Any compound that is able to protect normal cells from the damage caused by radiation therapy.
Member | Definition | Class |
1,2,3,4,6-pentakis-O-galloyl-beta-D-glucose | A galloyl-beta-D-glucose compound having five galloyl groups in the 1-, 2-, 3-, 4- and 6-positions. | 1,2,3,4,6-pentakis-O-galloyl-beta-D-glucose |
16,16-dimethylprostaglandin e2 | A prostanoid that is prostaglandin E2 in which both of the hydrogens at position 16 have been replaced by methyl groups. A synthetic analogue of prostaglandin E2, it is a potent inhibitor of pancreatic function and growth of experimental tumors. It also protects the gastric mucosa, prevents ulceration, and promotes the healing of peptic ulcers. | 16,16-dimethylprostaglandin E2 |
5-methoxytryptamine | A member of the class of tryptamines that is the methyl ether derivative of serotonin. | 5-methoxytryptamine |
amifostine anhydrous | An organic thiophosphate that is the S-phospho derivative of 2-[(3-aminopropyl)amino]ethanethiol. A prodrug for the free thiol, WR-1065, which is used as a cytoprotectant in cancer chemotherapy and radiotherapy. | amifostine |
androstenediol | A 3beta-hydroxy-Delta(5)-steroid that is 3beta-hydroxyandrost-5-ene carrying an additional hydroxy group at position 17beta. | androst-5-ene-3beta,17beta-diol |
cysteamine | An amine that consists of an ethane skeleton substituted with a thiol group at C-1 and an amino group at C-2. | cysteamine |
estramustine | A carbamate ester obtained by the formal condensation of the hydroxy group of 17beta-estradiol with the carboxy group of bis(2-chloroethyl)carbamic acid. | estramustine |
ferrostatin-1 | An ethyl ester resulting from the formal condensation of the carboxy group of 3-amino-4-(cyclohexylamino)benzoic acid with ethanol. It is a potent inhibitor of ferroptosis, a distinct non-apoptotic form of cell death caused by lipid peroxidation. It is also a radical-trapping antioxidant and has the ability to reduce the accumulation of lipid peroxides and chain-carrying peroxyl radicals. | ferrostatin-1 |
gamma-tocotrienol | A tocotrienol that is chroman-6-ol substituted by methyl groups at positions 2, 7 and 8 and a farnesyl chain at position 2. A vitamin E family member that has potent anti-cancer properties against a wide-range of cancers. | gamma-tocotrienol |
succinic acid | An alpha,omega-dicarboxylic acid resulting from the formal oxidation of each of the terminal methyl groups of butane to the corresponding carboxy group. It is an intermediate metabolite in the citric acid cycle. | succinic acid |
tempace | A piperidinecarboxamide that is TEMPO carrying an acetamido group at position 4. | 4-acetamido-TEMPO |
tocotrienol, delta | A tocotrienol that is chroman-6-ol substituted by methyl groups at positions 2 and 8 and a farnesyl chain at position 2. | delta-tocotrienol |
wr 1065 | An alkanethiol that is the N-3-aminopropyl derivative of cysteamine. Used as the S-phosphorylated prodrug, amifostine, for cytoprotection in cancer chemotherapy and radiotherapy. | WR-1065 |
zingerone | A methyl ketone that is 4-phenylbutan-2-one in which the phenyl ring is substituted at positions 3 and 4 by methoxy and hydroxy groups respectively. The major pungent component in ginger. | zingerone |
Protein | Taxonomy | Measurement | Average (mM) | Bioassay(s) | Drugs |
acetylcholinesterase | Homo sapiens (human) | Potency | 3.4708 | 1 | 2 |
activating transcription factor 6 | Homo sapiens (human) | Potency | 26.0820 | 2 | 2 |
AR protein | Homo sapiens (human) | Potency | 6.5032 | 5 | 9 |
arylsulfatase A | Homo sapiens (human) | Potency | 8.4921 | 1 | 1 |
ATP-dependent phosphofructokinase | Trypanosoma brucei brucei TREU927 | Potency | 0.0107 | 1 | 1 |
Bloom syndrome protein isoform 1 | Homo sapiens (human) | Potency | 136.7250 | 3 | 4 |
bromodomain adjacent to zinc finger domain 2B | Homo sapiens (human) | Potency | 70.7946 | 1 | 1 |
Cellular tumor antigen p53 | Homo sapiens (human) | Potency | 10.9061 | 2 | 5 |
Chain A, ATP-DEPENDENT DNA HELICASE Q1 | Homo sapiens (human) | Potency | 8.1349 | 1 | 1 |
Chain A, JmjC domain-containing histone demethylation protein 3A | Homo sapiens (human) | Potency | 50.1187 | 1 | 1 |
Chain A, MAJOR APURINIC/APYRIMIDINIC ENDONUCLEASE | Homo sapiens (human) | Potency | 0.0251 | 1 | 1 |
Chain A, TYROSYL-DNA PHOSPHODIESTERASE | Homo sapiens (human) | Potency | 7.2503 | 1 | 1 |
chromobox protein homolog 1 | Homo sapiens (human) | Potency | 50.1187 | 1 | 1 |
cytochrome P450 2C9, partial | Homo sapiens (human) | Potency | 22.1282 | 1 | 2 |
cytochrome P450 2D6 | Homo sapiens (human) | Potency | 9.5221 | 1 | 1 |
cytochrome P450 3A4 isoform 1 | Homo sapiens (human) | Potency | 1.0000 | 2 | 2 |
cytochrome P450 family 3 subfamily A polypeptide 4 | Homo sapiens (human) | Potency | 22.2033 | 1 | 3 |
