Shopping Cart
  • Remove All
  • TargetMol
    Your shopping cart is currently empty
Filter
Applied FilterClear all
TargetMol | Tags By Target
  • DNA/RNA Synthesis
    (433)
  • Apoptosis
    (191)
  • Topoisomerase
    (139)
  • Antibacterial
    (124)
  • Antibiotic
    (110)
  • Autophagy
    (88)
  • Endogenous Metabolite
    (86)
  • ADC Cytotoxin
    (69)
  • Nucleoside Antimetabolite/Analog
    (59)
  • Others
    (1160)
Filter
Search Result
Results for "

dna

" in TargetMol Product Catalog
  • Inhibitors & Agonists
    2535
    TargetMol | Inhibitors_Agonists
  • Compound Libraries
    15
    TargetMol | Compound_Libraries
  • Peptide Products
    48
    TargetMol | Peptide_Products
  • Inhibitory Antibodies
    12
    TargetMol | Inhibitory_Antibodies
  • Dye Reagents
    139
    TargetMol | Dye_Reagents
  • PROTAC Products
    34
    TargetMol | PROTAC
  • Natural Products
    396
    TargetMol | Natural_Products
  • Reagent Kits
    20
    TargetMol | Reagent_Kits
  • Recombinant Protein
    360
    TargetMol | Recombinant_Protein
  • Isotope Products
    41
    TargetMol | Isotope_Products
  • Antibody Products
    115
    TargetMol | Antibody_Products
  • Disease Modeling
    17
    TargetMol | Disease_Modeling_Products
  • Cell Research
    104
    TargetMol | Inhibitors_Agonists
Cyclophosphamide
T0707L50-18-0
Cyclophosphamide is an alkylating agent type of anti-tumor drug, and its main target is DNA. Cyclophosphamide inhibits the proliferation of tumor cells by undergoing alkylation reactions with DNA, interfering with the replication and transcription processes of DNA.
  • $35
In Stock
Size
QTY
TargetMol | Inhibitor Hot
aoh1996
T775202089314-64-5In house
AOH1996 is an orally active ligand for the replicasome component PCNA (proliferating cell nuclear antigen), targeting the transcription-replication conflict (TRC). It interferes with the interaction of PCNA with its binding proteins, leading to DNA replication stress and apoptosis. AOH1996 causes proteasome-dependent rpb1 degradation and lethal DNA damage by stabilizing the interaction between PCNA and RNA polymerase II, and acts synergistically with DNA damaging agents to inhibit tumor cell growth.
  • $60
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Carboxy-pyridostatin 2HCl
Carboxy-pyridostatin 2HCl(1417638-60-8 Free base)
T30745L In house
Carboxy-pyridostatin 2HCl has potential antitumor activity with high affinity for DNA at DNA G4s.
  • $228
In Stock
Size
QTY
Tallimustine HCl
Tallimustine HCl(115308-98-0 Free base)
T68151L118438-45-2In house
Tallimustine HCl is a DNA inhibitor, an AT-specific alkylated antitumor derivative of diamycin.Tallimustine HCl can be used in severe combined immunodeficiency mouse models of adult myelogenous leukemia, which can be used for the treatment of leukemia.
  • $195
In Stock
Size
QTY
Quinacrine dihydrochloride
SN-390, Quinacrine 2HCl, Mepacrine dihydrochloride
T094269-05-6
Quinacrine dihydrochloride (Mepacrine dihydrochloride) is the dihydrochloride salt of the 9-aminoacridine derivative quinacrine with potential antineoplastic and antiparasitic activities.
  • $41
In Stock
Size
QTY
Hydroxychloroquine sulfate
HCQ sulfate, Acidum iopanoicum
T0951747-36-4
Hydroxychloroquine sulfate (Acidum iopanoicum) inhibits plasmodial heme polymerase. It is a chemotherapeutic agent that acts against erythrocytic forms of malarial parasites. Hydroxychloroquine appears to concentrate in food vacuoles of affected protozoa.
  • $35
In Stock
Size
QTY
Methoxsalen
Xanthotoxin, NCI-C55903, 8-MOP, 8-Methoxypsoralen
T1548298-81-7
Methoxsalen (NCI-C55903) is a Photoactivated Radical Generator and Psoralen. The mechanism of action of methoxsalen is as a Photoabsorption. The physiologic effect of methoxsalen is by means of Photosensitizing Activity.
  • $29
In Stock
Size
QTY
Norharmane
β-Carboline, 2-Azacarbazole, 2,9-Diazafluorene
T4024244-63-3
Norharmane (β-Carboline) is a natural β-carboline first isolated from plants of the Zygophyllaceae family.
  • $30
In Stock
Size
QTY
Cyclophosphamide hydrate
Cyclophosphamide monohydrate
T07076055-19-2
Cyclophosphamide hydrate is a synthetic alkylating agent structurally related to nitrogen mustards, with antitumor and immunosuppressive activities. It is widely used in the treatment of various cancers and is also commonly employed to induce animal models of premature ovarian failure, myelosuppression, cystitis, and myocarditis.
  • $33
In Stock
Size
QTY
BCL6-IN-3
T104872253878-44-1
BCL6-IN-3 is a potent BCL6 inhibitor with GI50 of 70 nM in SU-DHL4 cells. BCL6-in-3 regulates cell activation, differentiation, DNA damage and apoptosis, and has antitumor activity.
  • $117
In Stock
Size
QTY
AGI-24512
T141412201066-53-5
AGI-24512 is a potent inhibitor of methionine adenylyltransferase 2α (MAT2A) (IC50: 8 nM).AGI-24512 shows antiproliferative activity in MTAP-deficient cancer cells.AGI-24512 inhibits MAT2A, which causes DNA damage in MTAP, and is often used in conjunction with anticancer compounds in cancer research.
