Format
Sort by

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 114

1.

Two new oxidation products obtained from the biotransformation of asiatic acid by the fungus Fusarium avenaceum AS 3.4594.

Huang FX, Lin XH, He WN, Song W, Ye M, Yang WZ, Guo DA.

J Asian Nat Prod Res. 2012;14(11):1039-45. doi: 10.1080/10286020.2012.702761. Epub 2012 Oct 29.

PMID:
23106376
2.

Microbial transformation of asiatic acid.

Guo FF, Feng X, Chu ZY, Li DP, Zhang L, Zhang ZS.

J Asian Nat Prod Res. 2013;15(1):15-21. doi: 10.1080/10286020.2012.741124. Epub 2012 Dec 11.

PMID:
23227815
3.

Microbial transformation of asiatic acid by Alternaria longipes.

He WN, Dai JG, Ye M, Wu LJ, Guo DA.

J Asian Nat Prod Res. 2010 Sep;12(9):760-4. doi: 10.1080/10286020.2010.501505.

PMID:
20839122
4.

Unusual microbial lactonization and hydroxylation of asiatic acid by Umbelopsis isabellina.

Gao ZH, Dong XR, Gao RR, Sun DA.

J Asian Nat Prod Res. 2015;17(11):1059-64. doi: 10.1080/10286020.2015.1054377. Epub 2015 Jul 20.

PMID:
26194478
5.

New terpenes from Salvia palaestina Benth. and Salvia syriaca L. growing wild in Jordan.

Al-Jaber HI, Abrouni KK, Al-Qudah MA, Abu Zarga MH.

J Asian Nat Prod Res. 2012;14(7):618-25. doi: 10.1080/10286020.2012.682151. Epub 2012 May 10.

PMID:
22574636
6.

Multihydroxylation of ursolic acid by Pestalotiopsis microspora isolated from the medicinal plant Huperzia serrata.

Fu SB, Yang JS, Cui JL, Meng QF, Feng X, Sun DA.

Fitoterapia. 2011 Oct;82(7):1057-61. doi: 10.1016/j.fitote.2011.06.009. Epub 2011 Jul 2.

PMID:
21767617
7.

Biotransformation of betulinic and betulonic acids by fungi.

Bastos DZ, Pimentel IC, de Jesus DA, de Oliveira BH.

Phytochemistry. 2007 Mar;68(6):834-9. Epub 2007 Jan 26.

PMID:
17258248
8.

Structural determination of two new triterpenoids from Potentilla discolor Bunge by NMR techniques.

Yang J, Chen XQ, Liu XX, Cao Y, Lai MX, Wang Q.

Magn Reson Chem. 2008 Aug;46(8):794-7. doi: 10.1002/mrc.2253.

PMID:
18509870
9.

Biotransformation of ursolic acid by Syncephalastrum racemosum CGMCC 3.2500 and anti-HCV activity.

Fu SB, Yang JS, Cui JL, Sun DA.

Fitoterapia. 2013 Apr;86:123-8. doi: 10.1016/j.fitote.2013.02.007. Epub 2013 Feb 17.

PMID:
23425601
10.

Hydroxylation at carbon-2 of ent-16-oxo-17-norkauran-19-oic acid by Fusarium proliferatum.

Rocha AD, dos Santos GC, Fernandes NG, Pfenning LH, Takahashi JA, Boaventura MA.

J Nat Prod. 2010 Aug 27;73(8):1431-3. doi: 10.1021/np100134f.

PMID:
20617817
11.

New ursane-type triterpene with NO production suppressing activity from Nauclea officinalis.

Tao JY, Dai SJ, Zhao F, Liu JF, Fang WS, Liu K.

J Asian Nat Prod Res. 2012;14(2):97-104. doi: 10.1080/10286020.2011.628839.

PMID:
22296148
12.

Natural products inhibiting Candida albicans secreted aspartic proteases from Lycopodium cernuum.

Zhang Z, ElSohly HN, Jacob MR, Pasco DS, Walker LA, Clark AM.

J Nat Prod. 2002 Jul;65(7):979-85.

PMID:
12141856
13.

Microbiological transformation of two 15α-hydroxy-ent-kaur-9(11),16-diene derivatives by the fungus Fusarium fujikuroi.

Fraga BM, González-Vallejo V, Guillermo R, Amaro-Luis JM.

Phytochemistry. 2013 May;89:39-46. doi: 10.1016/j.phytochem.2013.01.006. Epub 2013 Feb 8.

PMID:
23398890
14.

Microbial transformation of the anti-diabetic agent corosolic acid.

Feng X, Li DP, Zhang ZS, Chu ZY, Luan J.

Nat Prod Res. 2014;28(21):1879-86. doi: 10.1080/14786419.2014.955485. Epub 2014 Sep 5.

PMID:
25190540
15.

Biotransformation of two ent-Pimara-9(11),15-diene derivatives by Gibberella fujikuroi.

Fraga BM, Guillermo R, Hernández MG, Chamy MC, Garbarino JA.

J Nat Prod. 2009 Jan;72(1):87-91. doi: 10.1021/np800647v.

PMID:
19128148
16.

A new triterpenoid from the rhizomes of Nelumbo nucifera.

Chaudhuri PK, Singh D.

Nat Prod Res. 2013;27(6):532-6. doi: 10.1080/14786419.2012.676549. Epub 2012 Apr 19.

PMID:
22512662
17.

Triterpenes from Astilbe chinensis.

Hu JY, Yao Z, Xu YQ, Takaishi Y, Duan HQ.

J Asian Nat Prod Res. 2009;11(3):236-42. doi: 10.1080/10286020802682866.

PMID:
19408147
18.

Microbial transformation of oleanolic acid by Fusarium lini and alpha-glucosidase inhibitory activity of its transformed products.

Choudhary MI, Batool I, Khan SN, Sultana N, Shah SA, Ur-Rahman A.

Nat Prod Res. 2008 Apr 15;22(6):489-94. doi: 10.1080/14786410601083787.

PMID:
18415855
19.

Pentacyclic triterpenoids from the mangrove plant Rhizophora stylosa.

Li DL, Li XM, Wang BG.

Nat Prod Res. 2008 Jun 15;22(9):808-13. doi: 10.1080/14786410701640452.

PMID:
18569720
20.

New lanostane-type triterpenoids from Ganoderma applanatum.

Shim SH, Ryu J, Kim JS, Kang SS, Xu Y, Jung SH, Lee YS, Lee S, Shin KH.

J Nat Prod. 2004 Jul;67(7):1110-3.

PMID:
15270562
Items per page

Supplemental Content

Write to the Help Desk