-
1
-
-
84884674744
-
-
Moon HS, Yoo MH, Kim SH, et al. Novel phenylpropionic acid derivatives as peroxisome proliferator-activated gamma receptor modulators, method of the same, and pharmaceutical composition comprising the same: WO, 2008108602 [P]. 2008-12-09.
-
Moon HS, Yoo MH, Kim SH, et al. Novel phenylpropionic acid derivatives as peroxisome proliferator-activated gamma receptor modulators, method of the same, and pharmaceutical composition comprising the same: WO, 2008108602 [P]. 2008-12-09.
-
-
-
-
2
-
-
0041335381
-
Progress in studies on antidiabetic agents [J]
-
Tang L, Yang YS, Ji RY. Progress in studies on antidiabetic agents [J]. Acta Pharm Sin, 2001, 36: 711-715.
-
(2001)
Acta Pharm Sin
, vol.36
, pp. 711-715
-
-
Tang, L.1
Yang, Y.S.2
Ji, R.Y.3
-
3
-
-
0029946714
-
Structure-activity relationships of boronic acid inhibitors of dipeptidyl peptidase IV. 1. Variation of the P2 position of Xaa-boroPro dipeptides [J]
-
Courts SJ, Kelly TA, Snow RJ, et al. Structure-activity relationships of boronic acid inhibitors of dipeptidyl peptidase IV. 1. Variation of the P2 position of Xaa-boroPro dipeptides [J]. J Med Chem, 1996, 39: 2087-2094.
-
(1996)
J Med Chem
, vol.39
, pp. 2087-2094
-
-
Courts, S.J.1
Kelly, T.A.2
Snow, R.J.3
-
4
-
-
34548091662
-
-
Shen L, Zhang Y, Wang AH, et al. Synthesis and identification of [1, 2, 4] thiadiazole derivatives as a new series of potent and orally active dual agonists of peroxisome proliferators -activated receptors α and delta [J]. J Med Chem, 2007, 50: 3954-3963.
-
Shen L, Zhang Y, Wang AH, et al. Synthesis and identification of [1, 2, 4] thiadiazole derivatives as a new series of potent and orally active dual agonists of peroxisome proliferators -activated receptors α and delta [J]. J Med Chem, 2007, 50: 3954-3963.
-
-
-
-
5
-
-
3242766018
-
Substituted 3-imidazo [1, 2-a] pyridin-3-yl-4-(l, 2, 3, 4-tetrahydro-[l, 4] diazepino-[6, 7, 1-hi] indol-7-yl) pyrrole-2, 5-diones as highly selective and potent inhibitors of glycogen synthase kinase-3 [J]
-
Engler TA, Henry JR, Malhotra S, et al. Substituted 3-imidazo [1, 2-a] pyridin-3-yl-4-(l, 2, 3, 4-tetrahydro-[l, 4] diazepino-[6, 7, 1-hi] indol-7-yl) pyrrole-2, 5-diones as highly selective and potent inhibitors of glycogen synthase kinase-3 [J]. J Med Chem, 2004,47: 3934-3937.
-
(2004)
J Med Chem
, vol.47
, pp. 3934-3937
-
-
Engler, T.A.1
Henry, J.R.2
Malhotra, S.3
-
6
-
-
47349106390
-
Flavonol caffeoylglycosides as α-glucosidase inhibitors from spiraea cantoniensis flower [J]
-
Yoshida K, Hishida A, Iida O, et al. Flavonol caffeoylglycosides as α-glucosidase inhibitors from spiraea cantoniensis flower [J]. J Agric Food Chem, 2008, 56: 4367-4371.
-
(2008)
J Agric Food Chem
, vol.56
, pp. 4367-4371
-
-
Yoshida, K.1
Hishida, A.2
Iida, O.3
-
7
-
-
84884669745
-
Studies on selective PPARγ modulators antidiabetic agents in the treatment of type 2 diabetes [J]
-
Zhang XG, Li ZX, Zhang HJ, et al. Studies on selective PPARγ modulators antidiabetic agents in the treatment of type 2 diabetes [J]. Prog Pharm Sci, 2005, 29: 550-557.
