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Filtered Search Results
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000669787 Z-INDIRUBIN STAND 10MG
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Medchemexpress LLC 3-pyrrolidinol, 1-(phenylmethyl)-, (3S)- | 101385-90-4 | MFCD00075485 | 99.9% | 177.25 g·mol⁻¹ | C11H15NO | 10 G
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(S)-1-Benzylpyrrolidin-3-ol (CAS 101385-90-4) is a chiral pyrrolidinol intermediate used in small-molecule synthesis and impurity characterization. Manufacturer documentation provides solubility, storage, and handling guidance for research applications and formulation testing.
- Chiral pyrrolidinol intermediate for synthetic chemistry.
- Molecular formula C11H15NO.
- Molecular weight 177.25 g·mol⁻¹.
- High purity (reported ~99.9%).
- Soluble in DMSO (200 mg/mL in vitro) and compatible with common in vivo vehicles.
- Suggested storage: pure form -20°C (long term) or 4°C (shorter term).
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Medchemexpress LLC (11-((4-hydroxy-3-methoxybenzoyl)oxy)undecyl)triphenylphosphonium bromide | 1254044-38-6 | 99.8% | C37H44BrO4P | 10MG
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Mito-apocynin (C11) is a mitochondria-targeted derivative of apocynin in which the apocynin moiety is conjugated to a triphenylphosphonium cation. It is supplied as a high-purity research reagent intended for preclinical studies of mitochondrial oxidative stress, neuroprotection, and related mitochondrial metabolism pathways.
- Targets mitochondria via a triphenylphosphonium moiety.
- Provides antioxidant activity to mitigate mitochondrial oxidative stress.
- Suitable for in vitro and in vivo preclinical research applications.
- High purity, approximately 99.8%.
- Available in milligram-scale quantities for laboratory use.
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eMolecules N-BOC-6-BROMOHEXYLAMINE 1G
5000161240 N-BOC-6-BROMOHEXYLAMINE 1G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000383317 S R S -AHPC-C6-NH2 50MG
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Medchemexpress LLC Doxorubicin-SMCC 5mg | 400647-59-8 | 5 MG
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Doxorubicin-SMCC is an antibody-drug conjugate (ADC) drug-linker conjugate that links the anthracycline topoisomerase II inhibitor doxorubicin to a non-cleavable SMCC linker for research use. It is supplied as a solid or as a DMSO solution and is intended for in vitro ADC research and linker-drug evaluation.
- Contains non-cleavable SMCC linker
- Delivers anthracycline topoisomerase II inhibitor doxorubicin
- High purity suitable for research applications
- Available as solid and as 10 mM solution in DMSO
- Soluble in DMSO at up to 125 mg/mL with ultrasonic assistance
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Apexbio Technology LLC Rac GTPase fragment 5mg
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Rac GTPase fragment is a synthetic peptide representing a segment of the small signaling protein Rac a member of the Rho family of GTPases It is designed to serve as a molecular tool to investigate Rac-mediated modulation of actin dynamics and kinase activation processes essential for cytoskeletal rearrangement cell-cycle progression differentiation and cell adhesion Rac GTPase fragment exerts its biological activity by serving as a probe for Rac-driven signaling pathways Based on these pharmacological properties Rac GTPase fragment holds research potential in studying tumor biology particularly the development and progression of melanoma and non-small-cell lung carcinoma
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eMolecules 3S-HYDROXYMETHYL-PYRROLI 25G
5000161464 3S-HYDROXYMETHYL-PYRROLI 25G
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MEDCHEMEXPRESS LLC RUBOXISTAURIN HYDROCHLORIDE
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501871934 RUBOXISTAURIN HYDROCHLORIDE
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eMolecules TERT-BUTYL 3S-3-HYDROXYM 1G
5000224760 TERT-BUTYL 3S-3-HYDROXYM 1G
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eMolecules (R)-2-N-CBZ-AMINO-PENTANE-1,5-DIOL | 478646-28-5 | MFCD03426376 | 1g
AstaTech | (R)-2-N-CBZ-AMINO-PENTANE-1,5-DIOL | 1g | 200611390 | 57862 | 97.000 | 478646-28-5 | MFCD03426376 | 253.298 | C13H19NO4
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eMolecules (2R,4R)-1-(TERT-BUTOXYCARBONYL)-4-(TRIFLUOROMETHYL)PYRROLIDINE-2-CARBOXYLIC ACID | 497103-78-3 | MFCD26521847 | 1g
AstaTech | (2R,4R)-1-(TERT-BUTOXYCARBONYL)-4-(TRIFLUOROMETHYL)PYRROLIDINE-2-CARBOXYLIC ACID | 1g | 268502152 | 72966 | 95.000 | 497103-78-3 | MFCD26521847 | 283.247 | C11H16F3NO4
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Selleck Chemical LLC Z-Guggulsterone
Z-Guggulsterone a constituent of Ayurvedic medicinal plant Commiphora mukul inhibits angiogenesis in vitro and in vivo Z-Guggulsterone exhibits anti-inflammatory effects in microglia Z-Guggulsterone induces apoptosis in gastric cancer cells through the intrinsic mitochondria-dependent pathway
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Medchemexpress LLC Z-WEHD-FMK | 210345-00-9 | 98.0% | 763.77 | 25 MG
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Z-WEHD-FMK is a potent, cell-permeable, and irreversible caspase-1/5 inhibitor. It also demonstrates a robust inhibitory effect on cathepsin B activity with an IC50 of 6 μM, and can be utilized to investigate cells for evidence of apoptosis.
- Potent, cell-permeable, and irreversible caspase-1/5 inhibitor
- Demonstrates a robust inhibitory effect on cathepsin B activity
- Utilized to investigate cells for evidence of apoptosis
- Appears as a light yellow to yellow solid
- Soluble in DMSO
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eMolecules 1S 4S-2-BOC-2 5-DIAZABI 100G
5000217262 1S 4S-2-BOC-2 5-DIAZABI 100G
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