All ProductsDisplaying Products Alphabetically by Name (M)
Cat. No. | Product Name / Activity |
---|---|
5807 | M 084 hydrochloride |
TRPC4 and TRPC5 inhibitor; antidepressant and anxiolytic | |
1941 | m-3M3FBS |
Phospholipase C activator | |
1942 | o-3M3FBS |
Inactive analog of m-3M3FBS (Cat. No. 1941) | |
3425 | M40 |
Potent, non-selective galanin receptor antagonist | |
7754 | M4K2163 dihydrochloride |
Potent and selective ALK2 inhibitor | |
2697 | M617 |
Selective GAL1 agonist | |
5324 | M8 B hydrochloride |
Potent and selective TRPM8 channel blocker | |
2698 | M871 |
Selective GAL2 antagonist | |
6618 | MB 05032 |
Potent FBPase inhibitor; promotes HSC expansion | |
4077 | MC 1568 |
Selective HDAC class IIa inhibitor | |
5727 | MC 1742 |
Potent class I and IIb HDAC inhibitor | |
3806 | MCH (human, mouse, rat) |
Potent endogenous MCH agonist | |
0336 | (RS)-MCPG |
Non-selective mGlu antagonist | |
3696 | (RS)-MCPG disodium salt |
Non-selective mGlu antagonist; disodium salt of (RS)-MCPG (Cat. No. 0336) | |
0337 | (S)-MCPG |
Non-selective mGlu antagonist; active isomer of (RS)-MCPG (Cat. No. 0336) | |
7195 | MCU i4 |
Negative modulator of mitochondrial Ca2+ uniporter (MCU) | |
7503 | MD13 |
Potent MIF Degrader (PROTAC®) | |
7504 | MD15 |
Negative control for MD13 (Cat. No. 7503) | |
4173 | MDL 100907 |
Potent and selective 5-HT2A antagonist | |
0870 | MDL 11,939 |
5-HT2A antagonist | |
0640 | MDL 72222 |
5-HT3 antagonist | |
5887 | MES, free acid |
Commonly used buffer | |
6718 | ±-MF 094 |
Selective USP30 inhibitor | |
1748 | MG 132 |
Proteasome and calpain inhibitor. Inhibits NF-κB activation | |
6033 | (R)-MG 132 |
Potent 20S proteasome inhibitor | |
5604 | MI 14 |
Potent and selective PI 4-kinase IIIβ inhibitor | |
4848 | MI 2 (MALT1 inhibitor) |
MALT1 inhibitor | |
3362 | MIRA-1 |
Restores mutant p53 activity; proapoptotic | |
5272 | MK 0677 |
High affinity ghrelin receptor agonist | |
4622 | MK 1903 |
Potent and selective GPR109A (HCA2) agonist | |
0941 | MK 212 hydrochloride |
5-HT2C agonist | |
7850 | MK 2206 dihydrochloride |
Potent and selective allosteric Akt1, Akt2 and Akt3 inhibitor | |
5842 | MK 386 |
Potent, selective human type 1 5α-reductase inhibitor | |
2338 | MK 571 |
Potent CysLT1 (LTD4) inverse agonist. Also MRP1 inhibitor | |
0924 | (+)-MK 801 maleate |
Non-competitive NMDA antagonist; acts at ion channel site | |
0955 | (-)-MK 801 maleate |
NMDA antagonist; less active enantiomer of (+)-MK 801 | |
1311 | MK 886 |
Inhibitor of 5-lipoxygenase-activating protein (FLAP) | |
5547 | MK6-83 |
TRPML channel activator | |
4621 | MKT 077 |
Binds mot-2; selectively cytotoxic in cancer cells | |
4854 | ML 00253764 hydrochloride |
Melanocortin MC4 receptor antagonist; brain penetrant | |
4899 | ML 120B dihydrochloride |
Novel IKK2-selective inhibitor | |
4549 | ML 133 hydrochloride |
Kir2 channel blocker | |
4266 | ML 141 |
Selective Cdc42 Rho family inhibitor | |
4172 | ML 145 |
GPR35 antagonist | |
7821 | ML 162 |
Inhibits glutathione peroxidase (GPX4); induces ferroptosis | |
4957 | ML 179 |
Selective liver receptor homolog 1 (LRH1) inverse agonist | |
6668 | ML 184 |
Selective GPR55 agonist; also promotes NSC proliferation and differentiation | |
4866 | ML 190 |
Selective κ opioid receptor antagonist | |
