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Tetrahydrofuran

Tetrahydrofuran is an organic, polar, water-miscible, cyclic ether and aprotic solvent with low viscosity. Available in various quantities, purities, and reagent grades, it has applications including use in polymer science and reversed phase chromatography.

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1

Medchemexpress LLC N-Vanillyldecanamide | 31078-36-1 | MFCD01233545 | 50 MG
SDP

N-Vanillyldecanamide is a capsaicinoid isolated from the fruits of Capsicum annuum. It significantly reduced the radical length of Lactuca sativa seedling in a dose-dependent manner. This product is for research use only.

  • Purity of 99.86%
  • Molecular weight of 307.43
  • Molecular formula C18H29NO3
  • Appears as a white to off-white solid
  • Exhibits agonist activity at rat TRPV1 in CHO cells with an EC50 of 83 nM

ENCOMPASS_PREFERRED
2

Medchemexpress LLC AST5902 trimesylate | 2929417-90-1 | 98.8% | 842.88 | 50 MG
SDP

AST5902 trimesylate is the principal metabolite of Alflutinib (AST2818) both in vitro and in vivo. It exerts antineoplastic activity. Alflutinib is an EGFR inhibitor.

  • Principal metabolite of Alflutinib
  • Exerts antineoplastic activity
  • EGFR inhibitor
  • Yellow to orange solid
  • Store at 4°C, sealed, away from moisture and light
  • In solvent: -80°C for 6 months; -20°C for 1 month

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3

Medchemexpress LLC SU 5214 | 186611-04-1 | 98.29% | 251.28 | 50 MG
SDP

SU5214 is a potent VEGFR2 inhibitor extracted from patent US5834504A. It has IC50s of 14.8 μM for FLK-1 and 36.7 μM for EGFR. This product is suitable for various laboratory applications.

  • Potent VEGFR2 inhibitor
  • IC50s of 14.8 μM for FLK-1
  • IC50s of 36.7 μM for EGFR
  • Extracted from patent US5834504A

ENCOMPASS_PREFERRED
4

Medchemexpress LLC PD-1/PD-L1-IN-23 | 2597056-04-5 | 99.9% | C32H30BrCl2N3O6 | 50 MG
SDP

PD-1/PD-L1-IN-23 is a potent and orally active inhibitor of PD-1/PD-L1. It is an ester proagent of L7, a benzo[c]oxadiazole derivative biologically evaluated as an inhibitor of PD-L1. It has shown significant antitumor effects in tumor models of syngeneic and PD-L1 humanized mice.

  • Potent and orally active inhibitor of PD-1/PD-L1
  • Ester proagent of L7, a benzo[c]oxadiazole derivative
  • Displays significant antitumor effects in tumor models
  • For research use only

ENCOMPASS_PREFERRED
5

Medchemexpress LLC D-serine, N-[[2-[(3-cyanophenyl)methoxy]-4-...]] hydrochloride (1:1) | 2113650-04-5 | 98.0% | 50 MG
SDP

BMS-1001 hydrochloride is a small-molecule inhibitor of the PD-1/PD-L1 interaction supplied as the hydrochloride salt for research use. It is described as orally active and exhibits low cellular toxicity, and is provided as a solid with high purity suitable for cellular assays and interaction studies.

  • Orally active PD-1/PD-L1 interaction inhibitor.
  • High purity (98.0%).
  • Molecular weight 631.11 g·mol⁻1.
  • Solid appearance; store sealed and away from moisture.
  • Storage in solvent: -80°C up to 6 months, -20°C up to 1 month.
  • Available in small milligram pack sizes for research use.

ENCOMPASS_PREFERRED
6

Medchemexpress LLC N,N'-1,3-phenylenebis[2,3-dihydroxy-benzamide] | 368449-04-1 | 98.6% | 50 MG
SDP

MST-312 (Telomerase Inhibitor IX) is a small-molecule telomerase inhibitor derived from epigallocatechin gallate (EGCG). It is supplied as a white to off-white solid for laboratory research in oncology and telomerase studies.

  • Telomerase inhibitor for cancer research.
  • Chemically modified derivative of epigallocatechin gallate (EGCG).
  • Molecular formula C20H16N2O6 and molecular weight 380.35 g·mol⁻1.
  • Purity 98.6%.
  • Supplied as a solid with common solubility in DMSO for solution preparation.

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7

Medchemexpress LLC 1-(1-(3-methoxyphenyl)-7-propoxyindolizin-3-yl)ethanone | 1693766-04-9 | MFCD30186082 | 99.5% | 323.39 | C20H21NO3 | 50 MG
SDP

GSK8573 is a small-molecule inactive control compound used in epigenetic reader-domain research and biochemical assays. Supplied as a solid for research use only, it is intended for use as a control in binding studies and compound screening. Store and handle according to the supplier safety data sheet and batch certificate of analysis.

ENCOMPASS_PREFERRED
8

Medchemexpress LLC N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide | 2922283-38-1 | 98.0% | C93H177N3O3 | 50 MG
SDP

N1,N3,N5-Tris(4-dodecylhexadecyl)benzene-1,3,5-tricarboxamide is an analogue of TT3, an ionizable lipid-like material used for mRNA delivery. It presents as an oil, with a color ranging from off-white to light yellow.

