Hydrochlorides
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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Apexbio Technology LLC Terbinafine HCl 78628-80-5 10mM (in 1mL DMSO)
Terbinafine hydrochloride (CAS 78628-80-5) is a small-molecule inhibitor targeting squalene epoxidase It is designed to selectively inhibit this key enzyme within the fungal sterol biosynthesis pathway thereby disrupting cell membrane integrity Terbinafine hydrochloride exerts its biological activity primarily through non-competitive inhibition of squalene epoxidase In experimental studies Terbinafine hydrochloride demonstrates potent antifungal activity with reported IC50 values against fungal squalene epoxidase in the nanomolar range Based on these pharmacological properties Terbinafine hydrochloride holds research potential in antifungal drug mechanism studies fungal sterol metabolism and therapeutic strategies against fungal pathogens in experimental models
Apexbio Technology LLC Tirofiban hydrochloride monohydrate 150915-40-5 5mg
Tirofiban hydrochloride monohydrate (CAS 150915-40-5) is a small-molecule inhibitor targeting platelet glycoprotein IIb/IIIa receptors It is designed to reversibly antagonize the binding of fibrinogen to these receptors thereby inhibiting platelet aggregation and thrombus formation Tirofiban hydrochloride monohydrate exerts its biological activity primarily through selective reversible inhibition of glycoprotein IIb/IIIa-mediated platelet aggregation Based on these pharmacological properties tirofiban hydrochloride monohydrate holds research potential in antithrombotic therapy and the investigation of unstable angina and thrombus-associated cardiovascular conditions
Matrix Scientific 4,4-DIFLUOROPIPERIDINE HYDR-1G
4,4-Difluoropiperidine hydrochloride, 95%; 1g,C5H10ClF2N, MFCD03095381, mw 157.59, [144230-52-4]
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
Apexbio Technology LLC Nitrocaramiphen hydrochloride 98636-73-8 10mg
Nitrocaramiphen hydrochloride (CAS 98636-73-8) is a small molecule that acts as a selective antagonist of muscarinic acetylcholine M1 receptors exhibiting a Ki of 5 5 nM Studies indicate that it effectively inhibits the hyperpolarizing effects induced by muscarinic agonists in muscle fibers Due to its receptor specificity nitrocaramiphen hydrochloride is widely utilized in neurobiological research to investigate cholinergic signaling pathways and the physiological roles of M1 receptor modulation
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
Medchemexpress LLC Iso-H7 dihydrochloride | 140663-38-3 | 99.1% | 364.29 | 25 MG
Iso-H7 dihydrochloride is an inhibitor of protein kinase with IC50 values of 22 and 34 μM for PKC and PKA, respectively. It has a negative control effect on PKA in satellite cell myogenesis.
- Protein kinase inhibitor.
- Inhibits PKC (IC50 = 22 μM).
- Inhibits PKA (IC50 = 34 μM).
- Negative control of PKA on satellite cell myogenesis.
Apexbio Technology LLC VU 0361737 1161205-04-4 100mg
VU 0361737 (CAS 1161205-04-4) is a selective brain-penetrant positive allosteric modulator of the metabotropic glutamate receptor 4 (mGluR4) It demonstrates high selectivity for mGluR4 over other mGluR subtypes with EC50 values of 240 nM for human and 110 nM for rat mGluR4 and shows minimal to no activity at mGluR1 mGluR2 mGluR3 mGluR6 and mGluR7 while exhibiting weak activity at mGluR5 and mGluR8 VU 0361737 crosses the blood-brain barrier and achieves significant brain exposure (brain plasma ratio of 4 1) with a short half-life (T1/2 20 min) following administration in rats This compound is utilized in studies exploring the modulation of basal ganglia neurotransmission and the pathophysiology of Parkinson s disease
Medchemexpress LLC UAMC-3203 hydrochloride | 2271358-65-5 | 98.1% | 508.12 | 100 MG
UAMC-3203 hydrochloride is a potent and selective ferroptosis inhibitor with an IC50 of 12 nM. It is for research use only and not sold to patients.
- No toxicity observed in mice after repeated injections.
- Available in solid and solution forms.
- Ships at room temperature in continental US.
- Store at 4°C, sealed, away from moisture and light.
- When in solvent, store at -80°C for 6 months or -20°C for 1 month, sealed, away from moisture and light.
Cayman Chemical 1Deoxynojirimycin hydrochlor
An inhibitor of α-glucosidase I and II (IC50s = ~2 µM for both); inhibits virus spread in HIV-infected lymphocyte cultures at 0.4 mM
Medchemexpress LLC Iso-H7 dihydrochloride | 140663-38-3 | 99.1% | 364.29 | 50 MG
Iso-H7 dihydrochloride is an inhibitor of protein kinase with IC50 values of 22 and 34 μM to PKC and PKA respectively. It has negative control of PKA on satellite cell myogenesis. This product offers high purity and is suitable for various research applications.
- Inhibits protein kinase with IC50 values of 22 and 34 μM to PKC and PKA.
- Exhibits negative control of PKA on satellite cell myogenesis.
- Boasts a high purity of 99.06%.
- Has a molecular weight of 364.29.
- Presents as a white to off-white solid.
- Readily soluble in water and DMSO.
- Recommended shipping at room temperature and storage at 4°C.