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16
Angiogenesis
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BTK
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test3
demo333
8
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8
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12
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19
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4
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10
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20
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5
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17
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16
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8
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4
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2
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2
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Products starting with 'S'
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H406405
SU11606
SU11606 is a potent c-MET inhibitor with potential anticancer activity.
H402150
SU11274
featured
SU11274 is a selective Met tyrosine kinase inhibitor with IC50 of 10 nM. SU11274 increases tumorigen…
H406406
SU11271
SU11271 is a potent c-MET inhibitor with potential anticancer activity.
H406731
SU6656
featured
SU6656 is a potent and selective dual inhibitor of Src family kinases and Aurora kinase. SU6656 modu…
H406473
SU5402
featured
SU5402 is a potent and selective vascular endothelial growth factor receptor (VEGFR) and fibroblast …
H406474
SU4984
new
featured
SU4984 is a cell-permeable, reversible, and ATP-competitive inhibitor of the tyrosine kinase activit…
H406526
STX-0119
featured
STX-0119 is a potent STAT3 inhibitor. STX-0119 is an efficient therapeutic to overcome TMZ resistanc…
H406525
STA-21
featured
STA-21 is a promising STAT-3 inhibitor that reciprocally regulates Th17 and Treg cells, inhibits ost…
H406585
ST7612AA1
ST7612AA1 is a new and potent HDCA inhibitor with potential anticancer activity. ST7612AA1 showed an…
H406480
SRT2183
SRT2183 is a Sirt1 activator, currently being developed by Sirtris Pharmaceuticals. SRT2183 has simi…
H402110
SRT-1720 free base
featured
SRT-1720, also known as CAY10559 and is a drug developed by Sirtris Pharmaceuticals intended as a s…
H406236
SP-600125
featured
SP-600125 is a specific JNK inhibitor. SP-600125 kills p53-deficient cells more efficiently than the…
H406226
SNX-7081
NX-7081 is a novel small molecule inhibitor of Hsp90, which blocks components of inflammation, inclu…
H406117
SN-28049
SN-28049 SN is a DNA intercalating drug that binds selectively to GC-rich DNA and shows curative act…
H406186
SN-23862
SN-23862 is a bioreductive agent with potential anticancer activity. SN-23862 is analogue of CB-1954…
H406468
SLR080811 HCl
SLR080811 is a SphK inhibitor. Sphingosine-1-phosphate (S1P) is a ubiquitous, endogenous small molec…
H401920
SL0101
featured
SL0101 is a highly specific RSK inhibitor. SL0101 showed improved in vitro biological stability whil…
H401980
SKLB1002
featured
SKLB1002 is a new potent VEGFR2 inhibitor, which could significantly inhibit HUVEC proliferation, mi…
H401970
SKLB610
featured
SKLB610 is a VEGFR inhibitor that potently suppresses human tumor angiogenesis. SKLB610 inhibited an…
H401950
SK1071
SK1071 is a novel migrastatin analogs, which demonstrated improved performance over migrastatin, wit…
H406130
Sirtinol
featured
Sirtinol is a SIRT inhibitor. Sirtinol significantly increased the acetylation of p53, which has bee…
H401915
SIM010603
SIM010603 is a structurally novel, oral, multi-targeted receptor tyrosine kinase inhibitor. SIM01060…
H406159
SH-5
SH-5 is a novel potent inhibitor of SARS-CoV-2 3CLpro.
H406442
SGC-CBP30
featured
SGC-CBP30 is a potent and selective inhibitor of CREBBP (CBP) and EP300; which are general transcrip…
H406721
SG2057
SG2057 is a pentyldioxy linked PBD dimer which binds sequence selectively in the minor groove of DNA…
H406446
Scytonemin
Scytonemin is a biological pigment synthesized by many strains of cyanobacteria, including Calothrix…
H406167
SCH1473759 free base
SCH-1473759 is a potent and selective Aurora A/B inhibitor with IC50 sub-nanomolar. SCH 1473759 was…
H406225
SC-44463
SC-44463 is an MMP inhibitor, also a collagenase inhibitor , and HDAC inhibitor.
H406445
SBE-13 HCl
new
featured
SBE-13 is a selective inhibitor of PLK1 (IC50 values are 200 pM, 875 nM and 66 μ M for PLK1, PLK3 an…
H406109
SB-590885
featured
SB-590885 is a novel triarylimidazole that selectively inhibits Raf kinases with more potency toward…
H406415
SB525334
featured
SB525334 is a potent and selective inhibitor of the transforming growth factor-beta1 (TGF-beta1) rec…
H406135
SB505124
featured
SB505124: SB505124 is a selective inhibitor of transforming growth factor-β type I receptor (ALK5, …
H406337
SB239063
featured
SB239063 is a potent p38MAPK inhibitor. SB 239063 had an IC(50) of 44 nM for inhibition of recombina…
H406348
SB-218078
featured
SB-218078 is a potent and selective indolocarbazole chk1 inhibitor.
H401903
SB-216763
featured
SB-216763 is a glycogen synthase kinase-3 (GSK3) inhibitor, which can maintain mouse embryonic stem …
H406594
SAR156497
SAR156497 is an exquisitely selective Aurora A, B, and C inhibitor with in vitro and in vivo efficac…
H406347
SAR-020106
featured
SAR-020106 is an ATP-competitive, potent, and selective CHK1 inhibitor with an IC(50) of 13.3 nmol/L…
H406545
Salinomycin
new
featured
Salinomycin is an antibacterial and coccidiostat ionophore agent. Salinomycin suppresses T24 cells b…
H406140
sinbaglustat (OGT2378)
sinbaglustat (OGT2378) is a GCS inhibitor (Glucosyl Ceramide Synthase Inhibitor) with potential ant…
H206206
Seviteronel
Seviteronel, also known as VT-464 and INO-464, is an orally available non-steroidal, lyase-selective…
H206080
Savolitinib
featured
Savolitinib, also known as Volitinib, AZD6094 or HMPL-504, is an orally bioavailable inhibitor of th…
H206091
Supinoxin
featured
Supinoxin, also known as RX-5902, is orally bioavailable small molecule inhibitor of phosphorylated-…
H205995
Sulofenur
Sulofenur is a diarylsulfonylurea with potential antineoplastic activity. Sulofenur's antineoplastic…
H202713
Sulforaphane
featured
Sulforaphane, also known as BroccoPhane; Sulphoraphane; Detoxophane, is a naturally-occurring phyt…
H206205
Sulfatinib
new
featured
Sulfatinib, also known as surufatinib, is an orally bioavailable, small molecule inhibitor of vascul…
H202708
Stannsoporfin
featured
Stannsoporfin ( SnMP), also known as Tin mesoporphyrin, is a porphyrin-Sn(IV) complex, is also a pot…
H206189
STA-9584
STA-9584 is a potent vascular disrupting agent, which exhibits potent antitumor activity by selectiv…
H202715
STA-1474
STA-1474 is a water soluble prodrug of ganetespib (formerly STA-9090). STA-1474 will metabolized to …
H202702
SSR97225
SSR97225 is Tubulin-binding agent with potential antineoplastic activity. SSR97225 binds to tubulin,…
H205881
SRT2104
featured
SRT2104, also known as GSK2245840, is a novel, first-in-class, highly selective small molecule acti…
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