sb-431542

346  

Sb 431542
20-abx182645
  • EUR 1497.00
  • EUR 370.00
  • 100 mg
  • 10 mg
SB 431542
A8249-10 10 mg
EUR 139
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.
SB 431542
A8249-5.1 10 mM (in 1mL DMSO)
EUR 166
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.
SB 431542
A8249-50 50 mg
EUR 431
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.
SB 431542
A8249-S Evaluation Sample
EUR 81
Description: SB431542 is a selective ATP-competitive inhibitor of ALK5 (activin receptor-like kinase 5) with an IC50 value of 94 nM [1].SB431542 showed most potent efficacy among the series of hits screened out.
SB-431542
1674-1
EUR 169
SB-431542
1674-5
EUR 446
SB 431542, > 98%
BC261-005 5 mg
EUR 232
SB 431542, > 98%
BC261-010 10 mg
EUR 313
SB 431542, > 98%
BC261-050 50 mg
EUR 928
EZSolution? SB-431542
1872-1
EUR 158
EZSolution? SB-431542, Sterile-Filtered
1992-1
EUR 272
SB-423562
HY-15105 10mg
EUR 11800
SB-269970
HY-15370 50mg
EUR 712
SB 415286
HY-15438 50mg
EUR 608
SB-222200
HY-15722 10mg
EUR 229
SB 204990
HY-16450 10mM/1mL
EUR 277
SB 242235
HY-18306 100mg
EUR 1703
SB-616234A
HY-19477 10mg
EUR 13535
SB-265610
HY-50688 10mM/1mL
EUR 1502
SB-408124
HY-70068 10mM/1mL
EUR 128
SB-705498
HY-10633 100mg
EUR 1496
SB-657510
HY-10656 10mg
EUR 946
SB-649868
HY-10806 100mg
EUR 4114
SB-277011
HY-10847 50mg
EUR 1096
SB-334867
HY-10895 50mg
EUR 491
SB-674042
HY-10898 10mM/1mL
EUR 200
SB-590885
HY-10966 10mM/1mL
EUR 255
SB 239063
HY-11068 10mM/1mL
EUR 143
SB 216763
HY-12012 100mg
EUR 546
SB 525334
HY-12043 10mg
EUR 173
SB-743921
HY-12069 100mg
EUR 1359
SB-366791
HY-12245 10mg
EUR 147
SB-3CT
HY-12354 50mg
EUR 567
SB 242084
HY-13409 50mg
EUR 807
SB-505124
HY-13521 50mg
EUR 628
SB-568849
HY-100308 10mg
EUR 2809
SB 203580
HY-10256 100mg
EUR 215
SB 202190
HY-10295 200mg
EUR 277
SB 258719
HY-U00443 10mg
EUR 371
SB 743921
E1KS2182 10mg
EUR 1504
SB 216763
E1KS1075 5 mg
EUR 206
SB 203580
E1KS1076 25 mg
EUR 284
SB 202190
E1KS1077 25 mg
EUR 284
SB 525334
E1KS1476 5mg
EUR 325
SB-408124
E1KS1545 5mg
EUR 325
SB 202190
GK2422-1MG 1 mg
EUR 106
SB 202190
GK2422-25MG 25 mg
EUR 424
SB 202190
GK2422-5MG 5 mg
EUR 160
SB 203580
GK9716-1MG 1 mg
EUR 112
SB 203580
GK9716-25MG 25 mg
EUR 401
SB 203580
GK9716-5MG 5 mg
EUR 181
SB-366791
GL6242-5MG 5 mg
EUR 131
SB-366791
GL6242-25MG 25 mg
EUR 321
SB 216763
GL9739-25MG 25 mg
EUR 269
SB-366791
20-abx076632
  • EUR 314.00
  • EUR 857.00
  • 10 mg
  • 50 mg
SB 204741
B6708-10 10 mg
EUR 302
SB 204741
B6708-50 50 mg
EUR 1114
SB 228357
B6709-10 10 mg
EUR 366
SB 228357
B6709-50 50 mg
EUR 1379
SB 218795
B6710-10 10 mg
EUR 383
SB 218795
B6710-50 50 mg
EUR 1455
SB 221284
B6713-10 10 mg
EUR 324
SB 221284
B6713-50 50 mg
EUR 1211
SB 205384
B6770-10 10 mg
EUR 366
Description: SB-205384 is a selective and positive GABAA receptor modulator with EC50 values of 280, 695 and 730 nM on ?6, ?3 and ?5-subunit-containing receptors, respectively [1].
