Catalog No. Size 价格库存数量
S0766-2 2mg solid ¥95
售罄
不可用
S0766-10 10mg solid ¥285
售罄
不可用

详情描述

WT-161 is a potent and selective HDAC6 inhibitor with an IC50 of 0.40 nM.

Product information

CAS Number: 1206731-57-8

Molecular Weight: 458.55

Formula: C27H30N4O3

Chemical Name: 7-{N'-[(1E)-[4-(diphenylamino)phenyl]methylidene]hydrazinecarbonyl}-N-hydroxyheptanamide

Smiles: ONC(=O)CCCCCCC(=O)N/N=C/C1C=CC(=CC=1)N(C1C=CC=CC=1)C1C=CC=CC=1

InChiKey: KXWWYFKVBFUVIZ-SGWCAAJKSA-N

InChi: InChI=1S/C27H30N4O3/c32-26(15-9-1-2-10-16-27(33)30-34)29-28-21-22-17-19-25(20-18-22)31(23-11-5-3-6-12-23)24-13-7-4-8-14-24/h3-8,11-14,17-21,34H,1-2,9-10,15-16H2,(H,29,32)(H,30,33)/b28-21+

Technical Data

Appearance: Solid Power

Purity: ≥98% (or refer to the Certificate of Analysis)

Solubility: DMSO : ≥ 100 mg/mL (218.08 mM)

Shipping Condition: Shipped under ambient temperature as non-hazardous chemical or refer to Certificate of Analysis

Storage Condition: Dry, dark and -20 oC for 1 year or refer to the Certificate of Analysis.

Shelf Life: ≥360 days if stored properly.

Stock Solution Storage: 0 - 4 oC for 1 month or refer to the Certificate of Analysis.

Drug Formulation: To be determined

HS Tariff Code: 382200

How to use

In Vitro:

WT161 selectively inhibits HDAC6 and dramatically increases levels of acetylated α-tubulin (Ac-α-tubulin) with little effect on global lysine acetylation. WT161 induces significant toxicity in all multiple myeloma cell lines tested, with IC50s between 1.5 and 4.7 µM . WT161 in combination with bortezomib triggers significant accumulation of polyubiquitinated proteins and cell stress, followed by caspase activation and apoptosis. More importantly, this combination treatment is effective in bortezomib-resistant cells and in the presence of bone marrow stromal cells, which have been shown to mediate multiple myeloma cell drug resistance.

In Vivo:

WT161 shows toxicity at 100 mg/kg i.p., but WT161 is well tolerated at 50 mg/kg i.p.. Bortezomib combined with WT161 demonstrates a significant antitumor effect.

References:

  1. Hideshima T, et al. Discovery of selective small-molecule HDAC6 inhibitor for overcoming proteasome inhibitor resistance in multiple myeloma. Proc Natl Acad Sci U S A. 2016 Nov 15;113(46):13162-13167.

Products are for research use only. Not for human use.

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