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UNC0638 - ≥98%, high purity , CAS No.1255580-76-7, Inhibitor of euchromatic histone lysine methyltransferase 1;Inhibitor of euchromatic histone lysine methyltransferase 2

  • Moligand™
  • ≥98%
Item Number
U275196
Grouped product items
SKUSizeAvailabilityPrice Qty
U275196-1mg
1mg
In stock
$18.90
U275196-5mg
5mg
In stock
$77.90
U275196-10mg
10mg
In stock
$116.90
U275196-50mg
50mg
In stock
$325.90
U275196-250mg
250mg
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$1,467.90

Potent, selective and reversible G9 and GLP histone methyltransferase inhibitor

Basic Description

Synonyms1255580-76-7|UNC0638|UNC-0638|UNC 0638|2-Cyclohexyl-N-(1-isopropylpiperidin-4-yl)-6-methoxy-7-(3-(pyrrolidin-1-yl)propoxy)quinazolin-4-amine|1255517-77-1|2-cyclohexyl-6-methoxy-N-(1-propan-2-ylpiperidin-4-yl)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine
Specifications & Purity≥98%
SourceSynthetic
Storage TempStore at -20°C,Desiccated
Shipped InDry ice
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of euchromatic histone lysine methyltransferase 1;Inhibitor of euchromatic histone lysine methyltransferase 2
Product Description

Description
UNC0638 is a potent, selective and cell-penetrant chemical probe for G9a and GLP histone methyltransferase with IC50 of <15 nM and 19 nM, respectively, shows selectivity over a wide range of epigenetic and non-epigenetic targets. UNC0638 has anti-viral activities.
Application
In MDA-MB-231 cells, in a concentration-dependent manner, exposure to UNC0638 for 48 h reduced H3K9me2 levels with an IC50 value of 81 ± 9 nM. Cellular levels of H3K9me2 were progressively reduced from 1 d to 4 d exposure to UNC0638 at the concentrations of 80 nM (IC50), 250 nM (IC90) and 500 nM (2 × IC90). The reductions of H3K9me2 levels with 250 nM and 500 nM treatments after 4 d were equal or very close to that of G9a and GLP knockdown cells. The effects of UNC0638 were long-lasting. In cells with 2 d exposure to UNC0638, levels of H3K9me2 remained low after washout of compound followed by 2 d incubation without the inhibitor.

Associated Targets

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 2 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EHMT1 Tchem Histone-lysine N-methyltransferase EHMT1 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name 2-cyclohexyl-6-methoxy-N-(1-propan-2-ylpiperidin-4-yl)-7-(3-pyrrolidin-1-ylpropoxy)quinazolin-4-amine
INCHI InChI=1S/C30H47N5O2/c1-22(2)35-17-12-24(13-18-35)31-30-25-20-27(36-3)28(37-19-9-16-34-14-7-8-15-34)21-26(25)32-29(33-30)23-10-5-4-6-11-23/h20-24H,4-19H2,1-3H3,(H,31,32,33)
InChi Key QOECJCJVIMVJGX-UHFFFAOYSA-N
Canonical SMILES CC(C)N1CCC(CC1)NC2=NC(=NC3=CC(=C(C=C32)OC)OCCCN4CCCC4)C5CCCCC5
Isomeric SMILES CC(C)N1CCC(CC1)NC2=NC(=NC3=CC(=C(C=C32)OC)OCCCN4CCCC4)C5CCCCC5
PubChem CID 46224516
Molecular Weight 509.73

Certificates

Certificate of Analysis(COA)

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5 results found

Lot NumberCertificate TypeDateItem
L2107128Certificate of AnalysisJun 14, 2023 U275196
L2107129Certificate of AnalysisJun 14, 2023 U275196
L2107132Certificate of AnalysisJun 14, 2023 U275196
L2107120Certificate of AnalysisJun 14, 2023 U275196
L2107152Certificate of AnalysisJun 14, 2023 U275196

Chemical and Physical Properties

Solubility≥25.5 mg/mL in DMSO; insoluble in H2O; ≥48.2 mg/mL in EtOH

Related Documents

Solution Calculators