Pachysandra terminalis

Details

Ethnobotanical Use

General Uses

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Gallery

Contributors

Collections

Details Top

Internal ID	UUID6440220008c28340195729
Scientific name	Pachysandra terminalis
Authority	Siebold & Zucc.
First published in	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 142 (1845)

Ethnobotanical Use Top

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General Uses Top

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Common products:
- Live plants sold by nurseries as rooted cuttings, liners, plugs, container‑grown stock, and finished flats for use as a low‑maintenance evergreen groundcover (listed in national horticultural databases such as USDA PLANTS and the RHS Plant Finder).
- Cut foliage used by florists as a filler in bouquets and wreaths; the glossy, dark‑green leaves retain turgidity after cutting.
- Plant material supplied to natural‑product research laboratories for isolation of alkaloids of the pachysandrine series (e.g., Matsumoto et al., J. Nat. Prod. 2003) and for use as reference standards in phytochemical profiling; the material is sold as dried leaf or stem.
- Whole‑plant specimens employed in controlled experiments on shade tolerance, groundcover performance, and ecosystem service assessments (e.g., studies on understory planting in horticultural science journals).

Industrial and craft applications:
- Groundcover mats and slope‑stabilization projects exploit the species’ dense rhizomatous growth to reduce soil erosion, limit runoff, and suppress weed establishment on embankments and landscaped slopes (documented in landscape engineering literature).

Properties relevant to use:
- Evergreen habit with leathery, glossy leaves that retain color under low light, providing year‑round visual coverage.
- Compact growth habit (typically 15–30 cm tall) and spreading rhizomes create a dense mat that fills gaps quickly.
- High shade tolerance, maintaining vigor in 30 % ambient light, enabling planting beneath trees and in deeply shaded garden beds.
- Rapid rooting from stem cuttings and compatibility with tissue‑culture micropropagation, facilitating reliable nursery propagation and consistent cultivar production.
- Hardy in USDA zones 5–9; tolerates a range of soil pH (5.5–7.5) and moderate drought once established, allowing use in varied climatic conditions.

Sustainability and sourcing:
- Commercial material is produced almost entirely by nursery propagation; wild harvesting is minimal and generally discouraged.
- Propagation by vegetative cuttings or tissue culture preserves clonal fidelity, reduces genetic erosion, and limits pressure on native populations.
- The species is not listed in CITES or regional conservation concern inventories, and its cultivation contributes to local horticulture economies without documented significant environmental impact.
- Recommended practices include sourcing nursery‑grown stock, recycling potting media, and avoiding over‑collection from natural sites to maintain sustainable supplies.

Synonyms Top

No known synonyms.

Common names Top

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Filter by language:

Language	Common/alternative name
English	japanese pachysandra
English	japanese spurge
Welsh	pren bocs carped
Danish	vinterglans
German	dickmännchen
German	japanischer ysander
German	dickanthere
Finnish	idänvarjoyrtti
Finnish	varjoyrtti
Upper Sorbian	japanska pachysandra
Japanese	フッキソウ
Japanese	フッキソウ属
Korean	수호초
Dutch	dikkemanskruid
Polish	runianka japońska
Swedish	skugg-gröna
Chinese	頂花板凳果
Chinese	富贵草
Chinese	顶蕊三角咪
Chinese	顶花板凳果
Chinese	雪山林
Chinese	粉蕊黄杨
Chinese	长青草

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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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 North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
- Russian Far East
  - Sakhalin

Europe click to expand
- Middle Europe
  - Austria
  - Germany
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Yugoslavia

