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16
Angiogenesis
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8
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11
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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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4
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9
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9
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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 'J'
or product name starting with:
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H525316
JNJ-26146900
JNJ-26146900 is a nonsteroidal androgen receptor (AR) ligand with tissue-selective activity in rats.…
H525315
JNJ-26076713
JNJ-26076713 is an orally active alpha V integrin antagonist. JNJ-26076713 represents a potential th…
H525313
JNJ-20788560
JNJ-20788560 is a delta opioid agonist analgesics, exhibited high DOR affinity, with K(i) values of …
H525312
JNJ-19567470
JNJ-19567470 is a selective, non-peptide CRF receptor 1 antagonist. It is a novel target for develop…
H525309
JNJ-17203212
featured
JNJ-17203212 is a reversible, competitive and potent TRPV1 antagonist (pKi values are 6.5, 7.1 and 7…
H525307
JNJ-17156516
JNJ-17156516 is a novel, potent, and selective cholecystokinin 1 receptor antagonist. JNJ-17156516 e…
H525306
JNJ-17029259
JNJ-17029259 is an orally selective, nanomolar inhibitors of the vascular endothelial growth factor …
H525305
JNJ-1661010
featured
JNJ-1661010 is a selective, reversible inhibitor of fatty acid amide hydrolase (FAAH) (IC50 = 12 nM)…
H525304
JNJ-1250132
JNJ-1250132 is a steroidal progesterone receptor modulator that inhibits binding of the receptor to …
H525303
JNJ-10397049
featured
JNJ-10397049 is a potent and selective OX2 receptor antagonist (pIC50 = 7.4 for chimeric OX2 recepto…
H525302
JNJ-10329670
JNJ-10329670 represents a novel class of immunosuppressive compounds. JNJ 10329670 is a highly poten…
H525301
JNJ-10311795
JNJ-10311795 is a dual inhibitor of the leukocyte Proteases Cathepsin G and Chymase. It has therapeu…
H525299
JNJ-10258859
JNJ-10258859 is a novel, potent, and selective phosphodiesterase type 5 inhibitor. JNJ-10258859 inhi…
H525298
JNJ-10229570
JNJ-10229570 is a novel MC1R and MC5R antagonist was used to treat primary human sebaceous cells. It…
H525297
JNJ-10191584
new
featured
JNJ-10191584 is a drug which acts as a potent and selective antagonist at the histamine H4 receptor.…
H525296
JNJ-10181457
new
featured
JNJ-10181457 is a histamine H3 receptor antagonist (pKi values are 8.15 and 8.93 for rat and human H…
H406760
JPH203 free base
featured
JPH203, also known as KYT-0353, is a potent and selective LAT1 selective ( L-type amino acid transp…
H526662
JNJ-5207852
featured
JNJ-5207852 is a potent and selective H3 antagonist with high affinity at the rat (pKi=8.9) and huma…
H406740
JNK-IN-8
featured
JNK-IN-8, also known as JNK Inhibitor XVI, is a selective JNK inhibitor that inhibits phosphorylatio…
H523108
JNJ 63533054
new
featured
JNJ 63533054 is a potent and selective GPR139 agonist (EC50 = 16 nM) that is brain and cell penetran…
H522678
JNJ-42041935
new
featured
JNJ-42041935 is a potent (pK(I) = 7.3-7.9), 2-oxoglutarate competitive, reversible, and selective i…
H407269
JH-IX-179
JH-IX-179 is a novel type I ATP competitive, extremely potent and selective FLT3 inhibitor. JH-IX-1…
H522652
JJKK048
featured
JJKK048 is an ultrapotent and highly selective inhibitors of monoacylglycerol lipase. JJKK-048 poten…
H522586
JTE-013
new
featured
JTE-013 is a potent, selective sphingosine-1-phosphate 2 (S1P2) receptor antagonist that binds to th…
H522579
JZP-430
featured
JZP-430 is a potent and selective ABHD6 inhibitor. P-430 potently and irreversibly inhibited hABHD6 …
H522518
JTP-4819
JTP-4819 is a potent and selective prolyl endopeptidase (PEP) inhibitor with potential for treating …
H522481
JNJ-38431055
new
featured
JNJ-38431055, also known as APD597, is a potent and selective GPR119 agonist, which is potential use…
H522477
JNJ-42165279
new
featured
JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. JNJ-42165279 cov…
H522475
JTC-801 HCl
featured
JTC-801 is an opioid analgesic drug used in scientific research. JTC-801 is a selective antagonist f…
H522462
JH-II-127
featured
JH-II-127 is a potent and selective inhibitor of both wild-type and G2019S mutant LRRK2. JH-II-127 s…
H522417
JZL195
featured
JZL195 is a potent and selective dual inhibitor of FAAH and monacylglycerol lipase (MAGL). JZL195 ha…
H522409
JNJ7777120
featured
JNJ7777120 is a potent and selective histamine H4 receptor antagonist. JNJ7777120 induces increases …
H522384
J147
featured
J147 is a potent neuroprotective and neurotrophic compound. J147 protects against neurotoxicity in c…
H522359
JM6
featured
JM6 is a prodrug inhibitor of kynurenine 3-monooxygenase (KMO) that increases kynurenic acid levels …
H406500
JW74
featured
JW74 is a tankyrase-specific inhibitor. JW74 affects cell cycle progression and induces apoptosis an…
H406502
JW55
featured
JW55 is a tankyrase 1 and tankyrase 2 (TNKS1/2) inhibitor. JW55 functions via inhibition of the PARP…
H406426
JSH-23
featured
JSH-23 is a nuclear factor-kappa B (NF-κB) nuclear translocation inhibitor. JSH-23 inhibits LPS and …
H406161
JNJ-7706621
featured
JNJ-7706621 is a novel cell cycle inhibitor that showed potent inhibition of several cyclin-dependen…
H406201
JNJ-28312141
JNJ-28312141 is an orally active CSF1R inhibitor (Colony-stimulating factor-1 receptor, CRF1R) and a…
H406104
JH295
JH295 is an irreversible, cysteine-targeted inhibitors of the human centrosomal kinase, Nek2. JH295 …
H201615
JNJ-38877605
featured
JNJ-38877605 is an orally bioavailable, small-molecule receptor tyrosine kinase inhibitor with poten…
H201613
JNJ-26483327
featured
JNJ-26483327, also known as BGB102, is an orally bioavailable, small-molecule, multitargeted reversi…
H201611
JI-101 free base
featured
JI-101, also known as CGI-1842, is an orally active inhibitor of vascular endothelial growth factor …
H510320
JZL184
new
featured
JZL184 is highly selective, and potent MAGL inhibitor ( monoacylglycerol lipase inhibitor). JZL184 i…
H510336
JNJ-31020028
featured
JNJ-31020028 is a selective brain penetrant small molecule antagonist of the neuropeptide Y Y(2) rec…
H406601
JIB-04
featured
JIB-04, also known as NSC 693627, is a Jumonji histone demethylase inhibitor. JIB-04 selectively blo…
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