4860 | ML 193 |
Potent, selective GPR55 antagonist | |
4732 | ML 204 |
Selective TRPC4 inhibitor | |
5987 | (±)-ML 209 |
RORγt inverse agonist; suppresses Th17 cell differentiation | |
6429 | ML 210 |
Selectively kills mutant HRAS-expressing cells; glutathione peroxidase inhibitor; induces ferroptosis | |
4519 | ML 213 |
KV7.2 and KV7.4 channel opener | |
4507 | ML 218 hydrochloride |
CaV3.x blocker | |
4748 | ML 221 |
Apelin antagonist | |
5966 | ML 233 |
Non-peptide apelin agonist | |
4829 | ML 239 |
Breast cancer stem cell inhibitor | |
5153 | ML 240 |
ATP-competitive inhibitor of p97 ATPase | |
4687 | ML 252 |
Potent and selective KV7.2 inhibitor; brain penetrant | |
4777 | ML 277 |
Selective KV7.1 (KCNQ1) potassium channel activator; augments IKs current | |
4880 | ML 281 |
STK33 inhibitor | |
5380 | ML 297 |
Selective Kir3.1/3.2 (GIRK1/2) channel activator | |
4894 | ML 299 |
Potent inhibitor of PLD1 and PLD2; CNS penetrant | |
5700 | ML 315 hydrochloride |
Inhibitor of Clk and DYRK kinases | |
6435 | ML 323 |
Potent and selective USP1-UAF1 allosteric inhibitor | |
5625 | ML 334 |
Inhibitor of Keap1- Nrf2 interaction | |
6887 | ML 335 |
Selective K2P2.1 (TREK-1) and K2P10.1 (TREK-2) activator | |
4982 | ML 337 |
Selective negative allosteric modulator of mGlu3 receptors | |
5943 | ML 339 |
Potent and selective hCXCR6 antagonist | |
4945 | ML 347 |
Potent and selective ALK1 and ALK2 inhibitor | |
6448 | ML 351 |
Selective 12/15 LOX inhibitor; active in vivo | |
5337 | ML 365 |
Potent and selective K2P3.1 (TASK-1) channel blocker | |
5738 | ML 382 |
MRGPRX1 positive allosteric modulator | |
6243 | ML 385 |
Nrf2 inhibitor; phenotypically lethal | |
6889 | ML 418 |
Kir 7.1 inhibitor; also inhibits Kir 6.2 | |
6886 | ML 67-33 |
K2P2.1 (TREK-1), K2P10.1 (TREK-2) and K2P4.1 (TRAAK) channel activator | |
4310 | ML 7 hydrochloride |
Selective inhibitor of myosin light chain kinase | |
0431 | ML 9 hydrochloride |
Myosin light chain kinase inhibitor | |
4746 | ML SA1 |
Activator of TRPML channels | |
8119 | ML T7 |
Inhibitor of phosphatidylserine/CEACAM1 binding to Tim-3 | |
1885 | MLCK inhibitor peptide 18 |
Selective inhibitor of myosin light chain kinase | |
3345 | MLN 4760 |
Potent and selective angiotensin-converting enzyme 2 (ACE2) inhibitor | |
6499 | MLN 4924 |
Potent and selective NEDD8 activating enzyme (NAE) inhibitor; cell permeable | |
4582 | MLR 1023 |
Selective allosteric activator of Lyn kinase | |
6171 | MLS 1547 |
G protein-biased D2 partial agonist | |
5756 | MLi-2 |
Potent and selective LRRK2 inhibitor | |
5307 | MM 102 |
Potent WDR5/MLL interaction inhibitor | |
3822 | MM 11253 |
RARγ-selective antagonist | |
5992 | MM 54 |
Potent apelin antagonist | |
6858 | MMG 11 |
TLR2 antagonist | |
4388 | MNI 137 |
Selective negative allosteric modulator of group II mGlu receptors | |
1490 | MNI-caged-L-glutamate |
Stable photoreleaser of L-glutamate | |
6871 | MO-I-500 |
FTO inhibitor; anticonvulsant | |
2568 | MOG (35-55) |
Encephalitogenic myelin oligodendrocyte glycoprotein fragment | |
7926 | MOMBA |
Selective orthostatic agonist of hFFA2-DREADDs | |
5770 | MONNA |
Potent TMEM16A (Anoctamin-1) blocker | |
8802 | MPD 2 New |
SARS-CoV-2 Mpro Degrader (PROTAC®) | |
