Drug Standards
Sigma Aldrich Fine Chemicals Biosciences Econazole Related Compound A United States Pharmacopeia (USP) Reference Standard | 24155-42-8 | 15MG
Econazole Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 257.12 | 24155-42-8 | 15MG
Chemscene ChemScene | 6-Methoxynaphthalen-2-ol | 1G | CS-W017504 | 0.98 | 5111-66-0| MFCD00088677 | 174.2
ChemScene | 6-Methoxynaphthalen-2-ol | 1G | CS-W017504 | 0.98 | 5111-66-0| MFCD00088677 | 174.2
Medchemexpress LLC Tenofovir hydrate | 206184-49-8 | MFCD11519982 | 99.9% | 305.23 g/mol | C9H16N5O5P | 5 MG
Tenofovir hydrate is the analytical standard form of tenofovir, a nucleotide reverse transcriptase inhibitor used in HIV and chronic hepatitis B research. Supplied as a high-purity hydrate for analytical and method development applications, it is intended for laboratory research use only and not for human consumption.
- High reported purity (≈99.88%) for reliable analytical results.
- Monohydrate form with molecular formula C9H16N5O5P and molecular weight 305.23 g/mol.
- Supplied in small weighed quantities suitable for standards and validation.
- Suitable as an analytical standard for HPLC and method development.
- Accompanied by a certificate of analysis for batch traceability.
Selleck Chemical LLC Tacedinaline10mg
Tacedinaline (CI994, PD-123654, GOE-5549, Acetyldinaline) is a selective class I HDAC inhibitor with IC50 of 0.9, 0.9, 1.2, and >20 ?M for human HDAC 1, 2, 3, and 8, respectively. Phase 3. *For Research & Development use only. Product is not intended for drug, household, or human consumption.
Sigma Aldrich Fine Chemicals Biosciences Alitame - Alanine Amide Impurity United States Pharmacopeia (USP) Reference Standard | 80875-07-6 | 25MG
Alitame - Alanine Amide Impurity United States Pharmacopeia (USP) Reference Standard | Mol Wt: 216.34 | 80875-07-6 | 25MG
Sigma Aldrich Fine Chemicals Biosciences Altizide impurity B European Pharmacopoeia (EP) Reference Standard | 84522-35-0 |
Altizide impurity B European Pharmacopoeia (EP) Reference Standard | Mol Wt: 162.25 | 84522-35-0 |
Sigma Aldrich Fine Chemicals Biosciences Ganoderic acid A United States Pharmacopeia (USP) Reference Standard | 81907-62-2 | 50MG
Ganoderic acid A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 516.67 | 81907-62-2 | 50MG
Apexbio Technology LLC Procaine 59-46-1 5g
Procaine (CAS 59-46-1) is a small-molecule inhibitor targeting voltage-gated sodium channels It is designed to block these channels thereby inhibiting neuronal action potential propagation and suppressing nerve signal transmission Procaine exerts its biological activity primarily through reversible inhibition of voltage-gated sodium channel currents In in vitro studies Procaine demonstrates sodium channel inhibition with reported IC50 values typically ranging from 250 to 400 M depending on the experimental system Based on these pharmacological properties Procaine holds research potential in studies of electrophysiology ion channel pharmacology and neurological signaling pathways
Selleck Chemical LLC LY2584702 Tosylate
LY2584702 Tosylate is a selective ATP-competitive p70S6K inhibitor with IC50 of 4 nM Phase 1
Medchemexpress LLC 2,6-Benzothiazolediamine, 4,5,6,7-tetrahydro-N6-propyl-, hydrochloride (1:2), (6S)- | 104632-25-9 | 98.0% | 284.25 | 100 MG
Pramipexole dihydrochloride is a selective and blood-brain barrier (BBB) penetrant dopamine D2-type receptor agonist, with Kis of 2.2 nM, 3.9 nM, 0.5 nM and 1.3 nM for D2-type receptor, D2, D3 and D4 receptors, respectively. It can be used for the research of Parkinson's disease (PD) and restless legs syndrome (RLS).
- Selective and blood-brain barrier (BBB) penetrant dopamine D2-type receptor agonist.
- Kis of 2.2 nM, 3.9 nM, 0.5 nM and 1.3 nM for D2-type receptor, D2, D3 and D4 receptors, respectively.
- Applicable for research into Parkinson's disease (PD) and restless legs syndrome (RLS).
Medchemexpress LLC Ivermectin B1b | 70209-81-3 | MFCD00866559 | 98.7% | 861.07 | C47H72O14 | 1MG
Ivermectin B1b is the minor component of ivermectin, a macrocyclic lactone antiparasitic agent supplied for research use. The compound has documented analytical data and literature reports of antiviral activity in cell culture; product listings include CAS, formula, molecular weight, and RP-HPLC documentation.
- Minor component of ivermectin with antiparasitic activity.
- Macrocyclic lactone structure suitable for research applications.
- Reported to inhibit replication of SARS-CoV-2 in cell culture.
- CAS number 70209-81-3 for unambiguous identification.
- Chemical formula C47H72O14; molecular weight ≈ 861.07.
- High purity reported (about 98.66%) with RP-HPLC documentation available.
- Available in small laboratory quantities (500 μg-10 mg) for research use.
Sigma Aldrich Fine Chemicals Biosciences Emedastine difumarate United States Pharmacopeia (USP) Reference Standard | 87233-62-3 | 100MG
Emedastine difumarate United States Pharmacopeia (USP) Reference Standard | Mol Wt: 534.56 | 87233-62-3 | 100MG
Sigma Aldrich Fine Chemicals Biosciences Citalopram hydrochloride European Pharmacopoeia (EP) Reference Standard | 85118-27-0 |
Citalopram hydrochloride European Pharmacopoeia (EP) Reference Standard | Mol Wt: 360.85 | 85118-27-0 |
eMolecules Sarafloxacin | 98105-99-8 | MFCD00865974 | 1g
Combi-Blocks | Sarafloxacin | 1g | 205406342 | QA-8020 | 97.000 | 98105-99-8 | MFCD00865974 | 385.371 | C20H17F2N3O3
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Selleck Chemical LLC Lenvatinib (E7080) 5mg 417716-92-8
Lenvatinib (E7080) is a multi-target inhibitor, mostly for VEGFR2(KDR)/VEGFR3(Flt-4) with IC50 of 4 nM/5.2 nM, less potent against VEGFR1/Flt-1, ~10-fold more selective for VEGFR2/3 against FGFR1, PDGFR?/? in cell-free assays. Lenvatinib (E7080) also inhibits FGFR1-4, PDGFR, Kit (c-Kit), RET (c-RET), and shows potent antitumor activities. Phase 3. *For Research & Development use only. Product is not intended for drug, household, or human consumption.