13250-98-1
Chemical Structure
Dibenz[a,h]anthracene-d14
Synonym(s): DBA-d14; 1,2,5,6-Dibenzanthracene-d14; Benzo[k]tetraphene-d14
- CAS No.: 13250-98-1
- Formula:C22D14
- Molecular Weight:292.43
IUPAC Name: benzo[k]tetraphene-d14
InChIKey: LHRCREOYAASXPZ-WZAAGXFHSA-N
SMILES: [2H]C1=C(C([2H])=C([2H])C2=C([2H])C([2H])=C([2H])C([2H])=C23)C3=C([2H])C4=C([2H])C([2H])=C(C([2H])=C([2H])C([2H])=C5[2H])C5=C41
Biological Activity: Dibenz[a,h]anthracene-d14 is the deuterium Dibenz[a,h]anthracene.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Dibenz[a,h]anthracene-d14 | Dibenz[a,h]anthracene-d14 is the deuterium Dibenz[a,h]anthracene. | |||||||||||||||||||||
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Dibenz[a,h]anthracene (Standard) | ≥98% | Dibenz[a,h]anthracene (Standard) is the analytical standard of Dibenz[a,h]anthracene. This product is intended for research and analytical applications. Dibenz[a,h]anthracene (DBA) is a polycyclic aromatic hydrocarbon (PAH) of considerable tumorigenicity. Dibenz[a,h]anthracene results in DNA adduct formation leading to the activation of a DNA damage response. Dibenz[a,h]anthracene induces cell cycle arrest and apoptosis via both Tp53-dependent and Tp53-independent mechanisms. | ||||||||||||||||||||
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Dibenz[a,h]anthracene | 98.0% | Dibenz[a,h]anthracene (DBA) is an orally active polycyclic aromatic hydrocarbon, a by-product of incomplete combustion of organic matter, a potent carcinogen, and an agonist of AhR. Dibenz[a,h]anthracene induces dose-dependent increases in DNA adduct formation and lacZ mutation frequency. Dibenz[a,h]anthracene upregulates St3gal5. Dibenz[a,h]anthracene can be used in cancer-related research. | ||||||||||||||||||||
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