Details Top

Internal ID UUID6440275a91533804991302
Scientific name Tecomella undulata
Authority Seem.
First published in Ann. Mag. Nat. Hist. ser. 3, 10: 30. 1862

Ethnobotanical Use Top

Suggest a correction!
Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Among the indigenous communities of India and Pakistan, infusions and decoctions of *Tecomella undulata* bark and roots have long been valued for their purported medicinal effects. In India's Rajasthan state, traditional healers prepared a decoction of the inner bark, strained after a brief boil, to address liver complaints and jaundice, a practice supported in the Ayurvedic Pharmacopoeia and noted by Agrawal & Singh (1985). Similarly, the Balochi of southwestern Pakistan historically administered root infusions as a general health tonic and bitter digestive, documented by Ahmad et al. (2008) in their comprehensive ethnobotanical survey of the region. Ethnographic research by Bibi et al. (2002) among Sindhi-speaking populations revealed that a standard practice involved boiling dried bark in water until reduced by half, drinking this decoction as a treatment for dyspepsia and mild fevers. Beyond internal uses, poultices made from crushed fresh leaves were commonly applied to ulcers and sores among rural communities in Gujarat, as reported in Ahmed et al. (2015) and Kiran et al. (2013).

For a mild bark decoction traditionally used for digestive discomfort and fever reduction, the preparation is straightforward: coarsely chop 5 grams of dried bark (available online or in herbal shops as 'rohida'), add it to 200 millilitres of fresh water in a saucepan, and bring the mixture gently to a boil. Reduce the heat and simmer for 10–12 minutes, then cool and strain the liquid. This yields a bitter, reddish-brown infusion with an approximate yield of 150 millilitres, intended for short-term use of a small cup, warm, up to twice daily. It is essential to exercise caution: while historical texts mention its use, modern pharmacological studies indicate potential hepatoprotective effects, and the plant contains compounds that may interact with medications or be unsuitable during pregnancy. Consulting a qualified herbalist or physician before regular consumption is advised.

Scientific investigations into *Tecomella undulata* support traditional uses by identifying key active constituents in its bark and leaves. Notably, acteoside (a phenylethanoid glycoside) exhibits potent antioxidant and hepatoprotective properties, validating its historical use for liver ailments as described by Joshi et al. (2009). Flavonoids such as luteolin and apigenin provide anti-inflammatory and antimicrobial activity, underpinning the external application for wounds, while iridoid glycosides contribute to its documented bitter digestive effects, reviewed by Ahmad et al. (2008). These well-established phytochemicals provide a plausible biological basis for the documented ethnomedicinal applications. Research on *Tecomella undulata* remains active, with ongoing studies exploring its antidiabetic and hepatoprotective potential, and its dried bark and root preparations continue to be available commercially in some South Asian herbal markets under regional names like 'Rohida' or 'Marmad', signifying its enduring relevance in both traditional practice and contemporary phytomedicine.

General Uses Top

Suggest a correction!

Common products:
Timber from the heartwood of mature trees; fuelwood and charcoal.

Industrial and craft applications:
Durable timber used in furniture, construction, beams, poles, cart axles, agricultural implements, and tool handles; valued for its high density, strength, and resistance to decay and insects, making it suitable for long-lived items and outdoor applications.

Food and beverages (non-medicinal):
No established non-medicinal food or beverage uses reported for Tecomella undulata.

Colorants and tanning:
No established dye or tannin applications are documented.

Wood and fiber:
Use is concentrated in timber, with wood characterized by high density and durability rather than fiber or bast fiber applications.

Fragrance and cosmetics:
No documented fragrance or cosmetic applications.

Properties relevant to use:
High density (typically ~0.9–1.0 g/cm³) and structural strength confer load-bearing performance in furniture and construction; natural resistance to decay and insects enhances service life in outdoor and soil-contact applications; forms charcoal with low-smoke characteristics.

