Benzamide, N-hydroxy-4-[(8-quinolinylamino)methyl]-, compd. with methanesulfonate (1:1)
- CAS No.
- 2151854-33-8
- Chemical Name:
- Benzamide, N-hydroxy-4-[(8-quinolinylamino)methyl]-, compd. with methanesulfonate (1:1)
- Synonyms
- MPT0G211 mesylate;Benzamide, N-hydroxy-4-[(8-quinolinylamino)methyl]-, compd. with methanesulfonate (1:1)
- CBNumber:
- CB710974040
- Molecular Formula:
- C18H19N3O5S
- Molecular Weight:
- 389.43
- MDL Number:
- MOL File:
- 2151854-33-8.mol
- MSDS File:
- SDS
- TDS File:
- TDS
Benzamide, N-hydroxy-4-[(8-quinolinylamino)methyl]-, compd. with methanesulfonate (1:1) Chemical Properties,Uses,Production
Uses
MPT0G211 mesylate is a potent, orally active and selective HDAC6 inhibitor (IC50=0.291 nM). MPT0G211 mesylate displays >1000-fold selective for HDAC6 over other HDAC isoforms. MPT0G211 mesylate can penetrate the blood-brain barrier. MPT0G211 mesylate ameliorates tau phosphorylation and cognitive deficits in an Alzheimer’s disease model. MPT0G211 mesylate has anti-metastatic and neuroprotective effects. Anticancer activities[1][2][3].
in vivo
MPT0G211 mesylate (50 mg/kg; p.o.; daily for 3 months) significantly ameliorates the spatial memory impairment[1].
MPT0G211 mesylate (25 mg/kg; i.p.; qd; day 73 post-tumor injection) reduces numbers of nodules and lung weights[2].
MPT0G211 mesylate treatment not only diminishes tau phosphorylation by inhibition GSK3β activity but also enhances the acetylation of Hsp90, which causes the downregulation of HDAC6/Hsp90 binding and facilitates proteasomal degradation of polyubiquitinated p-tau[1].
| Animal Model: | Triple transgenic (3×Tg-AD) mice (harboring APPSwe and tauP301L mutant transgenes[1] |
| Dosage: | 50mg/kg |
| Administration: | P.o.; daily for 3 months |
| Result: | Significantly ameliorated the spatial memory impairment. |
| Animal Model: | Female SCID mice (bearing MDA-MB-231 cells)[2] |
| Dosage: | 25mg/kg |
| Administration: | I.p.; qd; day 73 post-tumor injection |
| Result: | Significantly reduced numbers of nodules and lung weights. |
IC 50
HDAC6: 0.291 μM (IC50)
References
[1] Fan SJ, et al. The novel histone de acetylase 6 inhibitor, MPT0G211, ameliorates tau phosphorylation and cognitive deficits in an Alzheimer's disease model. Cell Death Dis. 2018;9(6):655. Published 2018 May 29. DOI:10.1038/s41419-018-0688-5
[2] Hsieh YL, et al. Anti-metastatic activity of MPT0G211, a novel HDAC6 inhibitor, in human breast cancer cells in vitro and in vivo. Biochim Biophys Acta Mol Cell Res. 2019;1866(6):992-1003. DOI:10.1016/j.bbamcr.2019.03.003
[3] Tu HJ, et al. The anticancer effects of MPT0G211, a novel HDAC6 inhibitor, combined with chemotherapeutic agents in human acute leukemia cells. Clin Epigenetics. 2018;10(1):162. Published 2018 Dec 29. DOI:10.1016/j.bbamcr.2019.03.003
Benzamide, N-hydroxy-4-[(8-quinolinylamino)methyl]-, compd. with methanesulfonate (1:1) Preparation Products And Raw materials
Raw materials
Preparation Products
Benzamide, N-hydroxy-4-[(8-quinolinylamino)methyl]-, compd. with methanesulfonate (1:1) Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
|---|---|---|---|---|---|
| BOC Sciences | 1-631-485-4226; 16314854226 | info@bocsci.com | United States | 9920 | 65 |
| TargetMol Chemicals Inc. | 15002134094 | marketing@targetmol.cn | China | 29874 | 58 |
| TargetMol Chemicals Inc. | 13564774135 | marketing@targetmol.com | United States | 19950 | 58 |
| Supplier | Advantage |
|---|---|
| BOC Sciences | 65 |
| TargetMol Chemicals Inc. | 58 |
| TargetMol Chemicals Inc. | 58 |
View Lastest Price from Benzamide, N-hydroxy-4-[(8-quinolinylamino)methyl]-, compd. with methanesulfonate (1:1) manufacturers
| Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
|---|---|---|---|---|---|---|---|---|
![]() |
2026-04-20 | MPT0G211 mesylate
2151854-33-8
|
$1520.00-2500.00 | 10g | TargetMol Chemicals Inc. |
-

- MPT0G211 mesylate
2151854-33-8
- $1520.00-2500.00
- TargetMol Chemicals Inc.




