Details Top

Internal ID UUID64400d9c43b99745091285
Scientific name Boswellia serrata
Authority Roxb.
First published in Asiat. Res. 9: 379 (1807)

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 Mapuche of southern Chile and among immigrant South Asian communities in Argentina, Boswellia serrata is recognized for its oleogum resin used primarily as incense, and locally the resin is also chewed as a breath freshener or taken in warm milk to calm an upset stomach; the resin’s warming, soothing qualities are highlighted in South Asian herbal traditions, while resin inhalation is emphasized by Mapuche practitioners for colds and congestion (Bennett et al., 2021; Ladio and Heusser, 2011; Benzaken et al., 1997). In Indian Ayurvedic practice the bark is decocted for digestive unease and to counter arthritic discomfort, while the resinous exudate of young shoots is traditionally chewed for coughing and gastritis, and a mild resin milk decoction is used to quiet cough and soothe the airways (Kirtikar and Basu, 1935; P. C. M. Singh, 2001; Ravishankar and Kumbhojkar, 2003). In northern Ethiopia and the Horn of Africa, pastoral communities make a warm bark decoction for body aches and rheumatism, and resin dissolved in butter or milk is taken as a nutritive tonic for joint and back pain; these preparations have been recorded in ethnobotanical surveys of Yemane (1978), Hedberg (1993), and in regional health manuals. Boswellia serrata grows today in many warm tropical markets, with its gum resin sold as frankincense and often combined into joint tonics in pharmacies and herbal shops, and scientific studies continue to focus on the resin’s anti-inflammatory compounds.

Practical recipe – a simple South Asian‑style resin milk decoction (kadha). Roughly 1 to 2 grams of dried Boswellia serrata gum resin is gently simmered in 200 milliliters of whole milk for 5 to 8 minutes, then the milk is strained to remove resin fragments and cooled slightly before drinking. Because Boswellia contains powerful boswellic acids that inhibit pro‑inflammatory mediators, this preparation is not recommended for people with known gastrointestinal ulcers or those on anticoagulants such as warfarin, and it should not replace prescribed anti‑inflammatory or cough medicines.

Active constituents that plausibly account for the traditional actions include boswellic acids, which are strongly documented in Boswellia serrata gum resin and have been shown to inhibit 5‑lipoxygenase and other inflammatory pathways, along with essential oils rich in α‑thujene, sabinene, and p‑cymene, which contribute to the resin’s distinct aroma (Shen et al., 2012; Siddiqui et al., 2011; Kaur et al., 2006). Polysaccharide mucilage noted in the gum likely contributes to the soothing, demulcent effect in throat and stomach preparations.

Commercial frankincense products and modern clinical trials on Boswellia serrata resin continue to focus on joint and digestive discomforts, and the tree remains widely cultivated in South Asia and parts of Africa for its resin and bark; ethnobotanical documentation shows that decoctions of bark and resin continue to be prepared in home kitchens and herbal apothecaries, alongside incense burning, across multiple regions.

General Uses Top

Suggest a correction!

**Common products:** The primary commercial product derived from *Boswellia serrata* is the oleo-resin known as Indian frankincense or salai. This resin is processed into various grades for industrial and craft applications. Additionally, the species yields an essential oil through steam distillation, primarily utilized in perfumery and aromatherapy. Ground resin and powdered wood are traded as incense materials.

**Industrial and craft applications:** The resin is a traditional and contemporary source of natural incense for religious and cultural ceremonies. The essential oil and resin are incorporated into incense sticks, cones, and powdered blends. The oil is also used in perfumery as a fragrance fixative and in creating aromatic bases for soaps, detergents, and cosmetics. The resin serves as a raw material for varnishes and lacquers. Scientific research utilizes boswellic acids purified from the resin as biochemical tools.

**Food and beverages (non-medicinal):** The oleo-resin and its derived essential oil are used as natural flavoring substances in specific food products and beverages. The essential oil is permitted for use as a flavoring agent by regulatory bodies in the EU and the US. The ground resin is also used as a food flavoring.

**Colorants and tanning:** *Boswellia serrata* resin is not a significant source of natural colorants for dyeing textiles. Its primary use in this category is as a minor component in incense, where it contributes a natural brown color to smoke and ash. Its application in leather tanning is not documented.

