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Results for "

carcinogen

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    53
    TargetMol | All_Pathways
  • Dye Reagents
    1
    TargetMol | All_Dye_Reagents
  • Natural Products
    15
    TargetMol | Natural_Products
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    TargetMol | Isotope_Products
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    5
    TargetMol | Disease_Modeling_Products
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    5
    TargetMol | Cell_Research_Reagents
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    5
    TargetMol | Standard_Products
N-Nitroso-N-methylurea
N-Methyl-N-nitrosourea, Methylnitrosourea, 1-Methyl-1-nitrosourea
T4169684-93-5
N-Nitroso-N-methylurea (NMU/MNU/NMH) is a nitrosourea compound with alkylating, carcinogenic, and mutagenic properties; as a direct-acting alkylating agent, it interacts with DNA and targets multiple animal organs to induce various cancers and degenerative diseases, and is commonly used to induce disease models such as gastric cancer and breast cancer in mice.
  • $36
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1-Hydroxyanthraquinone
T37101129-43-1
1-Hydroxyanthraquinone is an anthraquinone that has been found in Morinda officinalis and has genotoxic and carcinogenic activities. 1-Hydroxyanthraquinone generates strong DNA repair response.
  • $29
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(Iso)-Flavokawain A
Flavokavain A
T3S07373420-72-2
NSC-37445 has anti-tumor activity, such as inhibits growth of bladder tumor cells in a nude mice model , prevents the recurrence and progression of non-muscle-invasive urothelial cell carcinoma. NSC-37445 can significantly reduce the expression of CDK1-inhibitory kinases, Myt1 and Wee1, and cause cyclin B1 protein accumulation leading to CDK1 activation in T24 cells. 3. Flavokawain A (Flavokavain A) may exert anti-inflammatory responses by suppressing LPS-induced expression of pro-inflammatory mediators via blockage of NF-κB-AP-1-JNK/p38 MAPK signaling pathways in the murine macrophages.
  • $42
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TargetMol | Citations Cited
TFMB-(R)-2-HG
T170651445700-01-5
TFMB-(R)-2-HG is a cell membrane-permeable (R)-2-HG, an oncogenic factor in acute myeloid leukemia. It impairs SCF ER-Hoxb8 cell differentiation in response to estrogen withdrawal.
  • $70
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Macrozamin
T194126327-93-1
Macrozamin has carcinogenic, mutagenic, teratogenic and neurotoxic properties.Macrozamin is a natural product isolated from Cycads.
  • $39
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2,5-Dimethyl-3(2H)-furanone
2,5-Dimethyl-2,3-dihydrofuran-3-one
T2230914400-67-0
2,5-Dimethyl-3(2H)-furanone (2,5-Dimethyl-2,3-dihydrofuran-3-one) is a non-genotoxic flavoring substance [1].
  • $30
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Xanthone
Xanthenone, Genicide, Benzophenone oxide
T298290-47-1
Xanthone (Xanthenone) is currently used as ovicide for codling moth eggs and as a larvicide.
  • $29
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D-Saccharic acid 1,4-lactone hydrate
T4131961278-30-6
D-Saccharic acid 1,4-lactone hydrate is a potent β-glucuronidase inhibitor (IC50=48.4 μM) that possesses anticarcinogenic, detoxifying, and antioxidant properties[1][2].
  • $31
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TargetMol | Citations Cited
α-Angelica lactone
Alpha-Angelica Lactone
T7995591-12-8
α-Angelica lactone has cardiotonic activity, may exert their effects by providing an increased contraction-dependent calcium pool to be released upon systolic depolarization.
  • $29
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7-Hydroxyflavanone
T79996515-36-2
7-Hydroxyflavanone shows antimicrobial activity against Streptococcus pneumoniae clinical isolates.
  • $40
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Glyphosate
Lancer, Folusen, Atila
T198571071-83-6
Glyphosate (Atila) is an herbicide. It also is a possible carcinogen to humans.
  • $39
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TargetMol | Inhibitor Hot
Azoxymethane
AOM
T7371925843-45-2
Azoxymethane (AOM) is a colon-specific carcinogen that induces DNA damage and forms DNA adducts, and is commonly used to establish mouse models of colorectal cancer.
  • $169
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Oltipraz
RP 35972, NSC 347901
T015364224-21-1
Oltipraz (RP 35972) is a synthetic dithiolethione with potential chemopreventive and anti-angiogenic properties. Oltipraz induces phase II detoxification enzymes, such as glutathione S transferase (GST) and NAD(P)H: quinone oxidoreductase 1 (NQO1). The induction of detoxification enzymes enhances the detoxification of certain cancer-causing agents, thereby enhancing their elimination and preventing carcinogen-induced DNA damages. Although the exact mechanism through which the anti-angiogenesis effect remains to be fully elucidated, oltipraz maybe able to modulate the expression of a number of angiogenic factors, thereby blocking the sustained and focal neovascularization in multiple tumor cell types.