SB 205384
B6770-50 50 mg
EUR 1379
Description: SB-205384 is a selective and positive GABAA receptor modulator with EC50 values of 280, 695 and 730 nM on ?6, ?3 and ?5-subunit-containing receptors, respectively [1].
SB 366791
B6804-10 10 mg
EUR 239
SB 366791
B6804-5.1 10 mM (in 1mL DMSO)
EUR 142
SB 366791
B6804-50 50 mg
EUR 853
SB 218078
C3012-1 1 mg
EUR 209
Description: Targets:Chk1, cdc2 and PKCIC50:15, 250 and 1000 nM for Chk1, cdc2 and PKC respectivelySB 218078 is a potent inhibitor of checkpoint kinase 1, with the IC50 values of 15, 250 and 1000 nM for Chk1, cdc2 and PKC, respectively.
SB-3CT
B4792-100 100 mg
EUR 827
Description: SB-3CT is a potent and selective inhibitor of gelatinases with Ki values of 13.9 and 600 nM for MMP-2 and MMP-9, respectively. Gelatinases A (MMP-2) and B (MMP-9) belong to matrix metalloproteinases family and are involved in tumor metastasis and angiogenesis by hydrolyzing extracellular matrix.
SB-3CT
B4792-25 25 mg
EUR 444
Description: SB-3CT is a potent and selective inhibitor of gelatinases with Ki values of 13.9 and 600 nM for MMP-2 and MMP-9, respectively. Gelatinases A (MMP-2) and B (MMP-9) belong to matrix metalloproteinases family and are involved in tumor metastasis and angiogenesis by hydrolyzing extracellular matrix.
SB-3CT
B4792-5 5 mg
EUR 200
Description: SB-3CT is a potent and selective inhibitor of gelatinases with Ki values of 13.9 and 600 nM for MMP-2 and MMP-9, respectively. Gelatinases A (MMP-2) and B (MMP-9) belong to matrix metalloproteinases family and are involved in tumor metastasis and angiogenesis by hydrolyzing extracellular matrix.
SB 706504
B4937-10 10 mg
EUR 373
SB 706504
B4937-50 50 mg
EUR 1413
SB 204070
B5105-10 10 mg
EUR 405
SB 265610
B5333-1 1 mg
EUR 160
Description: SB 265610 is a potent CXCR2 antagonist that inhibits CINC-1-mediated Ca2+ mobilization with IC50 value of 3.4nM [1] [2]. CXCR2 is an integral membrane protein that specifically binds and responds to cytokines of the CXC chemokine family.
SB 265610
B5333-10 10 mg
EUR 303
Description: SB 265610 is a potent CXCR2 antagonist that inhibits CINC-1-mediated Ca2+ mobilization with IC50 value of 3.4nM [1] [2]. CXCR2 is an integral membrane protein that specifically binds and responds to cytokines of the CXC chemokine family.
SB 265610
B5333-5 5 mg
EUR 196
Description: SB 265610 is a potent CXCR2 antagonist that inhibits CINC-1-mediated Ca2+ mobilization with IC50 value of 3.4nM [1] [2]. CXCR2 is an integral membrane protein that specifically binds and responds to cytokines of the CXC chemokine family.
SB 242084
B5348-10 10 mg
EUR 267
SB 242084
B5348-50 50 mg
EUR 1044
SB 328437
B5467-10 10 mg
EUR 334
SB 328437
B5467-50 50 mg
EUR 1243
SB 297006
B5542-10 10 mg
EUR 224
SB 297006
B5542-25 25 mg
EUR 441