1212 | MPEP hydrochloride |
Potent mGlu5 antagonist; also positive allosteric modulator of mGlu4 receptors | |
1991 | MPP dihydrochloride |
Highly selective ERα antagonist | |
7695 | Mpro 61 |
Potent non-covalent inhibitor of SARS-CoV-2 main protease | |
7230 | MPro N3 |
Coronavirus Mpro inhibitor | |
7856 | MQAE |
Fluorescent Cl- indicator; membrane permeable | |
8122 | MR 24 New |
Potent and selective MST3 kinase binding inhibitor | |
3817 | MRK 016 |
α5-selective GABAA inverse agonist | |
4000 | MRK 560 |
γ-secretase inhibitor; attenuates amyloid plaque deposition | |
1217 | MRS 1220 |
Highly potent and selective hA3 antagonist | |
1385 | MRS 1334 |
Potent, highly selective hA3 antagonist | |
2752 | MRS 1754 |
Selective A2B antagonist | |
0900 | MRS 2179 tetrasodium salt |
Selective P2Y1 antagonist | |
2402 | MRS 2211 |
Competitive P2Y13 antagonist | |
2157 | MRS 2365 |
Highly potent and selective P2Y1 agonist | |
2159 | MRS 2500 tetraammonium salt |
Highly potent and selective P2Y1 antagonist | |
2146 | MRS 2578 |
Selective P2Y6 antagonist | |
2915 | MRS 2690 |
Potent P2Y14 agonist | |
2502 | MRS 2693 trisodium salt |
Selective P2Y6 agonist | |
3884 | MRS 2768 tetrasodium salt |
Selective P2Y2 agonist | |
5633 | MRS 2905 |
Potent and selective P2Y14 receptor agonist | |
4261 | MRS 4062 triethylammonium salt |
Selective P2Y4 receptor agonist | |
5134 | MRT 67307 dihydrochloride |
Salt inducible kinase (SIK) inhibitor; also ULK1 and 2 inhibitor | |
5067 | MRT 68601 hydrochloride |
Potent TBK inhibitor | |
5780 | MRT 68921 dihydrochloride |
ULK inhibitor | |
7488 | MRTX 849 |
Mutation-selective inhibitor of KRASG12C | |
5713 | MS 023 dihydrochloride |
Potent and selective type I PRMT inhibitor | |
8077 | MS 147 New |
PRC1 Degrader (PROTAC®); degrades BMI1 and RING1B | |
7395 | MS 154 |
Potent and selective cereblon-recruiting Degrader (PROTAC®) of mutant EGFR | |
7396 | MS 154N |
Negative control for MS 154 (Cat No. 7395) | |
8079 | MS 159 New |
NSD2 Degrader (PROTAC®) | |
6298 | MS 21570 |
GPR171 antagonist | |
6208 | MS 275 |
HDAC (Class I) inhibitor | |
8076 | MS 28 New |
Cyclin D1, CDK4/6 and cyclin D3 Degrader (PROTAC®) | |
7397 | MS 39 |
Potent and selective VHL-recruiting Degrader (PROTAC®) of mutant EGFR | |
7398 | MS 39N |
Negative control for MS 39 (Cat. No. 7397) | |
8080 | MS 4322 New |
Selective PRMT5 Degrader (PROTAC®) | |
8073 | MS 6105 New |
Potent lactate dehydrogenase Degrader (PROTAC®) | |
7353 | MSA 2 |
Non-nucleotide STING agonist; orally bioavailable | |
7927 | MSC 1186 |
Potent and selective SRPK family inhibitor | |
5641 | MSC 2032964A |
Potent and selective ASK1 inhibitor; orally bioavailable | |
8008 | MSC 4381 New |
Potent and selective monocarboxylate transporter 4 (MCT4) inhibitor | |
3013 | [Nle4,D-Phe7]-α-MSH |
Melanocortin receptor agonist | |
2584 | α-MSH |
Endogenous melanocortin receptor agonist | |
0803 | MSOP |
Specific group III mGlu antagonist | |
2921 | MTEP hydrochloride |
Potent and selective mGlu5 antagonist | |
7980 | MTK 458 |
PINK1 activator | |
5224 | MTT |
Reagent used in the measurement of cell proliferation | |
7979 | MU 1742 |
Potent and selective CK1α, CK1δ and CK1ε inhibitor | |
8109 | MYX 1715 |
N-myristoyltransferase (NMT) inhibitor | |
6154 | MZ 1 |
