Lardy H - Search Results

1

Ergosteroids IV: synthesis and biological activity of steroid glucuronosides, ethers, and alkylcarbonates.

Marwah P, Marwah A, Kneer N, Lardy H. Marwah P, et al. Among authors: lardy h. Steroids. 2001 Jul;66(7):581-95. doi: 10.1016/s0039-128x(00)00234-8. Steroids. 2001. PMID: 11322966

2

Ergosteroids V: preparation and biological activity of various D-ring derivatives in the 7-oxo-dehydroepiandrosterone series.

Reich IL, Reich HJ, Kneer N, Lardy H. Reich IL, et al. Among authors: lardy h. Steroids. 2002 Mar;67(3-4):221-33. doi: 10.1016/s0039-128x(01)00155-6. Steroids. 2002. PMID: 11856546

Several new steroids were synthesized and characterized by (1)H and (13)C NMR spectroscopy. The availability of a number of closely related compounds allowed detailed (13)C chemical shift correlations. ...Hydroxylation of dehydroepiandrosterone (DHEA) at the 16 alpha posit …

Several new steroids were synthesized and characterized by (1)H and (13)C NMR spectroscopy. The availability of a number of closely r …

3

Ergosteroids. VI. Metabolism of dehydroepiandrosterone by rat liver in vitro: a liquid chromatographic-mass spectrometric study.

Marwah A, Marwah P, Lardy H. Marwah A, et al. Among authors: lardy h. J Chromatogr B Analyt Technol Biomed Life Sci. 2002 Feb 15;767(2):285-99. doi: 10.1016/s1570-0232(01)00570-0. J Chromatogr B Analyt Technol Biomed Life Sci. 2002. PMID: 11885858

4

Transformations of DHEA and its metabolites by rat liver.

Lardy H, Marwah A, Marwah P. Lardy H, et al. Lipids. 2002 Dec;37(12):1187-91. doi: 10.1007/s11745-002-1019-7. Lipids. 2002. PMID: 12617473

5

Steroidal allylic fluorination using diethylaminosulfur trifluoride: a convenient method for the synthesis of 3 beta-acetoxy-7 alpha- and 7 beta-fluoroandrost-5-en-17-one.

Marwah P, Thoden JB, Powell DR, Lardy HA. Marwah P, et al. Among authors: lardy ha. Steroids. 1996 Aug;61(8):453-60. doi: 10.1016/0039-128x(96)00092-x. Steroids. 1996. PMID: 8870164

6

Ergosteroids. II: Biologically active metabolites and synthetic derivatives of dehydroepiandrosterone.

Lardy H, Kneer N, Wei Y, Partridge B, Marwah P. Lardy H, et al. Steroids. 1998 Mar;63(3):158-65. doi: 10.1016/s0039-128x(97)00159-1. Steroids. 1998. PMID: 9558717

7

Ergosteroids III. Syntheses and biological activity of seco-steroids related to dehydroepiandrosterone.

Reich IL, Lardy H, Wei Y, Marwah P, Kneer N, Powell DR, Reich HJ. Reich IL, et al. Among authors: lardy h. Steroids. 1998 Oct;63(10):542-53. doi: 10.1016/s0039-128x(98)00066-x. Steroids. 1998. PMID: 9800285

8

Ergosteroids: induction of thermogenic enzymes in liver of rats treated with steroids derived from dehydroepiandrosterone.

Lardy H, Partridge B, Kneer N, Wei Y. Lardy H, et al. Proc Natl Acad Sci U S A. 1995 Jul 3;92(14):6617-9. doi: 10.1073/pnas.92.14.6617. Proc Natl Acad Sci U S A. 1995. PMID: 7604042 Free PMC article.

9

Molecular differences caused by differentiation of 3T3-L1 preadipocytes in the presence of either dehydroepiandrosterone (DHEA) or 7-oxo-DHEA.

Gomez FE, Miyazaki M, Kim YC, Marwah P, Lardy HA, Ntambi JM, Fox BG. Gomez FE, et al. Biochemistry. 2002 Apr 30;41(17):5473-82. doi: 10.1021/bi012177r. Biochemistry. 2002. PMID: 11969408

10

C19-steroids as androgen receptor modulators: design, discovery, and structure-activity relationship of new steroidal androgen receptor antagonists.

Marwah P, Marwah A, Lardy HA, Miyamoto H, Chang C. Marwah P, et al. Among authors: lardy ha. Bioorg Med Chem. 2006 Sep 1;14(17):5933-47. doi: 10.1016/j.bmc.2006.05.022. Epub 2006 Jun 8. Bioorg Med Chem. 2006. PMID: 16759873

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