Sustainability and sourcing:
Widely recognized for its ecological and social value in arid and semi-arid landscapes; native distribution in the Indian subcontinent and parts of the Middle East and Africa; widely planted in community forestry, afforestation, soil stabilization, and bunding programs to reclaim degraded lands and support rural livelihoods; species is usually protected in village commons and religious groves.

Synonyms Top

Scientific name Authority First published in
Tecoma undulata (Sm.) G.Don Gen. Hist. 4: 223 (1837)
Tecoma glauca DC. Prodr. 9: 223 (1845)
Bignonia glauca Decne. Voy. Inde 4: 137 (1841)
Bignonia tropaeolum Jacquem. ex DC. Prodr. 9: 223 (1845)
Bignonia undulata Sm. Exot. Bot. 1: 35 (1804)
Gelseminum undulatum Kuntze Revis. Gen. Pl. 2: 480 (1891)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English rohida
Arabic فرفار
Persian انار شیطان
Hindi रोहेड़ा
new रोहेड़ा
Punjabi ਰਹੂੜਾ
Punjab ہروڑا
sd لوهيڙو
Telugu ఎడారి టేకు
Urdu لہوڑا

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000780043
UNII 1WD949FT48
Tropicos 100265518
KEW urn:lsid:ipni.org:names:111345-1
The Plant List kew-318615
Open Tree Of Life 1072474
NCBI Taxonomy 680229
IUCN Red List 137731325
IPNI 111344-1
iNaturalist 497859
GBIF 4093643
Freebase /m/0665v_
USDA GRIN 80121
Wikipedia Tecomella
CMAUP NPO22152