Northern America click to expand
- Eastern Canada
  - Ontario
- North-central U.S.A.
  - Illinois
  - Minnesota
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Massachusetts
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
- Southeastern U.S.A.
  - Delaware
  - District Of Columbia
  - Maryland
  - North Carolina
  - South Carolina
  - Virginia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000733029
Cornell Woody Plants	162
Canadensys	4139
USDA Plants	PATE11
UConn	298
Tropicos	4900004
INPN	717364
Flora of Italy	11723
KEW	urn:lsid:ipni.org:names:353208-1
The Plant List	kew-2868090
Missouri Botanical Garden	278317
PFAF	Pachysandra terminalis
Open Tree Of Life	314708
Observations.org	7136
NCBI Taxonomy	74825
NBN Atlas	NHMSYS0100002282
Nature Serve	2.158022
IPNI	353208-1
iNaturalist	142928
GBIF	2984676
Freebase	/m/03gxv7w
WisFlora	4396
EPPO	PCHTE
EOL	486257
Elurikkus	347975
USDA GRIN	26291
Wikipedia	Pachysandra_terminalis

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_031762675.1	ASM3176267v1	Scaffold	Iridian Genomes	2023-09-20	50	1.11 Gb

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

Interactive effects of two rodent species on the seed dispersal of Japanese walnut

Okawa R, Saitoh T, Noda T

Sci Rep

23-Oct-2023

PMCID:	PMC10593932
doi:	10.1038/s41598-023-44513-9
PMID:	37872180

Phytophthora : taxonomic and phylogenetic revision of the genus

Abad ZG, Burgess TI, Bourret T, Bensch K, Cacciola SO, Scanu B, Mathew R, Kasiborski B, Srivastava S, Kageyama K, Bienapfl JC, Verkleij G, Broders K, Schena L, Redford AJ

Stud Mycol

06-Oct-2023

PMCID:	PMC10825748
doi:	10.3114/sim.2023.106.05
PMID:	38298569

Complete Chloroplast Genomes and Phylogenetic Relationships of Bougainvillea spectabilis and Bougainvillea glabra (Nyctaginaceae)

Zhang H, Huang T, Zhou Q, Sheng Q, Zhu Z

Int J Mol Sci

22-Aug-2023

PMCID:	PMC10487864
doi:	10.3390/ijms241713044
PMID:	37685873

Four new species of Phyllosticta from China based on morphological and phylogenetic characterization

Sui XN, Guo MJ, Zhou H, Hou CL

Mycology

04-Jul-2023

PMCID:	PMC10424619
doi:	10.1080/21501203.2023.2225552
PMID:	37583457

Heteroverticillium phytelephatis gen. et sp. nov. intercepted from nuts of Phytelephas macrocarpa, with an updated phylogenetic assessment of Nectriaceae

Li X, Han SL, Zhang YY, Cai L, Zhao P

Mycology

11-Jun-2023

PMCID:	PMC10424595
doi:	10.1080/21501203.2023.2210603
PMID:	37583458

Differential Adaptation Has Resulted in Aggressiveness Variation of Calonectria pseudonaviculata on Hosts Buxus, Pachysandra, and Sarcococca

Kong P, Daughtrey ML, Hong C

J Fungi (Basel)

29-Jan-2023

PMCID:	PMC9966688
doi:	10.3390/jof9020181
PMID:	36836296

Freeze dehydration vs. supercooling of mesophyll cells: Impact of cell wall, cellular and tissue traits on the extent of water displacement

Stegner M, Flörl A, Lindner J, Plangger S, Schaefernolte T, Strasser A, Thoma V, Walde J, Neuner G

Physiol Plant

01-Nov-2022

PMCID:	PMC9828361
doi:	10.1111/ppl.13793
PMID:	36190477

Alkaloid Derivative (Z)-3β-Ethylamino-Pregn-17(20)-en Inhibits Triple-Negative Breast Cancer Metastasis and Angiogenesis by Targeting HSP90α

Liu XY, Wang YM, Zhang XY, Jia MQ, Duan HQ, Qin N, Chen Y, Yu Y, Duan XC

Molecules

21-Oct-2022

PMCID:	PMC9611734
doi:	10.3390/molecules27207132
PMID:	36296726

Comparative genomic analysis reveals contraction of gene families with putative roles in pathogenesis in the fungal boxwood pathogens Calonectria henricotiae and C. pseudonaviculata

