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Zuclopenthixol

Zuclopenthixol, also known as Cisordinol, Clopixol, Acuphase, zuclopentixol, is a ...

Zuclopenthixol acetate

Zuclopenthixol acetate is a typical antipsychotic drug of the thioxanthene class. ...

Zuclopenthixol decanoate

Zuclopenthixol decanoate is an anti-schizophrenia drug. Zuclopenthixol decanoate p...

Zuclopenthixol dihydrochloride

Zuclopenthixol, also known as Cisordinol, Clopixol, Acuphase, zuclopentixol, is a ...

ZUH280 is a potent and effective HDAC8 Degrader. SZUH280 effectively induced HDAC8...

Also known as Difluorocarboxyfluorescein Azide, 6-isomer. It is a bright, green-f...

Also known as 5(6)-Carboxyrhodamine 110 NHS Ester. It is the nonsulfonated analog ...

ZUN00609, also known as Azido-PEG9-NHS ester is a PEG Linker. PEG Linkers may be u...

ZUN04395, also known as GSK3β inhibitor XI, is a potent inhibitor of glycogen synt...

ZUN29814 is a CRBN modulator, which showed CRBN modulatory activity.

ZUN36901, also known asCompound 18, MPO-IN-28 and NPYLR7-agonist-18, is a novel p...

ZUN 42572, also known as N-(Azido-PEG3)-N-bis(PEG3-acid) HCl salt is a branched PE...

ZUN64390, also known as PI3Kδ-IN-1, is a potent, selective, and efficacious PI3Kδ ...

ZUN70743, also known as 7-Methoxy-8-(3-morpholin-4-ylpropoxy)-2,3-dihydroimidazo[1...

ZUN 89633, also known as Propargyl-PEG5-CH2CO2tBu is a PEG derivative containing a...

ZUN 91828, also known as Azido-PEG8-amine is a PEG derivative containing an amino ...

ZUN97585, also known as FGFR1/DDR2 inhibitor 1, is an orally active inhibitor of ...

Zunsemetinib

Zunsemetinib, also known as ATI-450 and CDD450, is a potent MK2 Inhibitor. ATI-450...

Zunsemetinib M-atropisomer

Zunsemetinib M-atropisomer is the inactive isomer of Zunsemetinib. Zunsemetinib, ...

Zuretinol, is the metabolite of Zuretinol acetate, which is also known as QLT09100...

Zurletrectinib

Zurletrectinib is a tyrosine kinase inhibitor with potential as an antineoplastic ...

Zuvotolimod

Zuvotolimod is a biochemical.

Z-VAD-FMK is a cell-permeable, irreversible pan-caspase inhibitor. Z-VAD-FMK inhib...

Z-VAD(OH)-FMK

Z-VAD(OH)-FMK, also known as Z-Val-Ala-Asp-(OH)-Fluoromethyl Ketone, is an irreve...

Z-VAE(OMe)-fmk

Z-VAE(OMe)-fmk is a cell-permeable and irreversible UCHL1 inhibitor. The inhibitor...

ZVN26391, also known as NLRP3-IN-10, is a IL-1β inhibitor for the treatment of inf...

ZW4864 is an Orally Bioavailable Small-Molecule Inhibitor for the β‑Catenin/B-Cell...

Zwittermicin A

Zwittermicin A is a natural antibiotic with diverse biological activities includin...

ZWM026 is a multi-target inhibitor, and an indolocarbazoles analogue derived from ...

ZWN 06769, also known as N-(Azido-PEG3)-N-Biotin-PEG4-methyl ester is a Biotin PEG...

ZX-29 is a potent and selective ALK inhibitor for ALK, ALK L1196M and ALK G1202R m...

ZXH-1-161 is a novel Selective Degrader of GSPT1. Due to its potency and selectivi...

ZXH-3-26 is a selective degrader of BRD4.

ZXH-3-26 HCl

ZXH-3-26 is a selective PROTAC BRD4 degrader.

ZXH-4-130 is a PROTAC compound.

ZXH-4-137 is a PROTAC compound.

ZX-J-19J is an inhibitor of Cyclophilin J (CyPJ) PPIase. ZX-J-19J demonstrates rem...

ZX-J-19L is an inhibitor of Cyclophilin J (CyPJ) PPIase. ZX-J-19L demonstrates rem...

ZXX2-77 is a cyclooxygenase-1 inhibitor.

ZY12201 is a novel potent and orally bioavailable TGR5 agonist.

Zy 15109 is an inhaled mast cell stabiliser.

ZYDPLA1 is a novel next generation orally active DPP-4 inhibitor to treat Type 2 D...

Zygosporin D

Zygosporin D is one of the cytochalasins was isolated from the culture filtrate of...

ZYH is a monoacylglycerol lipase (MAGL) inhibitor

ZYJ-25e is a histone deacetylase inhibitor (HDACi) with potent oral antitumor acti...

ZYJ-34c is a histone deacetylase inhibitor (HDACi) with potent oral antitumor acti...

ZYJ-34v is an oral active histone deacetylase inhibitor with potent antitumor acti...

Zylofuramine

Zylofuramine is a psychomotor stimulant.

Zymostenol is a late-stage precursor in the biosynthesis of cholesterol.

ZYN57939 is RNA polymerase I inhibitor for treating RNA polymerase I-mediated dis...