Rat Target Sites  Mouse Target Sites  TD_{50} (mg/kg/day)  
Male  Female  Male  Female  Rat  Mouse 
no positive  no positive  liv  liv  no positive  7.37^{m,P,v} 
Hamster Target Sites  TD_{50} (mg/kg/day) 

Male  Female  
no positive  no test  no positive 
Key to the Table Above
The Carcinogenic Potency Database (CPDB) is a unique and widely used international resource of the results of 6540 chronic, longterm animal cancer tests on 1547 chemicals. The CPDB provides easy access to the bioassay literature, with qualitative and quantitative analyses of both positive and negative experiments that have been published over the past 50 years in the general literature through 2001 and by the National Cancer Institute/National Toxicology Program through 2004. The CPDB standardizes the diverse literature of cancer bioassays that vary widely in protocol, histopathological examination and nomenclature, and in the published author’s choices of what information to provide in their papers. Results are reported in the CPDB for tests in rats, mice, hamsters, dogs, and nonhuman primates.
For each experiment, information is included on species, strain, and sex of test animal; features of experimental protocol such as route of administration, duration of dosing, dose level(s) in mg/kg body weight/day, and duration of experiment; experimental results are provided on target organ, tumor type, and tumor incidence; carcinogenic potency (TD_{50}) and its statistical significance; shape of the doseresponse, author’s opinion as to carcinogenicity, and literature citation.
Only tests with dosing for at least ¼ the standard lifespan of the species and experiment length at least ½ the lifespan are included in the CPDB. Only routes of administration with whole body exposure are included. Doses are standardized, average dose rates in mg/kg/day. A description of methods used in the CPDB to standardize the diverse literature of animal cancer tests is presented for: 1) Criteria for inclusion of experiments 2) Standardization of average daily dose levels and 3) TD_{50} estimation for a standard lifespan. See Methods for other details.
TD_{50} provides a standardized quantitative measure that can be used for comparisons and analyses of many issues in carcinogenesis. The range of TD_{50} values across chemicals that are rodent carcinogens is more than 100 millionfold. More than half the chemicals tested are positive in at least one experiment.
A plot of all results on each experiment in the CPDB for this chemical is presented below. These results are the source information for the Cancer Test Summary table above.
Chemical (Synonym) CAS # Species Sex Strain Route Xpo+Xpt PaperNum 0 Dose 1 Dose 2 Dose 3 Dose Literature Reference or NCI/NTP:Site Path Site Path Notes TD50 DR Pval AuOp LoConf UpConf Cntrl 1 Inc 2 Inc 3 Inc Brkly Code
