Bioactive Small Molecules
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Filtered Search Results
Cayman Chemical GCN2-IN-1, Purity: ≥90%, CAS: 1448693-69-3, 25 mg
An inhibitor of GCN2 (IC50 = ~0.2 µM for autophosphorylation); inhibits integrase phosphorylation (IC50 = ~0.2 µM for the HIV-1 enzyme); inhibits ELAV-like protein 1 protein dimerization (IC50 = 4.5 µM); decreases the viability in U251, XD456, U87, and LN-229 glioma cells (IC50s = 4.7, 2.8, 3.2, and 2.7 µM, respectively)
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Medchemexpress LLC PRSS3/Trypsin-3 Hum 10ug
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Recombinant human PRSS3 (Trypsin-3) is a serine protease that cleaves peptide bonds after arginine residues. This product is supplied as 10 μg of recombinant, polyhistidine-tagged protein intended for enzymatic assays, inhibitor screening, and biochemical characterization.
- Recombinant human enzyme for biochemical and enzymatic assays.
- Polyhistidine tag facilitates purification and detection.
- Supplied in a 10 μg unit size suitable for screening and pilot studies.
- Appropriate for activity assays and inhibitor profiling.
- Can be aliquoted and stored long term according to manufacturer instructions.
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Cayman Chemical Bourgeonal, Purity: ≥95%, CAS: 18127-01-0, 25 mg
An hOR17-4 agonist; increases cytosolic calcium levels in human spermatozoa at 5 μM; acts as a chemoattractant and increases swimming speed in sperm chemotaxis assays in a concentration-dependent manner
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Medchemexpress LLC HY-117930 25mg , Danicopan CAS:1903768-17-1 Purity:>98%
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HY-117930 25mg Danicopan CAS: 1903768-17-1 Danicopan (ACH-4471), a selective and orally active small-molecule factor D inhibitor, shows high binding affinity to human Factor D with Kd value of 0.54 nM. Danicopan (ACH-4471) inhibits alternative pathway of complement (APC) activity, has potential to block the alternative pathway of complement in paroxysmal nocturnal hemoglobinuria (PNH) and atypical hemolytic uremic syndrome (aHUS). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
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Cayman Chemical PI-828, Purity: ≥98%, CAS: 942289-87-4, 5 mg
A potent inhibitor of PI3K (IC50s = 9.8, 183, 227, and 1,967 nM for p110β, p110α, p110δ, and p110γ, respectively); has been immobilized on solid surface; interacts with non-PI3K cellular proteins such as mTOR, ALDH1, BRD4, CKIIα, and GSK-3β.
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TARGETMOL CHEMICALS INC EPIDERMAL GROWTH FACTOR 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg and bulk. Please contact Fisher for quotes. Epidermal Growth Factor binds to epidermal growth factor receptor (EGFR) and stimulates cell growth and proliferation. It is approved for the treatment of diabetic foot ulcers. purity: 100%
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Cayman Chemical Cercosporin, Purity: ≥95%, CAS: 35082-49-6, 5 mg
A cytotoxic phytotoxin; produces ROS in plant hosts; has light-activated cytotoxic effects (CC50s = 241, 282, and 174 nM in HeLa, A432, and MCF-7 cells, respectively); a selective inhibitor of PKC (IC50 = 600-1,300 nM) with no activity on PKA or PPK
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Medchemexpress LLC Hydrazinecarboselenoamide | 21198-79-8 | 95.0% | 50 MG
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Selenosemicarbazide, also known as Hydrazinecarboselenoamide, is a chemical compound with the molecular formula CH5N3Se and a molecular weight of 138.03. This off-white to gray solid has a purity of 95.0% by NMR. Derivatives of Selenosemicarbazide have shown indications of antimicrobial activity and potential anti-tumor effects.