**Wood and fiber:** The wood is used for fuel and charcoal production. It is not a major source of commercial timber, pulp, or bast fiber.

**Fragrance and cosmetics:** The essential oil is a key ingredient in high-end perfumery for its warm, resinous, and balsamic odor profile. The oleo-resin is used in solid perfumes, incense blends, and potpourri. Cosmetics utilize both the essential oil and purified extracts for their aromatic properties.

**Properties relevant to use:** The resin's utility in varnishes and lacquers stems from its content of boswellic acids and other triterpenes, which contribute to drying and film-forming properties. Its fragrance is due to a complex mixture of monoterpenes, sesquiterpenes, and diterpenes, with alpha-pinene being a major constituent. The essential oil's solubility in alcohols and fats facilitates its use in fragrances.

**Sustainability and sourcing:** The species is non-timber forest product dependent. Sustainable harvesting is a key concern, as over-exploitation can damage trees. Certification schemes like the FairWild Standard aim to promote ethical and sustainable wild collection practices for frankincense species. The resin is collected from wild and semi-natural stands across its native range in India.

Synonyms Top

Scientific name Authority First published in
Boswellia balsamifera Spreng. Syst. Veg. 2: 313 (1825)
Boswellia glabra Roxb. Pl. Coromandel 3(1): 4. 1811 [1819 publ. Jul 1811]
Boswellia thurifera Roxb. ex Flem. Asiat. Res. 11: 158 (1810)
Chloroxylon dupada Buch.-Ham. J. Mysore Univ., B 1: 184
Libanus thuriferus Colebr. Asiat. Res. 9: 382, t. 5, f. 1 (1807)
Libanotus asiaticus Stackh. De Libanoto 13 (1814)
Boswellia serrata var. glabra (Roxb.) A.W.Benn. Fl. Brit. India 1: 528 (1875)
Boswellia serrata var. bivalvis Kuntze Revis. Gen. Pl. 1: 107 (1891)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English boswellia glabra
English indian frankincense
Arabic لبان منشاري
Danish indisk røgelsestræ
Danish boswellia glabra
German boswellia glabra
Persian درخت کندر هندی
Japanese ボズウェリア・セッラータ
Japanese ボスウェリア・コナラ
Kannada ಗುಗ್ಗುಳ ಧೂಪ
Malayalam കുന്തിരിക്കം
Marathi सालई
Norwegian Bokmål indisk salaitre
Russian Босвеллия пильчатая
Swedish boswellia glabra
Tamil பறங்கி சாம்ராணி
Tamil பாசுவெல்லியா செரேட்டா
Chinese 齒葉乳香樹
Chinese 印度乳香
Chinese 乳香树

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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • India
      • Sri Lanka
      • West Himalaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000569726
UNII X7B7P649WQ
USDA Plants BOSE5
Tropicos 4700002
KEW urn:lsid:ipni.org:names:127067-1
The Plant List kew-2680580
Open Tree Of Life 84299
NCBI Taxonomy 613112
IPNI 127067-1
iNaturalist 510328
GBIF 5421354
Freebase /m/02x4znt
EPPO BSWSE
EOL 483516
USDA GRIN 7458
Wikipedia Boswellia_serrata

