Database	ID/link to page
World Flora Online	wfo-0001228174
Tropicos	50053707
KEW	urn:lsid:ipni.org:names:900105-1
The Plant List	tro-50053707
Open Tree Of Life	105454
NCBI Taxonomy	1202798
IUCN Red List	152824853
IPNI	900105-1
GBIF	7314066
EOL	5348306

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

Anticoronavirus Evaluation of Antimicrobial Diterpenoids: Application of New Ferruginol Analogues

Varbanov M, Philippot S, González-Cardenete MA

Viruses

09-Jun-2023

PMCID:	PMC10301393
doi:	10.3390/v15061342
PMID:	37376641

Plant-Based Natural Products and Extracts: Potential Source to Develop New Antiviral Drug Candidates

Thomas E, Stewart LE, Darley BA, Pham AM, Esteban I, Panda SS

Molecules

14-Oct-2021

PMCID:	PMC8537559
doi:	10.3390/molecules26206197
PMID:	34684782

Potential of diterpene compounds as antivirals, a review

Wardana AP, Aminah NS, Rosyda M, Abdjan MI, Kristanti AN, Tun KN, Choudhary MI, Takaya Y

Heliyon

12-Aug-2021

PMCID:	PMC8359577
doi:	10.1016/j.heliyon.2021.e07777
PMID:	34405122

Neottia wuyishanensis (Orchidaceae: Neottieae), a new species from Fujian, China

Chen BH, Jin XH

Plant Divers

04-Feb-2021

PMCID:	PMC8591140
doi:	10.1016/j.pld.2021.01.008
PMID:	34816068

Change the channel: CysLoop receptor antagonists from Nature

Tong G, Baker MA, Shenvi RA

Pest Manag Sci

22-Nov-2020

PMCID:	PMC8087819
doi:	10.1002/ps.6166
PMID:	33135373

The search for, and chemistry and mechanism of, neurotrophic natural products

Fukuyama Y, Kubo M, Harada K

J Nat Med

08-Jul-2020

PMCID:	PMC7456418
doi:	10.1007/s11418-020-01431-8
PMID:	32643028

The largest early-diverging angiosperm family is mostly pollinated by ovipositing insects and so are most surviving lineages of early angiosperms

Luo SX, Zhang LJ, Yuan S, Ma ZH, Zhang DX, Renner SS

Proc Biol Sci

03-Jan-2018

PMCID:	PMC5784199
doi:	10.1098/rspb.2017.2365
PMID:	29298936

Bio-Guided Isolation of Methanol-Soluble Metabolites of Common Spruce (Picea abies) Bark by-Products and Investigation of Their Dermo-Cosmetic Properties

Angelis A, Hubert J, Aligiannis N, Michalea R, Abedini A, Nuzillard JM, Gangloff SC, Skaltsounis AL, Renault JH

Molecules

21-Nov-2016

PMCID:	PMC6272914
doi:	10.3390/molecules21111586
PMID:	27879645

The antiviral effect of jiadifenoic acids C against coxsackievirus B3

Ge M, Wang H, Zhang G, Yu S, Li Y

Acta Pharm Sin B

16-Jul-2014

PMCID:	PMC4629087
doi:	10.1016/j.apsb.2014.06.008
PMID:	26579396

Total Synthesis of Jiadifenolide

Paterson I, Xuan M, Dalby SM

Angew Chem Int Ed Engl

23-May-2014

PMCID:	PMC4320761
doi:	10.1002/anie.201404224
PMID:	24861364

An Enantiospecific Synthesis of Jiadifenolide

Siler DA, Mighion JD, Sorensen EJ

Angew Chem Int Ed Engl

23-Apr-2014

PMCID:	PMC4153357
doi:	10.1002/anie.201402335
PMID:	24757120

Neurotrophic Natural Products: Chemistry and Biology

Xu J, Lacoske MH, Theodorakis EA

Angew Chem Int Ed Engl

18-Dec-2013

PMCID:	PMC3945720
doi:	10.1002/anie.201302268
PMID:	24353244

The first examples of seco-prezizaane-type norsesquiterpenoids with neurotrophic activity from Illicium jiadifengpi

