1-[(E)-4-chlorobut-2-enyl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane;chloride

Modify Date: 2026-06-26 13:27:14

1-[(E)-4-chlorobut-2-enyl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane;chloride Structure
1-[(E)-4-chlorobut-2-enyl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane;chloride structure
Common Name 1-[(E)-4-chlorobut-2-enyl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane;chloride
CAS Number 64401-41-8 Molecular Weight 265.18
Density N/A Boiling Point N/A
Molecular Formula C10H18Cl2N4 Melting Point N/A
MSDS N/A Flash Point N/A

 Names

Name 1-[(E)-4-chlorobut-2-enyl]-3,5,7-triaza-1-azoniatricyclo[3.3.1.13,7]decane;chloride

 Chemical & Physical Properties

Molecular Formula C10H18Cl2N4
Molecular Weight 265.18
InChIKey AXSUDOUXNCTJMM-TYYBGVCCSA-M
SMILES C1N2CN3CN1C[N+](C2)(C3)C/C=C/CCl.[Cl-]

 Bioassay

View more

Name: Inhibition of human CDK4/cyclin-D3 assessed as residual activity at 1 uM using RB-CTF...
Source: ChEMBL
Target: G1/S-specific cyclin-D3
External Id: CHEMBL4327628
Name: Inhibition of human CDK4/cyclin-D1 assessed as residual activity at 1 uM using RB pro...
Source: ChEMBL
Target: Cyclin-dependent kinase 4
External Id: CHEMBL4327627
Name: Inhibition of human CDK3/cyclin-E assessed as residual activity at 1 uM using histone...
Source: ChEMBL
Target: G1/S-specific cyclin-E1
External Id: CHEMBL4327626
Name: Inhibition of human CDK2/cyclin-O assessed as residual activity at 1 uM using histone...
Source: ChEMBL
Target: Cyclin-O
External Id: CHEMBL4327625
Name: Inhibition of human CDK2/cyclin-E assessed as residual activity at 1 uM using histone...
Source: ChEMBL
Target: G1/S-specific cyclin-E1
External Id: CHEMBL4327624
Name: Inhibition of human CDK2/cyclin-A assessed as residual activity at 1 uM using histone...
Source: ChEMBL
Target: Cyclin-A2
External Id: CHEMBL4327623
Name: Inhibition of human CDK18/cyclin-Y assessed as residual activity at 1 uM using RB pro...
Source: ChEMBL
Target: Cyclin-dependent kinase 18
External Id: CHEMBL4327622
Name: Inhibition of human CDK17/cyclin-Y assessed as residual activity at 1 uM using MBP pr...
Source: ChEMBL
Target: Cyclin-Y
External Id: CHEMBL4327621
Name: Inhibition of human CDK9/cyclin-T2 assessed as residual activity at 1 uM using KTFCGT...
Source: ChEMBL
Target: Cyclin-dependent kinase 9
External Id: CHEMBL4327636
Name: Inhibition of human CDK9/cyclin-T1 assessed as residual activity at 1 uM using KTFCGT...
Source: ChEMBL
Target: Cyclin-dependent kinase 9
External Id: CHEMBL4327635
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