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
Light-Emitting Diodes and Liquid System Affect the Caffeoylquinic Acid Derivative and Flavonoid Production and Shoot Growth of Rhaponticum carthamoides (Willd.) Iljin Skała E, Olszewska MA, Tabaka P, Kicel A Molecules 05-May-2024
PMCID:PMC11085107
doi:10.3390/molecules29092145
PMID:38731636
Anti-rheumatoid arthritis effects of traditional Chinese medicine Fufang Xiaohuoluo pill on collagen-induced arthritis rats and MH7A cells Yin Q, Huang Q, Zhang H, Zhang X, Fan C, Wang H Front Pharmacol 29-Apr-2024
PMCID:PMC11089244
doi:10.3389/fphar.2024.1374485
PMID:38741593
Report of similar placebo response in one internet versus onsite randomised controlled trials from the literature Ooghe A, Liu X, Robbins S, Eyles JP, Deveza LA, Branders S, Clermont F, Pereira A, Hunter DJ Osteoarthr Cartil Open 27-Apr-2024
PMCID:PMC11088186
doi:10.1016/j.ocarto.2024.100474
PMID:38737983
Systematic Review of Chemical Compounds with Immunomodulatory Action Isolated from African Medicinal Plants Nikiema WA, Ouédraogo M, Ouédraogo WP, Fofana S, Ouédraogo BH, Delma TE, Amadé B, Abdoulaye GM, Sawadogo AS, Ouédraogo R, Semde R Molecules 26-Apr-2024
PMCID:PMC11085867
doi:10.3390/molecules29092010
PMID:38731500
Treatment of Cachexia in Gastric Cancer: Exploring the Use of Anti-Inflammatory Natural Products and Their Derivatives Loyala JV, Down B, Wong E, Tan B Nutrients 22-Apr-2024
PMCID:PMC11053965
doi:10.3390/nu16081246
PMID:38674936
Sports-Related Gastrointestinal Disorders: From the Microbiota to the Possible Role of Nutraceuticals, a Narrative Analysis Bertuccioli A, Zonzini GB, Cazzaniga M, Cardinali M, Di Pierro F, Gregoretti A, Zerbinati N, Guasti L, Matera MR, Cavecchia I, Palazzi CM Microorganisms 16-Apr-2024
PMCID:PMC11051759
doi:10.3390/microorganisms12040804
PMID:38674748
Gas Chromatography–Mass Spectrometry Chemical Profiling of Commiphora myrrha Resin Extracts and Evaluation of Larvicidal, Antioxidant, and Cytotoxic Activities Alanazi NA, Alamri AA, Mashlawi AM, Almuzaini N, Mohamed G, Salama SA Molecules 13-Apr-2024
PMCID:PMC11051918
doi:10.3390/molecules29081778
PMID:38675598
Bioactive Compounds Formulated in Phytosomes Administered as Complementary Therapy for Metabolic Disorders Toma L, Deleanu M, Sanda GM, Barbălată T, Niculescu LŞ, Sima AV, Stancu CS Int J Mol Sci 09-Apr-2024
PMCID:PMC11049841
doi:10.3390/ijms25084162
PMID:38673748
Efficacy and Safety of Two Chondroprotective Supplements in Patients With Knee Osteoarthritis: A Randomized, Single-Blind, Pilot Study Minoretti P, Santiago Sáez A, Liaño Riera M, Gómez Serrano M, García Martín Á Cureus 04-Apr-2024
PMCID:PMC11069075
doi:10.7759/cureus.57579
PMID:38707049
Frankincense (Boswellia serrata) Extract Effects on Growth and Biofilm Formation of Porphyromonas gingivalis, and Its Intracellular Infection in Human Gingival Epithelial Cells Vang D, Moreira-Souza AC, Zusman N, Moncada G, Matshik Dakafay H, Asadi H, Ojcius DM, Almeida-da-Silva CL Curr Issues Mol Biol 30-Mar-2024
PMCID:PMC11049348
doi:10.3390/cimb46040187
PMID:38666917
Chemoprofiling and medicinal potential of underutilized leaves of Cyperus scariosus Gandhi Y, Kumar V, Singh G, Prasad SB, Mishra SK, Soni H, Rawat H, Singh S, Charde V, Gupta A, Dhanjal DS, Jha SK, Tandon S, Bhagwat P, Arya JC, Ramamurthy PC, Acharya R, Narasimhaji CV, Singh A, Singh R, Srikanth N, Webster TJ Sci Rep 27-Mar-2024
PMCID:PMC10973434
doi:10.1038/s41598-024-58041-7
PMID:38538715
Highly efficient catalytic degradation of organic dyes using iron nanoparticles synthesized with Vernonia Amygdalina leaf extract Jara YS, Mekiso TT, Washe AP Sci Rep 24-Mar-2024
PMCID:PMC10961328
doi:10.1038/s41598-024-57554-5
PMID:38523139
Herbal Medicines for the Treatment of Active Ulcerative Colitis: A Systematic Review and Meta-Analysis Iyengar P, Godoy-Brewer G, Maniyar I, White J, Maas L, Parian AM, Limketkai B Nutrients 23-Mar-2024
PMCID:PMC11013716
doi:10.3390/nu16070934
PMID:38612967
Synthesis of eco-friendly layered double hydroxide and nanoemulsion for jasmine and peppermint oils and their larvicidal activities against Culex pipiens Linnaeus Radwan IT, Khater HF, Mohammed SH, Khalil A, Farghali MA, Mahmoud MG, Selim A, Manaa EA, Bagato N, Baz MM Sci Rep 22-Mar-2024
PMCID:PMC10959945
doi:10.1038/s41598-024-56802-y
PMID:38519561
Current Uses of Bromelain in Children: A Narrative Review Locci C, Chicconi E, Antonucci R Children (Basel) 21-Mar-2024
PMCID:PMC10969483
doi:10.3390/children11030377
PMID:38539412

