Exact Mass: 278.1095

Exact Mass Matches: 278.1095

Found 17 metabolites which its exact mass value is equals to given mass value 278.1095, within given mass tolerance error 0.0002 dalton. Try search metabolite list with more accurate mass tolerance error 4.0E-5 dalton.

Dibenz[a,h]anthracene

pentacyclo[12.8.0.0^{3,12}.0^{4,9}.0^{15,20}]docosa-1,3,5,7,9,11,13,15,17,19,21-undecaene

C22H14 (278.1095)


D009676 - Noxae > D002273 - Carcinogens 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[1][2].

   

Benzo[b]chrysene

1,2:6,7-Dibenzophenanthrene

C22H14 (278.1095)


   

Dibenz[a,c]anthracene

pentacyclo[12.8.0.0^{2,7}.0^{8,13}.0^{16,21}]docosa-1(22),2,4,6,8,10,12,14,16,18,20-undecaene

C22H14 (278.1095)


   

Benzo[m]tetraphene

Dibenzo-1,2,7,8-anthracene

C22H14 (278.1095)


   

PICENE

Benzo[a]chrysene

C22H14 (278.1095)


   

BENZO[G]CHRYSENE

BENZO[G]CHRYSENE

C22H14 (278.1095)


   

Benzo(a)naphthacene

Benzo(a)naphthacene

C22H14 (278.1095)


   

Indeno[1,2,3-cd]pyrene

Indeno[1,2,3-cd]pyrene

C22H14 (278.1095)


   

(±)-[5]helicene

(±)-[5]helicene

C22H14 (278.1095)


   

Pentaphene

Pentaphene

C22H14 (278.1095)


   

1,4-BIS(PHENYLETHYNYL)BENZENE

1,4-BIS(PHENYLETHYNYL)BENZENE

C22H14 (278.1095)


   

Pentacene

Pentacene

C22H14 (278.1095)


   

Benzo[c]chrysene

Benzo[c]chrysene

C22H14 (278.1095)


   

Benzo[a]tetraphene

Benzo[a]tetraphene

C22H14 (278.1095)


   

benzo[f]tetraphene

Dibenz[a,c]anthracene

C22H14 (278.1095)


   

BENZO(B)CHRYSENE

Benzo[c]tetraphene

C22H14 (278.1095)


   

Benzo[k]tetraphene

1,2:5,6-Dibenzanthracene

C22H14 (278.1095)


D009676 - Noxae > D002273 - Carcinogens 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[1][2].