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p97

p97 also known as VCP ( Cdc48 in yeast) is a hexameric ATPase of the AAA family which disassembles SNARE proteins after membrane fusion. It is involved in a fusion of homotypic membranes, protein degradation, and activation of membrane-bound transcription factors.

Cat. No.	Product name	CAS No.	Purity
T3164	ML241	1346528-06-0
T3164	ML241 is a potent and selective inhibitors of p97 ATPase.
T79255	UPCDC30766	2152623-68-0	98%
T79255	UPCDC30766, a potent allosteric inhibitor of p97, exhibits an IC50 of 12 nM and is applicable for colon cancer research [1].
T12114	MSC1094308	2219320-08-6	98%
T12114	MSC1094308 is a reversible and allosteric inhibitor of the type II AAA ATPase.
T1969	DBEQ	177355-84-9	99.94%
T1969	DBEQ (JRF 12) is a selective, potent, reversible, and ATP-competitive p97 inhibitor.
T6796	CB-5083	1542705-92-9	99.92%
T6796	CB-5083 is a potent, selective, and orally bioavailable p97 AAA ATPase inhibitor ( IC50=11 nM).
T1853	NMS-873	1418013-75-8	99.71%
T1853	NMS-873 is a potent, selective allosteric VCP/p97 inhibitor.
T60193	CB-5339	1863952-15-1	98.5%
T60193	p97-IN-1 is a potent inhibitor of p97 with an IC 50 <30 nM [1].
T6594	MNS	1485-00-3	98.45%
T6594	MNS is a tyrosine kinases inhibitor, inhibits Syk, Src, p97 with IC50 of 2.5 μM, 29.3 μM and 1.7 μM, respectively.
T3535	ML240	1346527-98-7	100%
T3535	ML240 is a selective, ATP-competitive p97 inhibitor.
T4684	ML241 hydrochloride	2070015-13-1	98%
T4684	ML241 is a potent and selective inhibitors of p97 ATPase.ML241 inhibits degradation of a p97-dependent but not a p97-independent proteasome substrate in a dual-r...