PHENOBARBITAL (phenobarbitone) 50066 4891 H m syg eat 52w52 1804 0 46.0mg Stenback;jnci,76,327333;1986 liv mix er no dre P=1.  23.7mg n.s.s. 0/5 0/10 4892 M m b6c wat 52w52 1477m 0 83.3mg Becker;canr,42,39183923;1982 liv mix r noTD50 P<.006 + n.s.s. 11.5mg 5/16 16/16 4893 M m b6c eat 96w96 2398 0 60.0mg Nitta;jtxp,4,5561;1991/pers.comm. liv hpc 20.4mg P<.0005 + 12.3mg 37.4mg 10/46 43/50 liv mix 21.1mg P<.0005 + 12.5mg 40.2mg 12/46 43/50 lun mix no dre P=1. 184.mg n.s.s. 9/46 7/50 4894 M f c3l eat 52w52 235m 0 65.0mg Peraino;jnci,51,13491350;1973 liv tum r noTD50 P<.0005 + n.s.s. 5.36mg 5/39 29/29 4895 M f c3l eat 52w52 235n 0 65.0mg liv tum r 12.2mg P<.0005 + 5.45mg 46.2mg 1/16 10/16 4896 M m c3l eat 52w52 235m 0 60.0mg liv tum r 4.18mg P<.0005 + 1.52mg 19.0mg 25/37 35/36 4897 M m c3l eat 52w52 235n 0 60.0mg liv tum r 4.46mg P<.0005 + 1.56mg 21.4mg 7/17 16/17 4898 M m c5n wat 78w78 1477n 0 83.3mg Becker;canr,42,39183923;1982 liv tum r no dre P=1.  155.mg n.s.s. 0/16 0/16 4899 M m cb6 eat 53w53 2084m 0 60.0mg Diwan;carc,13,18931901;1992 liv hct r no dre P=1. 80.3mg n.s.s. 0/25 0/25 4900 M f cd1 wat 78w78 1582 0 100.mg Miller;canr,43,11241134;1983 liv hpt 559.mg P<.1 137.mg n.s.s. 0/30 2/30 lun ade no dre P=1. 210.mg n.s.s. 1/30 1/30 4901 M m cen wat 52w52 1477o 0 83.3mg Becker;canr,42,39183923;1982 liv mix kr noTD50 P<.3 n.s.s. n.s.s. 5/8 8/8 4902 M m cen wat 52w52 1477r 0 83.3mg liv mix r noTD50 P<.09 + n.s.s. n.s.s. 10/16 16/16 4903 M m cen eat 52w52 1992 0 60.0mg Fullerton;carc,11,13011305;1990 liv mix r 6.67mg P<.0005 + 3.75mg 13.3mg 2/30 24/30 liv hpc r 7.78mg P<.0005 + 4.47mg 14.7mg 0/30 22/30 lun mix r 139.mg P<.4 28.5mg n.s.s. 2/30 4/30 liv hpa r no dre P=1. 44.9mg n.s.s. 2/30 2/30 4904 M m chg eat 52w52 1891 0 24.0mg Mizutani;clet,39,233237;1988 liv tum r 5.56mg P<.002 + 2.31mg 38.5mg 42/139 14/21 4905 M m chh eat 52w52 1891 0 24.0mg liv tum r noTD50 P<.09 n.s.s. n.s.s. 42/56 31/31 4906 M m d2b eat 26m26 2227 0 60.0mg Diwan;clet,89,2935;1995/pers.comm. liv hpa er 42.4mg P<.0005 + 21.0mg 161.mg 9/29 23/30 liv mix er 42.4mg P<.0005 + 21.0mg 161.mg 9/29 23/30 liv hpb er 101.mg P<.0005 + 50.1mg 250.mg 0/29 11/30 liv hpc er 199.mg P<.02 + 78.1mg n.s.s. 1/29 7/30 4907 M m dba eat 53w53 2084n 0 60.0mg Diwan;carc,13,18931901;1992 liv hpa r 61.2mg P<.02 21.1mg n.s.s. 0/25 4/25 4908 R f aci eat 67w67 1448 0 25.0mg Uchida;zkko,100,231238;1981 liv tum no dre P=1.  25.7mg n.s.s. 0/10 0/12 tba mix 81.7mg P<.3 13.3mg n.s.s. 0/10 1/12 4909 R m aci eat 67w67 1448 0 20.0mg liv tum no dre P=1.  20.5mg n.s.s. 0/10 0/12 tba mix no dre P=1. 15.3mg n.s.s. 4/10 1/12 4910 R f f34 wat 76w76 1689 0 28.6mg Diwan;jnci,75,10991105;1985 liv hpa er 99.2mg P<.3 16.1mg n.s.s. 0/10 1/10 4911 R f f34 eat 89w91 2219 0 24.4mg Zavanella;carc,15,25312539;1994/pers.comm. liv hct r 46.5mg P<.06 12.5mg n.s.s. 1/24 3/11 4912 R m f34 wat 76w76 1689 0 25.0mg Diwan;jnci,75,10991105;1985 liv hpa er 86.8mg P<.3 14.1mg n.s.s. 0/10 1/10 4913 R m f34 wat 72w72 1690 0 25.0mg Diwan;jnci,74,509516;1985 liv hpa e 45.0mg P<.08 11.0mg n.s.s. 0/13 2/12 4914 R m f34 eat 17m24 1803 0 14.0mg Shivapurkar;carc,7,547550;1986 liv nnd e no dre P=1.  