-
(2005)
Prog Pharm Sci
, vol.29
, pp. 550-557
-
-
Zhang, X.G.1
Li, Z.X.2
Zhang, H.J.3
-
8
-
-
0027724063
-
Acarbose: An update of its pharmacology and therapeutic use in diabetes mellitus [J]
-
Balfour JA, McTavish D. Acarbose: an update of its pharmacology and therapeutic use in diabetes mellitus [J]. Drugs, 1993, 46: 1025-1054.
-
(1993)
Drugs
, vol.46
, pp. 1025-1054
-
-
Balfour, J.A.1
McTavish, D.2
-
9
-
-
0347131149
-
In vitro study of some medicinally important Mannich bases derived from antitubercular agent [J]
-
Joshi S, Khosla N, Tiwari P. In vitro study of some medicinally important Mannich bases derived from antitubercular agent [J]. Bioorg Med Chem Lett, 2004, 12: 571-576.
-
(2004)
Bioorg Med Chem Lett
, vol.12
, pp. 571-576
-
-
Joshi, S.1
Khosla, N.2
Tiwari, P.3
-
10
-
-
1642540579
-
Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: New pharmacological opportunities due to related binding site recognition [J]
-
Weber A, Casini A, Heine A, et al. Unexpected nanomolar inhibition of carbonic anhydrase by COX-2-selective celecoxib: new pharmacological opportunities due to related binding site recognition [J]. J Med Chem, 2004,47: 550-557.
-
(2004)
J Med Chem
, vol.47
, pp. 550-557
-
-
Weber, A.1
Casini, A.2
Heine, A.3
-
11
-
-
0013209248
-
Anticancer and antiviral sulfonamides [J]
-
Scozzafava A, Owa T, Mastrolorenzo A, et al. Anticancer and antiviral sulfonamides [J]. Curr Med Chem, 2003, 10: 925-953.
-
(2003)
Curr Med Chem
, vol.10
, pp. 925-953
-
-
Scozzafava, A.1
Owa, T.2
Mastrolorenzo, A.3
-
12
-
-
0001231790
-
Further advances in the chemistry of Mannich bases [J]
-
Tramontini M, Angiolini L. Further advances in the chemistry of Mannich bases [J]. Tetrahedron, 1990, 46: 1791-1837.
-
(1990)
Tetrahedron
, vol.46
, pp. 1791-1837
-
-
Tramontini, M.1
Angiolini, L.2
-
13
-
-
1842692952
-
Synthesis and anti-inflammatory and anticancer activities of 2-(E)-(un)substituted benzylidene cyclopentanones and their Mannich base hydrochlorides [J]
-
Chen HT, Jing YK, Ji ZZ, et al. Synthesis and anti-inflammatory and anticancer activities of 2-(E)-(un)substituted benzylidene cyclopentanones and their Mannich base hydrochlorides [J]. Acta Pharm Sin, 1991, 26: 183-192.
-
(1991)
Acta Pharm Sin
, vol.26
, pp. 183-192
-
-
Chen, H.T.1
Jing, Y.K.2
Ji, Z.Z.3
-
14
-
-
84884669356
-
-
Yang DC, Fan L, Liu HP, et al. A kind of new Mannich base compounds, their uses for the treatment and / or precaution against leukaemia: CN, 101381320 [P]. 2009-03-11.
-
Yang DC, Fan L, Liu HP, et al. A kind of new Mannich base compounds, their uses for the treatment and / or precaution against leukaemia: CN, 101381320 [P]. 2009-03-11.
-
-
-
-
15
-
-
24944587938
-
Synthesis of Mannich bases of some 2, 5-disubstituted 4-thiazolidinones and evaluation of their antimicrobial activities [J]
-
Altintas H, Ates Ö, Birteksöz S, et al. Synthesis of Mannich bases of some 2, 5-disubstituted 4-thiazolidinones and evaluation of their antimicrobial activities [J]. Turk J Chem, 2005, 29: 425-435.
-
(2005)
Turk J Chem
, vol.29
, pp. 425-435
-
-
Altintas, H.1
Ates, O.2
Birteksöz, S.3
-
16
-
-
43449101893
-
Discovery and biological characterization of a novel series of androgen receptor modulators [J]
-
Zhou C, Wu G, Feng Y, et al. Discovery and biological characterization of a novel series of androgen receptor modulators [J]. Br J Pharmaco, 2008, 154: 440-450.
