Scientific name	Authority	First published in
Ziziphus aubletii	D.Dietr.	Syn. Pl. 1: 810 (1839)
Aubletia ramosissima	Lour.	Fl. Cochinch. 1: 283. 1790 [Sep 1790]
Ziziphus ramosissima	Spreng.	Syst. Veg. 1: 771 (1824)
Paliurus aubletia	Roem. & Schult.	Syst. Veg., ed. 15 bis [Roemer & Schultes] 5: 343. 1819 [Dec 1819]

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	ハマナツメ
Chinese	棘盘子
Chinese	白棘
Chinese	簕子
Chinese	铁篱笆
Chinese	铜钱树
Chinese	雄虎刺
Chinese	马甲子
Chinese	马鞍树
Chinese	铁篱笆果
Chinese	馬甲子
Chinese	马甲子根

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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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
- Eastern Asia
  - Japan
  - Korea
  - Nansei-shoto
  - Taiwan

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

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001131369
Tropicos	27501231
KEW	urn:lsid:ipni.org:names:717703-1
The Plant List	tro-27501231
PFAF	Paliurus ramosissimus
Open Tree Of Life	371173
NCBI Taxonomy	345801
IPNI	717703-1
iNaturalist	629247
GBIF	5603062
EPPO	PLSRA
EOL	2889198
USDA GRIN	26366

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

Plant Foliar Geometry as a Biomimetic Template for Antenna Design

Lozano JI, Panduro MA, Méndez-Alonzo R, Alonso-Arevalo MA, Conte R, Reyna A

Biomimetics (Basel)

07-Nov-2023

PMCID:	PMC10669502
doi:	10.3390/biomimetics8070531
PMID:	37999172

Combined analysis of transcriptomics and metabolomics on the cumulative effect of nano-titanium dioxide on mulberry seedlings

Yu D, Lu Q, Wei Y, Hou D, Yin X, Cai K, Qiu C, Xu K

Front Plant Sci

14-Jun-2023

PMCID:	PMC10301732
doi:	10.3389/fpls.2023.1175012
PMID:	37389295

Ancient Rhamnaceae flowers impute an origin for flowering plants exceeding 250-million-years ago

He T, Lamont BB

iScience

18-Jun-2022

PMCID:	PMC9254029
doi:	10.1016/j.isci.2022.104642
PMID:	35800761

Mechanistic Insights into the Ameliorating Effect of Melanogenesis of Psoralen Derivatives in B16F10 Melanoma Cells

Lee Y, Hyun CG

Molecules

19-Apr-2022

PMCID:	PMC9102055
doi:	10.3390/molecules27092613
PMID:	35565964

Trunk spines of trees: a physical defence against bark removal and climbing by mammals?

Lefebvre T, Charles-Dominique T, Tomlinson KW

Ann Bot

24-Feb-2022

PMCID:	PMC9007100
doi:	10.1093/aob/mcac025
PMID:	35199147

Repellency of forty‐one aromatic plant species to the Asian citrus psyllid, vector of the bacterium associated with huanglongbing

Yan Z, Zhang Q, Zhang N, Li W, Chang C, Xiang Y, Xia C, Jiang T, He W, Luo J, Xu Y

Ecol Evol

03-Nov-2020

PMCID:	PMC7713936
doi:	10.1002/ece3.6876
PMID:	33304506

Benefits of jasmonate-dependent defenses against vertebrate herbivores in nature

Machado RA, McClure M, Hervé MR, Baldwin IT, Erb M

eLife

29-Jun-2016

PMCID:	PMC4927296
doi:	10.7554/eLife.13720
PMID:	27352734

Ethanol Extract of Cirsium japonicum var. ussuriense Kitamura Exhibits the Activation of Nuclear Factor Erythroid 2-Related Factor 2-dependent Antioxidant Response Element and Protects Human Keratinocyte HaCaT Cells Against Oxidative DNA Damage

Yoo OK, Choi BY, Park JO, Lee JW, Park BK, Joo CG, Heo HJ, Keum YS

J Cancer Prev

30-Mar-2016

PMCID:	PMC4819669
doi:	10.15430/JCP.2016.21.1.66
PMID:	27051652

Effects of ATRA combined with citrus and ginger-derived compounds in human SCC xenografts

Kleiner-Hancock HE, Shi R, Remeika A, Robbins D, Prince M, Gill JN, Syed Z, Adegboyega P, Mathis JM, Clifford JL

