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PCC0105003

PCC0105003 is a potent MARK inhibitor. PCC0105003 can be used in the study of neuropathic pain[1].

Product Specifications

UNSPSC

12352005

Target

MARK

Type

Reference compound

Related Pathways

Cell Cycle/DNA Damage

Field of Research

Neurological Disease

Assay Protocol

https://www.medchemexpress.com/pcc0105003.html

Purity

99.88

Solubility

DMSO : 100 mg/mL (ultrasonic)

Smiles

FC(F)(C1=CN=C(N=C1NCC2=NNC=C2)NC3=CC=C(C=C3)N4CCOCC4)F

Molecular Formula

C19H20F3N7O

Molecular Weight

419.40

References & Citations

[1]Shi YQ, et al. A novel role for microtubule affinity-regulating kinases in neuropathic pain. Br J Pharmacol. 2024 Jul;181 (13) :2012-2032.|[2]Shi YQ, et al. A novel role for microtubule affinity-regulating kinases in neuropathic pain. Br J Pharmacol. 2024 Jul;181 (13) :2012-2032.

Shipping Conditions

Room Temperature

Storage Conditions

4°C (Powder, protect from light)

Scientific Category

Reference compound1

Clinical Information

No Development Reported

Available Sizes

Frequently Asked Questions

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