  • $64
In Stock
Size
QTY
Dibenz[a,h]anthracene
NSC 22433, DB(a,h)A, CCRIS 208, AI3-18996
T3142553-70-3
Dibenz[a,h]anthracene (CCRIS 208) has induced DNA damage and gene mutations in bacteria and gene mutations and transformation in several types of mammalian cell cultures.
  • $30
In Stock
Size
QTY
4-Ethylcatechol
T775631124-39-6
4-Ethylcatechol is present in red wine and can be extracted from Glechoma longituba (NaKai) Kupr.4-Ethylcatechol induces DNA damage in the presence of Cu(II).4-Ethylcatechol is a potent antiplatelet compound.
  • $29
In Stock
Size
QTY
3,7,4'-Trihydroxyflavone
Resokaempferol, 5-Deoxykampferol
TN21432034-65-3
3,7,4'-Trihydroxyflavone(5-Deoxykampferol) is a DNA-breaking flavonoid isolated from rosewood heartwood. It inhibits osteoclast differentiation, actin ring formation, and bone resorption in RAW 264.7 cells and bone marrow macrophages induced by NF-κB ligand (RANKL) receptor activators.
  • $64
In Stock
Size
QTY
BTB09089
GPR65 agonist (BTB09089)
T67892245728-44-3In house
BTB09089 (GPR65 agonist ) is a T cell death-associated gene 8 (TDAG8 GPR65)-specific agonist.BTB09089 induces TDAG8 expression and regulates cytokine production in T cells and macrophages.
  • $65
In Stock
Size
QTY
Elinafide
T68061162706-37-8In house
Elinafide, a dinaphthylimide cytotoxic agent, is a DNA-targeted anticancer agent that has shown antitumor activity in in vitro and in vivo assays.
  • $41
In Stock
Size
QTY
TargetMol | Inhibitor Sale
Tunicamycin
T1322911089-65-9
Tunicamycin is a mixture of antibiotics that inhibit N-linked glycosylation by blocking GlcNAc phosphotransferase (GPT). Tunicamycin has antitumor activity, as well as anti-bacterial, anti-fungal, and anti-viral activity.
  • $65
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Cisplatin
cis-Diaminodichloroplatinum, CDDP
T156415663-27-1
Cisplatin (CDDP) is a chemotherapeutic agent with antitumor activity and is a classic DNA crosslinker. It inhibits DNA synthesis and induces DNA damage in cancer cells by forming DNA adducts, ultimately leading to cell death. In addition, Cisplatin can activate ferroptosis and induce autophagy. In animal studies, it is commonly used to establish models of chronic kidney injury and acute renal failure.
  • $30
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Suramin Sodium Salt
Suramin hexasodium salt, NF-060, BAY-205
T2160129-46-4
Suramin Sodium Salt (BAY-205) is a sodium salt form of suramin, a polysulphonated naphthylurea with potential antineoplastic activity. Suramin blocks the binding of various growth factors, including insulin-like growth factor I (IGF-I), epidermal growth factor (EGF), platelet-derived growth factor (PDGF), and tumor growth factor-beta (TGF-beta), to their receptors, thereby inhibiting endothelial cell proliferation and migration. This agent also inhibits vascular endothelial growth factor (VEGF)- and basic fibroblast growth factor (bFGF)-induced angiogenesis; retroviral reverse transcriptase; uncoupling of G-proteins from receptors; topoisomerases; cellular folate transport; and steroidogenesis.
  • $35
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Prexasertib
LY2606368
T43101234015-52-1
Prexasertib (LY2606368) is a selective checkpoint kinase 1 (CHK1) inhibitor (Ki 0.9 nM, IC50<1 nM). Prexasertib causes double-stranded DNA breaks and replication mutations, leading to apoptosis. Prexasertib has antitumor activity.
  • $46
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Elimusertib
BAY-1895344
T73181876467-74-1
Elimusertib (BAY-1895344) is a potent, highly selective, and orally available ATR inhibitor with an IC50 of 7 nM, demonstrating significant anti-tumor efficacy as a monotherapy and strong combination potential with targeted alpha therapy Radium-223 dichloride.
  • $31
In Stock
Size
QTY
TargetMol | Inhibitor Hot
Adenine
Vitamin B4, 6-Aminopurine
T006473-24-5
Adenine is a purine-derived nucleobase and one of the four bases of DNA. It is an important chemical component of both DNA and RNA, involved in cellular respiration, the formation of ATP and coenzymes NAD and FAD, as well as protein synthesis. Adenine is commonly used to induce chronic kidney injury models.
  • $50
In Stock
Size
QTY
Budesonide
Rhinocort, Pulmicort, Entocort
T009451333-22-3
Budesonide (Pulmicort), an anti-inflammatory corticosteroid, has shown the effective glucocorticoid activitie and few mineralocorticoid activities. According to reports, Budesonide has extensively inhibitory effects against multiple cells types and mediators referred to allergic and nonallergic-mediated inflammatory. What's more, the anti-inflammatory action of budesonide has been revealed to contribute to the effectiveness of asthma.
  • $50
In Stock
Size
QTY
Foscarnet sodium
Phosphonoformate
T022063585-09-1
Foscarnet sodium (Phosphonoformate) is an antiviral agent used in the treatment of cytomegalovirus retinitis. Foscarnet also shows activity against human herpesviruses and HIV.
  • $41
In Stock
Size
QTY