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Filtered Search Results
Medchemexpress LLC (Rac)-Rhododendrol ((Rac)-betuligenol) | 69617-84-1 | 99.8% | 166.22 | 1 ML
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(Rac)-Rhododendrol ((Rac)-Betuligenol) is an aromatic compound recognized for its pro-oxidant activity. It has potential applications in suppressing liver diseases. However, it can also be toxic to melanocytes, inducing cell death.
- Aromatic compound with pro-oxidant activity
- May be useful in the suppression of liver diseases
- Can be toxic to melanocytes, leading to cell death
- Metabolite, RD-quinone, is cytotoxic and causes enzyme inactivation and endoplasmic reticulum stress by binding to thiol proteins
- Derived melanin exhibits potent pro-oxidant activity and may cause oxidative stress
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Medchemexpress LLC (Rac)-Hydnocarpin | 51419-48-8 | 25 MG
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(Rac)-Hydnocarpin is a flavonoid isolated from *Hydnocarpus anthelminthica*. This compound exhibits moderate cytotoxic effects on cancer cells. It has a molecular formula of C25H20O9 and a molecular weight of 464.42.
- Isolated from *Hydnocarpus anthelminthica*.
- Exhibits moderate cytotoxic effects on cancer cells.
- Molecular formula: C25H20O9.
- Molecular weight: 464.42.
- Solid appearance.
- Off-white to yellow color.
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![Medchemexpress LLC (1S,2S)-2-[(1S)-1-amino-1-carboxy-2-(9H-xanthen-9-yl)ethyl]cyclopropane-1-carboxylic acid | 201943-63-7 | >98.0% | 353.4 g/mol | C20H19NO5 | 10 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000298149.png-250.jpg)
Medchemexpress LLC (1S,2S)-2-[(1S)-1-amino-1-carboxy-2-(9H-xanthen-9-yl)ethyl]cyclopropane-1-carboxylic acid | 201943-63-7 | >98.0% | 353.4 g/mol | C20H19NO5 | 10 MG
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Racemic LY341495 is a metabotropic glutamate receptor (mGluR) antagonist used as a research tool in neuroscience and pharmacology. It inhibits multiple mGlu receptor subtypes and is supplied as a crystalline solid for experimental use.
- Antagonist of metabotropic glutamate receptors, particularly potent at group II (mGlu2, mGlu3).
- Reported IC50s: mGlu2 = 21 nM, mGlu3 = 14 nM; higher micromolar activity at mGlu1a, mGlu5a, and mGlu4.
- High purity: ≥98%.
- Chemical formula C20H19NO5; molecular weight ≈ 353.4 g/mol.
- Supplied as a small-quantity research pack (10 mg) for laboratory use.
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eMolecules (S)-Pyrrolidine-3-carboxamide | 573704-64-0 | MFCD11849581 | 1g
Combi-Blocks, Inc. | (S)-Pyrrolidine-3-carboxamide | 1g | 603149789 | ST-1036 | 95.000 | 573704-64-0 | MFCD11849581 | 114.148 | C5H10N2O
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Accela Chembio Inc 1-boc-3-(hydroxymethyl)pyrrolidine | 5g | 114214-69-6 | MFCD02179040 | 95+% | Shelf Life: 900 Days | Light Sensitive/+4
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1-boc-3-(hydroxymethyl)pyrrolidine | 5g | 114214-69-6 | MFCD02179040 | 95+% | Shelf Life: 900 Days | Light Sensitive/+4
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![Medchemexpress LLC Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N,β,β-trimethyl- | 676487-35-7 | 99.1% | 307.39 | 1 ML](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000404826-logo.png-250.jpg){kind=logo}
Medchemexpress LLC Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-N,β,β-trimethyl- | 676487-35-7 | 99.1% | 307.39 | 1 ML
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(Rac)-Taltobulin intermediate-1 is an intermediate in the synthesis of Taltobulin. Taltobulin is a common toxin component in ADC preparation and a powerful tubulin inhibitor. It disrupts tubulin polymerization, induces mitotic arrest, and induces apoptosis.
- Intermediate in the synthesis of Taltobulin
- Common toxin component in ADC preparation
- Powerful tubulin inhibitor
- Disrupts tubulin polymerization
- Induces mitotic arrest
- Induces apoptosis
- Purity: 99.11%
- Appearance: Solid, white to off-white
- Solubility: DMSO : ≥ 100 mg/mL (325.32 mM)
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Medchemexpress LLC Rac-epoxiconazole | 135319-73-2 | >98.0% | 1 MG
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Rac-epoxiconazole is a chiral triazole fungicide supplied as the racemic mixture for research use. It inhibits fungal sterol demethylation, disrupting ergosterol biosynthesis and is used in biochemical and agricultural research to study antifungal activity and mode of action.