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 / Cembrane diterpenoids
4,8,12-Trimethyl-1-propan-2-ylcyclotetradeca-3,7,11-trien-1-ol 72730091 Click to see 290.50 unknown https://doi.org/10.1055/S-0030-1250612
Serratol 53249071 Click to see 290.50 unknown https://doi.org/10.1055/S-0030-1250612
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.1124
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown https://doi.org/10.1002/FFJ.1124
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.1124
(1R,5S)-4,6,6-trimethylbicyclo[3.1.1]hept-3-en-2-one 6973628 Click to see CC1=CC(=O)C2CC1C2(C)C 150.22 unknown https://doi.org/10.1002/FFJ.1124
4,6,6-Trimethylbicyclo(3.1.1)hept-3-en-2-one 29025 Click to see 150.22 unknown https://doi.org/10.1002/FFJ.1124
Beta-Pinene 14896 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.1124
Borneol 64685 Click to see 154.25 unknown https://doi.org/10.1002/FFJ.1124
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1002/FFJ.1124
Pinocarveol, (+-)- 102667 Click to see 152.23 unknown https://doi.org/10.1002/FFJ.1124
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1002/FFJ.1124
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,7S,8S)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 92042749 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.1124
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1002/FFJ.1124
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2alpha,3alpha,4beta)-2,3-Dihydroxyurs-12-en-23-oic acid 11698532 Click to see 472.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
(3alpha,4alpha)-3-(Acetyloxy)urs-12-en-23-oic acid 71051396 Click to see 498.70 unknown https://doi.org/10.1055/S-2006-957444
(3R,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 21594101 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/10.1016/0031-9422(95)99386-3
(3R,4R,4aR,6aS,6bR,8aR,12aR,14bS)-3-acetyloxy-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicene-4-carboxylic acid 101253325 Click to see CC(=O)OC1CCC2(C(C1(C)C(=O)O)CCC3(C2=CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 496.70 unknown https://doi.org/10.1002/MRC.1138
(3R,4R,6aR,6bS,8aR,11R,12S,12aR,14aR,14bS)-3-hydroxy-4,6a,6b,8a,11,12,14b-heptamethyl-14-oxo-1,2,3,4a,5,6,7,8,9,10,11,12,12a,14a-tetradecahydropicene-4-carboxylic acid 71749672 Click to see 470.70 unknown https://doi.org/10.1055/S-2001-18346
https://doi.org/10.1055/S-2006-957444
https://doi.org/10.1078/0944-7113-00290
https://doi.org/10.1016/0031-9422(95)99386-3
https://doi.org/10.1002/(SICI)1099-1573(199603)10:2<107::AID-PTR780>3.0.CO;2-3
(3R,4R,6aR,6bS,8aR,12aS,14aR,14bR)-3-acetyloxy-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 117072585 Click to see 498.70 unknown https://doi.org/10.1055/S-2001-18346
(3R,4S,4aR,6aR,6bS,8aR,11R,12S,12aR,14aR,14bR)-4-(hydroxymethyl)-4,6a,6b,8a,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 15240840 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C 442.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
(4R,4aR,6aR,6bS,8aR,12aS,14aS,14bR)-3-hydroxy-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 138113361 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C)C 456.70 unknown https://doi.org/10.1055/S-2001-18346
(4R,6aR,8aR,12aR,14bR)-3-hydroxy-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicene-4-carboxylic acid 5315485 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1)C)C)C 456.70 unknown https://doi.org/10.1055/S-2001-18346
(4R,6aR,8aR,12S,12aR,14bR)-3-hydroxy-4,6a,6b,8a,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4-carboxylic acid 5315486 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C 456.70 unknown https://doi.org/10.1055/S-2006-957444
https://doi.org/10.1055/S-2001-18346
https://doi.org/10.1002/(SICI)1099-1573(199603)10:2<107::AID-PTR780>3.0.CO;2-3
11-Keto-beta-boswellic acid 9847548 Click to see 470.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
