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Items: 1 to 20 of 146

1.

11α-Ethoxy-β-boswellic acid and nizwanone, a new boswellic acid derivative and a new triterpene, respectively, from Boswellia sacra.

Al-Harrasi A, Ali L, Ur Rehman N, Hussain J, Hussain H, Al-Rawahi A, Shamim Rizvi T.

Chem Biodivers. 2013 Aug;10(8):1501-6. doi: 10.1002/cbdv.201200231.

PMID:
23939798
2.

A lupane triterpene from frankincense (Boswellia sp., Burseraceae).

Culioli G, Mathe C, Archier P, Vieillescazes C.

Phytochemistry. 2003 Feb;62(4):537-41.

PMID:
12560022
3.

Two new triterpenoids from the resin of Boswellia carterii.

Wang F, Li ZL, Cui HH, Hua HM, Jing YK, Liang SW.

J Asian Nat Prod Res. 2011 Mar;13(3):193-7. doi: 10.1080/10286020.2010.548808.

PMID:
21409679
4.

Immunomodulatory triterpenoids from the oleogum resin of Boswellia carterii Birdwood.

Badria FA, Mikhaeil BR, Maatooq GT, Amer MM.

Z Naturforsch C. 2003 Jul-Aug;58(7-8):505-16.

PMID:
12939036
6.

Anti-inflammatory activities of the triterpene acids from the resin of Boswellia carteri.

Banno N, Akihisa T, Yasukawa K, Tokuda H, Tabata K, Nakamura Y, Nishimura R, Kimura Y, Suzuki T.

J Ethnopharmacol. 2006 Sep 19;107(2):249-53. Epub 2006 Mar 17.

PMID:
16621377
7.

Hepatoprotective triterpenes from the gum resin of Boswellia carterii.

Wang YG, Ma QG, Tian J, Ren J, Wang AG, Ji TF, Yang JB, Su YL.

Fitoterapia. 2016 Mar;109:266-73. doi: 10.1016/j.fitote.2015.12.018. Epub 2015 Dec 29.

PMID:
26739386
8.

Ursane and tirucallane-type triterpenes of Boswellia rivae oleo-gum resin.

Manguro LO, Wagai SO.

J Asian Nat Prod Res. 2016 Sep;18(9):854-64. doi: 10.1080/10286020.2016.1165674. Epub 2016 Apr 5.

PMID:
27049028
9.
10.

Frankincense essential oil prepared from hydrodistillation of Boswellia sacra gum resins induces human pancreatic cancer cell death in cultures and in a xenograft murine model.

Ni X, Suhail MM, Yang Q, Cao A, Fung KM, Postier RG, Woolley C, Young G, Zhang J, Lin HK.

BMC Complement Altern Med. 2012 Dec 13;12:253. doi: 10.1186/1472-6882-12-253.

11.

[Chemical components of Boswellia carterii].

Zhou JY, Cui R.

Yao Xue Xue Bao. 2002 Aug;37(8):633-5. Chinese.

PMID:
12567779
12.

Survey on the Quality of the Top-Selling European and American Botanical Dietary Supplements Containing Boswellic Acids.

Meins J, Artaria C, Riva A, Morazzoni P, Schubert-Zsilavecz M, Abdel-Tawab M.

Planta Med. 2016 Apr;82(6):573-9. doi: 10.1055/s-0042-103497. Epub 2016 Apr 7.

PMID:
27054914
13.

In vitro metabolism, permeation, and brain availability of six major boswellic acids from Boswellia serrata gum resins.

Gerbeth K, Hüsch J, Fricker G, Werz O, Schubert-Zsilavecz M, Abdel-Tawab M.

Fitoterapia. 2013 Jan;84:99-106. doi: 10.1016/j.fitote.2012.10.009. Epub 2012 Oct 24.

PMID:
23103296
14.

Bioactive constituents from Boswellia papyrifera.

Atta-ur-Rahman, Naz H, Fadimatou, Makhmoor T, Yasin A, Fatima N, Ngounou FN, Kimbu SF, Sondengam BL, Choudhary MI.

J Nat Prod. 2005 Feb;68(2):189-93.

PMID:
15730241
15.

Cancer chemopreventive effects and cytotoxic activities of the triterpene acids from the resin of Boswellia carteri.

Akihisa T, Tabata K, Banno N, Tokuda H, Nishimura R, Nakamura Y, Kimura Y, Yasukawa K, Suzuki T.

Biol Pharm Bull. 2006 Sep;29(9):1976-9. Erratum in: Biol Pharm Bull. 2006 Dec;29(12):2536. Nishihara, Reiko [corrected to Nishimura, Reiko].

16.

Biotransformation of 11-keto-β-boswellic acid by Cunninghamella blakesleana.

Wang Y, Sun Y, Wang C, Huo X, Liu P, Wang C, Zhang B, Zhan L, Zhang H, Deng S, Zhao Y, Ma X.

Phytochemistry. 2013 Dec;96:330-6. doi: 10.1016/j.phytochem.2013.07.018. Epub 2013 Aug 17.

PMID:
23962801
18.

Hepatoprotective prenylaromadendrane-type diterpenes from the gum resin of Boswellia carterii.

Wang YG, Ren J, Wang AG, Yang JB, Ji TF, Ma QG, Tian J, Su YL.

J Nat Prod. 2013 Nov 22;76(11):2074-9. doi: 10.1021/np400526b. Epub 2013 Nov 6.

PMID:
24195447
19.

Workup-dependent formation of 5-lipoxygenase inhibitory boswellic acid analogues.

Schweizer S, von Brocke AF, Boden SE, Bayer E, Ammon HP, Safayhi H.

J Nat Prod. 2000 Aug;63(8):1058-61.

PMID:
10978197
20.

Identification of archaeological triterpenic resins by the non-separative techniques FTIR and 13C NMR: the case of Pistacia resin (mastic) in comparison with frankincense.

Bruni S, Guglielmi V.

Spectrochim Acta A Mol Biomol Spectrosc. 2014;121:613-22. doi: 10.1016/j.saa.2013.10.098. Epub 2013 Nov 7.

PMID:
24291439

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