UF-010
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    WARNING: This product is for research use only, not for human or veterinary use.

MedKoo CAT#: 406722

CAS#: 537672-41-6

Description: UF-010 is a Class I HDAC inhibitor (IC50 values are 0.06, 0.1, 0.5 and 1.5 μM for HDACs 3, 2, 1 and 8, respectively). UF010 inhibits cancer cell proliferation via class I HDAC inhibition. This causes global changes in protein acetylation and gene expression, resulting in activation of tumor suppressor pathways and concurrent inhibition of several oncogenic pathways. The isotype selectivity coupled with interesting biological activities in suppressing tumor cell proliferation support further preclinical development of the UF010 class of compounds for potential therapeutic applications.


Price and Availability

Size
Price

100mg
USD 750
1g
USD 3150
Size
Price

200mg
USD 1250
2g
USD 4950
Size
Price

500mg
USD 2250
5g
USD 6850

UF-010, purity > 98%, is in stock. Current shipping out time is about 2 weeks after order is received. CoA, QC data and MSDS documents are available in one week after order is received. Delivery time: overnight (USA/Canada); 3-5 days (worldwide).


Chemical Structure

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Theoretical Analysis

MedKoo Cat#: 406722
Name: UF-010
CAS#: 537672-41-6
Chemical Formula: C11H15BrN2O
Exact Mass: 270.0368
Molecular Weight: 271.158
Elemental Analysis: C, 48.72; H, 5.58; Br, 29.47; N, 10.33; O, 5.90


Synonym: UF-010, UF 010, UF010

IUPAC/Chemical Name: 4-Bromo-N'-butylbenzohydrazide

InChi Key: BVQCFCYPFJOOAV-UHFFFAOYSA-N

InChi Code: InChI=1S/C11H15BrN2O/c1-2-3-8-13-14-11(15)9-4-6-10(12)7-5-9/h4-7,13H,2-3,8H2,1H3,(H,14,15)

SMILES Code: O=C(NNCCCC)C1=CC=C(Br)C=C1


Technical Data

Appearance:
Crystalline solid

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, not in water

Shelf Life:
>2 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).

Harmonized System Code:
293490


References

1: Mahmud I, Liao D. Microarray gene expression profiling reveals potential mechanisms of tumor suppression by the class I HDAC-selective benzoylhydrazide inhibitors. Genom Data. 2015 Sep 1;5:257-259. PubMed PMID: 26217556; PubMed Central PMCID: PMC4513360.

2: Wang Y, Stowe RL, Pinello CE, Tian G, Madoux F, Li D, Zhao LY, Li JL, Wang Y, Wang Y, Ma H, Hodder P, Roush WR, Liao D. Identification of histone deacetylase inhibitors with benzoylhydrazide scaffold that selectively inhibit class I histone deacetylases. Chem Biol. 2015 Feb 19;22(2):273-84. doi:
10.1016/j.chembiol.2014.12.015. PubMed PMID: 25699604; PubMed Central PMCID: PMC4365786.