All ProductsDisplaying Products Alphabetically by Name (I)
Cat. No. | Product Name / Activity |
---|---|
7292 | I 432 |
TMPRSS2 Inhibitor | |
4650 | I-BET 151 dihydrochloride |
BET bromodomain inhibitor; also promotes differentiation of hiPSCs into megakaryocytes | |
6521 | I-BET 762 |
Potent and high affinity BET bromodomain inhibitor; anti-inflammatory; orally bioavailable. | |
5591 | I-BRD9 |
Potent and selective BRD9 inhibitor | |
7789 | IA |
SHAPE-JuMP monoadduct control for TBIA (Cat. No. 7788) | |
7015 | IA-Alkyne |
Broad spectrum cysteine reactive probe | |
1066 | IB-MECA |
A3 selective agonist | |
2845 | IBMX |
PDE inhibitor (non-selective) | |
4305 | ICA 069673 |
KV7.2/KV7.3 channel opener | |
4950 | ICA 110381 |
KV7.2/7.3 activator; displays anticonvulsant properties | |
5066 | ICA 121431 |
Potent and selective NaV1.3 and NaV1.1 channel blocker | |
4505 | ICG 001 |
Inhibits TCF/β-catenin-mediated transcription | |
7749 | ICG-d7 |
Near-infrared (NIR) fluorescent dye; partially deuterated form of Indocyanine Green (Cat. No. 7510), suitable for in vivo imaging. | |
0821 | ICI 118,551 hydrochloride |
Highly selective β2 inverse agonist | |
0820 | ICI 174,864 |
δ selective peptide antagonist | |
1047 | ICI 182,780 |
Estrogen receptor antagonist | |
0778 | ICI 199,441 hydrochloride |
Potent κ agonist | |
0822 | ICI 204,448 hydrochloride |
κ agonist, acts peripherally | |
4015 | IDE 1 |
Induces definitive endoderm formation in mouse and human ESCs | |
7866 | IDR 1002 |
Innate defence regulator peptide | |
1636 | IEM 1460 |
Open-channel blocker of AMPA currents; selective for non-GluA2-containing receptors | |
4198 | IEM 1925 dihydrobromide |
Voltage- and use-dependent open-channel AMPA blocker | |
5554 | IHR 1 |
Potent Smo antagonist | |
2539 | IKK 16 |
Selective inhibitor of IKK | |
2611 | IMD 0354 |
Inhibitor of IKKβ; also exhibits antibacterial activity | |
6016 | IN 1130 |
Potent and selective inhibitor of TGF-βRI | |
2162 | INCA-6 |
Inhibitor of calcineurin-substrate association | |
6007 | INCB 024360-analog |
Potent indoleamine 2,3-dioxygenase (IDO) inhibitor | |
4306 | INCB 3284 dimesylate |
Selective CCR2 antagonist | |
7685 | IND 1316 |
AMPK activator | |
4997 | INDY |
DYRK1A/B inhibitor | |
6341 | INF 39 |
Irreversible NLRP3 inhibitor | |
6172 | INF 4E |
Caspase-1 and NLRP3 inflammasome inhibitor | |
7870 | ING-2 AM |
Fluorescent sodium ion (Na+) indicator, membrane permeable | |
7423 | INT 131 |
PPARγ partial agonist | |
4464 | IOX 1 |
Histone demethylase inhibitor; cell permeable | |
4451 | IOX 2 |
Potent, selective HIF-1α prolyl hydroxylase-2 (PHD2) inhibitor | |
5699 | IP7e |
Potent Nurr1 activator | |
3622 | IPA 3 |
Group I PAK inhibitor | |
7871 | IPG-4 AM |
Fluorescent potassium ion (K+) indicator, membrane permeable | |
3429 | 4-IPP |
Inhibitor of macrophage migration inhibitory factor (MIF); suicide substrate | |
5509 | IPTG |
Used in cloning procedures with X-GAL | |
5665 | IRAK1/4 Inhibitor I |
IRAK4 and IRAK1 inhibitor | |
7983 | IRAK3 Degrader 23 |
IRAK3 Degrader (PROTAC® | |
4288 | ISO 1 |
Macrophage migration inhibitory factor (MIF) inhibitor | |
5284 | trans-ISRIB |
Integrated stress response (ISR) inhibitor | |
4439 | ISX 9 |
Neurogenic agent; induces neuronal differentiation of SVZ progenitors and also induces cardiomyogenic differentiation | |
4596 | IT1t dihydrochloride |
Potent CXCR4 antagonist | |
5068 | ITD 1 |
Selective inhibitor of TGF-β signaling; induces cardiomyocyte differentiation in ESCs | |
1803 | ITE |
Endogenous agonist for the transcription factor aryl hydrocarbon receptor | |
5692 | ITH 12575 |
Mitochondrial Na+/Ca2+ exchange (mNCX) inhibitor | |
5279 | IWP 12 |
Potent PORCN inhibitor; active in vivo | |
3533 | IWP 2 |
PORCN inhibitor; inhibits Wnt processing and secretion | |
5214 | IWP 4 |