(+)-JQ1 based Degrader (PROTAC®) that preferentially degrades BRD4 | |
7855 | Mag-Fura-2 AM |
Magnesium (Mg2+) indicator, membrane permeable | |
7681 | Mandi |
Highly efficient chemical inducer of proximity (CIP) | |
6856 | α-Mangostin |
Inhibits proliferation and induces apoptosis selectively in pancreatic CSCs and cancer cell lines | |
3756 | Maraviroc |
Selective CCR5 antagonist | |
2631 | Marimastat |
Broad spectrum MMP inhibitor | |
7705 | Masitinib |
Potent colony-stimulating factor 1 receptor (CSF-1R) tyroine kinase inhibitor | |
4949 | MaxiPost |
Potassium channel modulator; exerts subtype-specific effects | |
1384 | McN-A 343 |
Selective M1 muscarinic agonist | |
3982 | Mdivi 1 |
Selective dynamin inhibitor; attenuates mitochondrial division and apoptosis | |
7634 | Me VH 032, amine |
Amine functionalized VHL ligand for PROTAC® research | |
3873 | MeBIO |
Inactive analog of BIO (Cat. No. 3194) | |
2281 | 2'-MeCCPA |
Highly selective and potent A1 receptor agonist | |
2843 | Mecamylamine hydrochloride |
Non-competitive nAChR antagonist | |
4245 | Meclizine dihydrochloride |
Human pregnane X receptor agonist; H1 antagonist | |
5160 | Medetomidine hydrochloride |
Potent and highly selective α2 agonist | |
6819 | Mefloquine hydrochloride |
Cx36 and Cx50 gap channel blocker; also antimalarial and antischistosomal | |
6285 | Megestrol Acetate |
Synthetic progesterone analog | |
2566 | Melanotan II |
High affinity melanocortin receptor agonist | |
3550 | Melatonin |
Endogenous hormone; agonist at MT1 and MT2 | |
1193 | Melittin |
Inhibits Gs and stimulates Gi activity | |
0773 | Memantine hydrochloride |
NMDA antagonist; acts at ion channel site | |
0660 | Mepyramine maleate |
Selective H1 inverse agonist | |
7577 | 3-Mercaptopicolinic acid hydrochloride |
Phospoenolpyruvate carboxykinase (PEPCK) inhibitor; inhibits gluconeogenesis | |
3053 | Mesopram |
Orally active PDE4 inhibitor | |
1644 | Mesulergine hydrochloride |
5-HT2A and 5-HT2C antagonist; also D2-like partial agonist | |
1443 | Metastin (human) |
Potent, endogenous ligand for kisspeptin receptor | |
2864 | Metformin hydrochloride |
Activator of LKB1/AMPK; antidiabetic agent | |
1230 | Methotrexate |
Cytotoxic agent | |
4920 | Methoxy-X04 |
Brain penetrant fluorescent amyloid β probe. Used for: detection and quantification of plaques, tangles and cerebrovascular amyloid. Application: confocal microscopy, suitable for in vivo imaging | |
7320 | Methoxyluteolin |
Inhibitor of pro-inflammatory mediator release from mast cells | |
5698 | 1-Methyl-D-tryptophan |
Indoleamine 2,3-dioxygenase (IDO) inhibitor | |
3977 | 3-Methyladenine |
Class III PI 3-kinase inhibitor; also inhibits autophagy | |
3209 | α,β-Methyleneadenosine 5'-triphosphate trisodium salt |
Non-selective P2 agonist | |
0549 | Methylergometrine maleate |
Active metabolite of methysergide (Cat. No. 1064) | |
0569 | (R)-(-)-α-Methylhistamine dihydrobromide |
Potent, standard H3 agonist | |
2342 | 4-Methylhistamine dihydrochloride |
Selective, high affinity H4 agonist | |
1029 | Methyllycaconitine citrate |
Selective α7 neuronal nAChR antagonist | |
4979 | Methylmalonate |
Succinate dehydrogenase inhibitor | |
4819 | Methylprednisolone |
Glucocorticoid receptor agonist | |
3017 | 1-Methylpsilocin |