Rogers LW, Koehler AM, Crouch JA, Cubeta MA, LeBlanc NR

BMC Ecol Evol

21-Jun-2022

PMCID:	PMC9210730
doi:	10.1186/s12862-022-02035-4
PMID:	35725368

Chemistry and bioactivities of natural steroidal alkaloids

Xiang ML, Hu BY, Qi ZH, Wang XN, Xie TZ, Wang ZJ, Ma DY, Zeng Q, Luo XD

Nat Prod Bioprospect

15-Jun-2022

PMCID:	PMC9198197
doi:	10.1007/s13659-022-00345-0
PMID:	35701630

Genera of phytopathogenic fungi: GOPHY 4

Chen Q, Bakhshi M, Balci Y, Broders KD, Cheewangkoon R, Chen SF, Fan XL, Gramaje D, Halleen F, Jung MH, Jiang N, Jung T, Májek T, Marincowitz S, Milenković I, Mostert L, Nakashima C, Nurul Faziha I, Pan M, Raza M, Scanu B, Spies CF, Suhaizan L, Suzuki H, Tian CM, Tomšovský M, Úrbez-Torres JR, Wang W, Wingfield BD, Wingfield MJ, Yang Q, Yang X, Zare R, Zhao P, Groenewald JZ, Cai L, Crous PW

Stud Mycol

02-Jun-2022

PMCID:	PMC9365048
doi:	10.3114/sim.2022.101.06
PMID:	36059898

Discovery of the interfamily grafting capacity of Petunia, a floricultural species

Kurotani KI, Huang C, Okayasu K, Suzuki T, Ichihashi Y, Shirasu K, Higashiyama T, Niwa M, Notaguchi M

Hortic Res

20-Jan-2022

PMCID:	PMC8969063
doi:	10.1093/hr/uhab056
PMID:	35048114

A new strain of Volutella citrinella with nematode predation and nematicidal activity, isolated from the cysts of potato cyst nematodes in China

Zhang X, Zhang H, Jiang Z, Bai Q, Wu S, Wang Y, Li C, Zeng X, Gan X, Xie X, Li Z, Yang Z

BMC Microbiol

22-Nov-2021

PMCID:	PMC8607719
doi:	10.1186/s12866-021-02385-x
PMID:	34809566

The homogenous alternative to biomineralization: Zn- and Mn-rich materials enable sharp organismal “tools” that reduce force requirements

Schofield RM, Bailey J, Coon JJ, Devaraj A, Garrett RW, Goggans MS, Hebner MG, Lee BS, Lee D, Lovern N, Ober-Singleton S, Saephan N, Seagal VR, Silver DM, Som HE, Twitchell J, Wang X, Zima JS, Nesson MH

Sci Rep

01-Sep-2021

PMCID:	PMC8410824
doi:	10.1038/s41598-021-91795-y
PMID:	34471148

The complete chloroplast genome sequence of Buxus megistophylla Levl. (Buxaceae Dumort.)