Potent inhibitor of Wnt/β-catenin signaling | |
4992 | IWP L6 |
Potent PORCN inhibitor | |
TB3532-RMU | endo-IWR 1 |
endo-IWR 1 synthesized to Ancillary Material Grade | |
3532 | endo-IWR 1 |
Wnt/β-catenin signaling inhibitor; axin stabilizer | |
1086 | Iberiotoxin |
KCa (BK) channel blocker | |
0285 | Ibotenic acid |
NMDA agonist; also non selective mGlu agonist | |
6813 | Ibrutinib |
Potent and selective BTK inhibitor | |
1694 | Ibudilast |
PDE inhibitor (non-selective) | |
3908 | Ibutilide hemifumarate |
Blocks IKr, hERG and L-type Ca2+ channels; class III antiarrhythmic | |
1531 | Icilin |
Activates cold receptors. Cooling agent | |
6904 | Idasanutlin |
Potent MDM2 inhibitor; inhibits MDM2-p53 interaction | |
7631 | Idelalisib |
Potent PI 3-Kinase δ isoform inhibitor | |
0545 | Ifenprodil hemitartrate |
Non-competitive NMDA antagonist; also σ ligand | |
2332 | (+)-Igmesine hydrochloride |
Selective σ1 ligand; antidepressant | |
5906 | Imatinib mesylate |
Potent and selective v-Abl tyrosine kinase inhibitor; also inhibits PDGFR and c-kit | |
0729 | Imetit dihydrobromide |
Standard H3 and H4 agonist (H3 > H4) | |
0986 | Imiloxan hydrochloride |
Highly selective α2B antagonist | |
7841 | Imipramine hydrochloride |
Potent inhibitor of 5-HT and noradrenalin transporters; promotes immunostimulatory tumor microenvironment | |
3700 | Imiquimod |
Toll-like receptor 7 (TLR7) agonist | |
0932 | Immepip dihydrobromide |
Standard H3 agonist. Also H4 agonist | |
1588 | Indatraline hydrochloride |
Potent 5-HT uptake inhibitor; also inhibits dopamine and noradrenalin uptake | |
3728 | Indibulin |
Microtubule destabilizer | |
7196 | Indinavir sulfate |
Potent and selective HIV-1 and HIV-2 protease inhibitor | |
6782 | Indisulam |
Molecular glue; pre-mRNA splicing modulator | |
6704 | Indo 1AM |
Fluorescent Ca2+ indicator | |
7510 | Indocyanine green |
Near-infrared (NIR) fluorescent dye; suitable for in vivo imaging | |
1708 | Indomethacin |
Cyclooxygenase inhibitor (COX-1 > COX-2) | |
1482 | D-myo-Inositol 1,4,5-trisphosphate, hexapotassium salt |
Ca2+ mobilizing second messenger | |
3435 | Insulin (human) recombinant, expressed in yeast |
Endogenous peptide agonist | |
0737 | 2-Iodomelatonin |
High affinity melatonin agonist | |
0779 | Iodophenpropit dihydrobromide |
Potent, selective H3 antagonist | |
1745 | 5-Iodotubercidin |
Potent adenosine kinase inhibitor; also inhibits nucleoside transporters and a range of other kinases | |
0307 | (S)-(-)-5-Iodowillardiine |
Highly potent and subtype-selective kainate agonist | |
1704 | Ionomycin calcium salt |
Calcium ionophore | |
2092 | Ionomycin free acid |
Calcium ionophore | |
1869 | Ipsapirone |
Selective 5-HT1A agonist | |
5798 | Irbesartan |
Potent AT1 antagonist | |
3000 | Iressa |
Orally active, selective EGFR inhibitor | |
4695 | Ischemin sodium salt |
CBP inhibitor; cell permeable | |
6483 | Isoginkgetin |
Pre-mRNA splicing inhibitor; cell permeable | |
0235 | Isoguvacine hydrochloride |
Selective GABAA agonist | |
1747 | Isoproterenol hydrochloride |
Standard selective β agonist | |
5408 | Ispinesib |
High affinity and selective allosteric KSP inhibitor | |
2004 | Isradipine |
CaV1.x blocker | |
5147 | Istradefylline |
Potent and selective A2A antagonist | |
5981 | Itraconazole |
SMO antagonist; acts at different binding site to cyclopamine (Cat No. 1623) | |
6542 | Ivabradine hydrochloride |
HCN channel blocker; inhibits If pacemaker current | |
7887 | Ivacaftor |
Potent and selective CFTR potentiator | |
1260 | Ivermectin |
Positive allosteric modulator of α7 nAChRs; also positive allosteric modulator of P2X4 receptors | |
7761 | Ivosidenib |
Potent inhibitor of mutant isocitrate dehydrogenase (mIDH1) |
Tocris Products by Catalog Number
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