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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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Products starting with 'K'
or product name starting with:
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H522701
KM11060
featured
KM11060 is a mutated F508del cystic fibrosis transmembrane conductance regulator (CFTR) corrector. T…
H407309
K-858
new
featured
K-858 is a novel inhibitor of mitotic kinesin Eg5 and antitumor agent, induces cell death in cancer …
H558226
Ko-143
featured
Ko-143 is a potent and selective breast cancer resistance protein multidrug transporter (BCRP) inhib…
H522674
KN-93 phosphate
featured
KN-93 is a CaMKII inhibitor. KN-93 suppresses ventricular arrhythmia induced by LQT2 without decrea…
H318082
Ketotifen fumarate
featured
Ketotifen is a second-generation noncompetitive H1 antihistamine and mast cell stabilizer. It is mos…
H318081
Ketorolac
featured
Ketorolac or ketorolac tromethamine is a non-steroidal anti-inflammatory drug (NSAID) in the family …
H318080
Ketoprofen
featured
Ketoprofen is one of the propionic acid class of nonsteroidal anti-inflammatory drugs (NSAID) with a…
H318079
Ketoconazole
featured
Ketoconazole is a synthetic imidazole antifungal drug used primarily to treat fungal infections. It …
H522633
KLS-13019
KLS-13019 is a Cannabidiol-Derived Neuroprotective Agent with Improved Potency, Safety, and Permeabi…
H319621
Kebuzone
Kebuzone is a non-steroidal anti-inflammatory drug. Kebuzone also known shown analgesic, antipyretic…
H522570
KL001
new
featured
KL001 is a Cryptochrome protein (CRY) stabilizer. KL001 prevented ubiquitin-dependent degradation o…
H206491
K-11777
K-11777, also known as APC 3316; and K 777, is a a potent, irreversible cysteine protease inhibitor …
H522519
KYP-2047
featured
KYP-2047 is a very potent, selective inhibitor of Prolyl oligopeptidase (POP), also known as prolyl …
H558220
KAI-407
KAI407 is a potent non-8-aminoquinoline compound that kills Plasmodium cynomolgi early dormant liver…
H407214
KPU-300
KPU-300 is a potent and selective antimicrotubule agent. KPU-300 exhibited a potent cytotoxicity wit…
H522435
KY02111
featured
KY02111 is a potent and selective inhibitor of Wnt. KY02111 promotes differentiation of hPSCs by inh…
H407173
KRH-1636
KRH-1636 is an orally active, selective and extremely potent CXC chemokine receptor 4 antagonist. KR…
H522400
KB-R7943 mesylate
new
featured
KB-R7943 is a potent, selective inhibitor of the reverse mode of the Na+/Ca2+ exchanger (IC50 = 0.7 …
H522382
kb NB 142-70
featured
kb NB 142-70 is a selective protein kinase D (PKD) inhibitor with IC50 values are 28.3, 58.7 and 53…
H558221
KNK437
featured
KNK437 is a novel inhibitor of acquisition of thermotolerance and heat shock protein. KNK437 inhibit…
H406541
KX1-141
KX1-141 is an Src-protein tyrosine kinase inhibitor, which may reduce cisplatin ototoxicity while pr…
H406540
KX1-004
featured
KX1-004 is an Src-protein tyrosine kinase inhibitor to reduce cisplatin ototoxicity while preserving…
H406441
KU-60019
featured
KU-60019 is a potent and selective ATM inhibitor. KU-60019 is 10-fold more effective than KU-55933 a…
H406358
KU-0058684
KU-0058684 is a potent PARP and DNA-PK inhibitors.
H406725
KRN383
KRN383 also inhibited the proliferation of the ITD-positive cell lines with IC(50) values of < or =2…
H406512
KRIBB3
KRIBB3 is novel and potent microtubule inhibitor with potential anticancer activity. KRIBB3 has anti…
H406114
KRC-108
KRC-108 is a multiple kinase inhibitor. KRC-108 is a potent inhibitor of Ron, Flt3 and TrkA as well …
H406356
KR30031
KR30031 is a novel P-glycoprotein inhibitor with potential anticancer activity. KR30031 is a verapam…
H558212
KP372-1
KP372-1 is a synthetic small molecule AKT inhibitor. KP372-1 is consisted of two isomers: KP372-1 A …
H406351
Ki8751
featured
Ki8751 is a potent, selective inhibitor of VEGFR-2 tyrosine kinase (IC50 = 0.9 nM). Displays some in…
H406404
KI-328
KI-328 is a novel KIT inhibitor. KI-328 shows selective potency against KIT kinase for the in vitro …
H401515
KCN1
KCN1, a novel synthetic sulfonamide, is a HIF pathway inhibitor with potential anticancer activity i…
H206196
KX2-361
KX02, also known as KX2-361, is a lipophilic, orally available inhibitor of both Src kinase activity…
H205506
KW-2478 free base
featured
KW-2478 is an agent that targets the human heat-shock protein 90 (Hsp90) with potential antineoplast…
H205908
KW-2450 Tosylate
KW-2450 is an orally bioavailable inhibitor of insulin-like growth factor 1 receptor (IGF-1R) and in…
H206213
KW-2449
featured
KW-2449 is a novel multikinase inhibitor, which suppresses the growth of leukemia cells with FLT3 mu…
H558240
KU-2285
KU-2285 is a potent hypoxic cell radiosensitizer. At less than 100 mg/kg, KU-2285 sensitized SCCVII …
H205776
KU-0063794
featured
KU-0063794 is a potent and selective mTOT inhibitor, which inhibits both mTORC1 and mTORC2 with an I…
H203060
KRX-0601
featured
KRX-0601, also known as UCN-01, is a synthetic derivative of staurosporine with antineoplastic activ…
H201670
KRX-0402
KRX-0402 (O6-benzyl guanine or O6-BG) is a small molecule that was specifically designed to block th…
H205775
KRP-203 HCl
KRP-203 is a selective Sphingosine-1-phosphate receptor agonist that has been shown to reduce periph…
H201650
KOS-1584
KOS-1584 is a second-generation epothilone with potential antineoplastic activity. Epothilone KOS-15…
H201630
Karenitecin
Karenitecin, also known as Cositecan, is a synthetic silicon-containing agent related to camptotheci…
H510310
Kartogenin
featured
Kartogenin induces the selective differentiation of multipotent mesenchymal stem cells (MSCs) into c…
H510307
K02288
featured
K02288 is a potent inhibitor of BMP signaling. K02288 has in vitro activity against ALK2 at low nano…
H406550
Kenpaullone
featured
Kenpaullone is a potent inhibitor of CDK1/cyclin B (IC50 = 400 nM), CDK2/cyclin A (IC50 = 680 nM), C…
H406294
KU59403
featured
KU59403 is a potent and selective ATM (Ataxia telangiectasia mutated) inhibitor with with potential …
H201681
KU-55933
featured
KU-55933 is an ATM inhibitor, which blocks the phosphorylation of Akt induced by insulin and insulin…
H406288
KRN633
featured
KRN633 is a potent and selective VEGFR inhibitor. which inhibits tyrosine phosphorylation of VEGFR-2…
H401517
Ki23057
Ki23057 is a a FGFR2 inhibitor, which enhances the chemosensitivity of drug-resistant gastric cancer…
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