Wrightia tinctoria, also known as Pala indigo plant or dyer's oleander, is a flowering plant species found in India, southeast Asia and Australia. It is a small to medium-sized deciduous shrub or tree, ranging from 3–15 m (10–49 ft) in height but also reaching up to 18 m. The bark is smooth, yellowish-brown and about 10 mm thick, producing a milky-white latex. Leaves are simple, oppositely arranged, ovate, obtusely acuminate and are 10–20 cm long and 5 cm wide. White flowers appear in corymb-like cymes, 5–15 cm across, at the end of branches. The plant contains wrightial, a triterpenoid phytochemical, along with cycloartenone, cycloeucalenol, β-amyrin, and β-sitosterol isolated from the methanol extract of the immature seed pods. Various parts of the plant have been used in traditional medicine, but there is no scientific evidence it is effective or safe for treating any disease. The wood is used for turnery, carving, toy making

Synonyms Top

Scientific name	Authority	First published in
Nerium jaspideum	Span.	Linnaea 15: 325 (1841)
Nerium tinctorium	Roxb.	Orient. Repert. 1: 40 (1791)
Alstonia oleandrifolia	Lodd. ex Loudon	Hort. Brit. [Loudon] 67. 1830

Common names Top

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Filter by language:

Language	Common/alternative name
Hindi	मीठा इन्द्रजौ
Malayalam	വെൺപാല
Malayalam	sweet indrajao
Malayalam	അയ്യപ്പാല
Malayalam	ഗന്ധപ്പാല
Malayalam	വെട്ടുപാല
Malayalam	ദന്തപ്പാല
Punjabi	ਕਮੀਲਾ
Punjab	کمیلا
Tamil	வெப்பாலை

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Wrightia tinctoria subsp. rothii	(G.Don) Ngan	Ann. Missouri Bot. Gard. 52: 144 (1965)
Wrightia tinctoria subsp. tinctoria		Unknown

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-tropical click to expand
- Indian Subcontinent
  - Bangladesh
  - India
- Indo-China
  - Myanmar
- Malesia
  - Lesser Sunda Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000334581
Tropicos	1804348
KEW	urn:lsid:ipni.org:names:82890-1
The Plant List	kew-214955
Open Tree Of Life	842381
NCBI Taxonomy	653463
IPNI	82890-1
iNaturalist	489308
GBIF	5536686
Freebase	/m/09v6tk_
EPPO	WRITI
USDA GRIN	42065
Wikipedia	Wrightia_tinctoria
CMAUP	NPO3463

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

Use of Medicinal Plants in the Process of Wound Healing: A Literature Review

Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL

Pharmaceuticals (Basel)

27-Feb-2024

PMCID:	PMC10975678
doi:	10.3390/ph17030303
PMID:	38543089

Characterization of carbon fluxes, stock and nutrients in the sacred forest groves and invasive vegetation stands within the human dominated landscapes of a tropical semi-arid region

Akil Prasath RV, Mohanraj R, Balaramdas KR, Jhony Kumar Tagore A, Raja P, Rajasekaran A

Sci Rep

24-Feb-2024

PMCID:	PMC10894248
doi:	10.1038/s41598-024-55294-0
PMID:	38402350

Diverse origins of fibrinolytic enzymes: A comprehensive review

Hazare C, Bhagwat P, Singh S, Pillai S

Heliyon

22-Feb-2024

PMCID:	PMC10907686
doi:	10.1016/j.heliyon.2024.e26668
PMID:	38434287

Paclitaxel and its semi-synthetic derivatives: comprehensive insights into chemical structure, mechanisms of action, and anticancer properties

Sati P, Sharma E, Dhyani P, Attri DC, Rana R, Kiyekbayeva L, Büsselberg D, Samuel SM, Sharifi-Rad J

Eur J Med Res

30-Jan-2024

PMCID:	PMC10826257
doi:	10.1186/s40001-024-01657-2
PMID:	38291541

Research Advances in Clinical Applications, Anticancer Mechanism, Total Chemical Synthesis, Semi-Synthesis and Biosynthesis of Paclitaxel

