)OC	315.40	unknown	via CMAUP database
> Alkaloids and derivatives / Cephalotaxus alkaloids
(2R,6S)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-ol	11809221	Click to see COC1=CC23CCCN2CCC4=CC5=C(C=C4C3C1O)OCO5	315.40	unknown	via CMAUP database
(2S,3S,6R)-3-hydroxy-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-9-one	11461634	Click to see COC1=CC23CCC(=O)N2CCC4=CC5=C(C=C4C3C1O)OCO5	329.30	unknown	via CMAUP database
(2S,6S)-4-Methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-one	10892366	Click to see COC1=CC23CCCN2CCC4=CC5=C(C=C4C3C1=O)OCO5	313.30	unknown	via CMAUP database
(6S)-3-Hydroxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),2,13,15(19)-tetraen-4-one	10086100	Click to see C1CC23CC(=O)C(=C2C4=CC5=C(C=C4CCN3C1)OCO5)O	299.32	unknown	https://doi.org/10.1021/NP0203178
1-O-(4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl) 4-O-methyl (2R,3S)-2,3-dihydroxy-2-(3-methylbutyl)butanedioate	9871679	Click to see CC(C)CCC(C(C(=O)OC)O)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O	531.60	unknown	via CMAUP database
1-O-[(2S,3S,6R)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl] 4-O-methyl (2S)-2-hydroxy-2-(3-hydroxy-3-methylbutyl)butanedioate	29927670	Click to see CC(C)(CCC(CC(=O)OC)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O)O	531.60	unknown	via CMAUP database
1-O-[(2S)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl] 4-O-methyl (2S)-2-hydroxy-2-(3-methylbutyl)butanedioate	56840949	Click to see CC(C)CCC(CC(=O)OC)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O	515.60	unknown	via CMAUP database
3-Hydroxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),13,15(19)-trien-4-one	5316516	Click to see C1CC23CC(=O)C(C2C4=CC5=C(C=C4CCN3C1)OCO5)O	301.34	unknown	via CMAUP database
4H-Cyclopenta[a][1,3]dioxolo[4,5-h]pyrrolo[2,1-b][3]benzazepin-1-ol, 1,5,6,8,9,14b-hexahydro-2-methoxy-	278679	Click to see COC1=CC23CCCN2CCC4=CC5=C(C=C4C3C1O)OCO5	315.40	unknown	https://doi.org/10.1021/NP0203178
Cephalotaxine, 2,11-epoxy-1,2-dihydro-, (2alpha,11alpha)-	424504	Click to see COC12CC34CCCN3CC(O1)C5=CC6=C(C=C5C4C2O)OCO6	331.40	unknown	https://doi.org/10.1021/NP0203178
Cephalotaxine, 4-methyl 2-hydroxy-2-(4-hydroxy-4-methylpentyl)butanedioate (ester), [3(R)]-	3628	Click to see CC(C)(CCCC(CC(=O)OC)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O)O	545.60	unknown	via CMAUP database
Cephalotaxine, 4-methyl 2,3-dihydroxy-2-(3-methylbutyl)butanedioate (ester)	626936	Click to see CC(C)CCC(C(C(=O)OC)O)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O	531.60	unknown	https://doi.org/10.1021/NP0203178
Drupacine	21586622	Click to see COC12CC34CCCN3CC(O1)C5=CC6=C(C=C5C4C2O)OCO6	331.40	unknown	https://doi.org/10.1021/NP0203178
Epi-homoharringtonine	56841046	Click to see CC(C)(CCCC(CC(=O)OC)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O)O	545.60	unknown	via CMAUP database
> Alkaloids and derivatives / Erythrina alkaloids / Homoerythrinane alkaloids
3-Epischelhammericine	5317117	Click to see COC1CC=C2CCN3C2(C1)C4=C(CCC3)C5=C(C=C4)OCO5	313.40	unknown	via CMAUP database
> Alkaloids and derivatives / Hasubanan alkaloids
3,4,7,8-Tetramethoxy-17-methyl-7,8-didehydrohasubanan-6-one	628879	Click to see CN1CCC23C1(CCC4=C2C(=C(C=C4)OC)OC)C(=C(C(=O)C3)OC)OC	373.40	unknown	via CMAUP database
> Hydrocarbon derivatives / Tropones
