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(6)
By Target- PROTAC Linker
- Adrenergic Receptor(1)
- Autophagy(1)
- Calcium Channel(1)
- Dehydrogenase(1)
- PKA(1)
- PKC(1)
- Prostaglandin Receptor(1)
- ROCK(1)
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Results for "
T1606
" in TargetMol Product Catalog.- Inhibitors & Agonists11
- PROTAC Products6
- Antibody Products1
- Cell Research1
- FasudilHA-1077, AT877T1606103745-39-7Fasudil (HA-1077) is a potent inhibitor of ROCK1, PKA, PKC, and MLCK.
- $33
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Cited - Methyltetrazine-PEG5-NHS esterT160601802907-92-1Methyltetrazine-PEG5-NHS ester is a PROTAC linker belonging to the group of PEGs and is used for the synthesis of PROTAC molecules.
- $34
SizeQTY - Methyltetrazine-PEG8-acidT160612183440-33-5Methyltetrazine-PEG8-acid is a polyethylene glycol (PEG) derivative commonly employed as a linker in the synthesis of proteolysis-targeting chimeras (PROTACs)[1].
- Inquiry Price
SizeQTY - Methyltetrazine-PEG8-NHS esterT160622183440-34-6Methyltetrazine-PEG8-NHS ester is a polyethylene glycol (PEG) derivative specifically designed as a PROTAC linker for synthesizing Proteolysis Targeting Chimeras (PROTACs)[1].
- Inquiry Price
SizeQTY - Methyltetrazine-Ph-NHS esterT160631644644-96-1Methyltetrazine-Ph-NHS ester is an alkyl/ether-based linker used in synthesizing PROTACs (proteolysis-targeting chimeras)[1].
- Inquiry Price
SizeQTY - Methyltetrazine-Ph-PEG4-azideT160641802908-04-8Methyltetrazine-Ph-PEG4-azide is a PEG-based azide linker used in PROTAC synthesis [1].
- Inquiry Price
SizeQTY - Methyltetrazine-propylamineT160651802978-47-7Methyltetrazine-propylamine, an alkyl chain-based PROTAC linker, is utilized in the synthesis of PROTACs [1].
- Inquiry Price
SizeQTY - Metipranolol hydrochlorideT1606636592-77-5Metipranolol hydrochloride is a non-selective β-adrenergic receptor blocking agent.
- $77
SizeQTY - Metrizoic acidMetrizoateT160671949-45-7Metrizoic acid is an ionic contrast medium with high osmolality and carries a risk of inducing allergic reactions.
- $30
SizeQTY - MF-438T16068921605-87-0MF-438 is an effective and orally bioavailable stearoyl-CoA desaturase 1 (SCD1) inhibitor (EC50: 2.3 nM for rSCD1).
- $98
SizeQTY - MF498T16069915191-42-3MF498 is a novel and selective E prostanoid receptor 4 (EP4 receptor) antagonist, displayed a strong binding affinity for the EP4 receptor (Ki: 0.7 nM).
- $246
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