Drug Standards
Medchemexpress LLC Elacridar hydrochloride | 143851-98-3 | >98.0% | 600.10 | C34H34ClN3O5 | 10 MG
Elacridar hydrochloride is an orally active inhibitor of P-glycoprotein (P-gp) and breast cancer resistance protein (BCRP), used in research to study efflux transporter-mediated drug distribution, including blood-brain barrier penetration and multidrug resistance in cancer. Supplied as the hydrochloride salt for research applications.
- Orally active P-gp and BCRP inhibitor
- Used to evaluate efflux transporter effects on drug distribution and blood-brain barrier penetration
- Provided as hydrochloride salt for improved handling
- Available in small research sizes for analytical and preclinical studies
- Documented solubility and storage conditions for reproducible results
Sigma Aldrich Fine Chemicals Biosciences Delta-3-cefaclor European Pharmacopoeia (EP) Reference Standard | 152575-13-8 |
Delta-3-cefaclor European Pharmacopoeia (EP) Reference Standard | Mol Wt: 367.81 | 152575-13-8 |
Sigma Aldrich Fine Chemicals Biosciences Dacarbazine Related Compound B United States Pharmacopeia (USP) Reference Standard | 4656-86-4 (anhydrous) | 50MG
Dacarbazine Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 155.11 | 4656-86-4 (anhydrous) | 50MG
Sigma Aldrich Fine Chemicals Biosciences Diethylstilbestrol monomethyl ether European Pharmacopoeia (EP) Reference Standard | 7773-60-6 |
Diethylstilbestrol monomethyl ether European Pharmacopoeia (EP) Reference Standard | Mol Wt: 282.38 | 7773-60-6 |
Med Vet International Imatinib Mesylate (Gleevec) 400mg Tablet Yl Ovl 30 Tablets
VET LICENSE NEEDS TO BE PROVIDED IN 3-4 BUSINESS DAYS OR ORDER WILL BE CANCELLED
Imatinib Mesylate (Gleevec) 400mg Tablet Yl Ovl 30 Tablets.
TARGETMOL CHEMICALS INC Citalopram hydrobromide 100MG
Also available in 10 mg, 25 mg, 50 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Citalopram hydrobromide (XU-62-320) , a selective serotonin reuptake inhibitor (SSRI), selectively inhibits the CNS neuronal reuptake of serotonin, thereby potentiating serotonergic activity in the central nervous system (CNS). Citalopram hydrobromide is the orally bioavailable hydrobromide salt of the racemic bicyclic phthalene derivative citalopram with antidepressant activity. This agent has minimal effects on the CNS neuronal reuptake of norepinephrine (NE) and dopamine (DA). Purity 99.35%
eMolecules Ambeed / 2-(3-Ethylphenyl)-4455-tetramethyl-132-dioxaborolane / 250mg / 731677081 / A771497 / / 1075719-83-3 / MFCD18734472 / 232.130 / C14H21BO2
Ambeed / 2-(3-Ethylphenyl)-4455-tetramethyl-132-dioxaborolane / 250mg / 731677081 / A771497 / / 1075719-83-3 / MFCD18734472 / 232.130 / C14H21BO2
Apexbio Technology LLC MDV3100 (Enzalutamide), 915087-33-1, MFCD14155804, 10 mg
MF: C21H16F4N4O2S, MW: 464.4, Synonyms: Enzalutamide, MDV3100, MDV-3100, MDV 3100. Solubility: 23.22mg/mL in DMSO. MDV3100, known as Enzalutamide, is a second-generation androgen receptor (AR) signaling inhibitor. It has been demonstrated impressive affinity to the AR compared to the first-generation AR inhibitors. It is able to inhibit binding of androgens to the AR, AR nuclear translocation, and the association of the AR with DNA.
Apexbio Technology LLC Lenalidomide hydrochloride 1243329-97-6 50mg
Lenalidomide hydrochloride is a small-molecule immunomodulator that inhibits TNF- secretion It is designed to modulate immune signaling pathways thereby regulating T cell activation and cytokine production Lenalidomide hydrochloride exerts its biological activity primarily by inhibiting TNF- secretion (IC50 13 nM) enhancing IL-2 and soluble IL-2 receptor (sIL-2R) production and inducing CD28 tyrosine phosphorylation followed by NF- B activation in T cells It also impairs autoubiquitination of cereblon (CRBN) a substrate receptor of the E3 ligase complex affecting downstream protein expression including c-Myc IRF4 and p21(WAF-1) Based on these pharmacological properties lenalidomide hydrochloride holds research potential in oncology and inflammation studies focusing on immune modulation
Sigma Aldrich Fine Chemicals Biosciences Astemizole >=98% (HPLC) | 68844-77-9 | MFCD00153919 | 50MG
Astemizole >=98% (HPLC) | Purity: >=98% (HPLC) | Mol Wt: 458.57 | 68844-77-9 | MFCD00153919 | 50MG
Sigma Aldrich Fine Chemicals Biosciences Irinotecan Related Compound B United States Pharmacopeia (USP) Reference Standard | 86639-52-3 | MFCD00871873 | 10MG
Irinotecan Related Compound B United States Pharmacopeia (USP) Reference Standard | Mol Wt: 392.4 | 86639-52-3 | MFCD00871873 | 10MG
Medchemexpress LLC 4,5-dichloro-3,6-dihydroxybenzene-1,2-dicarbonitrile | 4640-41-9 | 50mg
Brexpiprazole impurity 1 is an impurity of Brexpiprazole (HY-15780)
Sigma Aldrich Fine Chemicals Biosciences Mepivacaine hydrochloride European Pharmacopoeia (EP) Reference Standard | 1722-62-9 | MFCD00144738 |
Mepivacaine hydrochloride European Pharmacopoeia (EP) Reference Standard | Mol Wt: 282.81 | 1722-62-9 | MFCD00144738 |
Avachem Scientific LLC Bortezomib, 179324-69-7, MFCD09056737, 10mg
Molecular Formula: C19H25BN4O4, Molecular Weight 384.241, Smiles: CC(C)C[C@@H](NC(=O)[C@H](Cc1ccccc1)NC(=O)c2cnccn2)B(O)O
Sigma Aldrich Fine Chemicals Biosciences Ramipril impurity C European Pharmacopoeia (EP) Reference Standard | 99742-35-5 |
Ramipril impurity C European Pharmacopoeia (EP) Reference Standard | Mol Wt: 422.56 | 99742-35-5 |