-
1
-
-
30144443660
-
Structure of UDP-glucuronosyltransferases in membranes
-
Radominska-Pandya, A.; Ouzzine, M.; Fournel-Gigleux, S.; Magdalou, J. Structure of UDP-glucuronosyltransferases in membranes. Methods Enzymol. 2005, 400, 116-147.
-
(2005)
Methods Enzymol
, vol.400
, pp. 116-147
-
-
Radominska-Pandya, A.1
Ouzzine, M.2
Fournel-Gigleux, S.3
Magdalou, J.4
-
2
-
-
10744227696
-
Glucuronidation and the UDP-glucuronosyltransferases in health and disease
-
Wells, P. G.; Mackenzie, P. I.; Chowdhury, J. R.; Guillemette, C.; Gregory, P. A.; Ishii, Y.; Hansen, A. J.; Kessler, F. K.; Kim, P. M.; Chowdhury, N. R.; Ritter, J. K. Glucuronidation and the UDP-glucuronosyltransferases in health and disease. Drug Metab. Dispos. 2004, 32, 281-290.
-
(2004)
Drug Metab. Dispos
, vol.32
, pp. 281-290
-
-
Wells, P.G.1
Mackenzie, P.I.2
Chowdhury, J.R.3
Guillemette, C.4
Gregory, P.A.5
Ishii, Y.6
Hansen, A.J.7
Kessler, F.K.8
Kim, P.M.9
Chowdhury, N.R.10
Ritter, J.K.11
-
3
-
-
0035209568
-
The role of hepatic and extrahepatic UDP-glucuronosyltransferases in human drug metabolism
-
Fisher, M. B.; Paine, M. F.; Strelevitz, T. J.; Wrighton, S. A. The role of hepatic and extrahepatic UDP-glucuronosyltransferases in human drug metabolism. Drug Metab. Rev. 2001, 33, 273-297.
-
(2001)
Drug Metab. Rev
, vol.33
, pp. 273-297
-
-
Fisher, M.B.1
Paine, M.F.2
Strelevitz, T.J.3
Wrighton, S.A.4
-
4
-
-
30144437158
-
UDP-glucuronosyltransferases: Gene structures of UGT1 and UGT2 families
-
Owens, I. S.; Basu, N. K.; Banerjee, R. UDP-glucuronosyltransferases: gene structures of UGT1 and UGT2 families. Methods Enzymol. 2005, 400, 1-22.
-
(2005)
Methods Enzymol
, vol.400
, pp. 1-22
-
-
Owens, I.S.1
Basu, N.K.2
Banerjee, R.3
-
5
-
-
6944221357
-
Drug-drug interactions for UDP-glucuronosyltransferase substrates: A pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios
-
Williams, J. A.; Hyland, R.; Jones, B. C.; Smith, D. A.; Hurst, S.; Goosen, T. C.; Peterkin, V.; Koup. J.; Ball, S. E. Drug-drug interactions for UDP-glucuronosyltransferase substrates: a pharmacokinetic explanation for typically observed low exposure (AUCi/AUC) ratios. Drug Metab. Dispos. 2004, 32, 1201-1208.
-
(2004)
Drug Metab. Dispos
, vol.32
, pp. 1201-1208
-
-
Williams, J.A.1
Hyland, R.2
Jones, B.C.3
Smith, D.A.4
Hurst, S.5
Goosen, T.C.6
Peterkin, V.7
Koup, J.8
Ball, S.E.9
-
6
-
-
0037396292
-
-
The term catalytic promiscuity has been used to describe the ability of an enzyme to catalyze an adventitious secondary activity at the active site responsible for the primary activity. However, in the case of metabolic enzymes like UGTs, the term has been used to depict their overlapping substrate selectivities. Cf. Copley, S. D. Enzymes with extra talents: moonlighting functions and catalytic promiscuity. Curr. Opin. Chem. Biol. 2003, 7, 265-272
-
The term catalytic promiscuity has been used to describe the ability of an enzyme to catalyze an adventitious secondary activity at the active site responsible for the primary activity. However, in the case of metabolic enzymes like UGTs, the term has been used to depict their overlapping substrate selectivities. Cf. Copley, S. D. Enzymes with extra talents: moonlighting functions and catalytic promiscuity. Curr. Opin. Chem. Biol. 2003, 7, 265-272.