Yao X, Meng X, Meng F, Zhang J, Wu J, Guo X, Xing S

Mitochondrial DNA B Resour

22-Aug-2021

PMCID:	PMC8386718
doi:	10.1080/23802359.2021.1966332
PMID:	34447883

Phytochemical Profile Top

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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 / Monoterpenoids / Acyclic monoterpenoids
(6E)-2'-O-Methylmyxalamide D	11474697	Click to see	387.60	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(3S,4R,4aS,6aS,6aS,6bR,12aS,14aS,14bS)-4,4a,6a,6b,8,11,11,14a-octamethyl-2,3,4,5,6,6a,10,12,12a,13,14,14b-dodecahydro-1H-picen-3-ol	101643003	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(C=C(C5=CCC(CC54)(C)C)C)C)C)C)C)O	424.70	unknown	https://doi.org/10.1248/CPB.29.2531
(3S,4R,4aS,6aS,6aS,6bR,12aS,14aS,14bS)-4,4a,6a,6b,8,11,11,14a-octamethyl-2,3,4,5,6,6a,7,12,12a,13,14,14b-dodecahydro-1H-picen-3-ol	101643002	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(=C5C4CC(C=C5)(C)C)C)C)C)C)C)O	424.70	unknown	https://doi.org/10.1248/CPB.29.2531
(3S,4R,4aS,6aS,6aS,6bS,12aS,14aS,14bS)-4,4a,6a,6b,8,11,11,14a-octamethyl-2,3,4,5,6,6a,10,12,12a,13,14,14b-dodecahydro-1H-picen-3-ol	162871051	Click to see	424.70	unknown	https://doi.org/10.1248/CPB.29.2531
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(3R,4aR,6aS,6aS,8aS,12aR,14aS,14bS)-4,4,6a,6a,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,8,9,10,12,12a,13,14,14a-tetradecahydropicen-3-ol	6573164	Click to see	426.70	unknown	https://doi.org/10.1248/YAKUSHI1947.90.8_1051
4,4,6a,8a,11,11,12b,14b-Octamethyl-1,2,3,4,4a,5,6,6a,8,8a,9,10,11,12,12a,12b,13,14,14a,14b-icosahydropicen-3-ol	344467	Click to see	426.70	unknown	https://doi.org/10.1248/YAKUSHI1947.90.8_1051
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2R,3R,4R,4aS,6aS,6aS,6bR,8S,8aS,12aS,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene-2,3,8-triol	163022863	Click to see	460.70	unknown	https://doi.org/10.1016/S0040-4039(01)97294-6
(3,8-Diacetyloxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-2-yl) acetate	162878573	Click to see	586.80	unknown	https://doi.org/10.1248/YAKUSHI1947.93.10_1378
(3S,4R,4aR,6aS,6aS,6bR,8aS,12aS,14aS,14bR)-8a-(hydroxymethyl)-4,4a,6a,6b,11,11,14a-heptamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-3-ol	162979967	Click to see	444.70	unknown	https://doi.org/10.1248/YAKUSHI1947.105.7_690
(3S,4R,4aS,6aS,6aS,6bR,8aR,9R,12aS,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene-3,9-diol	162976766	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5O)(C)C)C)C)C)C)C)O	444.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
(3S,4R,4aS,6aS,6aS,6bR,8S,8aS,12aS,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene-3,8-diol	101306869	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(C5(C4CC(CC5)(C)C)C)O)C)C)C)C)O	444.70	unknown	https://doi.org/10.1248/CPB.33.4223
(4R,4aS,6aS,6aS,6bR,8S,8aS,12aR,14aS,14bS)-8-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	163015245	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(C5(C4CC(CC5)(C)C)C)O)C)C)C)C	442.70	unknown	https://doi.org/10.1248/CPB.33.4223
(4R,4aS,6aS,6aS,6bR,8S,8aS,12aS,14aS,14bS)-8-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	21636455	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(C5(C4CC(CC5)(C)C)C)O)C)C)C)C	442.70	unknown	https://doi.org/10.1248/CPB.33.4223
(4R,4aS,6bR,8S,8aS,12aS,14aS)-8-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	5320371	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(C5(C4CC(CC5)(C)C)C)O)C)C)C)C	442.70	unknown	https://doi.org/10.1248/CPB.33.4223
[(2R,3R,4R,4aS,6aS,6aS,6bR,8S,8aS,12aR,14aS,14bR)-3,8-diacetyloxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicen-2-yl] acetate	162878574	Click to see	586.80	unknown	https://doi.org/10.1248/YAKUSHI1947.93.10_1378
4,4a,6a,6b,8a,11,11,14a-Octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene-2,3,8-triol	163022862	Click to see	460.70	unknown	https://doi.org/10.1016/S0040-4039(01)97294-6
