J22352
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 462481

CAS#: 2252395-44-9

Description: J22352 is a PROTAC (proteolysis-targeting chimeras)-like and highly selective HDAC6 inhibitor. J22352 promotes HDAC6 degradation and induces anticancer effects by inhibiting autophagy and eliciting the antitumor immune response in glioblastoma cancers, and leading to the restoration of host antitumor activity by reducing the immunosuppressive activity of PD-L1.

Chemical Structure

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J22352
CAS# 2252395-44-9
Handing Instruction

Theoretical Analysis

MedKoo Cat#: 462481
Name: J22352
CAS#: 2252395-44-9
Chemical Formula: C24H21N3O4
Exact Mass: 415.1532
Molecular Weight: 415.449
Elemental Analysis: C, 69.39; H, 5.10; N, 10.11; O, 15.40

Size Price Shipping out time Quantity
5mg USD 300 2 Weeks
10mg USD 480 2 Weeks
50mg USD 1000 2 Weeks
Inquire bulk and customized quantity
Pricing updated 2021-03-02. Prices are subject to change without notice.

J22352 is in stock.

Synonym: J22352; J-22352; J 22352

IUPAC/Chemical Name: 4-((2,4-dioxo-3-phenethyl-3,4-dihydroquinazolin-1(2H)-yl)methyl)-N-hydroxybenzamide

InChi Key: JBJIKUXUKSADFV-UHFFFAOYSA-N

InChi Code: InChI=1S/C24H21N3O4/c28-22(25-31)19-12-10-18(11-13-19)16-27-21-9-5-4-8-20(21)23(29)26(24(27)30)15-14-17-6-2-1-3-7-17/h1-13,31H,14-16H2,(H,25,28)

SMILES Code: O=C(C1=CC=CC=C1N2CC3=CC=C(C(NO)=O)C=C3)N(CCC4=CC=CC=C4)C2=O

Appearance:
Solid powder

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

Shipping Condition:
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.

Storage Condition:
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility:
Soluble in DMSO

Shelf Life:
>3 years if stored properly

Drug Formulation:
This drug may be formulated in DMSO

Stock Solution Storage:
0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code:
2934.99.9001

Handling Instructions:
View handling instruction

Preparing Stock Solutions

The following data is based on the product molecular weight 415.449 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Select a batch to recalculate based on the batch molecular weight:
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL

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1: Liu JR, Yu CW, Hung PY, Hsin LW, Chern JW. High-selective HDAC6 inhibitor promotes HDAC6 degradation following autophagy modulation and enhanced antitumor immunity in glioblastoma. Biochem Pharmacol. 2019;163:458-471. doi:10.1016/j.bcp.2019.03.023

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J22352

5mg / USD 300