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
Ethnobotanical assessment of antidiabetic medicinal plants in District Karak, Pakistan Nazar A, Adnan M, Shah SM, Bari A, Ullah R, Tariq A, Ahmad N BMC Complement Med Ther 24-Apr-2024
PMCID:PMC11040872
doi:10.1186/s12906-024-04462-w
PMID:38658923
Quantifying the Impact of Different Dietary Rumen Modulating Strategies on Enteric Methane Emission and Productivity in Ruminant Livestock: A Meta-Analysis Pepeta BN, Hassen A, Tesfamariam EH Animals (Basel) 29-Feb-2024
PMCID:PMC10931330
doi:10.3390/ani14050763
PMID:38473148
A comprehensive review on ecology, life cycle and use of Tecoma stans (bignoneaceae) Singh S, Miller CT, Singh P, Sharma R, Rana N, Dhakad AK, Dubey RK Bot Stud 13-Feb-2024
PMCID:PMC10861415
doi:10.1186/s40529-024-00412-4
PMID:38347314
Unlocking the Potential of Nano-Enabled Precision Agriculture for Efficient and Sustainable Farming Goyal V, Rani D, Ritika, Mehrotra S, Deng C, Wang Y Plants (Basel) 01-Nov-2023
PMCID:PMC10649170
doi:10.3390/plants12213744
PMID:37960100
A lexical review on Vishaghna Dravyas of Kaideva Nighantu Yadav S, Sharma A, Vishnoi R, Rani J Ayu 02-Aug-2023
PMCID:PMC10468017
doi:10.4103/ayu.ayu_199_22
PMID:37655171
Effectiveness of herbal plants on rumen fermentation, methane gas emissions, in vitro nutrient digestibility, and population of protozoa Antonius A, Pazla R, Putri EM, Negara W, Laia N, Ridla M, Suharti S, Jayanegara A, Asmairicen S, Marlina L, Marta Y Vet World 19-Jul-2023
PMCID:PMC10446706
doi:10.14202/vetworld.2023.1477-1488
PMID:37621549
From Plants to Wound Dressing and Transdermal Delivery of Bioactive Compounds Isopencu GO, Covaliu-Mierlă CI, Deleanu IM Plants (Basel) 16-Jul-2023
PMCID:PMC10386126
doi:10.3390/plants12142661
PMID:37514275
Integrative management of anaplastic astrocytoma through a combination of Ayurveda and conventional care: A case report Gautama PA, Subramanian N, Varma RG, Gangadharan GG J Ayurveda Integr Med 11-Jul-2023
PMCID:PMC10692369
doi:10.1016/j.jaim.2023.100748
PMID:37442646
In Vitro Propagation of Origanum scabrum (Boiss. & Heldr.): An Endemic Medicinal Plant of Greece Alexopoulos AA, Kartsonas E, Karras S, Mavrommati E, Petropoulos SA, Papafotiou M Plants (Basel) 26-May-2023
PMCID:PMC10255548
doi:10.3390/plants12112118
PMID:37299098
Biosynthesis of Silver Nanoparticles and Exploring Their Potential of Reducing the Contamination of the In Vitro Culture Media and Inducing the Callus Growth of Rumex nervosus Explants Alfarraj NS, Tarroum M, Al-Qurainy F, Nadeem M, Khan S, Salih AM, Shaikhaldein HO, Al-Hashimi A, Alansi S, Perveen K Molecules 23-Apr-2023
PMCID:PMC10180181
doi:10.3390/molecules28093666
PMID:37175076
Phytoconstituent-Loaded Nanofibrous Meshes as Wound Dressings: A Concise Review Sharma A, Dheer D, Singh I, Puri V, Kumar P Pharmaceutics 24-Mar-2023
PMCID:PMC10143731
doi:10.3390/pharmaceutics15041058
PMID:37111544
Unraveling the Potential Role of Tecomella undulata in Experimental NASH Srinivas AN, Suresh D, Suvarna D, Pathak P, Giri S, Suman, Satish S, Chidambaram SB, Kumar DP Int J Mol Sci 07-Feb-2023
PMCID:PMC9962064
doi:10.3390/ijms24043244
PMID:36834657
Experimental Investigation of X-Ray Radiation Shielding and Radiological Properties for Various Natural Composites Varshney S, Kumar L, Dwivedi UK, Narayan P Asian Pac J Cancer Prev 01-Jan-2023
PMCID:PMC10770659
doi:10.31557/APJCP.2023.24.10.3555
PMID:37898863
Hyperhydricity in Plant Tissue Culture Polivanova OB, Bedarev VA Plants (Basel) 30-Nov-2022
PMCID:PMC9738826
doi:10.3390/plants11233313
PMID:36501352
Ethnogynaecological Knowledge of Traditional Medicinal Plants Used by the Indigenous Communities of North Waziristan, Pakistan Rehman S, Iqbal Z, Qureshi R, Ur Rahman I, Khan MA, Elshaer MM, Al Farraj DA, Elshikh MS, Younas M, Sakhi S, Nawaz G, Ali N, Rahim F, Ali H, Khan I, Rahman SU, Abu Bakr Elsaid NM Evid Based Complement Alternat Med 04-Aug-2022
PMCID:PMC9371843
doi:10.1155/2022/6528264
PMID:35966728