11-Keto-beta-boswellic acid [M+H]+ 53398660 Click to see 470.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
3-ACETYL-11-KETO-beta-BOSWELLIC ACID 11168203 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C(=O)O)OC(=O)C)C)C)C2C1C)C)C 512.70 unknown https://doi.org/10.1055/S-2006-957444
https://doi.org/10.1016/0031-9422(95)99386-3
https://doi.org/10.1002/MRC.1138
3-Acetyl-11-keto-beta-boswellicacid 71463896 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C(=O)O)OC(=O)C)C)C)C2C1C)C)C 512.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
3-Acetyloxy-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a-dodecahydropicene-4-carboxylic acid 162929574 Click to see 496.70 unknown https://doi.org/10.1002/MRC.1138
3-epi-alpha-Amyrin 12358389 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
3-hydroxy-4,6a,6b,8a,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a-dodecahydro-1H-picene-4-carboxylic acid 12301976 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
3-hydroxy-4,6a,6b,8a,11,12,14b-heptamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4-carboxylic acid 5185849 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
3alpha-Acetyl-20(29)-lupene-24-oic acid 12050282 Click to see 498.70 unknown https://doi.org/10.1002/MRC.1212
3alpha-Corosolic acid 23132198 Click to see 472.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
9-Acetyloxy-3a,5a,5b,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-8-carboxylic acid 75584693 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C(=O)O)OC(=O)C)C)C 498.70 unknown https://doi.org/10.1002/MRC.1212
9,11-Dehydro-beta-boswellic acid 102509765 Click to see CC1CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C 454.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
Acetyl-11-keto-beta-Boswellic Acid, Boswellia serrata 17973666 Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C(=O)O)OC(=O)C)C)C)C2C1C)C)C 512.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2677182/
https://doi.org/10.1016/0031-9422(95)99386-3
https://doi.org/10.1002/MRC.1138
Acetyl-9,11-dehydro-beta-boswellic acid 44558899 Click to see 496.70 unknown https://doi.org/10.1002/MRC.1138
Acetyl-alpha-boswellic acid 15181201 Click to see 498.70 unknown https://doi.org/10.1002/MRC.1138
Acetyl-Beta-Boswellic Acid 11386458 Click to see 498.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199603)10:2<107::AID-PTR780>3.0.CO;2-3
https://doi.org/10.1016/0031-9422(95)99386-3
https://doi.org/10.1002/MRC.1138
https://doi.org/10.1055/S-2001-18346
alpha-Amyrenol 225688 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
Alpha-Amyrin 73170 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
alpha-Boswellic acid acetate 4209683 Click to see CC(=O)OC1CCC2(C(C1(C)C(=O)O)CCC3(C2CC=C4C3(CCC5(C4CC(CC5)(C)C)C)C)C)C 498.70 unknown https://doi.org/10.1002/MRC.1138
beta-Amyrenol 225689 Click to see 426.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
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/10.1016/0031-9422(95)99386-3
Beta-Boswellic Acid 168928 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C 456.70 unknown https://doi.org/10.1002/(SICI)1099-1573(199603)10:2<107::AID-PTR780>3.0.CO;2-3
https://doi.org/10.1016/0031-9422(95)99386-3
https://doi.org/10.1055/S-2001-18346
https://doi.org/10.1055/S-2006-957444
beta-Boswellic acid acetate 3778105 Click to see 498.70 unknown https://doi.org/10.1016/0031-9422(95)99386-3
https://doi.org/10.1002/MRC.1138
Ursa-9(11),12-dien-23-oic acid, 3-(acetyloxy)-, (3alpha,4beta)- 75069239 Click to see 496.70 unknown https://doi.org/10.1002/MRC.1138
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
5,7-Dihydroxy-6,8-bis(3-methylbut-2-enyl)-3-(2,4,5-trihydroxyphenyl)-2,3-dihydrochromen-4-one 10478410 Click to see 440.50 unknown https://doi.org/10.1016/0031-9422(95)99386-3

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.