Zhang S, Ye T, Liu Y, Hou G, Wang Q, Zhao F, Li F, Meng Q

Molecules

10-Nov-2023

PMCID:	PMC10673093
doi:	10.3390/molecules28227517
PMID:	38005238

Wound tissue remodeling by latex exudate of Himatanthus drasticus: A plant species used in Brazilian folk medicine

Souza TF, Ramos MV, Pierdoná TM, Rabelo LM, Vasconcelos MS, Carmo LD, Rangel GF, Paiva YT, Sousa ET, Figueiredo IS, Alencar NM

Heliyon

31-Oct-2023

PMCID:	PMC10660522
doi:	10.1016/j.heliyon.2023.e21843
PMID:	38027902

Discovery and Mechanism of Novel 7-Aliphatic Amine Tryptanthrin Derivatives against Phytopathogenic Bacteria

Long X, Zhang G, Long H, Wang Q, Wang C, Zhu M, Wang W, Li C, Wang Z, Ouyang G

Int J Mol Sci

30-Jun-2023

PMCID:	PMC10341529
doi:	10.3390/ijms241310900
PMID:	37446077

HPTLC and GC–MS finger-printing of two potential multifunctional siddha tailams: Mathan and maha megarajanga tailam

Senthilnathan S, Jayaraman S, Priya Veeraraghavan V, Masood Khan J, Ahmed MZ, Ahmad A, Gnanamani A

Saudi J Biol Sci

01-Jun-2023

PMCID:	PMC10276281
doi:	10.1016/j.sjbs.2023.103700
PMID:	37333677

Targeting receptor tyrosine kinase signaling: Avenues in the management of cutaneous squamous cell carcinoma

Gopinatha Pillai MS, Aiswarya SU, Keerthana CK, Rayginia TP, Anto RJ

iScience

05-May-2023

PMCID:	PMC10206193
doi:	10.1016/j.isci.2023.106816
PMID:	37235052

Do carbon stocks and floristic diversity of tropical homegardens vary along an elevational gradient and based on holding size in central Kerala, India?

Kumar BM

Agrofor Syst

07-Apr-2023

PMCID:	PMC10081327
doi:	10.1007/s10457-023-00821-7
PMID:	37193256

Evaluation of Antibacterial and Anticancer Characteristics of Silver Nanoparticles Synthesized from Plant Extracts of Wrightia tinctoria and Acacia chundra

Jegadeeshwari A, Seelam NR, Myneni VR

Int J Anal Chem

20-Mar-2023

PMCID:	PMC10042639
doi:	10.1155/2023/6352503
PMID:	36992867

Antibacterial sensitizers from natural plants: A powerful weapon against methicillin-resistant Staphylococcus aureus

Li X, Cai Y, Xia Q, Liao Y, Qin R

Front Pharmacol

24-Feb-2023

PMCID:	PMC9998539
doi:	10.3389/fphar.2023.1118793
PMID:	36909155

Plant-Derived Compounds and Extracts as Modulators of Plasmin Activity—A Review

Kolodziejczyk-Czepas J, Czepas J

Molecules

09-Feb-2023

PMCID:	PMC9965408
doi:	10.3390/molecules28041677
PMID:	36838662

Active Compounds with Medicinal Potential Found in Maxillariinae Benth. (Orchidaceae Juss.) Representatives—A Review

Lipińska MM, Haliński ŁP, Gołębiowski M, Kowalkowska AK

Int J Mol Sci

01-Jan-2023

PMCID:	PMC9821772
doi:	10.3390/ijms24010739
PMID:	36614181

Huanglongbing Pandemic: Current Challenges and Emerging Management Strategies

Ghosh D, Kokane S, Savita BK, Kumar P, Sharma AK, Ozcan A, Kokane A, Santra S

Plants (Basel)

