Azobenzenes

Medchemexpress LLC D5D-IN-326 | 1236767-85-3 | 99.9% | 473.27 | C17H11F8N3O4 | 5 MG

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D5D-IN-326 is a selective, orally active delta-5 desaturase (D5D) inhibitor (CAS 1236767-85-3) with reported nanomolar potency in enzymatic and cell-based assays and demonstrated activity in preclinical metabolic disease models. The compound is supplied for research use in multiple formats and sizes and is characterized by high purity and defined storage stability.

• Selective inhibitor of delta-5 desaturase with nanomolar potency.
• Reduces insulin resistance and body weight in preclinical models.
• High purity (99.9%) for reliable experimental results.
• Available as powder and solution formats for flexible dosing.
• Stable under recommended storage conditions for long-term use.
• Supplied in small research quantities suitable for in vitro and in vivo studies.

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eMolecules​ AstaTech / 44-BIS(BROMOMETHYL)BIPHENYL / 1g / 448278113 / T70531 / 95.000 / 20248-86-6 / MFCD00094419 / 340.058 / C14H12Br2

AstaTech / 44-BIS(BROMOMETHYL)BIPHENYL / 1g / 448278113 / T70531 / 95.000 / 20248-86-6 / MFCD00094419 / 340.058 / C14H12Br2

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Medchemexpress LLC Orismilast | 1353546-86-7 | 99.9% | 510.29 g·mol⁻¹ | C19H15Cl2F2NO7S | 5 MG

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Orismilast is an orally active, selective phosphodiesterase 4 (PDE4) inhibitor used in preclinical research on inflammatory diseases. It demonstrates potent activity against PDE4B and PDE4D subtype splice variants and is supplied as a high-purity research compound.

• Selective phosphodiesterase 4 (PDE4) inhibitor.
• Orally active compound suitable for inflammatory disease research.
• Potent inhibition of PDE4B and PDE4D subtype splice variants.
• High purity solid supplied in a 5 mg package.
• Molecular weight 510.29 g·mol⁻¹; formula C19H15Cl2F2NO7S.

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eMolecules​ Ambeed / (4S4S)-44-Diisopropyl-11-di-m-tolyl-4455-tetrahydro-1H1H-22-biimidazole / 100mg / 714083376 / A1501171 / / 2374958-85-5 / [null] / 402.586 / C26H34N4

Ambeed / (4S4S)-44-Diisopropyl-11-di-m-tolyl-4455-tetrahydro-1H1H-22-biimidazole / 100mg / 714083376 / A1501171 / / 2374958-85-5 / [null] / 402.586 / C26H34N4

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eMolecules​ Ambeed / Anthra[219-def6510-def]diisoquinoline-13810(2H9H)-tetrone 29-bis[3-(dimethyloxidoamino)propyl]- / 100mg / 633419517 / A1156199 / / 1558023-86-1 / [null] / 592.652 / C34H32N4O6

Ambeed / Anthra[219-def6510-def]diisoquinoline-13810(2H9H)-tetrone 29-bis[3-(dimethyloxidoamino)propyl]- / 100mg / 633419517 / A1156199 / / 1558023-86-1 / [null] / 592.652 / C34H32N4O6

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Medchemexpress LLC 3H-pyrrolo[2,3-d]pyrimidine-4,6-dione derivative (pentafluoropropoxy, trifluoroethoxy phenyl) | 1236767-85-3 | 99.9% | 473.27 g·mol^-1 | C17H11F8N3O4 | 25 MG

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D5D-IN-326 is a selective, orally active delta-5 desaturase inhibitor provided for research use. It shows low-nanomolar activity against human and rat D5D and is used in biochemical, cellular, and in vivo studies related to fatty acid metabolism and metabolic disease models.

• Selective delta-5 desaturase inhibitor with IC50 ≈ 22 nM (human) and 72 nM (rat).
• High purity (99.9%) suitable for biochemical and cellular assays.
• Supplied as a laboratory-scale powder, typical quantity 25 MG.
• Molecular formula C17H11F8N3O4, molecular weight 473.27 g·mol^-1.
• Recommended storage: powder at -20°C for long-term stability.

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Medchemexpress LLC DB04760 | 544678-85-5 | 99.2% | 410.42 g·mol⁻¹ | C22H20F2N4O2 | 50MG

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DB04760 is a potent, highly selective, non-zinc-chelating MMP-13 inhibitor (IC50 = 8 nM) used as a research reagent in preclinical studies. It has been reported to reduce paclitaxel-induced neurotoxicity and to exhibit anticancer activity. The compound has formula C22H20F2N4O2, molecular weight 410.42 g·mol⁻¹, and is supplied in solid and solution forms with high purity suitable for biological assays.