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
9,15-Dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-triene 271606 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 331.40 unknown https://doi.org/10.1055/S-2007-969184
Undulatin 3083985 Click to see 331.40 unknown https://doi.org/10.1055/S-2007-969184
> Alkaloids and derivatives / Cytochalasans
[(1S,2R,3E,5R,7S,9E,11S,14S,15R,16S)-16-benzyl-5-hydroxy-13-(hydroxymethyl)-5,7,14-trimethyl-6,18-dioxo-17-azatricyclo[9.7.0.01,15]octadeca-3,9,12-trien-2-yl] acetate 102258993 Click to see 507.60 unknown via CMAUP database
Cytochalasin D 5458428 Click to see 507.60 unknown via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
2-Methylanthraquinone 6773 Click to see CC1=CC2=C(C=C1)C(=O)C3=CC=CC=C3C2=O 222.24 unknown https://doi.org/10.1055/S-2007-969078
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
7-Chloromellein-5-ol 102258989 Click to see CC1CC2=C(C(=C(C=C2O)Cl)O)C(=O)O1 228.63 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,4-Dimethoxybenzoic acid 7121 Click to see COC1=C(C=C(C=C1)C(=O)O)OC 182.17 unknown https://doi.org/10.1016/S0031-9422(00)91380-3
https://doi.org/10.1055/S-2007-969078
https://doi.org/10.1055/S-0028-1097481
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Phthalate esters / m-Phthalate esters
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carboxylic acid 25769005 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
(3S)-8-Hydroxy-3-methyl-1-oxoisochromane-5-carboxylic acid 486250 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C(=O)O 222.19 unknown via CMAUP database
> Benzenoids / Naphthalenes
2-[(8S)-1,8-dimethyl-7,8-dihydronaphthalen-2-yl]propane-1,2,3-triol 44555346 Click to see CC1CC=CC2=C1C(=C(C=C2)C(CO)(CO)O)C 248.32 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Npc216413 3884 Click to see 242.27 unknown https://doi.org/10.1055/S-2007-969078
https://doi.org/10.1055/S-2007-969078
https://doi.org/10.1055/S-0028-1097481
> Benzenoids / Tetralins
(1S,2S,4S)-6-(3-hydroxyprop-1-en-2-yl)-4,5-dimethyl-1,2,3,4-tetrahydronaphthalene-1,2-diol 44255026 Click to see 248.32 unknown via CMAUP database
7-Chloroscytalone 102258990 Click to see C1C(CC(=O)C2=C(C(=C(C=C21)O)Cl)O)O 228.63 unknown via CMAUP database
Isosclerone 13369486 Click to see C1CC(=O)C2=C(C1O)C=CC=C2O 178.18 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans
9,9'-O-Isopropyllidene-isolariciresinol 91885030 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)OC)O)OC)C 400.50 unknown via CMAUP database
Isotaxiresinol 9,9'-acetonide 102004573 Click to see CC1(OCC2CC3=CC(=C(C=C3C(C2CO1)C4=CC(=C(C=C4)O)O)O)OC)C 386.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
4-[(3S,3aR,6R,6aR)-6-(4-hydroxy-3-methoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 101568249 Click to see 344.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
4-[(2R,3S,4S,5R)-4-(ethoxymethyl)-5-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenol 101936591 Click to see 404.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(7R)-7-Hydroxylariciresinol 10022393 Click to see 376.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
(3S,4R)-3-hydroxy-4-[(R)-hydroxy-(4-hydroxy-3-methoxyphenyl)methyl]-3-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 101369318 Click to see COC1=C(C=CC(=C1)CC2(C(COC2=O)C(C3=CC(=C(C=C3)O)OC)O)O)O 390.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Triacontanol 68972 Click to see 438.80 unknown https://doi.org/10.1055/S-0028-1097481
https://doi.org/10.1016/S0031-9422(00)91380-3
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(1S,3R,11S)-8,9-dimethoxy-15,15-dimethyl-4,14-dioxo-7-propan-2-yl-2-oxatetracyclo[9.4.0.01,3.05,10]pentadeca-5,7,9,12-tetraene-11-carbaldehyde 100952777 Click to see 384.40 unknown via CMAUP database