4,4a,6a,6b,8a,11,11,14a-Octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene-3,8-diol	12313887	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(C5(C4CC(CC5)(C)C)C)O)C)C)C)C)O	444.70	unknown	https://doi.org/10.1248/CPB.33.4223
4,4a,6a,6b,8a,11,11,14a-Octamethyl-1,2,3,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-hexadecahydropicene-3,9-diol	162976765	Click to see	444.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
8-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one	12313889	Click to see	442.70	unknown	https://doi.org/10.1248/CPB.33.4223
Epifriedelanol	119242	Click to see	428.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
Friedelan-3-one	244297	Click to see	426.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
Friedelanol	348029	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O	428.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
Friedelin	91472	Click to see	426.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
Pachysandiol A	21596127	Click to see	444.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids
E-Salignone	70688999	Click to see CC=C1C(=O)CC2C1(CCC3C2CCC4C3(CCC(C4)N(C)C)C)C	343.50	unknown	https://doi.org/10.1021/NP300207C
Z-Salignone	70697323	Click to see	343.50	unknown	https://doi.org/10.1021/NP300207C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
(10S,13S,17S)-17-[1-(dimethylamino)ethyl]-2',10,13-trimethylspiro[1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,3'-isoindole]-1'-one	374414	Click to see	462.70	unknown	https://doi.org/10.1055/S-2007-969070 https://doi.org/10.1248/CPB.23.416
(3R,10S,13S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2',10,13-trimethylspiro[1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,3'-isoindole]-1'-one	11972521	Click to see	462.70	unknown	https://doi.org/10.1055/S-2007-969070
(3R,5S,8R,9S,10S,13R,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2',10,13-trimethylspiro[1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,3'-isoindole]-1'-one	162990679	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC5(C4)C6=CC=CC=C6C(=O)N5C)C)C)N(C)C	462.70	unknown	https://doi.org/10.1248/CPB.23.416
(3R,5S,8S,9R,10S,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2',10,13-trimethylspiro[1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,3'-isoindole]-1'-one	162990670	Click to see	462.70	unknown	https://doi.org/10.1016/0031-9422(90)85362-J
(3S,5S,8R,9R,10S,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-2',10,13-trimethylspiro[1,2,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthrene-3,3'-isoindole]-1'-one	162990669	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC5(C4)C6=CC=CC=C6C(=O)N5C)C)C)N(C)C	462.70	unknown	https://doi.org/10.1016/S0040-4039(00)89747-6
(8R,10S,13S,17S)-17-[1-(dimethylamino)ethyl]-N,10,13-trimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-amine	5320362	Click to see	360.60	unknown	https://doi.org/10.1055/S-2007-969070
Epipachysamine A	16831	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)N(C)C)C)C)N(C)C(=O)C	402.70	unknown	https://doi.org/10.1248/BPB1978.7.263 https://doi.org/10.1055/S-2007-969070
Epipachysamine B	70688998	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)NC(=O)C5=CN=CC=C5)C)C)N(C)C	451.70	unknown	https://doi.org/10.1021/NP300207C https://doi.org/10.1248/BPB.23.262
Epipachysamine E	10048235	Click to see	428.70	unknown	https://doi.org/10.1021/NP300207C https://doi.org/10.1248/BPB.23.262
Isospiropachysine	500127	Click to see	462.70	unknown	https://doi.org/10.1016/0031-9422(90)85362-J https://doi.org/10.1016/S0040-4039(00)89747-6
N-[(3S,10S,13S)-17-[1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-3-methylbut-2-enamide	5317106	Click to see	428.70	unknown	https://doi.org/10.1021/NP300207C
N-[(3S,10S,13S)-17-[1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]pyridine-3-carboxamide	5317103	Click to see	451.70	unknown	https://doi.org/10.1021/NP300207C