• Potent MMP-13 inhibition with IC50 = 8 nM.
• Non-zinc-chelating mechanism for selective target studies.
• Shown to reduce paclitaxel-induced neurotoxicity in models.
• Reported anticancer activity in preclinical research.
• Available as solid and as 10 mM solution in DMSO for assay flexibility.
• High purity (~99%) appropriate for biological testing.

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eMolecules​ Ambeed / 2-(5-(Dimethylamino)naphthalene-1-sulfonamido)acetic acid / 250mg / 586458002 / A836722 / / 1091-85-6 / MFCD00037734 / 308.350 / C14H16N2O4S

Ambeed / 2-(5-(Dimethylamino)naphthalene-1-sulfonamido)acetic acid / 250mg / 586458002 / A836722 / / 1091-85-6 / MFCD00037734 / 308.350 / C14H16N2O4S

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eMolecules​ Ambeed / (R)-22-Bis(diphenylphosphino)-55667788-octahydro-11-binaphthyl / 50mg / 588342799 / A525018 / / 139139-86-9 / MFCD01630795 / 630.752 / C44H40P2

Ambeed / (R)-22-Bis(diphenylphosphino)-55667788-octahydro-11-binaphthyl / 50mg / 588342799 / A525018 / / 139139-86-9 / MFCD01630795 / 630.752 / C44H40P2

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eMolecules​ Ambeed / (4R5R)-45-Diphenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-45-dihydrooxazole / 100mg / 633418067 / A1349930 / / 2757082-86-1 / [null] / 368.359 / C21H15F3N2O

Ambeed / (4R5R)-45-Diphenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-45-dihydrooxazole / 100mg / 633418067 / A1349930 / / 2757082-86-1 / [null] / 368.359 / C21H15F3N2O

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eMolecules​ AstaTech / 14-DIAZASPIRO[5.5]UNDECAN-5-ONE / 1g / 718056409 / AT28656 / 95.000 / 86047-86-1 / MFCD07373481 / 168.240 / C9H16N2O

AstaTech / 14-DIAZASPIRO[5.5]UNDECAN-5-ONE / 1g / 718056409 / AT28656 / 95.000 / 86047-86-1 / MFCD07373481 / 168.240 / C9H16N2O

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eMolecules​ Ambeed / Nitromethylphenylsulfone / 250mg / 686660269 / A592579 / / 21272-85-5 / MFCD00015928 / 201.200 / C7H7NO4S

Ambeed / Nitromethylphenylsulfone / 250mg / 686660269 / A592579 / / 21272-85-5 / MFCD00015928 / 201.200 / C7H7NO4S

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Medchemexpress LLC HSP27 inhibitor J2 | 2133499-85-9 | 99.7% | 264.30 g/mol | C13H12O4S | 25MG

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HSP27 inhibitor J2 is a small-molecule research reagent that inhibits heat shock protein 27 (HSP27) by inducing abnormal dimer formation and disrupting HSP27 polymer function. It is supplied as a purified solid for biochemical and cellular studies with documented solubility and storage recommendations.

• High purity (99.7%).
• Molecular weight 264.30 g/mol.
• Chemical formula C13H12O4S.
• Soluble in DMSO at 20 mg/mL (75.67 mM); hygroscopic DMSO may affect solubility.
• Storage: powder -20°C (up to 3 years) or 4°C (up to 2 years); in solvent -80°C (up to 2 years) or -20°C (up to 1 year).
• Available in multiple pack sizes including 25 mg.

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Medchemexpress LLC Kansuinine A | 57701-86-7 | 99.8% | 730.75 g·mol⁻1 | C37H46O15 | 5 MG

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Kansuinine A is a natural diterpenoid research compound that inhibits IL-6-induced STAT3 activation and has reported antiviral and anticancer activity. It is supplied as a high-purity solid with documented solubility and storage profiles for in vitro experimentation and dosing accuracy.

• Inhibits IL-6-induced STAT3 activation
• Reported antiviral and anticancer activity
• High purity (≈99.8%) suitable for research applications
• Supplied as a white to off-white solid with high solubility in DMSO
• Stable when stored as powder at -20 °C and in solvent under recommended conditions
• Molecular weight 730.75 g·mol⁻1 and formula C37H46O15 for accurate dosing

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Medchemexpress LLC MEDCHEMEXPRESS LLC

5000417741 LUPIWIGHTEONE 5MG

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