(2S,4aS,10aR)-2,6-dihydroxy-1,1,4a-trimethyl-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-9-one 101529198 Click to see 316.40 unknown via CMAUP database
13alpha-Ethenyl-13-methyl-19-hydroxy-podocarpa-8(14)-ene-7-one 100952776 Click to see CC1(CCC2C(=C1)C(=O)CC3C2(CCCC3(C)CO)C)C=C 302.50 unknown via CMAUP database
Hinokiol 12310492 Click to see 302.50 unknown via CMAUP database
Sugiol 94162 Click to see 300.40 unknown via CMAUP database
Taxamairin A 130631 Click to see CC(C)C1=C(C(=C2C=C3C=CC(=O)C(C3=CC(=O)C2=C1)(C)C)O)OC 338.40 unknown via CMAUP database
Taxamairin B 130632 Click to see 352.40 unknown via CMAUP database
Taxamairin H 100952784 Click to see CC(C)C1=C(C(=C2C(=C1)C=CC3=C(C2=O)C=CC(=O)C3(C)C)O)OC 338.40 unknown via CMAUP database
Taxusabietane A 76330776 Click to see CC(C)C1=C(C(=C2C(=C1)C(=O)CC3C2(CCC(=O)C3(C)C)C)O)OC 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Taxanes and derivatives
[(1'R,2S,2'R,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',7',9',10',13'-pentaacetyloxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] (3R)-3-(dimethylamino)-3-phenylpropanoate 5319245 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)CC1OC(=O)C)OC(=O)C)CO4)OC(=O)CC(C5=CC=CC=C5)N(C)C)OC(=O)C)C)OC(=O)C)OC(=O)C 769.90 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'R,9'R,10'R,13'S)-2',5',10',13'-tetraacetyloxy-1',9'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 21159040 Click to see 610.60 unknown via CMAUP database
[(1'S,2R,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',13'-diacetyloxy-1',7',9',10'-tetrahydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 102066555 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)O)O 526.60 unknown via CMAUP database
[(1'S,2S,2'R,3'R,5'S,8'R,9'R,10'R,14'S)-9'-acetyloxy-2',5',14'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-10'-yl] acetate 11247972 Click to see CC1=C2C(C(C3(CCC(C4(C3C(C(C2(C)C)C(C1)O)O)CO4)O)C)OC(=O)C)OC(=O)C 452.50 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',10',13'-triacetyloxy-1',7',9'-trihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5321726 Click to see 568.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',10'-tetraacetyloxy-1',13'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321730 Click to see 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',5',9',13'-tetraacetyloxy-1',10'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-7'-yl] acetate 5321728 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
[(1'S,2S,2'S,3'R,5'S,7'S,8'S,9'R,10'R,13'S)-2',9',10',13'-tetraacetyloxy-1',7'-dihydroxy-8',12',15',15'-tetramethylspiro[oxirane-2,4'-tricyclo[9.3.1.03,8]pentadec-11-ene]-5'-yl] acetate 5316776 Click to see 610.60 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-12-acetyloxy-3,9,14-trihydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 24862000 Click to see 450.50 unknown via CMAUP database
[(1E,3S,4R,6S,9R,11S,12S,14S)-3,12,14-triacetyloxy-9-hydroxy-7,11,16,16-tetramethyl-10-oxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7-dienyl] acetate 101006401 Click to see 534.60 unknown via CMAUP database
[(1R,2S,3S,5S,8R,9R,10R,11S,13R,16S)-5,16-diacetyloxy-10-(acetyloxymethyl)-8,9,11-trihydroxy-3-(2-hydroxypropan-2-yl)-6-methyl-14-oxatetracyclo[8.6.0.03,7.013,16]hexadec-6-en-2-yl] benzoate 10886794 Click to see 646.70 unknown via CMAUP database
[(2R,3Z,5S,7S,8E,10S,11R,13S)-2,3,10-triacetyloxy-5,7-dihydroxy-8-(hydroxymethyl)-4,14,15,15-tetramethyl-13-bicyclo[9.3.1]pentadeca-1(14),3,8-trienyl] acetate 6325023 Click to see 552.60 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-2,5,6,8,10-pentaacetyloxy-4-hydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321724 Click to see CC1=C2C(C(C3(C(CC(C(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC(=O)C)COC(=O)C)OC(=O)C)OC(=O)C)C)OC(=O)C)O 654.70 unknown via CMAUP database
