3-Hydroxy-6-(hydroxymethyl)-2-[(2-pyridylamino)-3-thienylmethyl]pyran-4-one

Modify Date: 2026-06-19 09:30:53

3-Hydroxy-6-(hydroxymethyl)-2-[(2-pyridylamino)-3-thienylmethyl]pyran-4-one Structure
3-Hydroxy-6-(hydroxymethyl)-2-[(2-pyridylamino)-3-thienylmethyl]pyran-4-one structure
Common Name 3-Hydroxy-6-(hydroxymethyl)-2-[(2-pyridylamino)-3-thienylmethyl]pyran-4-one
CAS Number 690641-45-3 Molecular Weight 330.4
Density N/A Boiling Point N/A
Molecular Formula C16H14N2O4S Melting Point N/A
MSDS N/A Flash Point N/A

 Names

Name 3-Hydroxy-6-(hydroxymethyl)-2-[(2-pyridylamino)-3-thienylmethyl]pyran-4-one

 Chemical & Physical Properties

Molecular Formula C16H14N2O4S
Molecular Weight 330.4
InChIKey QUCBZTHJXHHFAW-UHFFFAOYSA-N
SMILES C1=CC=NC(=C1)NC(C2=CSC=C2)C3=C(C(=O)C=C(O3)CO)O

 Bioassay

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Name: Primary cell-based high-throughput screening assay for identification of compounds th...
Source: Johns Hopkins Ion Channel Center
Target: regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id: JHICC_RGS_Act_HTS
Name: uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
Source: Burnham Center for Chemical Genomics
Target: N/A
External Id: BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
Name: Small-molecule inhibitors of ST2 (IL1RL1)
Source: 20881
Target: interleukin-1 receptor-like 1 isoform [homo sapiens]
External Id: ST2_IL33_Inhibitors_Primary_Screening_77700
Name: Primary cell-based high-throughput screening for identification of compounds that all...
Source: Johns Hopkins Ion Channel Center
Target: MAS-related GPR member X1 [Homo sapiens]
External Id: JHICC_MrgX1_AlloAgonist_Primary
Name: Primary cell-based high-throughput screening for identification of compounds that ant...
Source: Johns Hopkins Ion Channel Center
Target: MAS-related GPR member X1 [Homo sapiens]
External Id: JHICC_MrgX1_Antagonist_Primary
Name: High throughput fluorescence intensity-based biochemical assay to screen for small mo...
Source: University of Pittsburgh Molecular Library Screening Center
Target: furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id: MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
Name: Antibacterial activity against Staphylococcus aureus
Source: ChEMBL
Target: Staphylococcus aureus
External Id: CHEMBL5228668
Name: uHTS identification of small molecule inhibitors of tim10-1 yeast via a luminescent a...
Source: Burnham Center for Chemical Genomics
Target: TPA: Essential protein of the mitochondrial intermembrane space, forms a complex with Tim9p (TIM10 complex) that delivers hydrophobic proteins to the TIM22 complex for insertion into the inner membrane [Saccharomyces cerevisiae S288c]
External Id: SBCCG-A413-tim10-1-Primary-Antagonist-Assay
Name: 384-well Z-Lyte format Hck-Nef inhibitor HTS run at the PMLSC
Source: University of Pittsburgh Molecular Library Screening Center
Target: N/A
External Id: MH083223 Targeting HIV-1 Nef with Small Molecules
Name: uHTS identification of APOBEC3A DNA Deaminase Inhibitors via a fluorescence-based sin...
Source: Burnham Center for Chemical Genomics
Target: probable DNA dC->dU-editing enzyme APOBEC-3A [Homo sapiens]
External Id: SBCCG-A539-APOBEC3A-Inhibitor-Primary-Assay
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