Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Schizandrin B phyproof(R) Reference Substance | 61281-37-6 | MFCD00210555 | 10MG
Schizandrin B phyproof(R) Reference Substance | Purity: >=95.0% (HPLC) | Mol Wt: 400.46 | 61281-37-6 | MFCD00210555 | 10MG
Medchemexpress LLC Tenofovir exalidex | 911208-73-6 | 99.8% | 569.72 | 50 MG
Tenofovir exalidex | 911208-73-6 | 99.8% | 569.72 | 50 MG
Medchemexpress LLC Enoxaparin | 679809-58-6 | 50 MG
Enoxaparin (PK 10169) is a low-molecular-weight heparin (LMWH) derivative that acts as an anticoagulant by inhibiting factor Xa and thrombin IIa through antithrombin III. It also demonstrates antioxidant and anti-inflammatory properties, protecting the rat hippocampus against traumatic brain injury (TBI). Enoxaparin is utilized in research for deep vein thrombosis (DVT), pulmonary embolism, TBI, and COVID-19.
- Exerts anticoagulant activity through antithrombin III, inhibiting factor Xa and thrombin IIa.
- Protects the rat hippocampus against TBI via antioxidant and anti-inflammatory properties.
- Can be used for research on deep vein thrombosis (DVT), pulmonary embolism, TBI, and COVID-19.
- In vitro, it enhances AAT (alpha-1-antitrypsin) inhibition of TMPRSS2 activity and HCoV-229E infection of hAEc.
- In vivo, it reduces oxidative damage, inflammation, and astrocytosis following TBI in rats.
Medchemexpress LLC Agouti-related Protein (AGRP) (83-132) Amide (human) TFA | 97.0% | 5676.57 (free base) | 1 MG
Agouti-related Protein (AGRP) (83-132) Amide (human) TFA is a fragment of agouti-related protein (AGRP) found in abundance in the arcuate nucleus of the hypothalamus. It primarily functions as an inverse agonist for the melanocortin-4 receptor (MC4R) to increase food intake.
- Fragment of agouti-related protein (AGRP)
- Acts as an inverse agonist for the melanocortin-4 receptor (MC4R)
- Increases food intake and decreases spontaneous locomotor activity in rats
- Solid, white to off-white appearance
- Soluble in DMSO up to 100 mg/mL with ultrasonic assistance
- Features a specific amino acid sequence with identified disulfide bridges
Medchemexpress LLC Gemcitabine monophosphate | 116371-67-6 | 99.98% | 343.18 | 10 MG
Gemcitabine monophosphate is an active intermediate of Gemcitabine. It demonstrates a synergistic anti-cancer effect and can be delivered through nanoparticle formulation. It is intended for research use only.
- Active intermediate of Gemcitabine.
- Exhibits synergistic anti-cancer effects.
- Can be delivered via nanoparticles.
- Induces tumor cell apoptosis (30-40%).
- Reduces tumor cell proliferation (8 times).
- Significantly reduces tumor microvessel density (MVD).
- Inhibits tumor mitosis.
Sigma Aldrich Fine Chemicals Biosciences Vigabatrin British Pharmacopoeia (BP) Reference Standard | 68506-86-5 | MFCD00274577 |
Vigabatrin British Pharmacopoeia (BP) Reference Standard | Mol Wt: 129.16 | 68506-86-5 | MFCD00274577 |
Sigma Aldrich Fine Chemicals Biosciences Bambuterol hydrochloride European Pharmacopoeia (EP) Reference Standard | 81732-46-9 | MFCD03427293 |
Bambuterol hydrochloride European Pharmacopoeia (EP) Reference Standard | Mol Wt: 403.9 | 81732-46-9 | MFCD03427293 |
Cayman Chemical Suc-AAPF-pNA 10mg
A chromogenic substrate that can be cleaved by cathepsin G (Km = 1.7 mM), subtilisins, chymotrypsin (Km = 60 µM), chymase (Km = 4 mM), and cyclophilin; used for inhibitor screening and kinetic analysis
Medchemexpress LLC Escitalopram oxalate | 219861-08-2 | MFCD06407826 | 100.0% | C22H23FN2O5 | 10MG
Escitalopram oxalate is the oxalate salt of escitalopram (the S-enantiomer of citalopram) supplied as a high-purity analytical standard for research and analytical applications. It is a selective serotonin reuptake inhibitor with high affinity for the serotonin transporter and is provided as a solid reference material for laboratory use only.
- High purity analytical standard (99.98%).
- CAS number 219861-08-2 for unambiguous identification.
- Intended for research and analytical applications, not for human use.
- Available in multiple small package sizes (5-500 mg) for method development.
- Reported high affinity for the serotonin transporter (Ki ≈ 0.89 nM).
Cayman Chemical RnItIdInhydrochlorIde 1g
A histamine H2 receptor antagonist; reverses histamine-induced relaxation of isolated rat uterine horn (pA2 = 6.9) as well as histamine-induced increases in contraction frequency in isolated guinea pig right atrium (pA2 = 7.2); inhibits histamine-and pentagastrin-induced gastric acid secretion in a dose-dependent manner in anesthetized rats from 0.03-3 mg/kg
Apexbio Technology LLC Alprostadil(Synonyms: Prostaglandin E1, PGE1, Alprostadilum, Edex, Caverject, Muse, Prostin VR, Liprostin), 10mg, CAS: 745-65-3.
Alprostadil (CAS 745-65-3) also known as prostaglandin E1 is an endogenous prostaglandin analog that exerts potent vasodilatory activity by binding and activating prostaglandin E-type (EP) receptors primarily EP2 and EP4 Upon receptor activation intracellular cyclic adenosine monophosphate (cAMP) levels rise mediating smooth muscle relaxation and vasodilation Clinically Alprostadil is investigated and utilized in research contexts addressing vascular biology erectile dysfunction mechanisms and cardiovascular function offering insights into prostaglandin signaling pathways
Medchemexpress LLC Sorafenib impurity 5 | 1379324-09-0 | 50mg
Sorafenib impurity 5 is an impurity of Sorafenib (HY-10201)
Medchemexpress LLC 6-[(2-iminopyrrolidin-1-yl)methyl]-1H-pyrimidine-2,4-dione | 2069937-25-1 | MFCD30741913 | 5mg
Tipiracil impurity 1 is an impurity of Tipiracil (HY-A0063A)