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16
Angiogenesis
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8
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19
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10
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20
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5
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17
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Products starting with 'J'
or product name starting with:
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H124991
JH-XII-03-02
JH-XII-03-02 is a PROTAC targeting LRRK2. JH-XII-03-0 displayed high potency and remarkable select…
H124950
JNJ-42165279 hydrochloride
JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. JNJ-42165279 cov…
H124934
JC-229
new
featured
JC-229 is a TbRPA1 inhibitor. JC-229 targets RPA1 in Trypanosoma brucei, the causative parasite of …
H124922
JAK Inhibitor 31
featured
JAK inhibitor 31 is an inhibitor of JAK2 (IC50 = 3.9 nM).
H124904
JNJ-42165279 dihydrochloride
JNJ-42165279 is a potent and selective fatty acid amide hydrolase (FAAH) inhibitor. JNJ-42165279 cov…
H124829
JNJ-40929837 succinate
JNJ-40929837 is an oral inhibitor of LTA4 hydrolase, which catalyzes LTB4 production.
H124749
J27
J27 is a NF-κB/MAPK inhibitor. J27decreased the release of TNF-αandIL-6 in mouse and human cells J77…
H124272
JPC0323
JPC0323 is a selective 5-HT2CR or dual 5-HT2CR/5-HT2AR positive allosteric modulator (PAM). JPC0323…
H124135
Jun9-62-2R
Jun9-62-2R is a SARS-CoV-2 Mpro inhibitor.
H123937
JET-209
JET-209 is an exceptionally potent PROTAC degrader of CBP/p300. JET-209, achieved a half-maximal deg…
H130606
JNJ-47909290
JNJ-47909290 is a novel antagonist of CCR2.
H123820
JUN82293
JUN82293 is also named as Boc-NH-PEG7-acetic acid. It is a PEG-based PROTAC linker.
H123793
JUN44830
JUN44830 is also named as Iodoacetamide-PEG5-NH2. It is a PEG-based PROTAC linker.
H123770
JUN55867
JUN55867 is also named as m-PEG11-Hydrazide. It is a PEG-based PROTAC linker .
H123755
JUN60475
JUN60475 is also named as S-acetyl-PEG12-alcohol. It is a PEG-based PROTAC linker
H130500
JAK/HDAC inhibitor 30
JAK/HDAC inhibitor 30 is a novel dual JAK/HDAC inhibitor. It potentially inhibits HDAC3/6 and JAK1/2…
H130499
JAK/HDAC inhibitor 21
JAK/HDAC inhibitor 21 is a HDAC3/6 and JAK1/2 inhibitor. It is selective for JAK2, presenting antipr…
H123645
JH530
JH-530 Is a potent Methuosis Inducer for the Treatment of Triple-Negative Breast Cancer. JH530 showe…
H123551
JB-170
featured
JB-170 is a PROTAC targeting Auora
H130465
JSD26
JSD26 is an inhibitor of SCoR2 with high selectivity over AKR1B1 (10-fold) for use in the treatment …
H123389
JNJ-78394355
JNJ-78394355 is a Mcl-1 inhibitor.
H130472
JG-2016
JG-2016 is an inhibitor of HAT1, displaying anticancer activities.
H130462
JH-LPH-50
JH-LPH-50, an LpxH inhibitor, has the potential to play a key role in the development of antibiotics…
H556219
J 3-54
new
featured
J 3-54, also known as LSD1-IN-24, is a selective LSD1 inhibitor with IC50 = 0.247 μM. J-3-54 can med…
H130461
JH-LPH-45
JH-LPH-45 is a LpxH inhibitor that chelates the active site dimanganese cluster of KpLpxH.
H130412
JHU94620
JHU94620 is a CB2R ligand.
H130423
JDH-2110
JDH-2110 is an allosteric human immunodeficiency virus type 1 integrase inhibitor (ALLINI), blocking…
H123042
JRJ00594
featured
Also known as 3'-Amino-3'-deoxyadenosine-5'-O-triphosphate (sodium salt). It is an amine-modified nu…
H123046
JDN18957
featured
Also known as 1-Stearoyl-2-Oleoyl-sn-glycero-3-PE. It is is a phospholipid that contains stearic a…
H130317
JH-XIV-68-3
JH-XIV-68-3 is a Dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A/ B (DYRK1A/B) inh…
H130321
JBI-589
JBI-589, an inhibitor of neutrophil peptidylarginine deiminase 4 (PAD4), has been shown to reduce th…
H122994
JB 300
featured
JB 300 is a potent and selective Aurora A Degrader
H122985
JWH181
featured
JWH181 is an analytical reference standard categorized as a synthetic cannabinoid.
H130278
JR2-298
JR2-298 is a σ2R ligand that binds to σ2R with a Ki of 10 nM. JR2-298 shows promise as a potential t…
H130277
JR1-157
JR1-157 is a σ2R ligand that binds σ2R with a Ki of 47 nM. JR1-157 shows promise as a potential trea…
H122937
JNJ-65234637
A protein-protein interaction inhibitor for a challenging-to-drug master transcription factor.
H130234
JJC8-091
JJC8-091 is a dopamine transporter (DAT) ligand and shows promise for use as a treatment for cocaine…
H130233
JJC8-088
JJC8-088 is a dopamine transporter (DAT) ligand and shows promise for use as a treatment for cocaine…
H130221
JC2-11
featured
JC2-11 is a pan-inflammasome inhibitor, with the potential to serve as a key agent in the treatment …
H130196
JZP-MA-11
JZP-MA-11 is the first PET ligand targeting the endocannabinoid α/β-hydrolase domain 6 (ABHD6) in vi…
H130207
JNJ-64413739
JNJ-64413739 is an antagonist of P2X7, more specifically a PET ligand for measuring P2X7 expression …
H130172
JS25
JS25 is a covalent inhibitor of Bruton’s tyrosine kinase (BTK) with the potential application as a t…
H122776
JOE azide, 5-isomer
featured
JOE azide, 5-isomer is a fluorescent dye with the emission in yellow region of the spectrum.
H130136
JTE-013-9d
JTE-013-9d is a S1PR2 antagonist (KD = 34.8 nM) derived from JTE-013 and has been shown to successfu…
H130138
JQ1-TCO
JQ1-TCO is a clickable BET inhibitor for use as a chemical probe in targeted cancer therapeutics, as…
H122732
JZN00688
featured
Also known as Carboxyrhodamine 110 LC Acid. It can be used to create bright and photostable green-fl…
H122730
JUN01107
featured
Also known as BP Fluor 546 DBCO. It is an azide-reactive probe that can be used for imaging azide-ta…
H122728
JUN00972
featured
Also known as BP Fluor 546 Azide. It is a bright, orange-fluorescent dye that reacts with terminal a…
H130126
JNJ-9350
JNJ-9350 is an inhibitor of SMOX ( IC50= 0.01 μM) with a negative control of JNJ-4545.
H130128
JNJ-6204
JNJ-6204 is a dual inhibitor of CSNK1D (IC50 = 2.3 nM) and CSNK1E (IC50 = 137 nM).
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