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16
Angiogenesis
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19
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4
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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 'P'
or product name starting with:
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H406195
PD318088
featured
PD318088 is a non-ATP competitive allosteric MEK1/2 inhibitor, binds simultaneously with ATP in a re…
H406196
PD184161
featured
PD184161 is an orally-active MEK inhibitor. PD184161 inhibited MEK activity (IC50 = 10-100 nM) in a …
H406175
PD180970
featured
PD180970 is a novel Bcr-Abl inhbiitor. PD180970 inhibited in vivo tyrosine phosphorylation of p210Bc…
H406164
PD-173955
new
featured
PD-173955 is a src tyrosine kinase inhibitor. PD173955 inhibited Bcr-Abl-dependent cell growth. PD17…
H406350
PD173074
featured
PD173074 is a small-molecule FGFR3-selective tyrosine kinase inhibitor (TKI), as a therapeutic modal…
H510236
PD-169316
featured
PD-169316 is a selective inhibitor of p38 MAPK. It inhibits p38 MAPK with an IC50 of 89 nM. PD169316…
H406105
PD-168393
featured
PD-168393 is a potent, cell-permeable, irreversible, ATP-competitive and selective inhibitor of EGF …
H406173
PD166326
featured
PD166326 is one of the most potent members of the pyridopyrimidine class of protein tyrosine kinase …
H406345
PD0166285
featured
PD0166285 is a potent Wee1 inhibitor and Chk1 inhibitor with activity at nanomolar concentrations. T…
H406363
PD-128763
PD-128763 is a selective inhibitor of poly(ADP-ribose) polymerase. PD-128763 has an IC50 value again…
H406313
PC-046
PC-046 is a potent tubulin-binding agent, which was originally identified for development based on s…
H203181
Pilaralisib
featured
Pilaralisib, also known as XL147, is a Class 1 PI3K kinase family inhibitor with potential antineopl…
H206217
PF-04929113 free base
featured
PF-04929113, also known as SNX-5422; is a synthetic prodrug targeting the human heat-shock protein 9…
H202370
Pyroxamide
featured
Pyroxamide is a synthetic derivative of hydroxamic acid with antineoplastic properties, Pyroxamide i…
H206201
Pyrotinib
Pyrotinibm, also known as SHR-1258, is an orally bioavailable, dual kinase inhibitor of the epiderm…
H202340
PX-12
PX-12 is an irreversible inhibitor of Trx-1 currently in clinical development as an antitumor agent.…
H205745
PWT33597 mesylate
PWT33597, also known as VDC-597, is an orally bioavailable dual inhibitor of phosphatidylinositide …
H205602
PV-10 sodium
featured
PV-10, also known as Acid Red 94 and Rose bengal disodium, an iodinated fluorescein derivative, with…
H205599
PTC299
PTC299, a VEGF inhibitor, is an orally bioavailable, small molecule inhibitor of vascular endotheli…
H202334
PRLX-93936
featured
PRLX 93936 is a structural analogue of erastin with potential antineoplastic activity. Erastin analo…
H202332
Prinomastat
featured
Prinomastat, also known as AG3340 amd KBR-9896, is a synthetic hydroxamic acid derivative with poten…
H205626
Pracinostat
featured
Pracinostat, also known as SB939, is an orally bioavailable, small-molecule histone deacetylase (HD…
H202331
PR-104
featured
PR-104 is a non-toxic, small-molecule, hypoxia-activated, 3,5-dinitrobenzamide nitrogen mustard pre-…
H202330
PPI-2458
PPI-2458 is a synthetic derivative of fumagillin with antineoplastic and cytotoxic properties. PPI-2…
H206168
PLX8394 (removed)
PLX8394 is an orally bioavailable inhibitor of serine/threonine-protein kinase B-raf (BRAF) protein …
H206074
PLX7486
PLX7486 is a selective inhibitor of the receptor tyrosine kinases colony-stimulating factor-1 recept…
H200150
Plitidepsin
new
featured
Plitidepsin is a cyclic depsipeptide isolated from the marine tunicate Aplidium albicans. Plitidepsi…
H202270
Plevitrexed
Plevitrexed is an orally bioavailable, small molecule, non-polyglutamatable, antifolate quinazoline …
H206073
PL225B
PL225B is an orally bioavailable inhibitor of the insulin-like growth factor 1 receptor (IGF-1R) wit…
H205989
PKI-179
featured
PKI-179 is a second generation, small-molecule mimetic of ATP that targets the mammalian target of r…
H205928
Pivanex
Pivanex, also known as AN-9, is a histone deacetylase inhibitor analog of butyric acid that causes a…
H205784
Piroxantrone
Piroxantrone, also known as CI942; PD111815, is a n anthrapyrazole antineoplastic antibiotic. Pirox…
H202240
Pipendoxifene
Pipendoxifene, also known as ERA-923, is a new antiestrogen with potential anticancer activity. ERA-…
H206030
Pimonidazole
featured
Pimonidazole, also known as Ro 03-8799 and PD 126675, is a nitroimidazole drug with hypoxic selectiv…
H202238
PIK-75
new
featured
PIK-75 was developed as part of a PI 3-kinase drug discovery program. PIK75 attenuates insulin stimu…
H202230
Picoplatin
featured
Picoplatin is a new generation organic platinum analog with an extended spectrum of antineoplastic a…
H202235
PI-103
new
featured
PI-103 is a potent, cell-permeable, ATP-competitive inhibitor of phosphatidylinositol 3-kinase (PI3K…
H206022
PH-797804
new
featured
PH-797804 is a potent and selectiove inhibitor of p38 mitogen-activated protein (MAP) kinase. PH-797…
H206024
PHA-793887
featured
PHA-793887 is an inhibitor of multiple cyclin dependent kinases (CDK) with activity against CDK2, CD…
H202231
PHA-665752
featured
PHA665752 is a potent and selective inhibitor of c-Met/HGF/SF (IC50 values are 9, 68, 200, 1400, 300…
H206166
PFK-158
new
featured
PFK-158, also known as ACT-PFK-158, is an inhibitor of 6-phosphofructo-2-kinase/fructose-2,6-bisphos…
H202227
PF-477736 HCl
PF-00477736, also known as PF-477736, is a potent CHK1 inhibitor with potential chemopotentiation ac…
H202226
PF-04691502
new
featured
PF-04691502 is a PI3K/mTOR kinase inhibitor , is also an agent targeting the phosphatidylinositol 3 …
H205987
PF-03814735
featured
PF-03814735 is an orally bioavailable, ATP-competitive, reversible small-molecule Aurora kinase inhi…
H205916
PF-00337210
PF-00337210 is an orally available ATP-competitive inhibitor of the vascular endothelial growth fact…
H205986
Peretinoin
featured
Peretinoin, also known as NIK-333 , orally available, acyclic retinoid with potential antineoplastic…
H202200
Pelitrexol
featured
Pelitrexol is a GARFT inhibitor, and is also a water soluble antifolate with anti-proliferative acti…
H202190
Pelitinib
featured
Pelitinib, also known as EKB569 and WAY-172569, is a 3-cyanoquinoline pan-ErbB tyrosine kinase inhi…
H206125
Peficitinib free base
featured
Peficitinib, also known as ASP015K and JNJ-54781532, is a novel potent JAK inhibitor, which demonstr…
H202174
PD-153035 free base
featured
PD153035 is a ATP-competitive EGFR inhibitor with an IC50 and Ki of 25 and 6 pM. PD153035 effectivel…
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