-
(2008)
Br J Pharmaco
, vol.154
, pp. 440-450
-
-
Zhou, C.1
Wu, G.2
Feng, Y.3
-
17
-
-
62749195205
-
Synthesis and α-glucosidase inhibitory activity of N-(1, 5-diaryl-3-pentone-1-yl)-4-aminobenzoic acid [J]
-
Xu J, Yan JF, Fan L, et al. Synthesis and α-glucosidase inhibitory activity of N-(1, 5-diaryl-3-pentone-1-yl)-4-aminobenzoic acid [J]. Acta Pharm Sin, 2009, 44: 48-55.
-
(2009)
Acta Pharm Sin
, vol.44
, pp. 48-55
-
-
Xu, J.1
Yan, J.F.2
Fan, L.3
-
18
-
-
9644291520
-
Synthesis and in vitro study of novel Mannich bases as antibacterial agents [J]
-
Joshi S, Khosla N, Khare D, et al. Synthesis and in vitro study of novel Mannich bases as antibacterial agents [J]. Bioorg Med Chem Lett, 2005, 15: 221-226.
-
(2005)
Bioorg Med Chem Lett
, vol.15
, pp. 221-226
-
-
Joshi, S.1
Khosla, N.2
Khare, D.3
-
19
-
-
84884669198
-
The replacement reaction of β-carbonyl ether and primary amine [J]
-
Hua WT, Ning FQ. The replacement reaction of β-carbonyl ether and primary amine [J]. Chem Bull, 1991, 7: 27-28.
-
(1991)
Chem Bull
, vol.7
, pp. 27-28
-
-
Hua, W.T.1
Ning, F.Q.2
-
20
-
-
62749147482
-
Synthesis and antitumor activities of 2-(E)-(4-cyclo-pentyloxy-3-methyl-benzylidene) cyclopentanone arylamine Mannich bases [J]
-
Ma YZ, Yin LN, Liu XY, et al. Synthesis and antitumor activities of 2-(E)-(4-cyclo-pentyloxy-3-methyl-benzylidene) cyclopentanone arylamine Mannich bases [J]. Chin J Med Chem, 2006, 16: 144-149.
-
(2006)
Chin J Med Chem
, vol.16
, pp. 144-149
-
-
Ma, Y.Z.1
Yin, L.N.2
Liu, X.Y.3
-
21
-
-
76049095251
-
-
J Beijing Normal Univ Nat Sci Ed
-
Zhao G, Shi M, Xu XJ. The exchange reaction of N, N-bis (benzotriazolylmethyl) hydroxylamine or N, N-bis (benzimidazolylmethyl) hydroxylamine with aryletones [J]. J Beijing Normal Univ (Nat Sci Ed), 1997, 33:221-225.
-
(1997)
The exchange reaction of N, N-bis (benzotriazolylmethyl) hydroxylamine or N, N-bis (benzimidazolylmethyl) hydroxylamine with aryletones [J]
, vol.33
, pp. 221-225
-
-
Zhao, G.1
Shi, M.2
Xu, X.J.3
-
22
-
-
0001125869
-
Mannich-type reaction with trifluoromethylated N, O-hemiacetal: Facile preparation of β-amino-β-trifluoromethyl carbonyl compounds [J]
-
Takaya J, Kagoshima H, Akiyama T. Mannich-type reaction with trifluoromethylated N, O-hemiacetal: facile preparation of β-amino-β-trifluoromethyl carbonyl compounds [J]. Org Lett, 2000,2: 1577-1579.
-
(2000)
Org Lett
, vol.2
, pp. 1577-1579
-
-
Takaya, J.1
Kagoshima, H.2
Akiyama, T.3
-
24
-
-
0041565548
-
The Mannich reaction among p-methoxyacetophenone, benzaldehyde or p-methoxybenzadehyde and arylamines [J]
-
Chen HL, Zou JH. The Mannich reaction among p-methoxyacetophenone, benzaldehyde or p-methoxybenzadehyde and arylamines [J]. J Southwest Chin Normal Univ (Nat Sci) , 1999, 24: 190-195.
-
(1999)
J Southwest Chin Normal Univ (Nat Sci)
, vol.24
, pp. 190-195
-
-
Chen, H.L.1
Zou, J.H.2
-
25
-
-
76049106966
-
Synthesis and Preliminary Study on Biological Activities of New Pharmaceuticals for Treatment of Diabetes [D]
-
Liu HP. Design, Synthesis and Preliminary Study on Biological Activities of New Pharmaceuticals for Treatment of Diabetes [D]. ChongQing: Southwest University, 2008.