-
-
-
-
7
-
-
30144436526
-
Isoform-selective probe substrates for in vitro studies of human UDP-glucuronosyltransferases
-
Court, M. H. Isoform-selective probe substrates for in vitro studies of human UDP-glucuronosyltransferases. Methods Enzymol. 2005, 400, 104-116.
-
(2005)
Methods Enzymol
, vol.400
, pp. 104-116
-
-
Court, M.H.1
-
8
-
-
0030790494
-
Non-enzymatic and enzymatic hydrolysis of alkyl halides: A haloalkane dehalogenation enzyme evolved to stabilize the gas-phase transition state of an SN2 displacement reaction
-
Lightstone, F. C.; Ya-Jun, Z.; Maulitz, A. H.; Bruice, T. C. Non-enzymatic and enzymatic hydrolysis of alkyl halides: a haloalkane dehalogenation enzyme evolved to stabilize the gas-phase transition state of an SN2 displacement reaction. Proc. Natl. Acad. Sci. U.S.A. 1997, 94, 8417-8420.
-
(1997)
Proc. Natl. Acad. Sci. U.S.A
, vol.94
, pp. 8417-8420
-
-
Lightstone, F.C.1
Ya-Jun, Z.2
Maulitz, A.H.3
Bruice, T.C.4
-
9
-
-
0023664326
-
A kinetic isotope effect study and transition state analysis of the S- adenosylmethionine synthetase reaction
-
Markham, G. D.; Parkin, D. W.; Mentch, F.; Schramm, V. L. A kinetic isotope effect study and transition state analysis of the S- adenosylmethionine synthetase reaction. J. Biol. Chem. 1987, 262, 5609-5615.
-
(1987)
J. Biol. Chem
, vol.262
, pp. 5609-5615
-
-
Markham, G.D.1
Parkin, D.W.2
Mentch, F.3
Schramm, V.L.4
-
10
-
-
9744244983
-
Enzymatic transition states: Thermodynamics, dynamics and analogue design
-
Schramm, V. L. Enzymatic transition states: thermodynamics, dynamics and analogue design. Arch. Biochem. Biophys. 2005, 433, 13-26.
-
(2005)
Arch. Biochem. Biophys
, vol.433
, pp. 13-26
-
-
Schramm, V.L.1
-
11
-
-
29444445067
-
Transition states and inhibitors of the purine nucleoside phosphorylase family
-
Taylor Ringia, E. A.; Schramm, V. L. Transition states and inhibitors of the purine nucleoside phosphorylase family. Curr. Top. Med. Chem. 2005, 5, 1237-1258.
-
(2005)
Curr. Top. Med. Chem
, vol.5
, pp. 1237-1258
-
-
Taylor Ringia, E.A.1
Schramm, V.L.2
-
12
-
-
0035061201
-
Natural and synthetic inhibitors of UDP-glucuronosyltransferase
-
Grancharov, K.; Naydenova, Z.; Lozeva, S.; Golovinsky, E. Natural and synthetic inhibitors of UDP-glucuronosyltransferase. Pharmacol. Ther. 2001, 89, 171-186.
-
(2001)
Pharmacol. Ther
, vol.89
, pp. 171-186
-
-
Grancharov, K.1
Naydenova, Z.2
Lozeva, S.3
Golovinsky, E.4
-
13
-
-
0030957158
-
Synthesis and inhibitory effect of a trisubstrate transition state analog for UDP glucuronosyltransferases
-
Timmers, C. M.; Dekker, M.; Buijsman, R. C.; van der Marel, G. A.; Ethell, B.; Anderson, G.; Burchell, B.; Mulder, G. J.; van Boom, J. H. Synthesis and inhibitory effect of a trisubstrate transition state analog for UDP glucuronosyltransferases. Bioorg. Med. Chem. Lett. 1997, 7, 1501-1506.