  • $31
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TargetMol | Citations Cited
Phenoxybenzamine hydrochloride
Phenoxybenzamine HCl, NSC 37448, NCI-c01661
T115863-92-3
Phenoxybenzamine hydrochloride (NCI-c01661) is the hydrochloride salt form of phenoxybenzamine, a synthetic, dibenzamine alpha-adrenergic antagonist with antihypertensive and vasodilatory properties. Phenoxybenzamine non-selectively and irreversibly blocks the postsynaptic alpha-adrenergic receptor in smooth muscle, thereby preventing vasoconstriction, relieving vasospasms, and decreasing peripheral resistance. Reflex tachycardia may occur and may be enhanced by blockade of alpha-2 receptors which enhances norepinephrine release. Phenoxybenzamine is reasonably anticipated to be a human carcinogen.
  • $29
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Phenazopyridine hydrochloride
Urodine, Pyridium, Phenazopyridine HCl
T1386136-40-3
Phenazopyridine hydrochloride (Pyridium) is used orally as a urinary tract analgesic. Side effects of phenazopyridine hydrochloride administration can include nausea, interference with the oxygen-carrying capacity of red blood cells (methemoglobinemia), hemolytic anemia as well as renal and hepatic toxicity. It is reasonably anticipated to be a human carcinogen.
  • $29
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Anthracene
T207084120-12-7
Anthracene is a polycyclic aromatic hydrocarbon (PAH) consisting of three fused benzene rings that presents as a colorless, solid, crystalline substance derived primarily from coal tar, known for its characteristic blue fluorescence under ultraviolet light and its extensive use as a fundamental raw material for producing anthraquinone dyes, synthetic fibers, and various other organic compounds. While Anthracene serves as a component in some wood preservatives and asphalt products, Anthracene is also a recognized environmental pollutant and is classified as a potential occupational carcinogen by some regulatory bodies.
    Inquiry
    4-Nitroquinoline 1-oxide
    NQO, NQNO, 4-NQO, 4Nqo, 4-Nitroquinoline-N-oxide, 4-Nitroquinoline 1-oxide
    T3536656-57-5
    4-Nitroquinoline 1-oxide (4-NQO) is a chemical carcinogen that induces mutations in bacteria, fungi, and animals through the formation of large amounts of purine adducts.
    • $37
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    N-Nitrosomorpholine
    T4068459-89-2
    N-Nitrosomorpholine is a light-sensitive nitrosamine with strong carcinogenicity in animals and is commonly used to induce liver cancer models.
    • $29
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    4-(Dimethylamino)benzaldehyde
    p-Dimethylaminobenzaldehyde
    T65645100-10-7
    4-(Dimethylamino)benzaldehyde (p-Dimethylaminobenzaldehyde) is a carcinogen that can induce liver cancer.
    • $29
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    2-Bromobiphenyl
    T79132052-07-5
    2-Bromobiphenyl is a persistent organic pollutant (POP) found primarily in soil and water. It is a known human carcinogen and has been linked to a variety of health effects including reproductive and developmental toxicity.
    • $39
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    TargetMol | Inhibitor Sale
    Lariciresinol
    TN185327003-73-2
    Lariciresinol is an enterolignan precursor, it possesses fungicidal activities by disrupting the fungal plasma membrane and therapeutic potential as a novel antifungal agent for the treatment of fungal infectious diseases in humans. Dietary lariciresinol
    • $172
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    TargetMol | Citations Cited
    AalphaC
    Aalpha-C, Aalpha C, 2-Amino-alpha-carboline
    T2088926148-68-5
    AalphaC (2-Amino-alpha-carboline) is a potential carcinogen.
    • $30
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    TargetMol | Inhibitor Sale
    PhIP
    T16525105650-23-5
    PhIP is a heterocyclic aromatic amine (HAA) from cooked meat. It belongs to pyridine heterocyclic amine and is a 2B carcinogen with estrogen activity. PhIP forms adducts with DNA that promote cancer.
    • $48
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    4-Aminobiphenyl
    T20604292-67-1
    4-Aminobiphenyl is a Class 1 carcinogen with cytotoxic effects on MCF-7 and RT-4 cells. It exhibits affinity as a substrate for UDP-glucuronosyltransferase 1A4 and can be used in related research in the field of life sciences.
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