Rat Target Sites | Mouse Target Sites | TD50 (mg/kg/day) | |||
Male | Female | Male | Female | Rat | Mouse |
adr liv pan pit | no positive | no positive | no positive | 9110 | no positive |
Hamster Target Sites | TD50 (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, long-term 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 (TD50) and its statistical significance; shape of the dose-response, 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) TD50 estimation for a standard lifespan. See Methods for other details.
TD50 provides a standardized quantitative measure that can be used for comparisons and analyses of many issues in carcinogenesis. The range of TD50 values across chemicals that are rodent carcinogens is more than 100 million-fold. 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
ETHYL ALCOHOL (ethanol) 64-17-5 2673 H m syg wat 29w78 2345 0 3.29gm 8.23gm McCoy;clet,33,151-159;1986 trh tum er no dre P=1. - 7.36gm n.s.s. 0/27 0/27 0/27 2674 M m amm wat 72w72 2081 0 16.7gm Anderson;carc,13,2107-2111;1992 liv hpa e 127.gm P<.4 27.8gm n.s.s. 1/47 3/48 lun ala e no dre P=1. 10.4gm n.s.s. 39/47 33/48 2675 M m bal wat 69w86 2510n 0 1.33gm Zariwala;ijeb,29,738-743;1991 for sqp no dre P=1. - 5.64gm n.s.s. 1/30 0/30 2676 M f c3s wat 86w86 1632 0 24.0gm Schrauzer;jsac,40,240-246;1979 mam adc Lr no dre P=1. 15.3gm n.s.s. 23/30 8/15 2677 M f swi wat 69w86 2510m 0 1.60gm Zariwala;ijeb,29,738-743;1991 for sqp s 10.9gm P<.1 - 2.67gm n.s.s. 0/30 2/30 tba mix s 21.4gm P<.6 - 2.94gm n.s.s. 1/30 2/30 2678 M m swi wat 69w86 2510m 0 1.33gm lun ade no dre P=1. - 3.40gm n.s.s. 1/30 1/30 2679 R m aci wat 52w52 2076 0 5.00gm Watanabe;gann,83,588-593;1992/pers.comm. for pam er 4.98gm P<.03 1.50gm n.s.s. 0/22 3/19 stg adc er no dre P=1. 4.89gm n.s.s. 0/22 0/19 2680 R f cdr wat 24m24 1962 0 2.86gm Cheever;faat,14,243-261;1990 liv nnd e no dre P=1. - 28.9gm n.s.s. 1/50 0/49 tba tum e no dre P=1. - 2.70gm n.s.s. 47/50 41/50 2681 R m cdr wat 24m24 1962 0 2.50gm liv nnd e 84.8gm P<.3 - 13.8gm n.s.s. 0/50 1/50 liv hpc e no dre P=1. - 25.8gm n.s.s. 1/50 0/50 tba tum e no dre P=1. - 1.38gm n.s.s. 42/50 42/50 2682 R m cdr wat 52w52 2074 0 5.00gm Watanabe;gann,83,1267-1272;1992/pers.comm. stg adc er no dre P=1. 3.86gm n.s.s. 0/12 0/15 2683 R m f3d wat 51w52 2564 0 4.90gm Wada;clet,124,127-134;1998 for tum er no dre P=1. - 4.04gm n.s.s. 0/15 0/16 stg tum er no dre P=1. - 4.04gm n.s.s. 0/15 0/16 2684 R f nbr wat 64w64 162a 0 5.71gm Yamamoto;ijcn,2,337-343;1967 liv tum no dre P=1. 8.92gm n.s.s. 0/20 0/20 2685 R m nbr wat 64w64 162a 0 5.00gm liv tum no dre P=1. 