Hydrochlorides
Sigma Aldrich Fine Chemicals Biosciences o-Phenylenediamine dihydrochloride tablet, 4 mg substrate per tablet | 615-28-1 | MFCD00012966 | 100TAB
o-Phenylenediamine dihydrochloride tablet, 4 mg substrate per tablet | Mol Wt: 181.06 | 615-28-1 | MFCD00012966 | 100TAB
Sigma Aldrich Fine Chemicals Biosciences 4-(Benzyloxy)aniline hydrochloride 98% | 51388-20-6 | MFCD00012995 | 100G
4-(Benzyloxy)aniline hydrochloride 98% | Purity: 98% | Mol Wt: 235.71 | 51388-20-6 | MFCD00012995 | 100G
Sigma Aldrich Fine Chemicals Biosciences O-Benzylhydroxylamine hydrochloride 99% | 2687-43-6 | MFCD00012952 | 100G
O-Benzylhydroxylamine hydrochloride 99% | Purity: 99% | Mol Wt: 159.61 | 2687-43-6 | MFCD00012952 | 100G
Sigma Aldrich Fine Chemicals Biosciences o-Phenylenediamine dihydrochloride tablet, 20 mg substrate per tablet | 615-28-1 | MFCD00012966 | 50TAB
o-Phenylenediamine dihydrochloride tablet, 20 mg substrate per tablet | Mol Wt: 181.06 | 615-28-1 | MFCD00012966 | 50TAB
Medchemexpress LLC Verubulin hydrochloride | 917369-31-4 | 98.7% | 100 MG
Verubulin hydrochloride is the hydrochloride salt of verubulin (MPC-6827), a blood-brain barrier permeable microtubule-disrupting agent with demonstrated in vitro and in vivo anticancer activity. It is supplied for research use in solid and solution formats.
- Blood-brain barrier permeable microtubule disruptor.
- Demonstrated cytotoxic activity in MX-1 breast and other xenograft models.
- Available as solid and as solution in DMSO; pack sizes typically range from 5 mg to 500 mg.
- High purity (approx. 98.7%).
- Molecular formula C17H18ClN3O; molecular weight 315.8 g/mol.
- For research use only; not for human or veterinary use.
Accela Chembio Inc 2-(methylsulfonyl)ethylamine Hydrochloride | 5g | 104458-24-4 | MFCD03840162 | 97+% | Shelf Life: 900 Days | Moisture Sensitive
2-(methylsulfonyl)ethylamine Hydrochloride | 5g | 104458-24-4 | MFCD03840162 | 97+% | Shelf Life: 900 Days | Moisture Sensitive
eMolecules 5-AMINOPYRROLIDIN-2-ONE TFA | | | 1g
AstaTech | 5-AMINOPYRROLIDIN-2-ONE TFA | 1g | 624127358 | D72820 | 98.000 | | | 214.144 | C6H9F3N2O3
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Accela Chembio Inc 3-pyridylacetic Acid Hydrochloride | 25g | 6419-36-9 | MFCD00012819 | 98% | Shelf Life: 1260 Days | Moisture Sensitive
3-pyridylacetic Acid Hydrochloride | 25g | 6419-36-9 | MFCD00012819 | 98% | Shelf Life: 1260 Days | Moisture Sensitive
eMolecules 2-PYRIDINEACETIC ACID, 3-AMINO-, ETHYL ESTER | 295327-27-4 | MFCD11616148 | 0.25g
AstaTech | 2-PYRIDINEACETIC ACID, 3-AMINO-, ETHYL ESTER | 0.25g | 417005744 | F18231 | 95.000 | 295327-27-4 | MFCD11616148 | 180.207 | C9H12N2O2
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Accela Chembio Inc 4-pyridineacetic Acid Hydrochloride | 5g | 6622-91-9 | MFCD00012827 | 97+% | Shelf Life: 900 Days | Light Sensitive/nitrogen Or Argon
4-pyridineacetic Acid Hydrochloride | 5g | 6622-91-9 | MFCD00012827 | 97+% | Shelf Life: 900 Days | Light Sensitive/nitrogen Or Argon
Medchemexpress LLC SKF89976A hydrochloride | 85375-15-1 | 98.7% | 371.90 | C22H26ClNO2 | 50 MG
SKF89976A hydrochloride is a selective inhibitor of the GABA transporter GAT-1 used in research to probe GABA uptake and transporter pharmacology. It exhibits high potency at GAT-1 with markedly lower potency at GAT-2 and GAT-3, and shows weak activity at monoamine transporters. Supplied as a solid for in vitro and in vivo preclinical studies.
- Selective GAT-1 inhibition with IC50 0.28 μM.
- Lower potency at GAT-2 and GAT-3 (IC50 137.34 μM and 202.8 μM).
- Weak activity at SERT, NET, and DAT consistent with transporter profiling.
- High purity solid suitable for biochemical assays (98.73%).
- Usable in both in vitro transporter assays and preclinical in vivo models.
Apexbio Technology LLC Tirofiban 144494-65-5 5mg
Tirofiban is a selective non-peptide antagonist targeting platelet glycoprotein (GP) IIb/IIIa receptors a heterodimeric complex abundantly expressed on platelet surfaces responsible for mediating fibrinogen binding and platelet aggregation It acts through competitive inhibition of fibrinogen binding at GP IIb/IIIa sites thereby suppressing platelet cross-linking and aggregation induced by agonists like ADP In vitro studies demonstrate that Tirofiban inhibits ADP-induced platelet aggregation with an IC50 value of approximately 9 nM showing significantly lower affinity for integrin v 3 (vitronectin receptor) Tirofiban is frequently applied in biomedical research investigating platelet aggregation mechanisms and thrombotic events
eMolecules (S)-(3-Aminopyrrolidin-1-yl)(cyclopropyl)methanone hydrochloride | 1286207-03-1 | MFCD17014261 | 1g
Oakwood Chemical | (S)-(3-Aminopyrrolidin-1-yl)(cyclopropyl)methanone hydrochloride | 1g | 537696164 | 063992 | | 1286207-03-1 | MFCD17014261 | 190.670 | C8H15ClN2O
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