-
(1997)
Bioorg. Med. Chem. Lett
, vol.7
, pp. 1501-1506
-
-
Timmers, C.M.1
Dekker, M.2
Buijsman, R.C.3
van der Marel, G.A.4
Ethell, B.5
Anderson, G.6
Burchell, B.7
Mulder, G.J.8
van Boom, J.H.9
-
14
-
-
0026009190
-
Selective inhibition of glucuronidation by 2,2,2-triphenylethyl-UDP in isolated rat hepatocytes: Conjugation of harmol, 3,3′,5-triiodothyronine, and N-hydroxy-2- acetylaminofluorene
-
Noort, D.; Meijer, E. A.; Visser, T. J.; Meerman, J. H. N.; van der Marel, G. A.; van Boom, J. H.; Mulder, G. J. Selective inhibition of glucuronidation by 2,2,2-triphenylethyl-UDP in isolated rat hepatocytes: conjugation of harmol, 3,3′,5-triiodothyronine, and N-hydroxy-2- acetylaminofluorene. Mol. Pharmacol. 1991, 40, 316-320.
-
(1991)
Mol. Pharmacol
, vol.40
, pp. 316-320
-
-
Noort, D.1
Meijer, E.A.2
Visser, T.J.3
Meerman, J.H.N.4
van der Marel, G.A.5
van Boom, J.H.6
Mulder, G.J.7
-
15
-
-
27944458409
-
Enzymatic transition states and transition state analogues
-
Schramm, V. L. Enzymatic transition states and transition state analogues. Curr. Opin. Struct. Biol. 2005, 15, 604-613.
-
(2005)
Curr. Opin. Struct. Biol
, vol.15
, pp. 604-613
-
-
Schramm, V.L.1
-
16
-
-
0031688282
-
Enzymatic transition states and transition state analog design
-
Schramm, V. L. Enzymatic transition states and transition state analog design. Annu. Rev. Biochem. 1998, 67, 693-720.
-
(1998)
Annu. Rev. Biochem
, vol.67
, pp. 693-720
-
-
Schramm, V.L.1
-
17
-
-
0026705819
-
Selective and potent inhibition of different hepatic UDP-glucuronosyltransferase activities by ω,ω, ω-triphenylalcohols and UDP derivatives
-
Said, M.; Noort, D.; Magdalou, J.; Ziegler, J. C.; van der Marel, G. A.; van Boom, J. H.; Mulder, G. J.; Siest, G. Selective and potent inhibition of different hepatic UDP-glucuronosyltransferase activities by ω,ω, ω-triphenylalcohols and UDP derivatives. Biochem. Biophys. Res. Commun. 1992, 187, 140-145.
-
(1992)
Biochem. Biophys. Res. Commun
, vol.187
, pp. 140-145
-
-
Said, M.1
Noort, D.2
Magdalou, J.3
Ziegler, J.C.4
van der Marel, G.A.5
van Boom, J.H.6
Mulder, G.J.7
Siest, G.8
-
18
-
-
0025265006
-
Inhibition of UDP- glucuronosyltransferase activity by possible transition-state analogues in rat-liver microsomes
-
Noort, D.; Coughtrie, M. W.; Burchell, B.; van der Marel, G. A.; van Boom, J. H.; van der Gen, A.; Mulder, G. J. Inhibition of UDP- glucuronosyltransferase activity by possible transition-state analogues in rat-liver microsomes. Eur. J. Biochem. 1990, 188, 309-312.
-
(1990)
Eur. J. Biochem
, vol.188
, pp. 309-312
-
-
Noort, D.1
Coughtrie, M.W.2
Burchell, B.3
van der Marel, G.A.4
van Boom, J.H.5
van der Gen, A.6
Mulder, G.J.7
-
19
-
-
33344473930
-
Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) "probes" for human UDP-glucuronosyltransferases
-
Uchaipichat, V.; Mackenzie, P. I.; Elliot, D. J.; Miners, J. O. Selectivity of substrate (trifluoperazine) and inhibitor (amitriptyline, androsterone, canrenoic acid, hecogenin, phenylbutazone, quinidine, quinine, and sulfinpyrazone) "probes" for human UDP-glucuronosyltransferases. Drug Metab. Dispos. 2006, 34, 449-456.