-
(2008)
ChongQing: Southwest University
-
-
Design, L.H.P.1
-
26
-
-
33847056248
-
5-catalyzed one-pot Mannich-type reaction: Three component synthesis of β-amino carbonyl compounds [J]
-
5-catalyzed one-pot Mannich-type reaction: three component synthesis of β-amino carbonyl compounds [J]. Tetrahedron Lett, 2007, 48: 2071-2073.
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 2071-2073
-
-
Wang, R.1
Li, B.G.2
Huang, T.K.3
-
28
-
-
33751190949
-
Mannich-type reactions in a colloidal solution formed by sodium tetrakis (3, 5-trifluoromethylphenyl)borate as a catalyst in water [J]
-
Chang CT, Liao BS, Liu ST. Mannich-type reactions in a colloidal solution formed by sodium tetrakis (3, 5-trifluoromethylphenyl)borate as a catalyst in water [J]. Tetrahedron Lett, 2006, 47: 9257-9259.
-
(2006)
Tetrahedron Lett
, vol.47
, pp. 9257-9259
-
-
Chang, C.T.1
Liao, B.S.2
Liu, S.T.3
-
29
-
-
0032518770
-
Novel one-pot Mannich-type reaction in water: Indium trichloride-catalyzed condensation of aldehydes, amines and silyl enol ethers for the synthesis of 3-amino ketones and esters [J]
-
Loh TP, Wei LL. Novel one-pot Mannich-type reaction in water: indium trichloride-catalyzed condensation of aldehydes, amines and silyl enol ethers for the synthesis of 3-amino ketones and esters [J]. Tetrahedron Lett, 1998, 39: 323-326.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 323-326
-
-
Loh, T.P.1
Wei, L.L.2
-
30
-
-
17144373290
-
Mannich-type reaction promoted by an ionic liquid [J]
-
Akiyama T, Suzuki A, Fuchibe K. Mannich-type reaction promoted by an ionic liquid [J]. Synlett, 2005: 1024-1026.
-
(2005)
Synlett
, pp. 1024-1026
-
-
Akiyama, T.1
Suzuki, A.2
Fuchibe, K.3
-
31
-
-
59049089913
-
Novel one-pot Cunanoparticles- catalyzed Mannich reaction [J]
-
Kidwai M, Mishra NK, Bansal V, et al. Novel one-pot Cunanoparticles- catalyzed Mannich reaction [J]. Tetrahedron Lett, 2009, 50: 1355-1358.
-
(2009)
Tetrahedron Lett
, vol.50
, pp. 1355-1358
-
-
Kidwai, M.1
Mishra, N.K.2
Bansal, V.3
-
32
-
-
62749137943
-
The Mannich reaction of 4-amino-benzoate with acetophenone and aromatic aldehydes [J]
-
Yang DC, Gu XY, Feng P. The Mannich reaction of 4-amino-benzoate with acetophenone and aromatic aldehydes [J]. J Southwest Chin Normal Univ (Nat Sci) , 1997, 22: 54-57.
-
(1997)
J Southwest Chin Normal Univ (Nat Sci)
, vol.22
, pp. 54-57
-
-
Yang, D.C.1
Gu, X.Y.2
Feng, P.3
-
33
-
-
62749134332
-
The Mannich reaction of 4-phenyl-2-butanone with aromatic aldehydes and acromatic amines [J]
-
Yang DC. The Mannich reaction of 4-phenyl-2-butanone with aromatic aldehydes and acromatic amines [J]. J Southwest Chin Normal Univ (Nat Sci) , 1996, 21: 354-359.
-
(1996)
J Southwest Chin Normal Univ (Nat Sci)
, vol.21
, pp. 354-359
-
-
Yang, D.C.1
-
34
-
-
28844488227
-
Design, virtual screening and synthesis of PPAR agonists [J]
-
Feng J, Guo YS, Lu Y, et al. Design, virtual screening and synthesis of PPAR agonists [J]. Acta Chim Sin, 2004, 62: 1544-1550.
-
(2004)
Acta Chim Sin
, vol.62
, pp. 1544-1550
-
-
Feng, J.1
Guo, Y.S.2
Lu, Y.3
|