Antibiotics
Compounds and substances that kill or slow the growth of bacteria; used as a means of preventing bacterial contamination in cell cultures; various formulations and volumes available.
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Type
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Physical Form
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Molecular Weight (g/mol)
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- (1)
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- (1)
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- (2)
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- (7)
Color
- (2)
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- (3)
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- (8)
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2,911
eMolecules Medchem Express / DCP-LA / 1mg / 451965217 / HY-108599 / / 28399-31-7 / MFCD09265251 / 308.506 / C20H36O2
Medchem Express / DCP-LA / 1mg / 451965217 / HY-108599 / / 28399-31-7 / MFCD09265251 / 308.506 / C20H36O2
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2,912
Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000379253 EST73502 MONOHYDROC 100MG
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2,913
U.S. Pharmacopeia FLUPHENAZINE HYDROCHLORIDE
Fluphenazine Hydrochloride (125 mg)
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2,914
MEDCHEMEXPRESS LLC CEFIXIME 5MG
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501874526 CEFIXIME 5MG
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2,915
MEDCHEMEXPRESS LLC FLORFENICOL 100MG
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501874524 FLORFENICOL 100MG
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2,916
MEDCHEMEXPRESS LLC DIIODOHYDROXYQUINOLINE 1G
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501874538 DIIODOHYDROXYQUINOLINE 1G
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2,917
Sigma Aldrich Fine Chemicals Biosciences Undecanoic acid >=99%, FG | 112-37-8 | MFCD00002730 |
Undecanoic acid >=99%, FG | Purity: >=99% | Mol Wt: 186.29 | 112-37-8 | MFCD00002730 |
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2,918
Sigma Aldrich Fine Chemicals Biosciences Amifostine disulfide United States Pharmacopeia (USP) Reference Standard | 10027-65-3 | 100MG
Amifostine disulfide United States Pharmacopeia (USP) Reference Standard | Mol Wt: 412.31 | 10027-65-3 | 100MG
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2,919
Selleck Chemical LLC NSC232003-E0351-5MG
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NSC232003 is a highly potent and cell-permeable UHRF1 inhibitor that binds to the 5mC binding pocket of the SRA domain of UHRF1 NSC232003 modulates DNA methylation in a cellular context
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2,920
Invivogen T3SS INNER ROD NLRC4 AGONIST
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T3SS Inner Rod protein fused to Lethal Factor - NLRC4 agonist
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2,921
eMolecules Medchem Express / IOX2 / 5mg / 446265749 / HY-15468 / / 931398-72-0 / MFCD22580424 / 352.346 / C19H16N2O5
Medchem Express / IOX2 / 5mg / 446265749 / HY-15468 / / 931398-72-0 / MFCD22580424 / 352.346 / C19H16N2O5
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2,922
Medchemexpress LLC A-381393 100mg | 726174-00-1 | 320.43 | C20H24N4 | 100 MG
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A-381393 is a potent, selective, brain-penetrant dopamine D4 receptor antagonist for research use in studies of dopaminergic signaling and neuronal pathways.
- Potent dopamine D4 antagonism with low-nanomolar Ki values (≈1.5-1.9 nM) against human D4 subtypes.
- High selectivity with >2,700-fold selectivity over D1, D2, D3, and D5 receptors.
- Moderate affinity at 5-HT2A (Ki ≈370 nM), useful for selectivity profiling.
- High reported purity (99.92%) and supplied in solid and DMSO solution formats.
- Good DMSO solubility (≈51.7 mg/mL) and documented in vivo formulation protocols.
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2,923
eMolecules Medchem Express / L-NIL / 50mg / 446260754 / HY-12116 / / 53774-63-3 / MFCD00792818 / 187.243 / C8H17N3O2
Medchem Express / L-NIL / 50mg / 446260754 / HY-12116 / / 53774-63-3 / MFCD00792818 / 187.243 / C8H17N3O2
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2,924
![eMolecules Pharmablock / 6-azaspiro[3.4]octane-25-dione / 25mg / 586151486 / PBU4897 / 0.000 / 2091102-07-5 / MFCD30002138 / 139.154 / C7H9NO2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502453165.PNG-250.jpg)
eMolecules Pharmablock / 6-azaspiro[3.4]octane-25-dione / 25mg / 586151486 / PBU4897 / 0.000 / 2091102-07-5 / MFCD30002138 / 139.154 / C7H9NO2
Pharmablock / 6-azaspiro[3.4]octane-25-dione / 25mg / 586151486 / PBU4897 / 0.000 / 2091102-07-5 / MFCD30002138 / 139.154 / C7H9NO2
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2,925
Medchemexpress LLC Oligomycin A | 579-13-5 | 99.91% | 791.06 | 100 MG
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Oligomycin A (MCH 32), produced by Streptomyces, functions as a mitochondrial F0F1-ATPase inhibitor with a Ki of 1 μM. It also demonstrates anti-fungal activity. For research use only; not sold to patients.
- Acts as a mitochondrial F0F1-ATPase inhibitor (Ki: 1 μM).
- Exhibits anti-fungal activity.
- Shows cytotoxic effects on NCI-60 cell lines with a GI50 of 10 nM.
- Inhibits the activity of Triton X-100-solubilized ATPase with a Ki of 0.1 μM.
- Inhibits the ability of spermatozoa to achieve feasible in vitro capacitation (IVC) at 2.4 μM.
- Suppresses progesterone-induced in vitro acrosome exocytosis (IVAE) and associated O2 consumption and ATP levels.
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