-
(2006)
Drug Metab. Dispos
, vol.34
, pp. 449-456
-
-
Uchaipichat, V.1
Mackenzie, P.I.2
Elliot, D.J.3
Miners, J.O.4
-
21
-
-
33947477067
-
Total synthesis of D,L-longifolene
-
Corey, E. J.; Ohno, M.; Vatakencherry, P. A.; Mitra, R. B. Total synthesis of D,L-longifolene. J. Am. Chem. Soc. 1961, 83, 1251-1253.
-
(1961)
J. Am. Chem. Soc
, vol.83
, pp. 1251-1253
-
-
Corey, E.J.1
Ohno, M.2
Vatakencherry, P.A.3
Mitra, R.B.4
-
22
-
-
0006826705
-
Novel synthesis of longifolene
-
Volkmann, R. A.; Andrews, G. C.; Johnson, W. S. Novel synthesis of longifolene. J. Am. Chem. Soc. 1975, 97, 4777-4779.
-
(1975)
J. Am. Chem. Soc
, vol.97
, pp. 4777-4779
-
-
Volkmann, R.A.1
Andrews, G.C.2
Johnson, W.S.3
-
23
-
-
0000628193
-
The intramolecular diene-carbene cycloaddition equivalence and an enantioselective Birch reduction-alkylation by the chiral auxiliary approach. Total synthesis of (±)-and (-)-longifolene
-
Schultz, A. G.; Puig, S. The intramolecular diene-carbene cycloaddition equivalence and an enantioselective Birch reduction-alkylation by the chiral auxiliary approach. Total synthesis of (±)-and (-)-longifolene. J. Org. Chem. 1985, 50, 915-916.
-
(1985)
J. Org. Chem
, vol.50
, pp. 915-916
-
-
Schultz, A.G.1
Puig, S.2
-
24
-
-
0001507831
-
-
Jadhav, P. K.; Brown, H. C. Dilongifolylborane: a new effective chiral hydroborating agent with intermediate steric requirements. J. Org. Chem. 1981, 46, 2988-2990.
-
Jadhav, P. K.; Brown, H. C. Dilongifolylborane: a new effective chiral hydroborating agent with intermediate steric requirements. J. Org. Chem. 1981, 46, 2988-2990.
-
-
-
-
25
-
-
0035844460
-
Chiral ferrocenes derived from (+)-longifolene - determination of the configuration by NMR spectroscopy and X-ray crystallography
-
Dimitrov, V.; Linden, A.; Hesse, M. Chiral ferrocenes derived from (+)-longifolene - determination of the configuration by NMR spectroscopy and X-ray crystallography. Tetrahedron: Asymmetry 2001, 12, 1331-1335.
-
(2001)
Tetrahedron: Asymmetry
, vol.12
, pp. 1331-1335
-
-
Dimitrov, V.1
Linden, A.2
Hesse, M.3
-
26
-
-
0000206111
-
Stereochemical aspects of sesquiterpene biosynthesis
-
Arigoni, D. Stereochemical aspects of sesquiterpene biosynthesis. Pure Appl. Chem. 1975, 41, 219-245.
-
(1975)
Pure Appl. Chem
, vol.41
, pp. 219-245
-
-
Arigoni, D.1
-
27
-
-
33646178621
-
Designed divergent evolution of enzyme function
-
Yoshikuni, Y.; Ferrin, T. E.; Keasling, J. D. Designed divergent evolution of enzyme function. Nature 2006, 440, 1078-1082.
-
(2006)
Nature
, vol.440
, pp. 1078-1082
-
-
Yoshikuni, Y.1
Ferrin, T.E.2
Keasling, J.D.3
-
28
-
-
0032124860
-
Identification of lipophilic pollutants discharged from a Finnish pulp and paper mill
-
Koistinen, J.; Lehtonen, M.; Tukia, K.; Soimasuo, M.; Lahtiperä, M.; Oikari, A. Identification of lipophilic pollutants discharged from a Finnish pulp and paper mill. Chemosphere 1998, 37, 219-235.