BMC Cancer

26-Jul-2010

PMCID:	PMC2916922
doi:	10.1186/1471-2407-10-394
PMID:	20659317

Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae)

Kurdelas RR, Lima B, Tapia A, Egly Feresin G, Gonzalez Sierra M, Rodríguez MV, Zacchino S, Enriz RD, Freile ML

Molecules

13-Jul-2010

PMCID:	PMC6257657
doi:	10.3390/molecules15074898
PMID:	20657398

Citrus auraptene suppresses cyclin D1 and significantly delays N-methyl nitrosourea induced mammary carcinogenesis in female Sprague-Dawley rats

Krishnan P, Yan KJ, Windler D, Tubbs J, Grand R, Li BD, Aldaz CM, McLarty J, Kleiner-Hancock HE

BMC Cancer

29-Jul-2009

PMCID:	PMC2724550
doi:	10.1186/1471-2407-9-259
PMID:	19640308

Two Triterpenes from Paliurus ramosissimus

Shoei-Sheng Lee, Cheng-Jen Lin, Karin C. Liu

American Chemical Society (ACS)

17-Mar-2005

doi:	10.1021/NP50083A007

Two New Triterpene Glucosides from Paliurus ramosissimus

Shoei-Sheng Lee, Whei-Chuan Su, Karin C. Liu

American Chemical Society (ACS)

17-Mar-2005

doi:	10.1021/NP50074A047

14‐Membered Cyclopeptides from <i>Paliurus ramosissimus</i> and <i>P. hemsleyanus</i>

Hui‐yi Lin, Chung‐Hsiung Chen, Karin C. S. Chen Liu, Shoei‐Sheng Lee

Wiley

06-Feb-2003

doi:	10.1002/HLCA.200390002

Cyclopeptide alkaloids from stems of Paliurus ramossisimus.