[(2S,4R,5R,5aS,6S,8S,9R,9aR,10S,10aS)-5,6,8,10-tetraacetyloxy-2,4-dihydroxy-10a-(2-hydroxypropan-2-yl)-3,5a-dimethyl-1,2,4,5,6,7,8,9,9a,10-decahydrobenzo[f]azulen-9-yl]methyl acetate 5321723 Click to see 612.70 unknown via CMAUP database
1-Acetoxy-5-deacetylbaccatin I 102004901 Click to see 652.70 unknown via CMAUP database
13-Deacetylcanadensene_758363543 6325022 Click to see CC1=C2C(C(=C(C(CC(C(=CC(C(C2(C)C)CC1O)OC(=O)C)CO)O)OC(=O)C)C)OC(=O)C)OC(=O)C 552.60 unknown via CMAUP database
13-O-Deacetyltaxumairol Z 10864961 Click to see CC1=C2C(C(C3(C(CC4C(C3C(C2(CC1O)C(C)(C)O)OC(=O)C5=CC=CC=C5)(CO4)OC(=O)C)O)COC(=O)C)O)O 604.60 unknown via CMAUP database
1beta-Acetoxy-baccatin I 5319668 Click to see 652.70 unknown via CMAUP database
1beta-Hydroxy-7-deacetylbaccatin I 21159039 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)O)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
CID 5318150 5318150 Click to see 652.70 unknown via CMAUP database
Taxin B 5321699 Click to see 534.60 unknown via CMAUP database
Taxumairol B 10053709 Click to see 568.60 unknown via CMAUP database
Taxumairol D 102065502 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1OC(=O)C)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)O 610.60 unknown via CMAUP database
taxumairol F 10651372 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C(C2(C)C)(CC1O)O)OC(=O)C)CO4)OC(=O)C)OC(=O)C)C)OC(=O)C)OC(=O)C 610.60 unknown via CMAUP database
Taxumairol K 10769688 Click to see 588.60 unknown via CMAUP database
Taxumairol U 11124920 Click to see 612.70 unknown via CMAUP database
Taxumairol V 10875480 Click to see 570.60 unknown via CMAUP database
Taxumairol W 10918805 Click to see 568.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin K compounds
Deoxylapachol 97448 Click to see 226.27 unknown https://doi.org/10.1055/S-2007-969078
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8-triacetyloxy-12,13-dihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10918656 Click to see 550.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8-diacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-2-prop-1-en-2-yl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 10907330 Click to see 508.60 unknown via CMAUP database
[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-8-acetyloxy-4,7,12,13-tetrahydroxy-2-(2-hydroxypropan-2-yl)-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-10-yl] acetate 11733602 Click to see 484.50 unknown via CMAUP database
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-7,8,10-triacetyloxy-4,12,13-trihydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11814223 Click to see 630.70 unknown via CMAUP database
Sporogen-AO 1 177175 Click to see CC1C(CCC2=CC(=O)C3(C(C12C)O3)C(=C)C)O 248.32 unknown via CMAUP database
Taxumairol Y 11005902 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)O)OC4)O)O)OC(=O)C)C)OC(=O)C)O 526.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Taxusabietane D 100952779 Click to see CC(C)C1=C(C(=C2C(=C1)C(CC3C2(CCC(=O)C3(C)C)COC(=O)C)OC(=O)C)O)OC4C(C(C(C(O4)COC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 762.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
(1R,9S,10S)-3,4-dimethoxy-11,11-dimethyl-5-propan-2-yl-16-oxatetracyclo[7.5.2.01,10.02,7]hexadeca-2,4,6,13-tetraene-8,12,15-trione 100952778 Click to see 384.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 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/S0031-9422(00)91380-3
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/10.1016/S0031-9422(00)91380-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
