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UNC669 - 10mM in DMSO, high purity , CAS No.1314241-44-5

    Grade & Purity:
  • 10mM in DMSO
In stock
Item Number
U421217
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U421217-1ml
1ml
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$105.90

Selective, competitive L3MBTL antagonist

View related series
Compound libraries (12325)

Basic Description

Synonyms 1314241-44-5 | UNC669 | UNC 669 | (5-bromopyridin-3-yl)(4-(pyrrolidin-1-yl)piperidin-1-yl)methanone | UNC-669 | (5-bromopyridin-3-yl)-(4-pyrrolidin-1-ylpiperidin-1-yl)methanone | CHEMBL1235119 | 3-Bromo-5-[(4-Pyrrolidin-1-Ylpiperidin-1-Yl)carbonyl]pyridine | C15H20BrN3O |
Specifications & Purity 10mM in DMSO
Biochemical and Physiological Mechanisms Selective, competitive L3MBTL antagonist (IC 50 = 5 µM). Inhibits L3MBTL induced transcription repression. Active in vitro .
Storage Temp Store at -80°C
Shipped In
Ice chest + Ice pads
This product requires cold chain shipping. Ground and other economy services are not available.
Product Description

Store at +4°C. The product can be stored for up to 12 months.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
Superclass Organoheterocyclic compounds
Class Pyridines and derivatives
Subclass Pyridinecarboxylic acids and derivatives
Intermediate Tree Nodes Not available
Direct Parent Pyridinecarboxylic acids and derivatives
Alternative Parents N-acylpiperidines  Aminopiperidines  N-alkylpyrrolidines  Aryl bromides  Tertiary carboxylic acid amides  Heteroaromatic compounds  Trialkylamines  Amino acids and derivatives  Azacyclic compounds  Organopnictogen compounds  Organooxygen compounds  Organobromides  Organic oxides  Hydrocarbon derivatives  
Molecular Framework Aromatic heteromonocyclic compounds
Substituents N-acyl-piperidine - Pyridine carboxylic acid or derivatives - 4-aminopiperidine - Aryl bromide - Aryl halide - Piperidine - N-alkylpyrrolidine - Heteroaromatic compound - Pyrrolidine - Tertiary carboxylic acid amide - Amino acid or derivatives - Carboxamide group - Tertiary aliphatic amine - Tertiary amine - Carboxylic acid derivative - Azacycle - Organooxygen compound - Organonitrogen compound - Organobromide - Organohalogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Amine - Organic nitrogen compound - Organopnictogen compound - Aromatic heteromonocyclic compound
Description This compound belongs to the class of organic compounds known as pyridinecarboxylic acids and derivatives. These are compounds containing a pyridine ring bearing a carboxylic acid group or a derivative thereof.
External Descriptors Not available

Associated Targets(Human)

AOX1 Tchem Aldehyde oxidase (429 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L3MBTL1 Tchem Lethal(3)malignant brain tumor-like protein 1 (14536 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L3MBTL3 Tchem Lethal(3)malignant brain tumor-like protein 3 (224 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
L3MBTL4 Tbio Lethal(3)malignant brain tumor-like protein 4 (125 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
MBTD1 Tbio MBT domain-containing protein 1 (145 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
SFMBT1 Tbio Scm-like with four mbt domains 1, isoform CRA_b (107 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PHF13 Tbio PHD finger protein 13 (2 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
CBX7 Tchem Chromobox protein homolog 7 (354 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
KDM5A Tchem Lysine-specific demethylase 5A (893 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
PHF23 Tbio PHD finger protein 23 (81 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
TP53BP1 Tbio Tumor suppressor p53-binding protein 1 (103 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
UHRF1 Tbio E3 ubiquitin-protein ligase UHRF1 (160 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Associated Targets(non-human)

Hdac6 Histone deacetylase 6 (222 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

IUPAC Name (5-bromopyridin-3-yl)-(4-pyrrolidin-1-ylpiperidin-1-yl)methanone
INCHI InChI=1S/C15H20BrN3O/c16-13-9-12(10-17-11-13)15(20)19-7-3-14(4-8-19)18-5-1-2-6-18/h9-11,14H,1-8H2
InChIKey CQERVFFAOOUFEQ-UHFFFAOYSA-N
Smiles C1CCN(C1)C2CCN(CC2)C(=O)C3=CC(=CN=C3)Br
Isomeric SMILES C1CCN(C1)C2CCN(CC2)C(=O)C3=CC(=CN=C3)Br
PubChem CID 46931242
Molecular Weight 338.24

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Chemical and Physical Properties

Molecular Weight 338.240 g/mol
XLogP3 2.100
Hydrogen Bond Donor Count 0
Hydrogen Bond Acceptor Count 3
Rotatable Bond Count 2
Exact Mass 337.079 Da
Monoisotopic Mass 337.079 Da
Topological Polar Surface Area 36.400 Ų
Heavy Atom Count 20
Formal Charge 0
Complexity 338.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 0
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
The total count of all stereochemical bonds 0
Covalently-Bonded Unit Count 1

Solution Calculators

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