Potent and selective 5-HT2C agonist | |
1624 | 2-Methylthioadenosine diphosphate trisodium salt |
Potent agonist at P2Y1, P2Y12 and P2Y13 | |
1062 | 2-Methylthioadenosine triphosphate tetrasodium salt |
Non-selective P2 agonist | |
1064 | Methysergide maleate |
5-HT1/5-HT2 antagonist | |
3256 | Metoprolol tartrate |
Selective β1 antagonist | |
3292 | Metyrapone |
11-β hydroxylase inhibitor | |
1526 | Mevastatin |
HMG-CoA reductase inhibitor | |
2596 | Mexiletine hydrochloride |
Na+ channel blocker; antiarrhythmic agent | |
2198 | Mibefradil dihydrochloride |
CaV3.x blocker | |
2832 | Midazolam hydrochloride |
Benzodiazepine agonist | |
1479 | Mifepristone |
Progesterone and glucocorticoid receptor antagonist | |
3117 | Miglustat hydrochloride |
α-glucosidase I and II inhibitor; also inhibits ceramide-specific glycosyltransferases and exhibits broad spectrum antiviral activity | |
1504 | Milrinone |
PDE3 inhibitor | |
3268 | Minocycline hydrochloride |
Antibiotic. Displays neuroprotective effects | |
0583 | Minoxidil |
Kir6 channel (KATP) opener | |
7070 | Mirabegron |
Potent and selective β3 agonist | |
3190 | Mirin |
MRN-ATM pathway inhibitor | |
7091 | Miro1 Reducer |
Promotes mitochondrial Rho GTPase 1 (Miro1) degradation | |
2018 | Mirtazapine |
Potent 5-HT2 antagonist; also 5-HT3, H1 and α2 antagonist; antidepressant | |
1489 | Mithramycin A |
Inhibitor of DNA and RNA polymerase | |
7641 | Mito-HE |
Red-fluorescent mitochondrial superoxide indicator. Used for: live cell imaging. Application: confocal microscopy, flow cytometry | |
7700 | MitoBrilliant™ 646 |
Universal red fluorescent mitochondrial stain for both live and fixed cells | |
7693 | MitoBrilliant™ Live 549 |
Orange fluorescent mitochondrial stain for live cells, Δψm dependent | |
7417 | MitoBrilliant™ Live 646 |
Red fluorescent mitochondrial stain for live cells, Δψm dependent | |
4428 | MitoPY1 |
Fluorescent mitochondrial hydrogen peroxide indicator. Used for: live cell imaging. Application: confocal microscopy | |
3258 | Mitomycin C |
DNA cross-linking antitumor agent | |
4395 | Moclobemide |
Reversible MAO-A inhibitor | |
1811 | Modafinil |
Psychostimulant | |
7586 | Molnupiravir |
Prodrug of antiviral nucleoside analog; inhibits SARS-CoV, SARS-CoV-2 and MERS-CoV infection | |
1305 | Monastrol |
Selective inhibitor of mitotic kinesin Eg5 | |
5904 | Montelukast sodium |
CysLT1 and GPR17 antagonist | |
5158 | Morphine hydrochloride |
Narcotic opioid analgesic | |
2264 | Motilin (human, porcine) |
Endogenous peptide regulator of gastrointestinal motility | |
7853 | Mpro 13b-H |
Negative control for Mpro 13b-K (Cat. No. 7228) | |
7228 | Mpro 13b-K |
Coronavirus Mpro inhibitor | |
8126 | Mpro Tracer New |
SARS-CoV-2 main protease fluorescent ligand; TR-FRET acceptor | |
5142 | Mps1-IN-1 dihydrochloride |
Selective Mps1 kinase inhibitor | |
3074 | (+)-Muscarine iodide |
Muscarinic receptor agonist | |
0289 | Muscimol |
Potent GABAA agonist; also GABAA-ρ partial agonist | |
4102 | Mycophenolate mofetil |
Inosine monophosphate dehydrogenase (IMPDH) inhibitor | |
1505 | Mycophenolic acid |
Inosine monophosphatase dehydrogenase (IMPDH) inhibitor |
Tocris Products by Catalog Number
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