Lee SS, Su WC, Liu KC

Phytochemistry

01-Dec-2001

doi:	10.1016/S0031-9422(01)00234-5
PMID:	11738421

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 / Triterpenoids
16-Hydroxy-17-(hydroxymethyl)-1,2,14,17-tetramethyl-8-prop-1-en-2-ylpentacyclo[11.7.0.02,10.05,9.014,18]icosane-5,15-dicarboxylic acid	74124644	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(C(C5(C)CO)O)C(=O)O)C)C)C(=O)O	502.70	unknown	https://doi.org/10.1021/NP50083A007
Betulinic Acid	64971	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O	456.70	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
Ceanothic acid	161352	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(C(C5(C)C)O)C(=O)O)C)C)C(=O)O	486.70	unknown	https://doi.org/10.1021/NP50074A047 https://doi.org/10.1016/S0031-9422(01)00234-5 https://doi.org/10.1021/NP50083A007 https://doi.org/10.1021/NP9800856
Emmolic acid	578549	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(C(C5(C)C)O)C(=O)O)C)C)C(=O)O	486.70	unknown	https://doi.org/10.1021/NP50083A007 https://doi.org/10.1021/NP9800856 https://doi.org/10.1021/NP50074A047 https://doi.org/10.1016/S0031-9422(01)00234-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
(2S,3R)-N-[(2S)-1-[(3S,7S,10S,13Z)-10-[(2R)-butan-2-yl]-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraen-6-yl]-1-oxo-3-phenylpropan-2-yl]-3-methyl-2-(methylamino)pentanamide	163194367	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC(=O)C(C(C)CC)NC	617.80	unknown	https://doi.org/10.1002/HLCA.200390002
(2S,3S)-N-[(2S)-1-[(3S,7S,10R,13E)-10-[(2S)-butan-2-yl]-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanamide	162953671	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC(=O)C(C(C)CC)N(C)C)OC	661.80	unknown	https://doi.org/10.1021/NP000136A
(2S)-N-[(2S,3S)-1-[(3S,7S,10R,13E)-10-[(2S)-butan-2-yl]-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-3-methyl-1-oxopentan-2-yl]-2-(dimethylamino)-3,3-dimethylbutanamide	163078246	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)NC(=O)C(C(C)(C)C)N(C)C)OC	627.80	unknown	https://doi.org/10.1021/NP000136A
(2S)-N-[(2S)-1-[(3S,10S,13E)-10-butan-2-yl-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(methylamino)-3-phenylpropanamide	101204325	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC(=O)C(CC5=CC=CC=C5)NC)OC	681.80	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
(3S,7S,10R,13E)-10-[(2S)-butan-2-yl]-6-[(2S)-2-(dimethylamino)-3-phenylpropanoyl]-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraene-8,11-dione	162898831	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)N(C)C)OC	548.70	unknown	https://doi.org/10.1021/NP000136A
(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-6-[(2S)-2-(dimethylamino)-3-phenylpropanoyl]-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraene-8,11-dione	101063136	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)N(C)C)OC	548.70	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
(3S,7S,10S,13Z)-10-[(2R)-butan-2-yl]-6-[(2S,3R)-2-(dimethylamino)-3-methylpentanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraene-8,11-dione	163188364	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)N(C)C	484.60	unknown	https://doi.org/10.1002/HLCA.200390002
(3S,7S,10S,13Z)-10-[(2R)-butan-2-yl]-6-[(2S)-2-(dimethylamino)-3-phenylpropanoyl]-16-hydroxy-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(17),13,15,18-tetraene-8,11-dione	163186710	Click to see CCC(C)C1C(=O)NC=CC2=C(C=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)N(C)C)O	534.60	unknown	https://doi.org/10.1002/HLCA.200390002
(3S,7S,10S,13Z)-10-[(2R)-butan-2-yl]-6-[(2S)-2-(dimethylamino)-3-phenylpropanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraene-8,11-dione	163193365	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)N(C)C	518.60	unknown	https://doi.org/10.1002/HLCA.200390002
(3S,7S,10S,13Z)-10-[(2R)-butan-2-yl]-6-[(2S)-2-(dimethylamino)-4-methylpentanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraene-8,11-dione	163193920	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC(C)C)N(C)C	484.60	unknown	https://doi.org/10.1002/HLCA.200390002
(3S,7S,10S,13Z)-10-[(2R)-butan-2-yl]-6-[(2S)-2-(methylamino)-3-phenylpropanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraene-8,11-dione	163190371	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC	504.60	unknown	https://doi.org/10.1002/HLCA.200390002
10-Butan-2-yl-6-[2-(dimethylamino)-4-methylpentanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(17),13,15,18-tetraene-8,11-dione	85244322	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC(C)C)N(C)C	484.60	unknown	https://doi.org/10.1002/HLCA.200390002
Paliurine B	101063132	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC(=O)C(C(C)CC)NC)OC	647.80	unknown	https://doi.org/10.1021/NP000136A https://doi.org/10.1016/S0031-9422(01)00234-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(2S,3S)-N-[(2S,3S)-1-[(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-3-methyl-1-oxopentan-2-yl]-2-(dimethylamino)-3-methylpentanamide	101063137	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)NC(=O)C(C(C)CC)N(C)C)OC	627.80	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
