Boswellia serrata, also known as Indian frankincense, is a plant that is native to India and the Punjab region of Pakistan. However, this plant is currently facing the threat of extinction due to unsustainable practices. It contains various derivatives of boswellic acid, which have been studied for their potential benefits in treating osteoarthritis and improving joint function. While the research has shown some positive results, further studies are needed to fully understand the effects of Boswellia serrata extracts. It is important to promote sustainable practices to ensure the preservation of this plant and its potential medicinal properties.

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

Common names Top

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Filter by language:

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

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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-tropical click to expand
- 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

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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 / Diterpenoids / Cembrane diterpenoids
(-)-Serratol	53249071	Click to see CC1=CCCC(=CCC(CCC(=CCC1)C)(C(C)C)O)C	290.50	unknown	https://doi.org/10.1055/S-0030-1250612
4,8,12-Trimethyl-1-propan-2-ylcyclotetradeca-3,7,11-trien-1-ol	72730091	Click to see CC1=CCCC(=CCC(CCC(=CCC1)C)(C(C)C)O)C	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 CC(=CCCC(=C)C=C)C	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 CC1=CC=C(C=C1)C(C)C	134.22	unknown	https://doi.org/10.1002/FFJ.1124
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(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
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol	64685	Click to see CC1(C2CCC1(C(C2)O)C)C	154.25	unknown	https://doi.org/10.1002/FFJ.1124
alpha-PINENE	6654	Click to see CC1=CCC2CC1C2(C)C	136.23	unknown	https://doi.org/10.1002/FFJ.1124
beta-Pinene	14896	Click to see CC1(C2CCC(=C)C1C2)C	136.23	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 CC1(C2CC1C(=C)C(C2)O)C	152.23	unknown	https://doi.org/10.1002/FFJ.1124
Verbenone	29025	Click to see CC1=CC(=O)C2CC1C2(C)C	150.22	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
(1R,3aR,5aR,5bR,7aR,8R,9R,11aR,11bR,13aR,13bR)-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	12050282	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
(2alpha,3alpha,4beta)-2,3-Dihydroxyurs-12-en-23-oic acid	11698532	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1C)C)C	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 CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)OC(=O)C)C)C)C2C1C)C)C	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 CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C	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,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-2001-18346 https://doi.org/10.1055/S-2006-957444 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 CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C	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/10.1016/0031-9422(95)99386-3 https://doi.org/10.1002/MRC.1138 https://doi.org/10.1055/S-2006-957444
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-Acetyl-beta-boswellic acid	11386458	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)OC(=O)C)C)C)C2C1C)C)C	498.70	unknown	https://doi.org/10.1002/MRC.1138 https://doi.org/10.1016/0031-9422(95)99386-3 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
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 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
3-alpha-O-acetyl-alpha-boswellic acid	15181201	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
3-epi-alpha-Amyrin	12358389	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	unknown	https://doi.org/10.1016/0031-9422(95)99386-3
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	53398660	Click to see CC1CCC2(CCC3(C(=CC(=O)C4C3(CCC5C4(CCC(C5(C)C(=O)O)O)C)C)C2C1C)C)C	470.70	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 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
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
3-O-Acetyl 9,11-dehydro beta-boswellic acid	44558899	Click to see CC1CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C(=O)O)OC(=O)C)C)C)C2C1C)C)C	496.70	unknown	https://doi.org/10.1002/MRC.1138
3-O-Acetyl-alpha-boswellic acid	117072585	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/10.1055/S-2001-18346
3alpha-Corosolic acid	23132198	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1C)C)C	472.70	unknown	https://doi.org/10.1016/0031-9422(95)99386-3
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol	225688	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	426.70	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://doi.org/10.1016/0031-9422(95)99386-3 https://doi.org/10.1002/MRC.1138 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2677182/
alpha-Amyrin	73170	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C	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-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/10.1055/S-2001-18346 https://doi.org/10.1016/0031-9422(95)99386-3 https://doi.org/10.1055/S-2006-957444 https://doi.org/10.1002/(SICI)1099-1573(199603)10:2<107::AID-PTR780>3.0.CO;2-3
beta-Boswellic acid acetate	3778105	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C(=O)O)OC(=O)C)C)C)C2C1C)C)C	498.70	unknown	https://doi.org/10.1016/0031-9422(95)99386-3 https://doi.org/10.1002/MRC.1138
Olean-12-en-3beta-ol	225689	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
Ursa-9(11),12-dien-23-oic acid, 3-(acetyloxy)-, (3alpha,4beta)-	75069239	Click to see CC1CCC2(CCC3(C(=CC=C4C3(CCC5C4(CCC(C5(C)C(=O)O)OC(=O)C)C)C)C2C1C)C)C	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 CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(CO2)C3=CC(=C(C=C3O)O)O)CC=C(C)C)O)C	440.50	unknown	https://doi.org/10.1016/0031-9422(95)99386-3

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Boswellia serrata

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