PlantaeDB Logo
Login Sign-up

Clerodendrum mandarinorum

We don't have an image yet. Upload an image!

Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644031ad649d6321355035
Scientific name Clerodendrum mandarinorum
Authority Diels
First published in Bot. Jahrb. Syst. 29: 549 (1900)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Clerodendrum bodinierii H.Lév. Repert. Spec. Nov. Regni Veg. 9: 325 (1911)
Clerodendrum cavaleriei H.Lév. Repert. Spec. Nov. Regni Veg. 10: 439 (1912)
Clerodendrum tsaii H.L.Li J. Arnold Arbor. 25: 315 (1944)
Clerodendrum kwangtungense var. puberulum H.L.Li J. Arnold Arbor. 25: 426. 1944
Clerodendrum bodinieri var. cavalieri (H.Lév.) H.Lév. Fl. Kouy-Tcheou 441. 1915

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Vietnamese ngọc nữ quan
Chinese 满大青
Chinese 牡丹树
Chinese 白灯笼
Chinese 线桐树
Chinese 铁枪桐
Chinese 鞋头树
Chinese 臭梧桐
Chinese 海通
Chinese 桐木树
Chinese 满大青；白灯笼
Chinese 小花泡桐
Chinese 木常山
Chinese 朴瓜树
Chinese 泡桐树

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000884070
Tropicos 33702301
KEW urn:lsid:ipni.org:names:862240-1
The Plant List kew-42822
Open Tree Of Life 261340
NCBI Taxonomy 54221
IUCN Red List 147653390
IPNI 862240-1
iNaturalist 1146879
GBIF 3891594
EOL 2893551

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
Biologically Active Diterpenoids in the Clerodendrum Genus—A Review Kuźma Ł, Gomulski J Int J Mol Sci 20-Sep-2022
PMCID:PMC9569547
doi:10.3390/ijms231911001
PMID:36232298
The Current State of Knowledge in Biological Properties of Cirsimaritin Benali T, Jaouadi I, Ghchime R, El Omari N, Harboul K, Hammani K, Rebezov M, Shariati MA, Mubarak MS, Simal-Gandara J, Zengin G, Park MN, Kim B, Mahmud S, Lee LH, Bouyahya A Antioxidants (Basel) 19-Sep-2022
PMCID:PMC9495358
doi:10.3390/antiox11091842
PMID:36139916
Exposed Rock Reduces Tree Size, but Not Diversity Li J, Zhang L, Li Y Front Plant Sci 07-Jun-2022
PMCID:PMC9210165
doi:10.3389/fpls.2022.851781
PMID:35747882
Complete chloroplast genome sequence and phylogenetic analysis of Clerodendrum japonicum (Thunb.) Sweet (Ajugoideae, Lamiaceae) Chen G, Wang LG, Wang YH Mitochondrial DNA B Resour 05-Jul-2021
PMCID:PMC8259852
doi:10.1080/23802359.2021.1944367
PMID:34263052
Increase in leaf organic acids to enhance adaptability of dominant plant species in karst habitats Tang S, Liu J, Lambers H, Zhang L, Liu Z, Lin Y, Kuang Y Ecol Evol 29-Jun-2021
PMCID:PMC8328463
doi:10.1002/ece3.7832
PMID:34367574
An interspecific variation in rhizosphere effects on soil anti-erodibility Wang Z, Chiarucci A, Fang H, Chen M Sci Rep 12-Feb-2020
PMCID:PMC7015890
doi:10.1038/s41598-020-58784-z
PMID:32051430
Betulinic acid augments the inhibitory effects of vincristine on growth and lung metastasis of B16F10 melanoma cells in mice Sawada N, Kataoka K, Kondo K, Arimochi H, Fujino H, Takahashi Y, Miyoshi T, Kuwahara T, Monden Y, Ohnishi Y Br J Cancer 23-Mar-2004
PMCID:PMC2409700
doi:10.1038/sj.bjc.6601746
PMID:15083202
Abietane diterpenoids from Clerodendrum mandarinorum T FAN, Z MIN, G SONG, M IINUMA, T TANAKA Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(99)00147-8
Chemical and biological investigation of the root bark of Clerodendrum mandarinorum. Zhu M, Phillipson JD, Greengrass PM, Bowery NG Planta Med 01-Oct-1996
doi:10.1055/S-2006-957923
PMID:9005449

