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16
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19
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10
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20
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17
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2
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Products starting with 'B'
or product name starting with:
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H401810
Bemcentinib
featured
Bemcentinib, also known as BGB-324 or R428, is a selective small molecule inhibitor of Axl kinase, w…
H406243
BTB-1
featured
BTB-1 is a novel small molecule inhibitor of the mitotic motor protein Kif18A, which was identified …
H406453
BSc2118
BSc2118 is a potent proteasome inhibitor. BSc2118 shows significant antimyeloma activity and may be …
H406179
BS-181 HCl
featured
BS-181 is a highly selective CDK inhibitor for CDK7 with an IC(50) of 21 nmol/L. Testing of other CD…
H401156
BRN-103
BRN-103 was found to suppress the VEGF-induced phosphorylation of VEGF receptor 2 (VEGR2) and the ac…
H406339
BPR1K653
BPR1K653 is a potent Aurora kinase inhibitor with potential anticancder activity. BPR1K653 specifica…
H406488
BPR1J-340
BPR1J-340 is a potent and selective FLT3 inhibitor with potential anticancer activity. BPR1J-340 was…
H406523
BP-1-102
featured
BP-1-102 is a potent, orally bioavailable and selective STAT3 inhibitor. BP-1-102 binds Stat3 with a…
H406506
BMS-645737
BMS-645737 is an inhibitor of vascular endothelial growth factor (VEGF) receptor-2 and fibroblast gr…
H406543
BMS-593214
BMS-593214 is an active-site, direct FVIIa inhibitor. BMS-593214 displayed direct, competitive inhib…
H406374
BMS-566419
featured
BMS-566419 is a novel chemically synthesized IMPDH inhibitor. The in vitro inhibitory activity of BM…
H406235
BMS-554417
BMS-554417 is a novel inhibitor of IGF-IR, which inhibits IGF-IR and insulin receptor kinase activit…
H406370
BMS-433796
BMS-433796 is a gamma-secretase inhibitor. BMS-433796 was identified with an acceptable pharmacodyna…
H406373
BMS-337197
BMS-337197 is a a potent inhibitor of IMPDH with potential anticancer activity.
H406234
BMS-317180
BMS-317180 is a potent, novel, orally effective growth hormone secretagogue (GHS) that shows an exce…
H401152
BMS-265246
featured
BMS-265246 is a potent CDK1/CDK2 selective inhibitor [(CDK1/cycB IC(50)=6 nM, CDK2/cycE IC(50)=9 nM)…
H406465
BMS-186511
BMS-186511 is a Farnesyltransferase (FT) inhibitor with potential anticancer activity. BMS-186511 is…
H406472
BML-258 HCl
BML-258 HCl was removed and discontinued.
H406178
BMI-1026
BMI-1026 is a potent cdk inhibitor with potential anticancer activity. BMI-1026 induced a strong cel…
H406417
BIM-46068
BIM-46068 is a potent and specific inhibitor of human farnesyltransferase. In regard to a panel of c…
H406464
BIM-46050
BIM-46050 is a potent and specific inhibitor of human farnesyltransferase. BIM-46050 is free acidic …
H406519
BIBR1532
featured
BIBR1532 is a selective telomerase inhibitor. BIBR1132 is highly selective for inhibition of telomer…
H406307
BI-4834
BI-4834 is a potent and selective Polo-like kinase 1 (PLK1) inhibitor. BI-4834 is also analogue (or …
H406369
BGP-15 HCl
new
featured
BGP-15 is a novel poly(ADP-ribose) polymerase inhibitor - protects against nephrotoxicity of cisplat…
H406437
Burapitant
Burapitant, also known as SSR 240600, is a potent and selective NK1 receptor antagonist. SSR240600 i…
H406436
Befetupitant
Befetupitant, also known as Ro 67-5930, is a potent and selective NK1 receptor antagonist. Befetupit…
H406223
BE-16627B
BE-16627B is a novel metalloproteinase (MP) inhibitor isolated from Streptomyces sp. BE16627B select…
H406177
BAY 61-3606
featured
BAY 61-3606 is a potent (Ki = 7.5 nM) and selective inhibitor of Syk kinase. BAY 61-3606 inhibited n…
H406452
b-AP15
new
featured
b-AP15 is a novel inhibitor of proteasome deubiquitination. b-AP15 displays antitumor activity in se…
H206146
Bimiralisib free base
new
featured
Bimiralisib, also known as PQR309, is an orally bioavailable pan inhibitor of phosphoinositide-3-ki…
H205864
Balixafortide TFA salt
featured
Balixafortide, also known as POL6326, is an orally bioavailable inhibitor of CXC chemokine receptor…
H205563
Briciclib
featured
Briciclib, also known as ON 013105 or ON 014185, is a benzyl styryl sulfone analog, and a disodium p…
H201922
Balamapimod (MKI-833)
Balamapimod, also known as MKI-822, is a Ras/Raf/MEK inhibitor. Balamapimod, may be potentially use…
H205531
Binimetinib (MEK-162)
featured
Binimetinib, also known as MEK162 (ARRY-162), is an oral, highly selective MEK inhibitor. In preclin…
H200584
BTZ043
featured
BTZ043 is a decaprenylphosphoryl-β-D-ribose 2'-epimerase (DprE1) inhibitor acting as a new antimycob…
H200580
Brostallicin HCl
Brostallicin is a synthetic, alpha-bromoacrylic, second-generation minor groove binder (MGB), relate…
H200570
Brivanib alaninate
featured
Brivanib alaninate is the alaninate ester of a vascular endothelial growth factor receptor 2 (VEGFR2…
H200569
Brivanib
featured
Brivanib is the hydrolyzed form of Brivanib alaninate, which is a vascular endothelial growth factor…
H205953
Brequinar
featured
Brequinar is a dihydroorotate dehydrogenase inhibitor (DHODH inhibitor) with antineoplastic propert…
H200561
BQS-481
BQS-481 is a bioactive chemical.
H205749
BNC105P
BNC105P is a benzofuran-based vascular disrupting agent (VDA) prodrug with potential anti-vascular a…
H204760
BNC-105
new
featured
BNC105 is a novel compound being developed by Bionomics as a Vascular Disrupting Agent (VDA) for tre…
H205827
BMS-906024
featured
BMS-906024 is a novel, potent Notch receptor inhibitor . Cancers have a tendency to relapse or to be…
H205767
BMS-911543
featured
BMS-911543 is an orally available small molecule targeting a subset of Janus-associated kinase (JAK)…
H206106
BMS-794833
featured
BMS-794833 is a potent ATP competitive inhibitor of Met/VEGFR2 with IC50 of 1.7 nM/15 nM. BMS-794833…
H200534
BMS-754807
featured
BMS-754807 is an orally bioavailable antagonist of human insulin-like growth factor type I receptor …
H200533
BMS-690514
BMS-690514 is a potent inhibitor of human epidermal growth factor receptor (HER) 1 (EGFR), 2, and 4,…
H200531
BMS-641988
BMS-641988 is a nonsteroidal androgen receptor (AR) antagonist with anti-androgenic and potential an…
H200521
BMS-536924
featured
BMS-536924 is a potent small molecule inhibitor of IGF-IR, which shows antitumor activity in multipl…
H200520
BMS-275183
BMS-275183 is an oral C-4 methyl carbonate analogue of paclitaxel that has the same mechanism of act…
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