29-Dec-2022

PMCID:	PMC9824665
doi:	10.3390/plants12010160
PMID:	36616289

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
> Benzenoids / Phenol ethers / Anisoles
Estragole	8815	Click to see COC1=CC=C(C=C1)CC=C	148.20	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(+)-Nortrachelogenin	479756	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	via CMAUP database
3-Hydroxy-3,4-bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one	321311	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	via CMAUP database
Nortrachelogenin	394846	Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)O	374.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
[(2R)-2,3-dihydroxypropyl] heptadecanoate	96367592	Click to see CCCCCCCCCCCCCCCCC(=O)OCC(CO)O	344.50	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,10aS)-1,4a-dimethyl-7-propan-2-yl-2,3,4,5,6,9,10,10a-octahydrophenanthrene-1-carboxylic acid	92166187	Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C	302.50	unknown	via CMAUP database
Abietic acid	10569	Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
Dehydroabietic acid	94391	Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C	300.40	unknown	via CMAUP database
Dextropimarinal	12304198	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C=O)C)C=C	286.50	unknown	via CMAUP database
Isopimara-7,15-dienal	12311183	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C=O)C)C1)C=C	286.50	unknown	via CMAUP database
Isopimaric Acid	442048	Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)O)C)C1)C=C	302.50	unknown	via CMAUP database
Levopimaric acid	221062	Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C	302.50	unknown	via CMAUP database
Neoabietic acid	221118	Click to see CC(=C1CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C	302.50	unknown	via CMAUP database
Palustric acid	443613	Click to see CC(C)C1=CC2=C(CC1)C3(CCCC(C3CC2)(C)C(=O)O)C	302.50	unknown	via CMAUP database
Pimaric acid	220338	Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C	302.50	unknown	via CMAUP database
Retene	10222	Click to see CC1=C2C=CC3=C(C2=CC=C1)C=CC(=C3)C(C)C	234.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
alpha-Fenchol	439711	Click to see CC1(C2CCC(C2)(C1O)C)C	154.25	unknown	via CMAUP database
Borneol	6552009	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
Limonene, (-)-	439250	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
Limonene, (+)-	440917	Click to see CC1=CCC(CC1)C(=C)C	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene	1796220	Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	13322124	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	454.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	13988619	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(=C)C	454.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
[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-yl] acetate	15921	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	454.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
[17-(5-ethyl-6-methylhept-6-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	13988618	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(=C)C	454.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Beta-Amyrin	73145	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	https://doi.org/10.1021/NP50100A022
beta-Sitosterol acetate	5354503	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Stigmast-5-en-3-yl acetate	521199	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	456.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Stigmasterol acetate	6437330	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C)C(C)C	454.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids
[(3S,5S,10S,13R,14R,17R)-10,13,14-trimethyl-17-[(2R)-6-methylhept-5-en-2-yl]-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate	162910859	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4)OC(=O)C)C)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
[10,13,14-Trimethyl-17-(6-methylhept-5-en-2-yl)-1,2,3,4,5,6,7,11,12,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl] acetate	14104199	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4)OC(=O)C)C)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
3b-Acetoxycholest-5,24-diene	10916916	Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Cholesta-5,24-dien-3beta-ol	313036	Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	384.60	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Cholesterol	5997	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	386.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Desmosterol	439577	Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	384.60	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Desmosterol acetate	520279	Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,8R,11R,12S,15R,16R)-7,7,12,16-tetramethyl-15-[(2R)-6-methylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-one	12305362	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	424.70	unknown	https://doi.org/10.1021/NP50100A022
CID 348093	348093	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	424.70	unknown	https://doi.org/10.1021/NP50100A022