-
(1998)
Chemosphere
, vol.37
, pp. 219-235
-
-
Koistinen, J.1
Lehtonen, M.2
Tukia, K.3
Soimasuo, M.4
Lahtiperä, M.5
Oikari, A.6
-
29
-
-
0030609785
-
Toxicity to Daphnia pulex and QSAR predictions for polycyclic hydrocarbons representative of Great Lakes contaminants
-
Passino-Reader, D. R.; Hickey, J. P.; Ogilvie, L. M. Toxicity to Daphnia pulex and QSAR predictions for polycyclic hydrocarbons representative of Great Lakes contaminants. Bull. Environ. Contam. Toxicol. 1997, 59, 834-840.
-
(1997)
Bull. Environ. Contam. Toxicol
, vol.59
, pp. 834-840
-
-
Passino-Reader, D.R.1
Hickey, J.P.2
Ogilvie, L.M.3
-
30
-
-
0019963537
-
-
Ishida, T.; Asakawa, Y.; Takemoto, T. Hydroxyisolongifolaldehyde: a new metabolite of (+)-longifolene in rabbits. J. Pharm. Sci. 1982, 71, 965-966.
-
Ishida, T.; Asakawa, Y.; Takemoto, T. Hydroxyisolongifolaldehyde: a new metabolite of (+)-longifolene in rabbits. J. Pharm. Sci. 1982, 71, 965-966.
-
-
-
-
31
-
-
27744481217
-
Trypanocidal activity of oleoresin and terpenoids isolated from Pinus oocarpa
-
Rubio, J.; Calderon, J. S.; Flores, A.; Castroa, C. Trypanocidal activity of oleoresin and terpenoids isolated from Pinus oocarpa. Z. Naturforsch. C 2005, 60, 711-716.
-
(2005)
Z. Naturforsch. C
, vol.60
, pp. 711-716
-
-
Rubio, J.1
Calderon, J.S.2
Flores, A.3
Castroa, C.4
-
32
-
-
0346134903
-
Products active on mosquitoes. Part VII. Synthesis and biological activity of longifolene derivatives
-
Sawaikar, D. D.; Sinha, B.; Hebbalkar, G. D.; Sharma, R. N.; Patwardhan, S. A. Products active on mosquitoes. Part VII. Synthesis and biological activity of longifolene derivatives. Indian J. Chem. B 1995, 34, 832-835.
-
(1995)
Indian J. Chem. B
, vol.34
, pp. 832-835
-
-
Sawaikar, D.D.1
Sinha, B.2
Hebbalkar, G.D.3
Sharma, R.N.4
Patwardhan, S.A.5
-
33
-
-
13844308927
-
Microbial transformation of (-)-isolongifolol and butyrylcholinesterase inhibitory activity of transformed products
-
Choudhary, M. I.; Musharraf, S. G.; Nawaz, S. A.; Anjum, S.; Parvez, M.; Fun, H.-K.; Atta-ur-Rahman. Microbial transformation of (-)-isolongifolol and butyrylcholinesterase inhibitory activity of transformed products. Bioorg. Med. Chem. Lett. 2005, 13, 1939-1944.
-
(2005)
Bioorg. Med. Chem. Lett
, vol.13
, pp. 1939-1944
-
-
Choudhary, M.I.1
Musharraf, S.G.2
Nawaz, S.A.3
Anjum, S.4
Parvez, M.5
Fun, H.-K.6
Atta-ur-Rahman7
-
34
-
-
33644855536
-
Stereochemical sensitivity of the human UDP-glucuronosyltransferases 2B7 and 2B17
-
Bichlmaier, I.; Siiskonen, A.; Finel, M.; Yli-Kauhaluoma, J. Stereochemical sensitivity of the human UDP-glucuronosyltransferases 2B7 and 2B17. J. Med. Chem. 2006, 49, 1818-1827.
-
(2006)
J. Med. Chem
, vol.49
, pp. 1818-1827
-
-
Bichlmaier, I.1
Siiskonen, A.2
Finel, M.3
Yli-Kauhaluoma, J.4
-
35
-
-
33645766962
-
Chiral distinction between the enantiomers of bicyclic alcohols by UDP-glucuronosyltransferases 2B7 and 2B17
-
Bichlmaier, I.; Siiskonen, A.; Kurkela, M.; Finel, M.; Yli-Kauhaluoma, J. Chiral distinction between the enantiomers of bicyclic alcohols by UDP-glucuronosyltransferases 2B7 and 2B17. Biol. Chem. 2006, 387, 407-416.