  • Analogue of TT3
  • Ionizable lipid-like material
  • Used for mRNA delivery
  • Appears as an oil
  • Off-white to light yellow color

ENCOMPASS_PREFERRED
9

Medchemexpress LLC 1-[[4-[4-[[4-(4-chloro-N-methylanilino)quinolin-1-ium-1-yl]methyl]phenyl]phenyl]methyl]-N-(4-chlorop | 850807-63-5 | 98.4% | 877.53 | C46H38Br2Cl2N4 | 50 MG
SDP

Selective choline kinase alpha (ChoKα) inhibitor for biochemical and cell-based cancer research. It demonstrates potent in vitro anti-proliferative activity and in vivo antitumor efficacy in xenograft models. Supplied as a solid for laboratory use in small-scale quantities.

  • Selective ChoKα inhibition (IC50 ≈ 1 μM).
  • Activity against multiple tumor-derived cell lines (IC50 ~1.3-7.1 μM).
  • High purity (98.4%).
  • Molecular weight 877.53; CAS 850807-63-5.
  • Storage: 4 °C sealed; in solvent -80 °C (6 months), -20 °C (1 month).

ENCOMPASS_PREFERRED
10

Medchemexpress LLC 2,2,2-trifluoro-N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(3-methoxyphenyl)propan-2-yl]acet | 1034148-04-3 | MFCD26142626 | 99.9% | 487.45 | C25H21F4N3O3 | 50 MG
SDP

AZD5423 is a non-steroidal, selective glucocorticoid receptor modulator provided as a research chemical for preclinical pharmacology and inhalation therapy studies. It is supplied for laboratory use only and has documented purity and storage recommendations.

  • Non-steroidal selective glucocorticoid receptor modulator for preclinical research.
  • High reported purity suitable for analytical and pharmacological studies.
  • Molecular formula C25H21F4N3O3 and molecular weight 487.45 g/mol.
  • Recommended storage conditions provided to maintain compound stability.
  • Available in multiple package sizes to support dose-ranging and formulation work.
  • Intended for laboratory research use only, not for clinical or human use.

ENCOMPASS_PREFERRED
11

Medchemexpress LLC 3-amino-4-{(3S)-3-[(2-ethoxyethoxy)methyl]piperidin-1-yl}thieno[2,3-b]pyridine-2-carboxamide | 2871872-79-4 | 99.9% | C18H26N4O3S | 50 MG
SDP

DS96432529 is a potent and orally active bone anabolic agent through CDK8 inhibition.

  • Potent bone anabolic agent
  • Orally active
  • Inhibits CDK8
  • For research use only

ENCOMPASS_PREFERRED
12

Medchemexpress LLC 5-(1-methyl-1H-pyrazol-4-yl)-N-(2-methyl-5-(3-(trifluoromethyl)benzamido)phenyl)nicotinamide | 2095849-04-8 | MFCD31813597 | 98.0% | 479.45 g/mol | C25H20F3N5O2 | 50 MG
SDP

CSF1R-IN-1 is a potent small-molecule inhibitor of the colony stimulating factor 1 receptor (CSF1R) with a reported IC50 of 0.5 nM. It shows good intestinal permeability in Caco-2 assays and favorable oral pharmacokinetics in mice. The compound is supplied as a solid for research use and includes standard storage recommendations and available solution formulations.

  • Potent CSF1R inhibition (IC50 0.5 nM).
  • Molecular formula C25H20F3N5O2; molecular weight 479.45 g/mol.
  • High purity (98.04%).
  • White to off-white solid physical form.
  • Stable storage: powder -20°C for up to 3 years; in solvent -80°C for 6 months, -20°C for 1 month.
  • Available in multiple sizes and as a 10 mM solution in DMSO.

ENCOMPASS_PREFERRED
13

Medchemexpress LLC Smyrindioloside | 87592-77-6 | 424.40 | 1 MG
SDP

Smyrindioloside is a natural product isolated from the bark of *Streblus indicus*. It is for research use only and not sold to patients.

  • High purity: 99.32%
  • White to off-white solid appearance
  • Available in various quantities, including 1 mg, 5 mg, 10 mg, and 50 mg
  • In-stock availability for 1 mg size
  • Detailed documentation available, including data sheet, COA, and SDS

ENCOMPASS_PREFERRED
14

Medchemexpress LLC Acrylodan | 86636-92-2 | 95.1% | 225.29 g/mol | C15H15NO | 5 MG
SDP

Acrylodan is a thiol-reactive, environment-sensitive fluorescent dye that covalently labels cysteine residues and reports on local dipolarity and conformational dynamics within binding pockets such as Cys34.

  • Reacts with thiols to form a covalent fluorescent adduct.
  • Sensitive to local dipolarity and protein dynamics.
  • Soluble in DMSO at approximately 50 mg/mL; ultrasonic agitation may be required.
  • Purity approximately 95.1%; molecular weight 225.29 g/mol.
  • Store protected from light; in solution store at -80°C (up to 6 months) or -20°C (up to 1 month).

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15

Medchemexpress LLC Rifalazil | 129791-92-0 | 99.6% | 941.07 | C51H64N4O13 | 50 MG
SDP

Rifalazil is a rifamycin-class antibiotic research compound that inhibits bacterial DNA-dependent RNA polymerase by binding the β-subunit. It demonstrates potent activity against a range of pathogens and is provided for research use only.

  • Inhibits bacterial RNA polymerase by targeting the β-subunit.
  • Exhibits high potency against mycobacteria and gram-positive bacteria.
  • Active against Helicobacter pylori, Chlamydia pneumoniae, and Chlamydia trachomatis.
  • High purity (~99.6%) suitable for research applications.
  • Available as a 50 MG solid package.
  • Stable when stored sealed at 4°C; in solvent store at -80°C (6 months) or -20°C (1 month).
  • Intended for research use only.

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