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16
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19
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10
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20
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Products starting with 'M'
or product name starting with:
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H620112
MDK71803
MDK71803 is an important intermediate or precursor for the synthesis of Cefiderocol. MDK71803 has CA…
H620111
MDK08445
MDK08445 is an important intermediate or precursor for the synthesis of Cefiderocol. MDK08445 has CA…
H406976
MS436
featured
MS436 is a BRD4 inhibitor. MS436, through a set of water-mediated interactions, exhibits low nanomo…
H530452
ML349
featured
ML349 is a reversible APT2 inhibitor with Ki = 120 nM. ML349 is highly selective within the serine …
H530450
MDK00245
featured
MDK00245, also known as TGR5 Receptor Agonist. MDK00245 has the CAS# 1197300-24-5. The last 5 digits…
H530449
ML161
featured
ML-161 is a potent and reversible inhibitor of proteinase-activated receptor 1 (PAR1) on platelets, …
H530446
ML226
ML226 is a DAGLα inhibitor.
H530439
MC-976
featured
MC-976 is an Vitamin D3 derivative.
H530436
MK-4256
MK-4256 is a potent and selective SSTR3 Antagonist as a Potential Treatment of Type 2 Diabetes. MK-4…
H530435
MitoPQ
featured
MitoPQ, also known as MitoParaquat, is a redox cycler. MitoParaquat (MitoPQ) that comprises a trip…
H530433
MK-1064
featured
MK-1064 is a potent, selective and orally active Orexin OX2 Receptor Antagonist for potential treatm…
H530212
MK-0703
MK-0703 is a selective cyclooxygenase-2 inhibitor investigated for the treatment of acute pain and i…
H531223
MRT68921 free base
featured
MRT68921 is an inhibitor of ULK1 and ULK2 (IC50s = 2.9 and 1.1 nM, respectively).
H531207
MDL 29951
featured
MDL 29951 is a novel glycine antagonist of NMDA receptor activation (Ki=0.14 mM, [3H]glycine binding…
H530205
Manifaxine
Manifaxine is a norepinephrine-dopamine reuptake inhibitor potentially for the treatment of attentio…
H329462
Meptazinol HCl
Meptazinol, also known as IL 22811 and WY 22811, is an opioid analgesic developed by Wyeth in the 19…
H530342
MK-8617
featured
MK-8617 is a potent, selective, orally bioavailabl Pan-Inhibitor of Hypoxia-Inducible Factor Prolyl …
H530335
MUN 08963
featured
MUN 08963, also known as Pyrrolidinedithiocarbamate ammonium, also known as PDTC, is a nuclear fact…
H206763
Marizomib
featured
Marizomib, also known as ML 858, NPI-0052 and Salinosporamide A, is a potent and selective 20S prote…
H406957
ML348
featured
ML348, also known as CID 3238952; SID 160654487, is a reversible LYPLA1 inhibitor with an IC50 value…
H406954
M2I-1
featured
M2I-1, also known as Mad2 Inhibitor-1, is Protein-Protein Interaction Inhibitor Targeting the Mitoti…
H530312
MDL-100240
MDL-100240 is a dual inhibitor of angiotensin-converting enzyme (ACE) and neprilysin. MDL 100240 is …
H530409
MK-0941 mesylate
featured
MK-0941 mesylate is a glucokinase activator (GKA) potentially for the treatment of type 2 diabetes. …
H526999
MK-0736
MK-0736 is a potent and selective 11β-HSD-1 inhibitor. Emerging data from animal and human studies i…
H206756
Merbarone
Merbarone, also known as NSC-336628; RLBN-1001, is a Type II DNA topoisomerase inhibitor potentially…
H526996
MCI-225 hydrochloride hydrate
MCI-225, also known as AA-10021; AA-10025; AA-10026; DDP-225, is a norepinephrine reuptake/5-HT3/5-H…
H526993
MEM-1003
MEM-1003, also known as BAY-Z-4406, is a calcium channel blocker potentially for treatment of bipola…
H328079
Mequitamium iodide
Mequitamium iodide, also known as LG-30435, is a platelet activating factor (PAF) inhibitor potentia…
H206755
Metesind
Metesind, also known as AG-331; AG-341, is a thymidylate synthase inhibitor potentially for the trea…
H328071
Mimopezil
Mimopezil, also known as ZT-1 and Debio-9902, is an acetylcholinesterase (AChE) inhibitor potentiall…
H527002
Mavacamten
featured
Mavacamten, also known as SAR-439152 and MYK-461, is a myosin inhibitor potentially for the treatmen…
H406847
MS453
MS453 is a potent and selective SETD8 inhibitor. MS453 specifically modifies a cysteine residue near…
H406846
MS2177
MS2177 is a potent and selective SETD8 inhibitor. MS2177 has an in vitro IC50 of 1.9 μM (σ = 1.05 μM…
H328044
Mivobulin Isethionate
Mivobulin, also known as CI-980; NSC-613863; NSC-635370; NSC-613862; NSC-350386; is a tubulin inhibi…
H328041
Modipafant racemate
Modipafant racemate, also known as UK-74505, is a potent and specific oral platelet activating facto…
H328033
Methylthioninium chloride hydrate
featured
Methylthioninium Chloride, also known as TRx-014 and Methylene blue, has many uses in biology and c…
H526935
ME-3221
ME-3221 is an angiotensin type 1 receptor antagonist potentially for the treatment of hypertension. …
H328029
Milfasartan
Milfasartan, also known as LR-B-081; LRB-081, is is a potent, selective and orally active antagonis…
H526919
ME-1111
ME-1111 is an antifungal agent for topical treatment of onychomycosis. ME1111 showed potent antifung…
H526907
MIPS-9922
MIPS-9922 is a potent and selective PI3Kβ inhibitor with antiplatelet activity. MIPS-9922 potently …
H526895
ML-324
new
featured
ML-324, also known as CID-44143209, is a potent JMJD2 demethylase inhibitor with demonstrated antivi…
H329103
Mosapramine
Mosapramine, also known as Clospipramine and Y-516, is a dopamine D2-receptor antagonist used for th…
H526893
MK-8998
MK-8998 is a T type calcium channel antagonist potentially for the treatment of schizophrenia. MK-89…
H328006
Maribavir
featured
Maribavir, also known as 1263W-94; BW-1263W-94; GW-1263; GW-257406X; SHP-620; VP-41263; BW-1263W94, …
H328915
Monoethanolamine Oleate
Monoethanolamine Oleate, also known as Ethamolin and FO-611, is a sclerosant used to treat varicose …
H406833
MK-4101
featured
MK-4101 is a potent and selective inhibitor of the Hedgehog Pathway. MK-401 Is Highly Active against…
H406828
MSC2530818
featured
MSC2530818 is a Potent, Selective, and Orally Bioavailable CDK8 Inhibitor with CDK8 IC50 = 2.6 nM; H…
H328612
Meprednisone
featured
Meprednisone, also known as NSC-63278 and Betapar, is a glucocorticoid receptor agonist used to trea…
H328611
Menatetrenone
featured
Menatetrenone (also known as Vitamin K-2[20], Vitamin MK-4, and E-3100) is a vitamin K compound used…
H328610
Mesalamine
featured
Mesalamine, also known as Asacol and 5-ASA, is an IkB kinase inhibitor structurally related to the s…
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