-
(2006)
Biol. Chem
, vol.387
, pp. 407-416
-
-
Bichlmaier, I.1
Siiskonen, A.2
Kurkela, M.3
Finel, M.4
Yli-Kauhaluoma, J.5
-
36
-
-
34548124595
-
Eudismic analysis of tricyclic sesquiterpenoid alcohols. Lead structures for the design of potent inhibitors of the human UDP-glucuronosyltransferase 2B7
-
submitted
-
Bichlmaier, I.; Kurkela, M.; Siiskonen, A.; Finel, M.; Yli-Kauhaluoma, J. Eudismic analysis of tricyclic sesquiterpenoid alcohols. Lead structures for the design of potent inhibitors of the human UDP-glucuronosyltransferase 2B7. Bioorg. Chem. (submitted).
-
Bioorg. Chem
-
-
Bichlmaier, I.1
Kurkela, M.2
Siiskonen, A.3
Finel, M.4
Yli-Kauhaluoma, J.5
-
37
-
-
31844432220
-
Hypervalent iodine(V) reagents in organic synthesis
-
Ladziata, U.; Zhdankin, V. V. Hypervalent iodine(V) reagents in organic synthesis. ARKIVOC: Arch. Org. Chem. 2006, ix, 26-58.
-
(2006)
ARKIVOC: Arch. Org. Chem
, vol.9
, pp. 26-58
-
-
Ladziata, U.1
Zhdankin, V.V.2
-
38
-
-
0033546262
-
A user friendly entry to 2-iodoxybenzoic acid (IBX)
-
Frigerio, M.; Santagostino, M.; Sputore, S. A user friendly entry to 2-iodoxybenzoic acid (IBX). J. Org. Chem. 1999, 64, 4537-4538.
-
(1999)
J. Org. Chem
, vol.64
, pp. 4537-4538
-
-
Frigerio, M.1
Santagostino, M.2
Sputore, S.3
-
39
-
-
15444373515
-
Catalytic reductive alkylation of secondary amine with aldehyde and silane by an iridium compound
-
Mizuta, T.; Sakaguchi, S.; Ishii, Y. Catalytic reductive alkylation of secondary amine with aldehyde and silane by an iridium compound. J. Org. Chem. 2005, 70, 2195-2199.
-
(2005)
J. Org. Chem
, vol.70
, pp. 2195-2199
-
-
Mizuta, T.1
Sakaguchi, S.2
Ishii, Y.3
-
40
-
-
0035935144
-
An improved preparation of epoxides from carbonyl compounds by using diiodomethane/methyllithium: Synthetic applications
-
Concellon, J. M.; Cuervo, H.; Fernandez-Fano, R. An improved preparation of epoxides from carbonyl compounds by using diiodomethane/methyllithium: synthetic applications. Tetrahedron 2001, 57, 8983-8987.
-
(2001)
Tetrahedron
, vol.57
, pp. 8983-8987
-
-
Concellon, J.M.1
Cuervo, H.2
Fernandez-Fano, R.3
-
41
-
-
0000240075
-
-
Li, Z.; Racha, S; Dan, L.; El-Subbagh, H.; Abushanab, E. A general and facile synthesis of β- and γ-hydroxyphosphonates from epoxides. J. Org. Chem. 1993, 58, 5779-5783.
-
Li, Z.; Racha, S; Dan, L.; El-Subbagh, H.; Abushanab, E. A general and facile synthesis of β- and γ-hydroxyphosphonates from epoxides. J. Org. Chem. 1993, 58, 5779-5783.
-
-
-
-
42
-
-
1842667316
-
2-terminal protein kinase with antiproliferative effects in neuronal tumor cells
-
2-terminal protein kinase with antiproliferative effects in neuronal tumor cells. J. Med. Chem. 2004, 47, 2710-2713.