Miwa Kubo, Kana Kobayashi, Jian-Mei Huang, Kenichi Harada, Yoshiyasu Fukuyama

Elsevier BV

11-Jan-2012

doi:	10.1016/J.TETLET.2011.12.107

Enantioselective Synthesis of (−)-Jiadifenin, a Potent Neurotrophic Modulator

Trzoss L, Xu J, Lacoske MH, Mobley WC, Theodorakis EA

Org Lett

03-Aug-2011

PMCID:	PMC3163030
doi:	10.1021/ol201742j
PMID:	21812392

Enantioselective Total Synthesis of (−)-Jiadifenolide

Xu J, Trzoss L, Chang WK, Theodorakis EA

Angew Chem Int Ed Engl

11-Mar-2011

PMCID:	PMC3159889
doi:	10.1002/anie.201100313
PMID:	21400650

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
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
Epitaraxerol	344467	Click to see CC1(CCC2(CC=C3C4(CCC5C(C(CCC5(C4CCC3(C2C1)C)C)O)(C)C)C)C)C	426.70	unknown	https://doi.org/10.1021/NP010571K
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(-)-Jiadifenolide	44542225	Click to see CC1CCC23C14CC(C5(C2(COC5=O)C)O)OC4(C(=O)O3)O	310.30	unknown	https://doi.org/10.1021/OL9021029
(1R,2R,3S,7R,8S,11R,13R,14S)-2,7-dihydroxy-3,14-dimethyl-5,9,12-trioxapentacyclo[6.6.1.12,13.01,11.03,7]hexadecane-6,10-dione	162939033	Click to see CC1C2CC3(C14CC(C5(C3(COC5=O)C)O)OC(=O)C4O2)O	310.30	unknown	https://doi.org/10.1021/OL9021029
(1R,2R,4R,5R,6S,10R,11R,14R)-4,5,10,14-tetrahydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione	162980859	Click to see CC1CC(C2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O)O	328.31	unknown	https://doi.org/10.1021/OL9021029
(1R,2R,4S,6S,7S,11R,12S,15R)-6,11,15-trihydroxy-2,7-dimethyl-3,9,13-trioxapentacyclo[10.3.1.01,6.02,4.07,11]hexadecane-10,14-dione	163029090	Click to see CC12COC(=O)C1(C3CC4(C2(CC5C4(O5)C)O)C(C(=O)O3)O)O	326.30	unknown	https://doi.org/10.1021/OL9021029
(1R,2R,5R,6S,10R,11R,14R)-5,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione	45269136	Click to see CC1CCC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O	312.31	unknown	https://doi.org/10.1021/OL9021029 https://doi.org/10.1021/NP010571K
(1R,2R,6R,10R,11R,14R)-10,14-dihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-4-ene-3,9,13-trione	11522412	Click to see CC1C(=O)C=C2C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O	308.28	unknown	https://doi.org/10.1021/NP010571K
(1R,2S,11R,14R)-10,14-dihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-4-ene-3,9,13-trione	163186509	Click to see CC1C(=O)C=C2C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O	308.28	unknown	https://doi.org/10.1021/NP010571K
(1R,2S,3R,5S,6S,10R,11R)-3,5,10-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.2.1.01,5.06,10]tetradecane-9,13-dione	57330139	Click to see CC1C(CC2(C13CC(C4(C2(COC4=O)C)O)OC3=O)O)O	298.29	unknown	https://doi.org/10.1016/J.TETLET.2011.12.107
(1R,2S,3R,6R,10R,11R,14R)-3,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-4-ene-9,13-dione	21629990	Click to see CC1C(C=C2C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O	310.30	unknown	https://doi.org/10.1021/NP010571K
(1R,2S,5R,6S,10R,11S,14R)-5,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-3-ene-9,13-dione	162942090	Click to see CC1C=CC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O	310.30	unknown	https://doi.org/10.1021/NP010571K
(1R,2S,6R,10R,11R,14R)-10,14-dihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadec-4-ene-3,9,13-trione	11659544	Click to see CC1C(=O)C=C2C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O	308.28	unknown	https://doi.org/10.1021/NP010571K
(1S,2R,4R,5R,6S,10R,11S,14R)-4,5,10,14-tetrahydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione	162980861	Click to see CC1CC(C2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O)O	328.31	unknown	https://doi.org/10.1021/NP010571K
