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16
Angiogenesis
Bcr-Abl
BTK
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FAK
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test3
demo333
8
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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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2
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Products starting with 'R'
or product name starting with:
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H123112
RPF101
RPF101 is a new capsaicin-like analogue. RPF101 disrupts the microtubule network accompanied by arre…
H123092
RL-603
RL-603 is a PDE3 inhibitor.
H130364
Rink Amide Linker
featured
Rink Amide Linker is a biochemical.
H123075
RIPK1-IN-7
featured
RIPK1-IN-7 is a potent and selective receptor-interacting serine/threonine-protein kinase 1 (RIPK1) …
H123040
RYJ80655
featured
Also known as 5-(3-Aminoallyl)-2'-deoxyuridine-5'-O-triphosphate (sodium salt). It is an amine-modif…
H123041
RRJ00594
featured
Also known as 2'-Amino-2'-deoxyadenosine-5'-O-triphosphate (sodium salt). It is an amino-substituted…
H123070
RO0505376
RO0505376 is a α4β1 integrin antagonist.
H123035
RYJ00611
featured
RYJ00611 is an amine-modified nucleotide that has been used in the synthesis of fluorescently labele…
H123005
RIPK2 inhibitor 1
featured
RIPK2 inhibitor 1 is a potent receptor-interacting protein kinase 2 (RIPK2) inhibitor.
H408196
RXN00442
new
featured
RXN00442, also known as EGFR-IN-11, is a fourth-generation EGFR-tyrosine kinase inhibitor (EGFR-TKI)…
H122986
R-DOTAP
featured
Also known as 1,2-Dioleoyl-3(R)-trimethylammoniumpropane (chloride). It is a cationic lipid and the …
H122953
RMC-4529
RMC-4529 has an IC50 value of 1.0 nM against p-4E-BP1-(T37/46) in mTOR kinase cellular assay.
H122949
RK-701
RK-701 is a structurally distinct potent inhibitor of G9a/GLP (IC50 = 27/53 nM). RK-701 exhibited re…
H122934
Rhyncophylline
featured
Rhyncophylline is an alkaloid that has been found in U. rhyncophylla and has diverse biological acti…
H122907
RUN00218
featured
Also known as p-Carboxyphenyl Sulfate. It is a sulfated phenolic acid that has been found in D. verm…
H130185
RJC00847
RJC00847 is a non-competitive PC2 inhibitor, in that it binds to an allosteric site of PC2.
H122725
RTI-122
RTI122 is a GPR88 agonist with IC50=11 nM). RTI-122 was more effective than RTI-13951-33 in attenuat…
H122709
RUN00767
featured
Also known as BP Fluor 568 Hydroxylamine. It reacts with aldehydes and ketones to yield oximes.
H130109
RyR1 inhibitor 1
RyR1 inhibitor 1 is a RyR1 inhibitor that was developed with the aim of increasing solubility as com…
H130101
RapiFluor-MS
RapiFluor-MS is a highly sensitive glycosylamine labelling reagent for the detection of O-glycans.
H130092
RA-1
RA-1 is a proteasome inhibitor with potential as a treatment for cervical cancer. It was suggested t…
H130079
R419
R419 is an indirect activator of AMPK with potential application as a method of glucose regulation.
H122669
RUN01075
featured
RUN01075 is an advanced fluorescent probe that incorporates a copper-chelating motif to raise the ef…
H556178
Ro 04-5595 free base
Ro 04-5595 is a selective antagonist of NMDA receptors NR2B subunits. Ro 04-5595 had an EC 50 of 186…
H130053
Rovadicitinib
Rovadicitinib is a Janus kinase inhibitor, also known as a JAK inhibitor. Rovadicitinib has potentia…
H130052
Rolusafine
Rolusafine is an antifungal.
H130051
Ritivixibat
Ritivixibat is an inhibitor of the ileal bile acid transporter (IBATi). IBATis have recently been us…
H130050
Risvodetinib
Risvodetinib, also known as IkT-148009., is a brain-penetrant c-Abl inhibitor with a favorable toxic…
H130049
Resencatinib
Resencatinib is a tyrosine kinase inhibitor with potential as an antineoplastic agent.
H130048
Relutrigine
Relutrigine is a sodium channel blocker.
H122599
RDN32136
featured
(S)-T-GNA phosphoramidite
H122435
RMC-6272
RMC-6272 is a Selective Bi-Steric Inhibitor of mTORC1 for the Treatment of mTORC1-Activated Tumors
H122434
RMC-5552
featured
RMC-5552 is a Selective Bi-Steric Inhibitor of mTORC1 for the Treatment of mTORC1-Activated Tumors. …
H122437
R05-2
R05-2 is an influenza PAN inhibitor
H471211
Ro 31-8425
featured
Ro 31-8425 is a cell-permeable, reversible, ATP-competitive protein kinase C (PKC) inhibitor.
H1008
RUN50765
RUN50765 is a chemical intermediate for drug synthesis such as Omidenepag Isopropyl. This product ha…
H121230
RTN00684
featured
RTN00684, also known as (S,R,S)-VL285 Phenol-C6-NH2 hydrochloride, is a ProTAC building block. This …
H121118
RP-6685 free base
featured
RP-6685 is a potent, selective, and orally bioavailable Polθ inhibitor that showed in vivo efficacy …
H121047
RNO-6
RNO-6 is a Rho-associated protein kinase (ROCK) inhibitor. RNO-6 maintained potent ROCK inhibitory a…
H208513
RMI-11877DA free base
RMI-11877DA free base is a biochemical
H208393
RHTB
RHTB is a biochemical
H121093
Resomelagon free base
Resomelagon, also known as AP1189, is a melanocortin receptor agonist, specifically MC1 and MC3. Res…
H121092
Razpipadon
Razpipadon is a dopamine receptor partial agonist.
H1041973
RUN48988
featured
RUN48988 is a chemical used for drug synthesis.
H1041948
RQN70319
featured
RQN70319 is a chemical for drug synthesis.
H1041930
RFN21609
featured
RFN21609 is a chemical for drug synthesis.
H1041929
RUN68808
featured
RUN68808 is a chemical for drug synthesis.
H1041879
RPN48119
featured
RPN48119 is a chemical for drug synthesis.
H1041866
RBN79768
featured
RBN79768 is a chemical for drug synthesis.
H1041854
RUN60879
featured
RUN60879 is a chemical for drug synthesis.
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