Drug Standards
Medchemexpress LLC Linagliptin impurity 9 | 2279114-27-9 | MFCD22035713 | 5mg
Linagliptin impurity 9 is an impurity of Linagliptin (HY-10284)
Selleck Chemical LLC Ifosfamide 50mg 3778-73-2 NSC109724, Isophosphamide
Ifosfamide (NSC109724, Isophosphamide) is a nitrogen mustard alkylating agent used in the treatment of cancer. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Medchemexpress LLC Diphenhydramine | 58-73-1 | 99.6% | 250 MG
Diphenhydramine is a first-generation histamine H1-receptor antagonist with an anti-cholinergic effect. Diphenhydramine hydrochloride can cross the ovine blood-brain barrier (BBB).
- Histamine H1-receptor antagonist
- Anti-cholinergic effect
- Can cross the ovine blood-brain barrier (BBB)
- Molecular weight: 255.35
- Molecular formula: C17H21NO
- Liquid appearance
- Colorless to light yellow
- In vitro solubility in DMSO: 100 mg/mL
- Targets H1 receptor and NMDA receptor
- IC50 for NMDA receptor: 24.6 μM
Medchemexpress LLC Latanoprost acid | 41639-83-2 | 95.1% | 390.51 | 10 MG
Latanoprost acid, an analog of prostaglandin (PG) F2α, is a selective prostanoid receptor (FP) agonist that specifically activates the FP-PG receptor. It inhibits RANKL-induced osteoclastogenesis and function by inhibiting the ERK, AKT, JNK, and p38 cascade, followed by the c-fos/NFATc1 pathway. Latanoprost acid is also a medication used to lower pressure inside the eyes.
- Selective prostanoid receptor (FP) agonist.
- Activates the FP-PG receptor.
- Inhibits RANKL-induced osteoclastogenesis and function.
- Lowers pressure inside the eyes.
- Inhibits ERK, AKT, JNK, and p38 cascade.
- Reduces protein expressions of c-fos and NFATc1 in bone marrow-derived macrophages cells (BMMs).
- Significantly inhibits mature osteoclast formation.
- Notably prevents LPS-induced bone destruction in 8-week-old C57BL/6J mice.
Enzo Life Sciences Amiloride hydrochloride dihydrate (1g). CAS: 17440-83-4
Selectively blocks low threshold (T-type) calcium channel (KD=30μM) with no effect on L-type channels or tetrodotoxin Na+ channels. Inhibits the epithelial tetrodotoxin insensitive Na+ channel (IC50 =1μM). Clinically useful K+ sparing diuretic. Alternative name: 3 5-Diamino-N-(aminoiminomethyl)-6-chloropyrazinecarboxamide HCl 2H2O. Purity: ≥98% (HPLC). Solubility: Soluble in DMSO (25mg/ml) or water (1mg/ml warm). Long Term Storage: Ambient.
TARGETMOL CHEMICALS INC FLUTRIMAZOLE 5MG
Also available in 1 mg 2 mg 10 mg 25 mg 50 mg 100 mg 500 mg and bulk. Please contact Fisher for quotes. Flutrimazole is a dual-action imidazole antifungal compound exhibiting both anti-inflammatory and antifungal properties. Notably flutrimazole demonstrates limited transdermal penetration making it particularly advantageous for topical applications in the treatment of fungal infections especially those accompanied by inflammation. purity: 98%
Apexbio Technology LLC Haloperidol hydrochloride 1511-16-6 50mg
Haloperidol hydrochloride is a small-molecule antagonist targeting dopamine D2 receptors It is designed to modulate dopaminergic neurotransmission thereby regulating neural pathways implicated in psychosis Haloperidol hydrochloride exerts its biological activity primarily through inverse agonist and antagonist effects on dopamine D2 receptors particularly within the mesocortical limbic and nigrostriatal pathways Based on these pharmacological properties haloperidol hydrochloride holds research potential in studying dopamine receptor functions dopamine-mediated neural circuits and the pathophysiological mechanisms underlying psychiatric disorders
Medchemexpress LLC 4-(3-aminophenyl)morpholin-3-one | 1082495-22-4 | MFCD11577324 | 100mg
Rivaroxaban impurity 67 is an impurity of Rivaroxaban (HY-50903)
Medchemexpress LLC 2-chloro-5-(2-fluorophenyl)-1H-pyrrole-3-carbaldehyde | 2169267-53-0 | 25mg
Vonoprazan impurity 46 is an impurity of Vonoprazan (HY-100007)
TARGETMOL CHEMICALS INC MONTELUKAST SODIUM 500MG
Also available in 50 mg 100 mg 1 mL 10 mM (in DMSO) and bulk. Please contact Fisher for quotes. Montelukast sodium (MK0476) is an orally available leukotriene receptor antagonist which is widely used for the prophylaxis and chronic treatment of asthma and has been linked to rare cases of clinically apparent liver injury. purity: 99%
Advanced Chemblocks Inc Alogliptin benzoate; 100MG; 98%
Chemical Name: Alogliptin benzoate CAS: 850649-62-6 MW: 461.53 MDL Number: MFCD09833195 Category: Reference Compound Synonym: Alogliptin benzoate
Medchemexpress LLC Zileuton sodium | 118569-21-4 | 98.02% | C₁₁H₁₁N₂NaO₂S | 50 MG
Zileuton sodium (A 64077 sodium) is a potent and selective inhibitor of 5-lipoxygenase, exhibiting inflammatory activities.
- Potent and selective inhibitor of 5-lipoxygenase.
- Exhibits inflammatory activities.
- Available in various quantities.
- Available as solid or in solution.
- For research use only.
eMolecules 496775-62-3 | Eltrombopag Olamine | Target Molecule | MFCD22380664 | 564.643 | C29H36N6O6 | 0.000 | NCCO.NCCO.CC1=NN(C(=O)\C1=N/Nc1cccc(-c2cccc(c2)C(O)=O)c1O)c1ccc(C)c(C)c1 | 100mg | 376018977
Eltrombopag Olamine | Target Molecule | 496775-62-3 | MFCD22380664 | 564.643 | C29H36N6O6 | 0.000 | NCCO.NCCO.CC1=NN(C(=O)\C1=N/Nc1cccc(-c2cccc(c2)C(O)=O)c1O)c1ccc(C)c(C)c1 | 100mg | 376018977
Selleck Chemical LLC Febantel S5092-25mg
Febantel (Rintal Combotel Oratel Bay Vh 5757 Negabot Plus) is a prodrug that is metabolized to fenbendazole and oxfendazole which are undoubtedly the active parasiticides
Sigma Aldrich Fine Chemicals Biosciences Irinotecan Related Compound E United States Pharmacopeia (USP) Reference Standard | 78287-27-1 | 15MG
Irinotecan Related Compound E United States Pharmacopeia (USP) Reference Standard | Mol Wt: 376.41 | 78287-27-1 | 15MG