(1S,2R,4S,6R,9R,10R,14S,15R)-10,15-dihydroxy-2,14-dimethyl-5,8,12-trioxapentacyclo[7.6.1.01,6.04,15.010,14]hexadecane-7,11-dione	44542226	Click to see CC1CC2C3(C14CC(C5(C3(COC5=O)C)O)OC(=O)C4O2)O	310.30	unknown	https://doi.org/10.1021/OL9021029
(1S,2R,5R,6S,10R,11S,14R)-5,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione	21672428	Click to see CC1CCC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O	312.31	unknown	https://doi.org/10.1021/NP010571K
(1S,2S,5R,6S,10R,11R,14R)-5,10,14-trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-3,9,13-trione	14564520	Click to see CC1C(=O)CC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O	326.30	unknown	https://doi.org/10.1021/NP010571K https://doi.org/10.1021/OL9021029
10,15-Dihydroxy-2,14-dimethyl-5,8,12-trioxapentacyclo[7.6.1.01,6.04,15.010,14]hexadecane-7,11-dione	75046197	Click to see CC1CC2C3(C14CC(C5(C3(COC5=O)C)O)OC(=O)C4O2)O	310.30	unknown	https://doi.org/10.1021/OL9021029
2,7-Dihydroxy-3,14-dimethyl-5,9,12-trioxapentacyclo[6.6.1.12,13.01,11.03,7]hexadecane-6,10-dione	162939032	Click to see CC1C2CC3(C14CC(C5(C3(COC5=O)C)O)OC(=O)C4O2)O	310.30	unknown	https://doi.org/10.1021/OL9021029
4,7a-Methano-1H,3H-cyclopenta[e]furo[3,4-c]oxocin-3,6(7H)-dione, heptahydro-3a,7,10,10a-tetrahydroxy-8,10b-dimethyl-	494843	Click to see CC1CC(C2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O)O	328.31	unknown	https://doi.org/10.1021/OL9021029 https://doi.org/10.1021/NP010571K
5,10,14-Trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-3,9,13-trione	14564519	Click to see CC1C(=O)CC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O	326.30	unknown	https://doi.org/10.1021/OL9021029
5,10,14-Trihydroxy-2,6-dimethyl-8,12-dioxatetracyclo[9.3.1.01,5.06,10]pentadecane-9,13-dione	15600080	Click to see CC1CCC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O	312.31	unknown	https://doi.org/10.1021/OL9021029
6,11,15-Trihydroxy-2,7-dimethyl-3,9,13-trioxapentacyclo[10.3.1.01,6.02,4.07,11]hexadecane-10,14-dione	163029089	Click to see CC12COC(=O)C1(C3CC4(C2(CC5C4(O5)C)O)C(C(=O)O3)O)O	326.30	unknown	https://doi.org/10.1021/OL9021029
6,9-Dihydroxy-2,11-dimethyl-4,8,14-trioxapentacyclo[7.4.2.17,10.01,10.02,6]hexadecane-5,15-dione	75046196	Click to see CC1CCC23C14CC(C5(C2(COC5=O)C)O)OC4(C(=O)O3)O	310.30	unknown	https://doi.org/10.1021/OL9021029
Majucin	3086559	Click to see CC1CC(C2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O)O	328.31	unknown	https://doi.org/10.1021/NP010571K
> Organoheterocyclic compounds / Lactones / Delta valerolactones
1,2-Dehydroneomajucin	11141421	Click to see CC1=CCC2(C13CC(C4(C2(COC4=O)C)O)OC(=O)C3O)O	310.30	unknown	https://doi.org/10.1021/NP010571K
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3aR,4R,8aS,8bR)-3a,4-dihydroxy-6,8b-dimethyl-4,5,8,8a-tetrahydro-1H-cyclopenta[e][2]benzofuran-3,7-dione	101792613	Click to see CC1=C2CC(C3(C(=O)OCC3(C2CC1=O)C)O)O	252.26	unknown	https://doi.org/10.1016/J.TETLET.2011.12.107
> Organoheterocyclic compounds / Oxepanes
Jiadifenin	11544617	Click to see CC1C(=O)C=C2C13CC(C4(C2(COC4=O)C)O)OC3(C(=O)OC)O	338.31	unknown	https://doi.org/10.1021/NP010571K
methyl rel-(3aR,4R,6S,6aR,7R,9bR)-3a,6-dihydroxy-7,9b-dimethyl-3,8-dioxo-1,3a,4,7,8,9b-hexahydro-3H-4,6a-methanocyclopenta[c]furo[3,4-e]oxepine-6-carboxylate	636731	Click to see CC1C(=O)C=C2C13CC(C4(C2(COC4=O)C)O)OC3(C(=O)OC)O	338.31	unknown	https://doi.org/10.1021/NP010571K

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Illicium jiadifengpi

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