cytochrome P450, family 19, subfamily A, polypeptide 1, isoform CRA_a | Homo sapiens (human) | Potency | 0.1188 | 1 | 1 |
DNA polymerase iota isoform a (long) | Homo sapiens (human) | Potency | 89.1251 | 1 | 1 |
DNA polymerase kappa isoform 1 | Homo sapiens (human) | Potency | 8.9125 | 1 | 1 |
dopamine D1 receptor | Homo sapiens (human) | Potency | 18.3564 | 1 | 1 |
estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 12.4792 | 9 | 17 |
estrogen receptor 2 (ER beta) | Homo sapiens (human) | Potency | 7.5416 | 3 | 4 |
estrogen-related nuclear receptor alpha | Homo sapiens (human) | Potency | 10.5909 | 1 | 1 |
euchromatic histone-lysine N-methyltransferase 2 | Homo sapiens (human) | Potency | 8.6188 | 1 | 3 |
farnesoid X nuclear receptor | Homo sapiens (human) | Potency | 41.3874 | 2 | 2 |
G | Vesicular stomatitis virus | Potency | 22.1282 | 1 | 2 |
GABA theta subunit | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit alpha-1 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit alpha-2 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit alpha-3 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit alpha-4 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit alpha-5 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit alpha-6 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit beta-1 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit beta-2 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit beta-3 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit delta | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit epsilon | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit gamma-1 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit gamma-2 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit gamma-3 | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
Gamma-aminobutyric acid receptor subunit pi | Rattus norvegicus (Norway rat) | Potency | 1.0000 | 1 | 1 |
geminin | Homo sapiens (human) | Potency | 16.7889 | 1 | 1 |
GLI family zinc finger 3 | Homo sapiens (human) | Potency | 31.5749 | 1 | 1 |
GLS protein | Homo sapiens (human) | Potency | 19.3512 | 2 | 2 |
glucocorticoid receptor [Homo sapiens] | Homo sapiens (human) | Potency | 6.0070 | 1 | 1 |
Glutamate receptor 2 | Rattus norvegicus (Norway rat) | Potency | 68.5896 | 1 | 1 |
heat shock protein beta-1 | Homo sapiens (human) | Potency | 0.0422 | 1 | 1 |
histone acetyltransferase KAT2A isoform 1 | Homo sapiens (human) | Potency | 12.5893 | 1 | 1 |
HLA class I histocompatibility antigen, B alpha chain | Homo sapiens (human) | Potency | 22.1282 | 1 | 2 |
hypoxia-inducible factor 1 alpha subunit | Homo sapiens (human) | Potency | 30.1065 | 1 | 1 |
Inositol hexakisphosphate kinase 1 | Homo sapiens (human) | Potency | 22.1282 | 1 | 4 |
Interferon beta | Homo sapiens (human) | Potency | 22.1282 | 1 | 2 |
lamin isoform A-delta10 | Homo sapiens (human) | Potency | 0.3162 | 1 | 1 |
Luciferase | Photinus pyralis (common eastern firefly) | Potency | 40.5334 | 1 | 1 |
Microtubule-associated protein tau | Homo sapiens (human) | Potency | 14.1254 | 1 | 1 |
muscarinic acetylcholine receptor M1 | Rattus norvegicus (Norway rat) | Potency | 0.0112 | 1 | 1 |
NFKB1 protein, partial | Homo sapiens (human) | Potency | 5.0119 | 2 | 2 |
nonstructural protein 1 | Influenza A virus (A/WSN/1933(H1N1)) | Potency | 0.3162 | 1 | 1 |
nuclear receptor subfamily 1, group I, member 2 | Rattus norvegicus (Norway rat) | Potency | 39.8107 | 1 | 1 |
nuclear receptor subfamily 1, group I, member 3 | Homo sapiens (human) | Potency | 61.1306 | 2 | 2 |
progesterone receptor | Homo sapiens (human) | Potency | 13.3332 | 1 | 1 |
RAR-related orphan receptor gamma | Mus musculus (house mouse) | Potency | 18.0746 | 1 | 2 |
regulator of G-protein signaling 4 | Homo sapiens (human) | Potency | 4.6014 | 1 | 2 |
retinoid X nuclear receptor alpha | Homo sapiens (human) | Potency | 27.0796 | 2 | 2 |
Spike glycoprotein | Severe acute respiratory syndrome-related coronavirus | Potency | 7.0795 | 1 | 1 |
TDP1 protein | Homo sapiens (human) | Potency | 25.8572 | 2 | 4 |
thioredoxin reductase | Rattus norvegicus (Norway rat) | Potency | 12.5341 | 4 | 4 |
thyroid stimulating hormone receptor | Homo sapiens (human) | Potency | 39.8107 | 2 | 3 |
USP1 protein, partial | Homo sapiens (human) | Potency | 50.1187 | 1 | 1 |
v-jun sarcoma virus 17 oncogene homolog (avian) | Homo sapiens (human) | Potency | 23.3226 | 2 | 2 |
vitamin D (1,25- dihydroxyvitamin D3) receptor | Homo sapiens (human) | Potency | 50.5758 | 2 | 2 |
vitamin D3 receptor isoform VDRA | Homo sapiens (human) | Potency | 46.9553 | 1 | 3 |
Voltage-dependent calcium channel gamma-2 subunit | Mus musculus (house mouse) | Potency | 68.5896 | 1 | 1 |