CID 10881512	10881512	Click to see CC1C(C2C3CC4=C5C3C1(CCC5=CC(=O)C=C4C)C(=O)O2)O	312.40	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(3E,5Z)-1,3,5-Tridecatriene-7,9,11-triyne	5322029	Click to see CC#CC#CC#CC=CC=CC=C	166.22	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin	72307	Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6	354.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(Z)-5-[[(2E,4E,6E)-7-thiophen-2-ylhepta-2,4,6-trienoyl]amino]pent-2-enyl] 3-methylbutanoate	72696081	Click to see CC(C)CC(=O)OCC=CCCNC(=O)C=CC=CC=CC1=CC=CS1	373.50	unknown	via CMAUP database
Docosanoic acid, pentyl ester	22608915	Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCC	410.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,6E)-N-Isobutyl-7-(2-Thienyl)-2,4,6-Heptatrienamide	73349612	Click to see CC(C)CNC(=O)C=CC=CC=CC1=CC=CS1	261.40	unknown	via CMAUP database
(2E,4E,6E)-N-Isopentyl-7-(2-Thienyl)-2,4,6-Heptatrienamide	72696080	Click to see CC(C)CCNC(=O)C=CC=CC=CC1=CC=CS1	275.40	unknown	via CMAUP database
(2E,4E,8Z)-N-(2-methylpropyl)tetradeca-2,4,8-trienamide	73355665	Click to see CCCCCC=CCCC=CC=CC(=O)NCC(C)C	277.40	unknown	via CMAUP database
(2E,4E)-N-isobutylundeca-2,4-dien-8,10-diynamide	5373537	Click to see CC(C)CNC(=O)C=CC=CCCC#CC#C	229.32	unknown	via CMAUP database
2,4-Dodecadienamide, N-(2-methylpropyl)-, (2E,4E)-	6443006	Click to see CCCCCCCC=CC=CC(=O)NCC(C)C	251.41	unknown	via CMAUP database
N-(2-methylpropyl)-7-thiophen-2-ylhepta-2,4,6-trienamide	71365555	Click to see CC(C)CNC(=O)C=CC=CC=CC1=CC=CS1	261.40	unknown	via CMAUP database
N-Isobutyl-(2E,4E)-tetradecadienamide	10731388	Click to see CCCCCCCCCC=CC=CC(=O)NCC(C)C	279.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Hexadeca-2,6,10,14-tetraen-1-ol, 3,7,11,16-tetramethyl-	5365865	Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C	290.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(1S,2S,3R,4S,7R,10S,12R,15S)-4,12-diacetyloxy-15-[(2R,3S)-3-benzamido-2-hydroxy-3-phenylpropanoyl]oxy-1,9-dihydroxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate	11320430	Click to see CC1=C2C(C(=O)C3(C(CC4C(C3C(C(C2(C)C)(CC1OC(=O)C(C(C5=CC=CC=C5)NC(=O)C6=CC=CC=C6)O)O)OC(=O)C7=CC=CC=C7)(CO4)OC(=O)C)O)C)OC(=O)C	853.90	unknown	via CMAUP database
[(1S,2S,3R,4S,7R,9S,10S,12R,15S)-4,12-diacetyloxy-1,9-dihydroxy-15-[2-hydroxy-3-[[(E)-2-methylbut-2-enoyl]amino]-3-phenylpropanoyl]oxy-10,14,17,17-tetramethyl-11-oxo-6-oxatetracyclo[11.3.1.03,10.04,7]heptadec-13-en-2-yl] benzoate	45358115	Click to see CC=C(C)C(=O)NC(C1=CC=CC=C1)C(C(=O)OC2CC3(C(C4C(C(CC5C4(CO5)OC(=O)C)O)(C(=O)C(C(=C2C)C3(C)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)O)O	831.90	unknown	via CMAUP database
Taxol B	6436208	Click to see CC=C(C)C(=O)NC(C1=CC=CC=C1)C(C(=O)OC2CC3(C(C4C(C(CC5C4(CO5)OC(=O)C)O)(C(=O)C(C(=C2C)C3(C)C)OC(=O)C)C)OC(=O)C6=CC=CC=C6)O)O	831.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
[(2R)-2-[(3S,3aS,5R,8R,8aS)-8,8a-dihydroxy-3,8-dimethyl-1,2,3,3a,4,5,6,7-octahydroazulen-5-yl]-2-hydroxypropyl] hydrogen sulfate	163035820	Click to see CC1CCC2(C1CC(CCC2(C)O)C(C)(COS(=O)(=O)O)O)O	352.40	unknown	https://doi.org/10.1080/10286020.2010.485934
[(2R)-2-[(3S,3aS,5R,8S,8aS)-3,8-dimethyl-1,2,3,3a,4,5,6,7,8,8a-decahydroazulen-5-yl]-2-hydroxypropyl] hydrogen sulfate	162973764	Click to see CC1CCC(CC2C1CCC2C)C(C)(COS(=O)(=O)O)O	320.40	unknown	https://doi.org/10.1080/10286020.2010.485934
[2-(3,8-Dimethyl-1,2,3,3a,4,5,6,7,8,8a-decahydroazulen-5-yl)-2-hydroxypropyl] hydrogen sulfate	162973763	Click to see CC1CCC(CC2C1CCC2C)C(C)(COS(=O)(=O)O)O	320.40	unknown	https://doi.org/10.1080/10286020.2010.485934