7.80gm n.s.s. 0/20 0/20 2686 R b sda wat 26m26 1264 0 9.45gm Schmahl;clet,1,215-218;1976 tba mal e no dre P=1. - 39.9gm n.s.s. 4/48 4/48 2687 R f sda wat 24m28 2257m 0 1.49gm Holmberg;txcy,96,133-145;1995/1994 pan ade Ie 21.9gm P<.04 6.63gm n.s.s. 0/50 3/50 mgl mix Ie 4.71gm P<.5 981.mg n.s.s. 38/50 41/50 mgl ben Ie 6.07gm P<.4 1.62gm n.s.s. 25/50 30/50 mgl fba Ie 8.79gm P<.5 1.98gm n.s.s. 22/50 26/50 liv hpc Ie no dre P=1. 20.4gm n.s.s. 1/50 0/50 liv mix Ie no dre P=1. 20.4gm n.s.s. 2/50 0/50 mgl car Ie no dre P=1. 5.29gm n.s.s. 13/50 11/50 liv hpa Ie no dre P=1. 20.4gm n.s.s. 1/50 0/50 tba ben Ie 3.15gm P<.2 1.08gm n.s.s. 30/50 37/50 tba mal Ie no dre P=1. 3.35gm n.s.s. 23/50 21/50 tba mix Ie no dre P=1. 340.mg n.s.s. 50/50 49/50 2688 R f sda wat 24m28 2257n 0 4.46gm pit nen Ie 5.48gm P<.02 2.40gm n.s.s. 29/50 40/50 liv hpa Ie 201.gm P<.3 32.8gm n.s.s. 0/50 1/50 liv hpc Ie no dre P=1. 61.1gm n.s.s. 0/50 0/50 pan mix Ie no dre P=1. 30.0gm n.s.s. 2/50 2/50 tba mix Ie 5.87gm P<.6 782.mg n.s.s. 48/50 49/50 tba ben Ie 12.1gm P<.3 3.71gm n.s.s. 29/50 35/50 tba mal Ie 61.0gm P<.7 7.94gm n.s.s. 19/50 21/50 2689 R m sda wat 30m30 1440 0 2.50gm Radike;enhp,41,59-62;1981 liv hnd e 8.26gm P<.0005 4.47gm 29.0gm 10/80 29/79 pit tum e 9.11gm P<.0005 + 4.89gm 32.1gm 8/80 26/79 adr tum e 13.7gm P<.0005 + 7.38gm 29.9gm 0/80 14/79 pan tum e 13.7gm P<.0005 + 7.38gm 29.9gm 0/80 14/79 liv hpc e 28.4gm P<.02 + 11.9gm n.s.s. 1/80 8/79 tba mix e 2.13gm P<.0005 1.42gm 3.51gm 16/80 61/79 2690 R m sda wat 24m28 2257m 0 1.21gm Holmberg;txcy,96,133-145;1995/1994 pan car Ie 17.5gm P<.2 4.90gm n.s.s. 1/50 4/50 liv hpc Ie no dre P=1. 16.6gm n.s.s. 2/50 0/50 liv hpa Ie no dre P=1. 16.6gm n.s.s. 0/50 0/50 tba mix Ie 1.21gm P<.3 305.mg n.s.s. 45/50 48/50 tba mal Ie 7.18gm P<.3 1.95gm n.s.s. 15/50 20/50 tba ben Ie no dre P=1. 1.36gm n.s.s. 35/50 35/50 2691 R m sda wat 24m28 2257n 0 3.64gm pan mix Ie 33.2gm P<.4 8.52gm n.s.s. 8/50 12/50 liv hpc Ie 164.gm P<.3 26.8gm n.s.s. 0/50 1/50 liv hpa Ie no dre P=1. 49.9gm n.s.s. 0/50 0/50 tba ben Ie no dre P=1. 6.88gm n.s.s. 30/50 27/50 tba mal Ie no dre P=1. 8.94gm n.s.s. 16/50 16/50 tba mix Ie no dre P=1. 2.25gm n.s.s. 44/50 44/50 2692 R m sls wat 28m28 2185 0 2.50gm 10.0gm Shibayama;extp,45,15-19;1993/pers.comm. liv mix er 33.8gm * P<.03 - 14.4gm n.s.s. 3/44 10/41 12/43 liv hpc er 93.9gm * P<.07 - 35.7gm n.s.s. 0/44 2/41 3/43 liv hpa er 56.1gm * P<.2 - 19.2gm n.s.s. 3/44 8/41 9/43 2693 R f wis wat 52w52 2028 0 4.08gm Yamagiwa;gann,82,771-778;1991 liv mix r no dre P=1. 2.10gm n.s.s. 0/5 0/10 2694 R m wis wat 91w91 1800 0 2.50gm Salmon;carc,7,1447-1450;1986 for sqc r no dre P=1. 3.94gm 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 TD10 (LTD10) are readily calculated from the TD50 and its lower confidence limit, which are reported in the CPDB. For researchers and regulatory agencies interested in LTD10 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.