SMILES, InChI and
Structure are below.
Rats and Mice: Cancer Test Summary
||eso liv sto vsc
Key to the Table Above
For each chemical with a positive (carcinogenic)
experiment in the Carcinogenic Potency
Database (CPDB), results are included on carcinogenic potency
(TD50) in each species and target sites in males and
females. Positivity is determined by an author’s opinion in a
published paper. If all experimental results in the CDPB are
negative in a sex-species group, “no positive” appears.
If the CPDB has no experiments in the sex-species group, “no
test” appears. The summary presents the strongest evidence of
carcinogenicity in each group. If there are both positive and
negative experiments in a sex-species, the negative results are
ignored in this Summary Table.
Codes: eso = esophagus. liv = liver. sto = stomach. vsc = vascular system. Target sites are listed
if any author of published experimental results concluded that
tumors were induced in that organ by the test agent. If there is
more than one positive experiment in a sex-species, target sites
listed may be from more than one experiment, e.g. if liver and lung
are both listed, then liver may have been a target in one
experiment and lung in another.
Our standardized measure of carcinogenic potency,
TD50, is the
daily dose rate in mg/kg body weight/day to induce tumors in half
of test animals that would have remained tumor-free at zero dose.
Whenever there is more than one positive experiment in a species,
the reported TD50 value is a Harmonic Mean
calculated using the TD50 value from the most potent
target site in each positive experiment.
Superscripts: m = There is more than one
positive experiment in the species, and TD50 values from
each positive experiment are used in the calculation of the
reported Harmonic mean of TD50. P = 100% of dosed animals had tumors at a target
site in an experiment in this species.
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
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
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.
Experiments and Citations in CPDB
The definition of each code in the plot below will appear in a
pop-up window when the field name in the header line is clicked,
e.g., Strain, Site, Path. Each numbered line
starts a new experiment and reports protocol information in black.
Average daily dose-rates per kg body weight per day are in
green. Remaining lines report
experimental results in blue.
Abbreviations of fields in header line: # = the line number in the plot of all CPDB chemicals; Xpo = duration of dosing; Xpt = duration of experiment; Site = tissue; Path = tumor type; DR = dose-response; AuOp = author’s opinion about
carcinogenicity; LoConf, UpConf =
confidence limits (99%) on TD50; Inc = tumor incidence for each dose
See Guide to reading the
plot for details on each field, using an example of one
See Help to improve
readability, or to fit the plot onto the screen or a printed
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
4463 R f f34 wat 6m30 1375m () 0 7.94ug 20.6ug 50.8ug .140mg .785mg 2.83mg Lijinsky;eaes,6,513-527;
ugi mix esy .142mg Z P<.0005 + 76.3ug .350mg 0/20 6/20 1/20 4/20 15/20 (17/20 15/20)
eso mix esy .216mg Z P<.0005 + .129mg .378mg 0/20 0/20 0/20 1/20 16/20 19/20 (15/20)
ugi car esy .271mg Z P<.0005 + .141mg .614mg 0/20 0/20 0/20 0/20 13/20 (10/20 8/20)
liv hes esy 4.04mg * P<.0005 + 2.14mg 8.91mg 0/20 0/20 0/20 0/20 0/20 0/20 14/20
liv hpc esy no dre P=1. + 12.8mg n.s.s. 0/20 2/20 6/20 4/20 2/20 0/20 2/20
liv mix esy no dre P=1. + 8.09mg n.s.s. 1/20 4/20 9/20 6/20 5/20 0/20 5/20
stn bcp esy no dre P=1. + 14.4mg n.s.s. 0/20 6/20 0/20 2/20 4/20 1/20 1/20
4464 R f f34 wat 16m23 1375n 0 .184mg
ugi mix es noTD50 P<.0005 + n.s.s. 62.0ug 0/20 20/20
ugi car es 96.6ug P<.0005 + 49.3ug .217mg 0/20 14/20
eso mix es .127mg P<.0005 + 63.3ug .303mg 0/20 12/20
liv hnd es 2.15mg P<.6 + .298mg n.s.s. 1/20 2/20
4465 R f f34 wat 23m30 1375o 0 31.8ug 82.6ug
ugi mix e 37.4ug * P<.0005 + 22.0ug 66.7ug 0/20 10/20 19/20
stn bcp e 55.1ug \ P<.0005 + 25.6ug .156mg 0/20 9/20 (3/20)
eso mix e 66.9ug / P<.0005 + 37.6ug .131mg 0/20 0/20 20/20
ugi car e 85.6ug / P<.0005 + 47.9ug .171mg 0/20 2/20 16/20
liv mix e .132mg * P<.003 + 66.5ug .852mg 1/20 7/20 9/20
eso sqc e .430mg * P<.005 + .163mg 3.43mg 0/20 0/20 5/20
liv hnd e .284mg * P<.03 + .115mg n.s.s. 1/20 3/20 6/20
SMILES Code for
InChI Code for
Source for SMILES and InChI: USEPA Distributed
Structure-Searchable Toxicity (DSSTox) Database
Chemical Structure for
Source for structure: National Library of
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 plot of the CPDB presents
results of 1547 experiments on 6540 chemicals in an easily readable
format that has been used in publications of the CPDB.
- A Screen version plot
for use on a single computer screen, with the same data.
- Excel version of the same
- Tab-separated versions of the
same data, which can be easily read into databases.
Dataset gives details on dosing and survival for each
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
PDF versions of our publications of analyses using the CPDB are
available, organized by year and by research topic.
Carcinogenic Potency Database Project
(CPDB) Home Page
For more information about this Web Page, contact Specialized Information
Last updated: October 3, 2007
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