(2S,3S)-N-[(2S)-1-[(3S,10S,13E)-10-benzyl-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-4-methyl-1-oxopentan-2-yl]-3-methyl-2-(methylamino)pentanamide	101204324	Click to see CCC(C)C(C(=O)NC(CC(C)C)C(=O)N1CCC2C1C(=O)NC(C(=O)NC=CC3=C(C=CC(=C3)O2)OC)CC4=CC=CC=C4)NC	647.80	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
(2S,3S)-N-[(2S)-1-[(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-1-oxo-3-phenylpropan-2-yl]-2-(dimethylamino)-3-methylpentanamide	101063131	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC(=O)C(C(C)CC)N(C)C)OC	661.80	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
(2S)-N-[(2S,3S)-1-[(3S,10S,13E)-10-butan-2-yl-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-3-methyl-1-oxopentan-2-yl]-4-methyl-2-(methylamino)pentanamide	101204207	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)NC(=O)C(CC(C)C)NC)OC	613.80	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
(2S)-N-[(2S,3S)-1-[(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-3-methyl-1-oxopentan-2-yl]-2-(dimethylamino)-3-phenylpropanamide	101063134	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)NC(=O)C(CC4=CC=CC=C4)N(C)C)OC	661.80	unknown	https://doi.org/10.1021/NP000136A https://doi.org/10.1016/S0031-9422(01)00234-5
(2S)-N-[(2S,3S)-1-[(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-3-methyl-1-oxopentan-2-yl]-2-(methylamino)-3-phenylpropanamide	101063135	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)NC(=O)C(CC4=CC=CC=C4)NC)OC	647.80	unknown	https://doi.org/10.1021/NP000136A https://doi.org/10.1016/S0031-9422(01)00234-5
(2S)-N-[(2S)-1-[(3S,10S,13E)-10-butan-2-yl-16-methoxy-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraen-6-yl]-3-methyl-1-oxobutan-2-yl]-2-(dimethylamino)-3-phenylpropanamide	101204206	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)C)NC(=O)C(CC4=CC=CC=C4)N(C)C)OC	647.80	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
(3S,10S,13E)-10-butan-2-yl-6-[(2S)-2-(dimethylamino)-3-phenylpropanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraene-8,11-dione	101229399	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)N(C)C	518.60	unknown	https://doi.org/10.1002/HLCA.200390002
(3S,10S,13E)-10-butan-2-yl-6-[(2S)-2-(methylamino)-3-phenylpropanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraene-8,11-dione	101229398	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC	504.60	unknown	https://doi.org/10.1002/HLCA.200390002
(3S,10S,13Z)-10-butan-2-yl-6-[(2S)-2-(dimethylamino)-3-phenylpropanoyl]-16-hydroxy-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(17),13,15,18-tetraene-8,11-dione	122404284	Click to see CCC(C)C1C(=O)NC=CC2=C(C=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)N(C)C)O	534.60	unknown	https://doi.org/10.1002/HLCA.200390002
(3S,7S,10S,13E)-10-[(2S)-butan-2-yl]-6-[(2S,3S)-2-(dimethylamino)-3-methylpentanoyl]-16-methoxy-2-oxa-6,9,12-triazatricyclo[13.3.1.03,7]nonadeca-1(19),13,15,17-tetraene-8,11-dione	101063133	Click to see CCC(C)C1C(=O)NC=CC2=C(C=CC(=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)N(C)C)OC	514.70	unknown	https://doi.org/10.1016/S0031-9422(01)00234-5
(3S,7S,10S,13Z)-10-butan-2-yl-6-[(2S)-2-(dimethylamino)-3-methylpentanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraene-8,11-dione	132582304	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)N(C)C	484.60	unknown	https://doi.org/10.1002/HLCA.200390002
10-Butan-2-yl-6-[2-(dimethylamino)-3-methylpentanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(17),13,15,18-tetraene-8,11-dione	162930422	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(C(C)CC)N(C)C	484.60	unknown	https://doi.org/10.1002/HLCA.200390002
10-Butan-2-yl-6-[2-(dimethylamino)-3-phenylpropanoyl]-16-hydroxy-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(17),13,15,18-tetraene-8,11-dione	163005261	Click to see CCC(C)C1C(=O)NC=CC2=C(C=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)N(C)C)O	534.60	unknown	https://doi.org/10.1002/HLCA.200390002
10-Butan-2-yl-6-[2-(dimethylamino)-3-phenylpropanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(17),13,15,18-tetraene-8,11-dione	162943384	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)N(C)C	518.60	unknown	https://doi.org/10.1002/HLCA.200390002
10-Butan-2-yl-6-[2-(methylamino)-3-phenylpropanoyl]-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(17),13,15,18-tetraene-8,11-dione	162952369	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC	504.60	unknown	https://doi.org/10.1002/HLCA.200390002
Mucronine J	10719669	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC(C)C)N(C)C	484.60	unknown	https://doi.org/10.1002/HLCA.200390002
N-[1-(10-butan-2-yl-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(17),13,15,18-tetraen-6-yl)-1-oxo-3-phenylpropan-2-yl]-3-methyl-2-(methylamino)pentanamide	162865570	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC(=O)C(C(C)CC)NC	617.80	unknown	https://doi.org/10.1002/HLCA.200390002
N-[1-[(3S,10S,13E)-10-butan-2-yl-8,11-dioxo-2-oxa-6,9,12-triazatricyclo[13.2.2.03,7]nonadeca-1(18),13,15(19),16-tetraen-6-yl]-1-oxo-3-phenylpropan-2-yl]-3-methyl-2-(methylamino)pentanamide	101229400	Click to see CCC(C)C1C(=O)NC=CC2=CC=C(C=C2)OC3CCN(C3C(=O)N1)C(=O)C(CC4=CC=CC=C4)NC(=O)C(C(C)CC)NC	617.80	unknown	https://doi.org/10.1002/HLCA.200390002

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Paliurus ramosissimus

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