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 / Diterpenoids
(2S,3S,4R,4aS,8aR)-3,4a,8,8-tetramethyl-4-[(2E)-3-methylpenta-2,4-dienyl]-2,4,5,6,7,8a-hexahydro-1H-naphthalene-2,3-diol 162949319 Click to see CC(=CCC1C2(CCCC(C2CC(C1(C)O)O)(C)C)C)C=C 306.50 unknown https://doi.org/10.1055/S-2006-957923
(4aS,10aS)-6-hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione 101034965 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O 314.40 unknown https://doi.org/10.1016/S0031-9422(99)00147-8
(9S,11bS)-7,11-dihydroxy-4,4,9,11b-tetramethyl-2,3,8,9-tetrahydro-1H-naphtho[2,1-f][1]benzofuran-6-one 15478793 Click to see CC1CC2=C(C3=C(C(=C2O1)O)C4(CCCC(C4=CC3=O)(C)C)C)O 328.40 unknown https://doi.org/10.1016/S0031-9422(99)00147-8
6-Hydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydrophenanthrene-2,9-dione 14239449 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O 314.40 unknown https://doi.org/10.1016/S0031-9422(99)00147-8
7,11-dihydroxy-4,4,9,11b-tetramethyl-1H-naphtho[2,1-f][1]benzofuran-6-one 162852530 Click to see CC1=CC2=C(C3=C(C(=C2O1)O)C4(CC=CC(C4=CC3=O)(C)C)C)O 324.40 unknown https://doi.org/10.1016/S0031-9422(99)00147-8
7,11-dihydroxy-4,4,9,11b-tetramethyl-2,3,8,9-tetrahydro-1H-naphtho[2,1-f][1]benzofuran-6-one 162966992 Click to see CC1CC2=C(C3=C(C(=C2O1)O)C4(CCCC(C4=CC3=O)(C)C)C)O 328.40 unknown https://doi.org/10.1016/S0031-9422(99)00147-8
Mandarone A 182295 Click to see CC(C)C1=C(C=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O 314.40 unknown https://doi.org/10.1016/S0031-9422(99)00147-8
Mandarone C 15478794 Click to see CC1=CC2=C(C3=C(C(=C2O1)O)C4(CC=CC(C4=CC3=O)(C)C)C)O 324.40 unknown https://doi.org/10.1016/S0031-9422(99)00147-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 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/10.1055/S-2006-957923
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/10.1055/S-2006-957923
Friedelan-3-one 244297 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2006-957923
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1055/S-2006-957923
Lup-20(29)-en-3-ol, (3beta)- 521518 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/10.1055/S-2006-957923
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/10.1055/S-2006-957923
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhepta-3,6-dien-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 73200193 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown https://doi.org/10.1055/S-2006-957923
22-Dehydroclerosterol 15608667 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 410.70 unknown https://doi.org/10.1055/S-2006-957923
5,25-Stigmastadienol 286499 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 412.70 unknown https://doi.org/10.1055/S-2006-957923
Clerosterol 5283638 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(=C)C 412.70 unknown https://doi.org/10.1055/S-2006-957923
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / C-glycosyl compounds
2-Ethoxy-2,5-bis(hydroxymethyl)oxolane-3,4-diol 14057170 Click to see CCOC1(C(C(C(O1)CO)O)O)CO 208.21 unknown https://doi.org/10.1055/S-2006-957923
Ethyl beta-D-fructofuranoside 11769694 Click to see CCOC1(C(C(C(O1)CO)O)O)CO 208.21 unknown https://doi.org/10.1055/S-2006-957923
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R,4S,5S,6R)-2-Ethoxy-6-hydroxymethyl-tetrahydro-pyran-3,4,5-triol 9815668 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown https://doi.org/10.1055/S-2006-957923
Ethyl glucoside 428040 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown https://doi.org/10.1055/S-2006-957923
Hex-2-ulofuranosyl hexopyranoside 1115 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1055/S-2006-957923
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1055/S-2006-957923
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
beta-D-glucose 64689 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2006-957923
Grape sugar 79025 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2006-957923
> Organoheterocyclic compounds / Lactones / Delta valerolactones
delta-Valerolactone 10953 Click to see C1CCOC(=O)C1 100.12 unknown https://doi.org/10.1055/S-2006-957923
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1055/S-2006-957923
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1055/S-2006-957923

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.