Cycloeucalenol	101690	Click to see CC1C2CCC3C4(CCC(C4(CCC35C2(C5)CCC1O)C)C(C)CCC(=C)C(C)C)C	426.70	unknown	https://doi.org/10.1021/NP50100A022
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylene,25-methylcholesta-5-en-3beta-ol	5283645	Click to see CC(CCC(=C)C(C)(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
24-Methylenecholesterol	92113	Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	398.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
CID 12358784	12358784	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids
3-(4,9,10,13-tetramethyl-3-propan-2-yl-15-prop-1-en-2-yl-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl)propanoic acid	74338889	Click to see CC(C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CCC4(C3C(CC4)C(=C)C)C)C)C	442.70	unknown	https://doi.org/10.1016/J.MOLSTRUC.2010.06.011
3-[(3S,4S,5R,8R,9R,10R,13R,14R,15R)-4,9,10,13-tetramethyl-3-propan-2-yl-15-prop-1-en-2-yl-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]propanoic acid	101449266	Click to see CC(C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CCC4(C3C(CC4)C(=C)C)C)C)C	442.70	unknown	https://doi.org/10.1016/J.MOLSTRUC.2010.06.011
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
[(1S,3R,6S,8S,11S,12S,15R,16R)-12,16-dimethyl-15-[(2R)-6-methylhept-5-en-2-yl]-6-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl] acetate	101288396	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5)OC(=O)C)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
[(3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methyl-5-methylideneheptan-2-yl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	11259252	Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R)-6,6-dimethyl-5-methylideneheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	13991212	Click to see CC(CCC(=C)C(C)(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	454.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
[10,13-dimethyl-17-(6-methyl-5-methylideneheptan-2-yl)-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	13991204	Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
[17-(6,6-dimethyl-5-methylideneheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate	13991211	Click to see CC(CCC(=C)C(C)(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	454.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
22-Dihydrobrassicasterol acetate	314396	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	442.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
9,19-Cyclocholest-24-en-3-ol, 14-methyl-, acetate, (3beta,5alpha)-	549810	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5)OC(=O)C)C)C	440.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Campesteryl acetate	13019955	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	442.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters / Cholesteryl esters
Cholest-5-en-3-yl acetate	222529	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	428.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
Cholesteryl acetate	2723897	Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C)C)C	428.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3beta,24xi)-Stigmast-5-en-3-ol	9823110	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
(8R,9S,10R,13R,14R)-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	137706654	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
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/10.1021/NP50100A022
24-Ethylcholest-5-en-3beta-ol	22012	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1021/NP50100A022
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/10.1016/0031-9422(88)80032-3
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/10.1016/0031-9422(88)80032-3
Isofucosterol	5281326	Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1016/0031-9422(88)80032-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Shikimic acids and derivatves
Shikimic acid	8742	Click to see C1C(C(C(C=C1C(=O)O)O)O)O	174.15	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
(3Z)-3-(3-oxo-1H-indol-2-ylidene)-1H-indol-2-one	5318433	Click to see C1=CC=C2C(=C1)C(=C3C(=O)C4=CC=CC=C4N3)C(=O)N2	262.26	unknown	https://doi.org/10.1016/J.JEP.2010.07.050
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-4-benzylsulfanyl-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol	10372558	Click to see C1=CC=C(C=C1)CSC2C(C(OC3=C(C(=CC(=C23)O)O)C4C(C(OC5=CC(=CC(=C45)O)O)C6=CC(=C(C=C6)O)O)O)C7=CC(=C(C=C7)O)O)O	700.70	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(4S)-Epicatechin benzylthioether	10645351	Click to see C1=CC=C(C=C1)CSC2C(C(OC3=CC(=CC(=C23)O)O)C4=CC(=C(C=C4)O)O)O	412.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
Pinobanksin	73202	Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	https://doi.org/10.1016/S0367-326X(02)00126-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1016/S0367-326X(02)00126-0
> Phenylpropanoids and polyketides / Stilbenes
3,5-Dimethoxystilbene	5316874	Click to see COC1=CC(=CC(=C1)C=CC2=CC=CC=C2)OC	240.30	unknown	via CMAUP database
Pinosylvin methyl ether	5281719	Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2	226.27	unknown	via CMAUP database

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Wrightia tinctoria

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