dibenz[a,h]acridine

Synonyms: "dibenz[a,h]acridine", "dibenz(A,H)acridine", "dibenzo[a,H]acridine", "dibenz(a,d)acridine", "1,2,5,6-dibenzacridine", "7-azadibenz(a,h)anthracene", "DB(a,h)AC", "1,2,5,6-dibenzoacridine", "1,2,5,6-dinaphthacridine", "7-azadibenz[A,H]antracene", "dibenz[a,d]acridine", "7-azadibenz[a,h]anthracene".

Source: Dibenz[a,h]acridine is formed during the incomplete burning of organic matter.

Identifiers:

IUPAC Name: 2-azapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),2,4,6,8,10,12,15,17,19,21-undecaene
CAS Number: 226-36-8
PubChem ID: 9183
InChiKey: JNCSIWAONQTVCF-UHFFFAOYSA-N
Canonical SMILES: C1=CC=C2C(=C1)C=CC3=C2C=C4C=CC5=CC=CC=C5C4=N3

Structural Properties:

Molecular Formula: C₂₁H₁₃N
Molecular Weight: 279.342

Pharmacophore Features:

Number of bond donors: 0
Number of bond acceptors: 1
Number of atoms different from hydrogen: 22

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3D structure (.sdf)
3D structure (.mol2)
3D structure (.pdb)
3D structure (.pdbqt)

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Evidence Supporting This Chemical as an Endocrine Disruptor
TEDX List of Potential Endocrine Disruptors

Benisek M, Blaha L, Hilscherova K. 2008. Interference of PAHs and their N-heterocyclic analogs with signaling of retinoids in vitro. Toxicol in Vitro 22(8):1909-1917. DOI: 10.1016/j.tiv.2008.09.009. URL: http://www.sciencedirect.com/science/article/pii/S0887233308002373?via%3Dihub.