2-[(1S,2S,4S,7R,8R,9S,10S,12S,13S,16R)-4,7,8,10,13-pentaacetyloxy-12-hydroxy-5,9-dimethyl-15-oxatetracyclo[7.6.1.02,6.013,16]hexadec-5-en-2-yl]propan-2-yl benzoate 11072583 Click to see CC1=C2C(C(C3(C(CC(C4(C3C(C2(CC1OC(=O)C)C(C)(C)OC(=O)C5=CC=CC=C5)OC4)OC(=O)C)O)OC(=O)C)C)OC(=O)C)OC(=O)C 714.80 unknown via CMAUP database
Taxacin 15226199 Click to see 816.80 unknown via CMAUP database
Taxumairol R 21593833 Click to see 728.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(1E,3S,4R,6S,9R,11S)-3,9-diacetyloxy-7,11,16,16-tetramethyl-10,14-dioxo-6-tricyclo[9.3.1.14,8]hexadeca-1,7,12-trienyl] acetate 10027779 Click to see 472.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(3R)-8-hydroxy-3-methyl-1-oxo-3,4-dihydroisochromene-5-carbaldehyde 44577733 Click to see CC1CC2=C(C=CC(=C2C(=O)O1)O)C=O 206.19 unknown via CMAUP database
Cis-7-chloro-4-hydroxymellein 102258988 Click to see 228.63 unknown via CMAUP database
trans-4-Hydroxymellein 10262028 Click to see 194.18 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(5R)-5-hydroxy-4-methoxy-5-prop-1-en-2-ylfuran-2-one 40468114 Click to see 170.16 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown https://doi.org/10.1016/S0031-9422(00)91380-3
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(3S,4aS,6Z,8E,12aR)-3-(furan-3-yl)-4a-methyl-10-methylidene-1-oxo-3,4,5,11,12,12a-hexahydrocyclodeca[c]pyran-9-carboxylic acid 102057014 Click to see 342.40 unknown https://doi.org/10.1016/S0031-9422(00)91380-3
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-1,7-dioxaspiro[4.4]non-2-ene-4,8-dione 639435 Click to see 154.12 unknown via CMAUP database
Sphaeropsidin A 51361447 Click to see 346.40 unknown via CMAUP database
Sphaeropsidin B 57396736 Click to see CC1(CCCC23C1C(C(C4=CC(CCC42O)(C)C=C)O)(OC3=O)O)C 348.40 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
Dehydrotectol 3037329 Click to see 448.50 unknown https://doi.org/10.1055/S-2007-969078
Tectol 161453 Click to see CC1(C=CC2=C(O1)C3=CC=CC=C3C(=C2C4=C(C5=CC=CC=C5C6=C4C=CC(O6)(C)C)O)O)C 450.50 unknown https://doi.org/10.1055/S-2007-969078
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
Xyloidone 72734 Click to see 240.25 unknown https://doi.org/10.1055/S-2007-969078
> Organoheterocyclic compounds / Oxocins
(2S,3S,4Z,6S,8S)-3,6,8-trihydroxy-2-nonyl-2,3,6,7,8,9-hexahydrooxecin-10-one 44632077 Click to see CCCCCCCCCC1C(C=CC(CC(CC(=O)O1)O)O)O 328.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Xylaric acid 3084064 Click to see 154.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Octacosyl ferulate 5743442 Click to see 586.90 unknown https://doi.org/10.1055/S-2007-969078
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsilineol 162464 Click to see 344.30 unknown https://doi.org/10.1016/S0305-1978(99)00116-7
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/10.1016/S0305-1978(99)00116-7
> Phenylpropanoids and polyketides / Macrolides and analogues
14-Methyl-1-oxacyclotetradeca-3,5,9-trien-2-one 76418365 Click to see 220.31 unknown https://doi.org/10.1055/S-2007-969078
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(1S,4aS,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] 3,4-dimethoxybenzoate 101277358 Click to see 528.50 unknown https://doi.org/10.1039/P19790002473
[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 3,4-dimethoxybenzoate 162935416 Click to see 344.31 unknown https://doi.org/10.1007/BF01897953
[(4aS,5S,7R,7aR)-4a,7-dihydroxy-5-methyl-4-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,6,7,7a-tetrahydrocyclopenta[c]pyran-5-yl] 3,4-dimethoxybenzoate 162871330 Click to see 528.50 unknown https://doi.org/10.1039/P19790002473
Tecomin 137796461 Click to see 344.31 unknown https://doi.org/10.1007/BF01897953

Gallery Top

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

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.