-
(2004)
J. Med. Chem
, vol.47
, pp. 2710-2713
-
-
Samadder, P.1
Bittman, R.2
Byun, H.-S.3
Arthur, G.4
-
43
-
-
0035907465
-
Aromatic inhibitors of dehydroquinate synthase: Synthesis, evaluation and implications for gallic acid biosynthesis
-
Chandran, S. S.; Frost, J. W. Aromatic inhibitors of dehydroquinate synthase: Synthesis, evaluation and implications for gallic acid biosynthesis. Bioorg. Med. Chem. Lett. 2001, 11, 1493-1496.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, pp. 1493-1496
-
-
Chandran, S.S.1
Frost, J.W.2
-
44
-
-
0142042926
-
Titanocene(III)-promoted Reformatsky additions
-
Parrish, J. D.; Shelton. D. R.; Little, R. D. Titanocene(III)-promoted Reformatsky additions. Org. Lett. 2003, 5, 3615-3617.
-
(2003)
Org. Lett
, vol.5
, pp. 3615-3617
-
-
Parrish, J.D.1
Shelton, D.R.2
Little, R.D.3
-
45
-
-
34250193360
-
-
Alternatively, gNOESY experiments could be used for the assignment of the absolute configuration at C(1′). The NOE correlation between C(1′)OH and endo-C(10)H was present when the OH group was pointing toward endo-C(10)H. In contrast, this NOE correlation was not found in its corresponding epimer in which the OH group was pointing away from endo-C(10)H. However, these correlations were often difficult to assign due to signal overlap, and, therefore, gHSQC analysis was superior because all corresponding signals were resolved.
-
Alternatively, gNOESY experiments could be used for the assignment of the absolute configuration at C(1′). The NOE correlation between C(1′)OH and endo-C(10)H was present when the OH group was pointing toward endo-C(10)H. In contrast, this NOE correlation was not found in its corresponding epimer in which the OH group was pointing away from endo-C(10)H. However, these correlations were often difficult to assign due to signal overlap, and, therefore, gHSQC analysis was superior because all corresponding signals were resolved.
-
-
-
-
47
-
-
0037423299
-
Expression and characterization of recombinant human UDP-glucuronosyltransferases (UGTs). UGT1A9 is more resistant to detergent inhibition than other UGTs and was purified as an active dimeric enzyme
-
Kurkela, M.; Garcia-Horsman, A.; Luukkanen, L.; Mörsky, S.; Taskinen, J.; Baumann, M.; Kostiainen, R.; Hirvonen, J.; Finel, M. Expression and characterization of recombinant human UDP-glucuronosyltransferases (UGTs). UGT1A9 is more resistant to detergent inhibition than other UGTs and was purified as an active dimeric enzyme. J. Biol. Chem. 2003, 278, 3536-3544.
-
(2003)
J. Biol. Chem
, vol.278
, pp. 3536-3544
-
-
Kurkela, M.1
Garcia-Horsman, A.2
Luukkanen, L.3
Mörsky, S.4
Taskinen, J.5
Baumann, M.6
Kostiainen, R.7
Hirvonen, J.8
Finel, M.9
-
48
-
-
0035873701
-
High-performance liquid chromatographic method combining radiochemical and ultraviolet detection for determination of low activities of uridine 5′-diphosphate-glucuronosyltransferase
-
Kaivosaari, S.; Salonen, J. S.; Mortensen, J.; Taskinen, J. High-performance liquid chromatographic method combining radiochemical and ultraviolet detection for determination of low activities of uridine 5′-diphosphate-glucuronosyltransferase. Anal. Biochem. 2001, 292, 178-187.
-
(2001)
Anal. Biochem
, vol.292
, pp. 178-187
-
-
Kaivosaari, S.1
Salonen, J.S.2
Mortensen, J.3
Taskinen, J.4
-
49
-
-
84943920736
-
Phase annealing in SHELX-90: Direct methods for larger structures
-
Sheldrick, G. M. Phase annealing in SHELX-90: direct methods for larger structures. Acta Crystallogr., Sect. A 1990, 46, 467-473.
-
(1990)
Acta Crystallogr., Sect. A
, vol.46
, pp. 467-473
-
-
Sheldrick, G.M.1
-
51
-
-
84944438568
-
On enantiomorph-polarity estimation
-
Flack, H. D. On enantiomorph-polarity estimation. Acta Crystallogr., Sect. A 1983, 39, 876-881.
-
(1983)
Acta Crystallogr., Sect. A
, vol.39
, pp. 876-881
-
-
Flack, H.D.1
|