AAAAAA
Results:
1-14
|
Results: 14
Authors:
Fernandez-Forner, D
Casals, G
Navarro, E
Ryder, H
Albericio, F
Citation: D. Fernandez-forner et al., Solid-phase synthesis of 4-aminopiperidine analogues using the Alloc protecting group: an investigation of Alloc removal from secondary amines, TETRAHEDR L, 42(27), 2001, pp. 4471-4474
Authors:
Crespo, MI
Gracia, J
Puig, C
Vega, A
Bou, J
Beleta, J
Domenech, T
Ryder, H
Segarra, V
Palacios, JM
Citation: Mi. Crespo et al., Synthesis and biological evaluation of 2,5-dihydropyrazolo[4,3-c]quinolin-3-ones, a novel series of PDE 4 inhibitors with low emetic potential and antiasthmatic properties, BIOORG MED, 10(23), 2000, pp. 2661-2664
Authors:
Garcia, M
Serra, A
Rubiralta, M
Diez, A
Segarra, V
Lozoya, E
Ryder, H
Palacios, JM
Citation: M. Garcia et al., Efficient method for the preparation of (S)-5-hydroxynorvaline, TETRAHEDR-A, 11(4), 2000, pp. 991-994
Authors:
Martinez, A
Castro, A
Gil, C
Miralpeix, M
Segarra, V
Domenech, T
Beleta, J
Palacios, JM
Ryder, H
Miro, X
Bonet, C
Casacuberta, JM
Azorin, F
Pina, B
Puigdomenech, P
Citation: A. Martinez et al., Benzyl derivatives of 2,1,3-benzo- and benzothieno[3,2-a]thiadiazine 2,2-dioxides: First phosphodiesterase 7 inhibitors, J MED CHEM, 43(4), 2000, pp. 683-689
Authors:
Puig, C
Crespo, MI
Godessart, N
Feixas, J
Ibarzo, J
Jimenez, JM
Soca, L
Cardelus, I
Heredia, A
Miralpeix, M
Puig, J
Beleta, J
Huerta, JM
Lopez, M
Segarra, V
Ryder, H
Palacios, JM
Citation: C. Puig et al., Synthesis and biological evaluation of 3,4-diaryloxazolones: A new class of orally active cyclooxygenase-2 inhibitors, J MED CHEM, 43(2), 2000, pp. 214-223
Authors:
Bloch, F
Ryder, H
Citation: F. Bloch et H. Ryder, Two-sided search, marriages, and matchmakers, INT ECON R, 41(1), 2000, pp. 93-115
Authors:
Santamaria, LF
Torres, R
Ryder, H
Beleta, J
Palacios, JM
Citation: Lf. Santamaria et al., Prostaglandin E2 inhibits SEB-mediated induction of the cutaneous lymphocyte-associated antigen, INT A AL IM, 118(2-4), 1999, pp. 351-352
Authors:
Bonjoch, J
Diaba, F
Puigbo, G
Sole, D
Segarra, V
Santamaria, L
Beleta, J
Ryder, H
Palacios, JM
Citation: J. Bonjoch et al., Synthesis and biological evaluation of a conformationally free seco-analogue of the immunosuppressant FR901483, BIO MED CH, 7(12), 1999, pp. 2891-2897
Authors:
Roe, M
Folkes, A
Ashworth, P
Brumwell, J
Chima, L
Hunjan, S
Pretswell, I
Dangerfield, W
Ryder, H
Charlton, P
Citation: M. Roe et al., Reversal of P-glycoprotein mediated multidrug resistance by novel anthranilamide derivatives, BIOORG MED, 9(4), 1999, pp. 595-600
Authors:
Donaldson, MJ
Skoumas, V
Watson, M
Ashworth, PA
Ryder, H
Moore, M
Coombes, RC
Citation: Mj. Donaldson et al., XR 3054, structurally related to limonene, is a novel inhibitor of farnesyl protein transferase, EUR J CANC, 35(6), 1999, pp. 1014-1019
Authors:
Segarra, V
Lopez, M
Ryder, H
Palacios, JM
Citation: V. Segarra et al., Prediction of drug permeability based on Grid calculations, QSAR, 18(5), 1999, pp. 474-481
Authors:
Segarra, V
Lopez, M
Ryder, H
Palacios, JM
Roberts, DJ
Citation: V. Segarra et al., Computer-assisted comparison of the structural and electronic dispositionsof ebastine and terfenadine, DRUG SAFETY, 21, 1999, pp. 45-61
Authors:
Santamaria, LF
Torres, R
Gimenez-Arnau, AM
Gimenez-Camarasa, JM
Ryder, H
Palacios, JM
Beleta, J
Citation: Lf. Santamaria et al., Rolipram inhibits staphylococcal enterotoxin B-mediated induction of the human skin-homing receptor on T lymphocytes, J INVES DER, 113(1), 1999, pp. 82-86
Authors:
Mistry, P
Plumb, J
Eccles, S
Watson, S
Dale, I
Ryder, H
Box, G
Charlton, P
Templeton, D
Bevan, PB
Citation: P. Mistry et al., In vivo efficacy of XR9051, a potent modulator of P-glycoprotein mediated multidrug resistance, BR J CANC, 79(11-12), 1999, pp. 1672-1678
Risultati:
1-14
|