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Angiogenesis
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19
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10
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20
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or product name starting with:
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H510228
VX-166
VX-166 is a broad caspase inhibitor, which can be used as a novel potential treatment for sepsis. VX…
H510229
Nivocasan
Nivocasan, also known as GS-9450 and LB-84451, a novel caspase-inhibitor has demonstrated hepatoprot…
H511221
IDN-1965
IDN-1965 is a potent, broad-spectrum, irreversible caspase inhibitor. IDN-1965 is markedly effective…
H510230
Emricasan
featured
Emricasan, also known as IDN 6556 and PF 03491390, is a first-in-class caspase inhibitor in clinical…
H406462
Y11
featured
Y11 is a small molecule inhibitor targeting Y397 site of FAK. Y11 significantly and specifically dec…
H406194
WP-1034
WP-1034 is a novel Jak-Stat inhibitor, which is active against AML blasts. WP-1034 effectively inhib…
H406330
VMY-1-103
VMY-1-103 is a potent CDK inhibitor, is also a novel dansylated analog of purvalanol B, was shown to…
H406400
Tetrabromobenzotriazole
featured
Tetrabromobenzotriazole, also known as TBB and NSC231634, is a potent protein kinase CK2 inhibitor,…
H406713
RO31-8220 mesylate
new
featured
Ro 31-8220 is a PKC-inhibitor, which inhibits stimulated fluid pinocytosis of human PMNs induced by …
H406119
MT477
MT477 is PKC-α inhibitor. MT477 interfered with PKC activity as well as phosphorylation of Ras and E…
H406513
MPT0B214
MPT0B214 is a novel and potent microtubule inhibitor with potential anticancer activity. MPT0B214 in…
H406364
ML-132
ML132, also known as CID-4462093 or NCGC-00183434, is the most potent caspase 1 inhibitor reported t…
H406485
MC2392
MC2392 is a potent and selective HDAC inhibitors. MC2392 induces changes in H3 acetylation at a smal…
H406297
Mahanine
Mahanine, a carbazole alkaloid (occurs in the edible part of Micromelum minutum, Murraya koenigii an…
H406500
JW74
featured
JW74 is a tankyrase-specific inhibitor. JW74 affects cell cycle progression and induces apoptosis an…
H406394
IWP-2
featured
IWP-2 is a potent WNT-3A inhibitor. IWP-2 can decrease MKN28 cell proliferation, migration and invas…
H406510
IG-105
IG-105 is a potent microtubule inhibitor with potential anticancer activity. IG-105 inhibits microtu…
H406528
HJC-0123
Downregulate phosphorylation of STAT3, increase the expression of cleaved caspase-3, inhibit cell cy…
H401430
Droxinostat
new
featured
Droxinostat, also known as NS 41080, is a selective inhibitor of HDAC3, HDAC6, and HDAC8. Droxinosta…
H406507
DAT-230
DAT-230 is a promising microtubule inhibitor that has great potential for the treatment of fibrosarc…
H406377
CGP74514A
CGP74514A is a CDK1 inhibitor with potential anticancer activity. In U937 cells, CGP74514A - induced…
H401218
Ivaltinostat
Ivaltinostat, also known as CG200745, is a novel hydroxamate-based pan-histone deacetylase inhibitor…
H402210
CDKI-83
CDKI-83 is a potent CDK9 inhibitor. The compound shows effective anti-proliferative activity in huma…
H406369
BGP-15 HCl
new
featured
BGP-15 is a novel poly(ADP-ribose) polymerase inhibitor - protects against nephrotoxicity of cisplat…
H406452
b-AP15
new
featured
b-AP15 is a novel inhibitor of proteasome deubiquitination. b-AP15 displays antitumor activity in se…
H205941
VRT-043198
featured
VRT-043198, the active metabolite of VX-765 (Belnacasan), is a Caspase inhibitor. VRT-043198 exhibit…
H558303
Valspodar
featured
Valspodar, also known as PSC-833, is an analogue of cyclosporin-A. Valspodar inhibits p-glycoprotein…
H203010
Triciribine
featured
Triciribine, also known as VQD-002, is a potent AKT inhibitor and a cell-permeable tricyclic nucleos…
H202713
Sulforaphane
featured
Sulforaphane, also known as BroccoPhane; Sulphoraphane; Detoxophane, is a naturally-occurring phyt…
H202180
Idronoxil
featured
Idronoxil, also known as Phenoxodiol, is a synthetic flavonoid derivative. Phenoxodiol activates the…
H202571
Pacritinib (SB1518)
featured
Pacritinib, also known as SB1518, is an orally bioavailable inhibitor of Janus kinase 2 (JAK2) and t…
H202090
Ortataxel
Ortataxel, also known as IDN5109, is novel seimsynthetic taxane with potential anticancer activity. …
H205885
MRK003
MRK003 is a γ-secretase inhibitor exhibits promising in vitro pre-clinical activity in multiple myel…
H201951
MPC-2130
MPC-2130 is a broad-acting, apoptosis-inducing, small molecule with potential antineoplastic activit…
H201930
MLN8054
featured
MLN8054 is an aurora kinase inhibitor MLN8054, which is an orally bioavailable, highly selective sma…
H205856
ME-344
ME-344 is an active metabolite of NV-128, a novel flavonoid small molecule inhibitor of the mammalia…
H201795
LY294002
featured
LY294002 is a morpholine derivative of quercetin. It is a potent inhibitor of phosphoinositide 3-kin…
H201500
Imexon
Imexon, also known as BM 06002 and NSC313425, is a cyanoaziridine derivatives with potential antican…
H205468
GDC-0917 (CUDC-427)
featured
CUDC-427, also known as, GDC-0917, is an orally available, monovalent mimetic of second mitochondria…
H205764
GDC-0152 free base
featured
GDC-0152 is a second mitochondrial activator of caspases (Smac) mimetic inhibitor of IAPs (Inhibitor…
H201310
Etalocib
new
featured
Etalocib, also known as LY293111 and VML295, is a novel diaryl ether carboxylic acid derivative, is …
H201266
Entinostat
featured
Entinostat, also known as MS-275 or SNDX-275, is a potent HDAC inhibitor with potential antineoplas…
H201110
E7974
E7974 is an analog of the sponge-derived anti-microtubule tripeptide hemiasterlin with antimitotic a…
H200900
Diethylnorspermine HBr
Diethylnorspermine, also known as DENSPM, BE-333, DE-333 and N(1),N(11)-Diethylnorspermine, is a hi…
H205748
Lexibulin
featured
Lexibulin, also known as CYT997, is a n orally bioavailable small-molecule with tubulin-inhibiting, …
H205834
CWP232204
CWP232204 is a metabolite of CWP232291. CWP232204 is a specific inhibitor of the canonical Wnt signa…
H206089
AZD-5582
featured
AZD5582 is a potent IAP inhibitor, which is a dimeric compound based on the AVPI motif of Smac. AZD5…
H205816
ARQ-761
ARQ-761 is a soluble prodrug of beta-lapachone with potential antineoplastic and radiosensitizing ac…
H205942
AKN-028
AKN-028, the FLT3/KIT kinase inhibitor, is an orally bioavailable protein tyrosine kinase inhibitor …
H200121
AG-490
new
featured
Tyrphostin AG490 is a JAK-2 specific inhibitor, which inhibits phosphorylation of EGFR and signal tr…
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