[2-(8,8a-Dihydroxy-3,8-dimethyl-1,2,3,3a,4,5,6,7-octahydroazulen-5-yl)-2-hydroxypropyl] hydrogen sulfate	163035819	Click to see CC1CCC2(C1CC(CCC2(C)O)C(C)(COS(=O)(=O)O)O)O	352.40	unknown	https://doi.org/10.1080/10286020.2010.485934
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
9-hydroxy-1-(hydroxymethyl)-5,8a-dimethyl-4,5,5a,9-tetrahydro-3aH-azuleno[6,7-b]furan-2,8-dione	3482907	Click to see CC1CC2C(=C(C(=O)O2)CO)C(C3(C1C=CC3=O)C)O	278.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(8R,10R,13R)-17-[(2R)-1,2-dihydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one	5316971	Click to see CC(=CCCC(CO)(C1CCC2(C1CCC3C2(CCC4C3(CCC(=O)C4(C)C)C)C)C)O)C	458.70	unknown	via CMAUP database
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	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
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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acid esters
[(3R)-3-(4-methoxy-5-methyl-6-oxopyran-2-yl)butyl] (2R)-5-oxopyrrolidine-2-carboxylate	163046143	Click to see CC1=C(C=C(OC1=O)C(C)CCOC(=O)C2CCC(=O)N2)OC	323.34	unknown	https://doi.org/10.1080/10286020.2011.615742
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(5-Acetyl-2-methoxy-phenyl)-3-methyl-butan-1-one	3009228	Click to see CC(C)CC(=O)C1=C(C=CC(=C1)C(=O)C)OC	234.29	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzazepines
Hainanensine	127616	Click to see CC1(C2=C3C(=CC4=C2OCO4)CCN5CCCC5=C3C1=O)O	299.32	unknown	via CMAUP database
> Organoheterocyclic compounds / Furopyrans
Harringtonolide	56841078	Click to see CC1C2C3C4C5C1(CCC6=CC(=O)C=C(C(=C56)C4O2)C)C(=O)O3	310.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / N-alkylindoles
2-[1-[[3-(2-Hydroxyethyl)indol-1-yl]methyl]indol-3-yl]ethanol	162878988	Click to see C1=CC=C2C(=C1)C(=CN2CN3C=C(C4=CC=CC=C43)CCO)CCO	334.40	unknown	https://doi.org/10.1080/10286020.2011.615742
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
8-Deoxylactucin	442196	Click to see CC1=C2C(C3C(CC1)C(=C)C(=O)O3)C(=CC2=O)CO	260.28	unknown	via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Hallolactone A	3084841	Click to see CC(C)C1=C2CC3C4C(C(C5C(C4(C2=CC(=O)O1)C)O5)O)(C(=O)O3)C	346.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Piperidines / N-acylpiperidines
(2E,4E,8Z)-1-Piperidino-2,4,8-tetradecatriene-1-one	11173777	Click to see CCCCCC=CCCC=CC=CC(=O)N1CCCCC1	289.50	unknown	via CMAUP database
(2E,4E)-1-(Piperidin-1-yl)tetradeca-2,4-dien-1-one	11130083	Click to see CCCCCCCCCC=CC=CC(=O)N1CCCCC1	291.50	unknown	via CMAUP database
1-[(2e,4e,6e)-7-(2-Thienyl)-2,4,6-heptatrienoyl]piperidine	11821786	Click to see C1CCN(CC1)C(=O)C=CC=CC=CC2=CC=CS2	273.40	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(2E,4E,6E)-1-(3,4-dihydro-2H-pyridin-1-yl)-7-thiophen-2-ylhepta-2,4,6-trien-1-one	73346583	Click to see C1CC=CN(C1)C(=O)C=CC=CC=CC2=CC=CS2	271.40	unknown	via CMAUP database
(2E,4E)-1-(3,4-dihydro-2H-pyridin-1-yl)undeca-2,4-dien-8,10-diyn-1-one	14427416	Click to see C#CC#CCCC=CC=CC(=O)N1CCCC=C1	239.31	unknown	via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-5-[(E)-3-oxoprop-1-enyl]-2,3-dihydro-1-benzofuran-3-yl]methyl 3-methylbutanoate	72696082	Click to see CC(C)CC(=O)OCC1C(OC2=C1C=C(C=C2OC)C=CC=O)C3=CC(=C(C=C3)O)OC	440.50	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
Umuhengerin	73648	Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O	388.40	unknown	via CMAUP database

Biological Material Top

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.

Cephalotaxus hainanensis

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top