Chemical structure
Cat.No.
Product Name
CAS no.
Target
YN320900 Dexamethasone 50-02-2
Dexamethasone (DHAP) is a potent synthetic member of the glucocorticoid class of steroid drugs, and an interleukin receptor modulator that has anti-inflammatory and immunosuppressant effects.
YN290415 Cyclophosphamide 50-18-0
Cyclophosphamide is a syntheticalkylatingagent chemically related to the nitrogen mustards with antineoplastic activity, a immunosuppressant.
YN321723 Hydrocortisone 50-23-7
Hydrocortisone is a steroid hormone or glucocorticoid produced by the adrenal gland.
YN480324 Benzo[a]pyrene 50-32-8
Benzo[a]pyrene showslung carcinogenicityin animal models, and it is frequently used in chemoprevention studies.
Thalidomide was introduced as a sedative drug, immunomodulatory agent and also is investigated for treating symptoms of many cancers. Thalidomide inhibits an E3 ubiquitin ligase, which is a CRBN-DDB1-Cul4A complex.
YN371768 6-Mercaptopurine 50-44-2
Mercaptopurine is a widely used antileukemic agent and immunosuppressive drug that inhibits de novo purine synthesis through incorporation of thiopurine methyltransferase metabolites into DNA and RNA.
YN481995 Estradiol benzoate 50-50-0
Estradiol benzoate is an estradiol analog which binds to the human, murine and chicken ERα with IC50 of 22-28 nM.
YN330348 Chloroquine phosphate 50-63-5
Chloroquine phosphate is a 4-aminoquinoline anti-malarial and anti-rheumatoid agent, also acting as an ATM activator.
Niclosamide can inhibit DNA replication and inhibit STAT3 with IC50 of 0.7 μM in a cell-free assay. Niclosamide selectively inhibited the phosphorylation of STAT3 and had no obvious inhibition against t...
YN374315 D-Ribose(mixture of isomers) 50-69-1
D-ribose is a naturally occurring sugar involved in producing energy in the body and is also the structural basis of DNA and RNA.
Floxuridine is an antineoplastic antimetabolite, used in the treatment of colon carcinoma and colorectal cancer that has metastasized to the liver.
YN290506 Procaine hydrochloride 51-05-8
Procaine is an inhibitor of sodium channel, NMDA receptor and nAChR with IC50 of 60 μM, 0.296 mM and 45.5 μM, which is also an inhibitor of 5-HT3 with KD of 1.7 μM.
YN251971 Benzimidazole 51-17-2
Benzimidazole is a heterocyclic aromatic organic compound and acts as an important pharmacophore in medicinal chemistry. Benzimidazole derivatives have been reported to possess various biological activities such as anti-cancer, anti-vir...
YN372699 5-Fluorouracil 51-21-8
Fluorouracil (5-Fluoracil, 5-FU) is a DNA/RNA synthesis inhibitor, which interrupts nucleotide synthetic by inhibiting thymidylate synthase (TS) in tumor cells.
YN321354 Histamine phosphate 51-74-1
Histamine acts directly on the blood vessels to dilate arteries and capillaries mediated by both H 1- and H 2-receptors.
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