38.2mg n.s.s. 2/28 2/28 4915 R m f34 eat 52w52 1834 0 20.0mg Leonard;jnci,79,13131319;1987/pers.comm. liv mix er no dre P=1.  20.6mg n.s.s. 0/20 0/20 4916 R m f34 eat 71w71 1951 0 20.0mg Diwan;carc,10,189194;1989 liv hpt e no dre P=1. 28.8mg n.s.s. 0/15 0/15 4917 R m f34 eat 71w71 2084m 0 20.0mg Diwan;carc,13,18931901;1992 liv hpa 76.6mg P<.1 18.8mg n.s.s. 0/25 2/25 4918 R m f34 eat 71w71 2109 0 20.0mg Diwan;artx,66,413422;1992 liv hpa e 44.6mg P<.04 11.0mg n.s.s. 0/27 2/15 4919 R m f34 eat 89w91 2219 0 19.6mg Zavanella;carc,15,25312539;1994/pers.comm. liv hct r 328.mg P<.8 22.7mg n.s.s. 1/21 1/13 4920 R m f34 eat 72w72 2322 0 20.0mg Diwan;carc,17,3743;1996 liv hpa 115.mg P<.3 18.7mg n.s.s. 0/18 1/18 4921 R m f34 eat 78w78 2535 0 20.0mg Allen;carc,18,11031107;1997/pers.comm. liv tum e no dre P=1.  64.9mg n.s.s. 0/28 0/28 4922 R m f34 eat 72w72 2657 0 20.0mg Diwan;ijtx,20,8187;2001 liv hpa 75.5mg P<.3  12.3mg n.s.s. 0/12 1/12 4923 R m f3d wat 40w78 2565 0 14.7mg Hasegawa;clet,123,185191;1998/pers.comm. liv tum e no dre P=1.  25.5mg n.s.s. 0/10 0/15 4924 R m fis eat 39w78 1653 0 10.0mg Carr;carc,5,15831590;1984 liv tum e no dre P=1.  6.96mg n.s.s. 0/12 0/6 tba tum e no dre P=1.  6.96mg n.s.s. 0/12 0/6 4925 R f sda ipj 24m24 1134 0 .286mg Schmahl;zkko,86,7784;1976 tba mal es no dre P=1.  1.25mg n.s.s. 3/33 1/30 4926 R m sda ipj 24m24 1134 0 .286mg liv hae es no dre P=1. 1.88mg n.s.s. 1/36 0/32 tba mal es 54.7mg P<1.  n.s.s. n.s.s. 1/36 1/32 4927 R m wis eat 59w59 2155 0 50.0mg KrauppGrasl;canr,51,666671;1991/pers.comm. liv mix e 303.mg P<.4 49.4mg n.s.s. 0/18 1/28 tba tum e 9.22mg P<.0005 5.07mg 20.4mg 1/18 20/28 4928 R f wsh wat 56w56 2659 0 57.1mg White;carc,22,553557;2001 liv tum Cr no dre P=1.  34.1mg n.s.s. 0/10 0/10
See full CPDB Summary Table on 1547 chemicals. See Full CPDB for all results on 6540 experiments of 1547 chemicals.
A complete list of CPDB chemicals, which is searchable by name or by CAS number, is available here.
For a compendium of CPDB results organized by target organ, which lists all chemicals in each species that induced tumors in each of 35 organs, see Summary Table by Target Organ.
The CPDB is available in several formats that permit printing and downloading into spreadsheets and statistical databases.
A Supplementary Dataset gives details on dosing and survival for each experiment.
Relatively precise estimates of the lower confidence limit on the TD_{10} (LTD_{10}) are readily calculated from the TD_{50} and its lower confidence limit, which are reported in the CPDB. For researchers and regulatory agencies interested in LTD_{10} values, we provide them in an Excel spreadsheet.
PDF versions of our publications of analyses using the CPDB are available, organized by year and by research topic.