- Off-white to gray solid
- Purity of 95.0%
- Potential for antimicrobial activity
- Potential for anti-tumor effects (derivatives)
- Store powder at -20°C for up to 3 years or 4°C for up to 2 years
- Store in solvent at -80°C for up to 6 months or -20°C for up to 1 month
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Cayman Chemical Cannabipiperidiethanone, Purity: ≥98%, CAS: 1345970-43-5, 5 mg
A synthetic CB that binds to the CB receptors CB1 and CB2 with IC50 values of 591 and 968 nM, respectively; intended for forensic purposes and research applications
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Cayman Chemical UAMC-3203 (hydrochloride), Purity: ≥98%, CAS: 2271358-65-5, 5 mg
A ferroptosis inhibitor (IC50 = 10 nM for erastin-induced ferroptosis in IMR-32 cells); decreases iron-induced plasma LDH levels in a mouse model of acute iron poisoning at 20 µmol/kg; not toxic to mice at 20 µmol/kg for four weeks
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Medchemexpress LLC AEBSF hydrochloride | 30827-99-7 | 99.87% | 200 MG
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AEBSF hydrochloride is an irreversible inhibitor of serine proteases, including chymotrypsin, kallikrein, plasmin, thrombin, and trypsin. It is for research use only and not sold to patients.
- Inhibits the constitutive production of Aβ by directly inhibiting β-secretase in various human cell lines.
- Inhibits the lysis of leukemic cells by human macrophages without affecting macrophage secretion of TNF-α and IL-1β.
- Disturbs the growth of blastocysts on endometrial cells and inhibits the adhesion of HeLa cells on HUVECs by altering protein secretion.
- Prolongs the survival of mice with lethal *T. gondii* infection *in vivo*.
- Reduces airway response and inflammation in a cockroach allergen-induced murine model.
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Cayman Chemical Acolbifene, Purity: ≥98%, CAS: 182167-02-8, 1 mg
A SERM; inhibits E2-induced transcriptional activity of ERα and ERβ (IC50s = 2 and 0.4 nM, respectively); binds to ERs in cytosol from human breast cancer and non-cancerous uterine cells (Kis = 0.047 and 0.042 nM, respectively); binds to ERs in cytosol from rat uterine cells (IC50 = 0.44 nM) but not to progesterone or androgen receptors in cytosol from rat uterine and ventral prostate cells (IC50s = 22,500 and >10,000 nM, respectively); inhibits E2-stimulated proliferation of T47D, ZR-75-1, and MCF-7 breast cancer cells (IC50s = 0.146, 0.75, and 0.321 nM, respectively); inhibits E1-stimulated tumor growth in a ZR-75-1 human breast cancer xenograft model in ovariectomized mice (50 μg per day); inhibits E1-stimulated endometrial epithelium thickening in vivo in ovariectomized mice (50 μg per day)
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Medchemexpress LLC Irinotecan hydrochloride | 100286-90-6 | 99.9% | 1 ML
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Irinotecan hydrochloride is a topoisomerase I inhibitor primarily used to treat colon cancer and rectal cancer. It is intended for research use only.
- Acts as a topoisomerase I inhibitor
- Inhibits tumor growth in various models
- Induces cell cycle arrest and apoptosis
- Suitable for in vitro and in vivo studies
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Medchemexpress LLC Methyl 2-((6S)-4-(4-chlorophenyl)-2-((5-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)amino) | 2243076-67-5 | 98.9% | 50 MG
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ZXH-3-26 is a proteolysis targeting chimera (PROTAC) that links a Cereblon ligand to a BRD4 ligand to induce selective BRD4 degradation, with a reported DC50/5h of approximately 5 nM. It is supplied as a 50 mg vial at high purity for use in chemical biology and targeted protein degradation research.
- Selective BRD4 degradation with DC50/5h ≈ 5 nM.
- Minimal degradation of BRD2 and BRD3 at tested concentrations.
- Molecular formula C38H37ClN8O7S and molecular weight 785.27.
- Purity 98.9% and supplied as a 50 mg quantity.
- Includes SMILES for cheminformatics and structure confirmation.
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Cayman Chemical MK-0812, Purity: ≥98%, CAS: 624733-88-6, 1 mg
A CCR2 antagonist (IC50 = 5 nM for the human receptor); inhibits mammosphere formation of BT-549 breast cancer cells; increases CCL2 levels and decreases CD11b+ monocytes in mouse blood at 0.03, 0.1, and 0.3 mg/kg
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