N-[17-[1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-3-methylbut-2-enamide	78384878	Click to see	428.70	unknown	https://doi.org/10.1248/BPB.23.262
Pachysamine A	197857	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)NC)C)C)N(C)C	360.60	unknown	https://doi.org/10.1055/S-2007-969070
Pachysamine E	10071262	Click to see	428.70	unknown	https://doi.org/10.1248/BPB.23.262
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3R)-1-[(3S,4R,10R,13S)-17-[(1S)-1-(dimethylamino)ethyl]-4-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-3-propan-2-ylazetidin-2-one	5320373	Click to see CC(C)C1CN(C1=O)C2CCC3(C(C2O)CCC4C3CCC5(C4CCC5C(C)N(C)C)C)C	458.70	unknown	https://doi.org/10.1021/NP300207C
Pachystermine B	70695310	Click to see	458.70	unknown	https://doi.org/10.1021/NP300207C
Terminamine E	70682697	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4O)N5CC(=C(C)C)C5=O)C)C)N(C)C	456.70	unknown	https://doi.org/10.1021/NP300207C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 16-hydroxysteroids
Terminamine B	70686928	Click to see	590.80	unknown	https://doi.org/10.1021/NP300207C
Terminamine C	70697321	Click to see	632.90	unknown	https://doi.org/10.1021/NP300207C
Terminamine D	70697322	Click to see CC(C1C(CC2C1(CCC3C2CCC4C3(CCC(C4O)N5CC(=C(C)C)C5=O)C)C)O)N(C)C	472.70	unknown	https://doi.org/10.1021/NP300207C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(3R)-1-[(3R,5R,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-4-oxo-1,2,3,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]-3-propan-2-ylazetidin-2-one	162945561	Click to see	456.70	unknown	https://doi.org/10.1248/BPB.23.262
1-[17-[1-(Dimethylamino)ethyl]-10,13-dimethyl-4-oxo-1,2,3,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]-3-propan-2-ylazetidin-2-one	634937	Click to see	456.70	unknown	https://doi.org/10.1248/BPB.23.262
2-Azetidinone, 1-(20-alpha-(dimethylamino)-4-oxo-5-alpha-pregnan-3-beta-yl)-3-isopropyl-, (3R)-	22532	Click to see	456.70	unknown	https://doi.org/10.1248/BPB.23.262 https://doi.org/10.1055/S-2007-969070 https://doi.org/10.1021/NP300207C
2-Azetidinone, 1-[(3beta,5alpha,20S)-20-(dimethylamino)-4-oxopregnan-3-yl]-3-(1-methylethyl)-, (3R)-	91745398	Click to see CC(C)C1CN(C1=O)C2CCC3(C4CCC5(C(C4CCC3C2=O)CCC5C(C)N(C)C)C)C	456.70	unknown	https://doi.org/10.1248/BPB.23.262 https://doi.org/10.1055/S-2007-969070
N-[(3S,5R,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-4-oxo-1,2,3,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]pyridine-3-carboxamide	10344442	Click to see	465.70	unknown	https://doi.org/10.1248/BPB.23.262
N-[17-[1-(dimethylamino)ethyl]-10,13-dimethyl-4-oxo-1,2,3,5,6,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]pyridine-3-carboxamide	85116242	Click to see	465.70	unknown	https://doi.org/10.1248/BPB.23.262
Pachystermine A	22296920	Click to see	456.70	unknown	https://doi.org/10.1021/NP300207C
Terminamine A	70693226	Click to see	472.70	unknown	https://doi.org/10.1021/NP300207C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
[(3R,4R,5R,8S,9S,10R,13S,14S,17S)-3-[benzoyl(methyl)amino]-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate	12313881	Click to see	522.80	unknown	https://doi.org/10.1055/S-2007-969070
[(4R,10R,13S)-3-[benzoyl(methyl)amino]-17-[1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate	5320366	Click to see	522.80	unknown	https://doi.org/10.1055/S-2007-969070
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Terminaline	177562	Click to see	363.60	unknown	https://doi.org/10.1021/NP300207C
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-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	12314479	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/S0040-4039(01)97003-0
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	412.70	unknown	https://doi.org/10.1016/S0040-4039(01)97003-0
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/S0040-4039(01)97003-0

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Pachysandra terminalis

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