- Chiral triazole fungicide supplied as a racemate.
- Inhibits fungal sterol demethylation (ergosterol biosynthesis).
- Broad-spectrum activity against multiple fungal classes.
- Molecular weight 329.76 and formula C17H13ClFN3O.
- Supplied in small pack sizes suitable for research (typical 1 mg).
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Medchemexpress LLC (Rac)-Rotigotine hydrochloride | 102120-99-0 | C19H26ClNOS | 50 MG
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(Rac)-Rotigotine hydrochloride is a racemate of Rotigotine, functioning as a full agonist of the dopamine receptor, a partial agonist of the 5-HT1A receptor, and an antagonist of the α2B-adrenergic receptor. It exhibits high selectivity for D3 receptors and is intended for research use only.
- Acts as a full agonist at all dopamine receptors
- Functions as a partial agonist of the 5-HT1A receptor
- Antagonizes the α2B-adrenergic receptor
- Demonstrates 10-fold selectivity for D3 receptors over D2, D4, and D5
- Provides significant protection against rotenone-induced cell death
- Inhibits rotenone-induced ROS production
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Medchemexpress LLC (Rac)-Acolbifene (EM-343; (Rac)-EM-652) | 151533-34-5 | 98.2% | 457.56 | 1 ML
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(Rac)-Acolbifene (EM-343; (Rac)-EM-652) is the racemic form of EM652, an estrogen receptor antagonist, exhibiting both anti-estrogenic and estrogenic activities. This compound contains a piperidine ring and demonstrates a good pharmacological profile with a relative binding affinity (RBA) of 380. It shows an inhibitory effect in T-47D cells and antiuterotrophic inhibitions in ovariectomized mice.
- Racemic form of EM652.
- Acts as an estrogen receptor antagonist.
- Exhibits anti-estrogenic and estrogenic activities.
- Contains a piperidine ring.
- Demonstrates a good pharmacological profile with a relative binding affinity (RBA) of 380.
- Inhibits T-47D cell growth with an IC50 value of 0.110 nM.
- Induces antiuterotrophic inhibitions in ovariectomized mice.
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eMolecules ChemScene 1-(tert-Butoxycarbonyl)-3 3-difluoropiperidine-4-carboxylic acid 100mg 346751360 CS-W001386 0 000 1303972-81-7 MFCD18909780 265 257 C11H17F2NO4
ChemScene 1-(tert-Butoxycarbonyl)-3 3-difluoropiperidine-4-carboxylic acid 100mg 346751360 CS-W001386 0 000 1303972-81-7 MFCD18909780 265 257 C11H17F2NO4
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![eMolecules Pharmablock / tert-butyl exo-3-(aminomethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate / 50mg / 586136424 / PB00291 / 0.000 / 273207-53-7 / MFCD20126200 / 240.347 / C13H24N2O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502516272.JPG-250.jpg)
eMolecules Pharmablock / tert-butyl exo-3-(aminomethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate / 50mg / 586136424 / PB00291 / 0.000 / 273207-53-7 / MFCD20126200 / 240.347 / C13H24N2O2
Pharmablock / tert-butyl exo-3-(aminomethyl)-8-azabicyclo[3.2.1]octane-8-carboxylate / 50mg / 586136424 / PB00291 / 0.000 / 273207-53-7 / MFCD20126200 / 240.347 / C13H24N2O2
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Medchemexpress LLC (Rac)-Reparixin | 957407-64-6 | C14H21NO3S | 25 MG
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(Rac)-Reparixin is identified for use as a laboratory chemical and in the manufacture of substances. This product has not been fully validated for medical applications and is intended for research use only by experienced personnel.
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Medchemexpress LLC (Rac)-Bepotastine besilate | 1415692-17-9 | 99.5% | C27H31ClN2O6S | 50 MG
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(Rac)-Bepotastine besilate is an isomer of Bepotastine besilate (HY-A0015) and serves as an experimental control. Bepotastine besilate is a selective, orally active second-generation histamine H1 receptor antagonist that suppresses the expression of nerve growth factor (NGF). It has potential for research related to allergic rhinitis, allergic conjunctivitis, and urticaria/pruritus.
- Isomer of Bepotastine besilate (HY-A0015)
- Used as an experimental control
- Selective and orally active second-generation histamine H1 receptor antagonist
- Suppresses nerve growth factor (NGF) expression
- Potential for research in allergic rhinitis, allergic conjunctivitis, and urticaria/pruritus
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Medchemexpress LLC TERT-BUTOXYCARBONYL 5G
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5000210271 TERT-BUTOXYCARBONYL 5G
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eMolecules 1- TERT-BUTOXYCARBONYL 10G
5000215973 1- TERT-BUTOXYCARBONYL 10G
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