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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4,336 – 4,350 of 7,111 results

4,336

Medchemexpress LLC 2-(4-methylphenyl)-1,2-benzisothiazol-3(2H)-one | 2514-30-9 | MFCD05856231 | 99.5% | 241.31 g/mol | C14H11NOS | 25 MG

PBIT is a research-grade small-molecule inhibitor of the Jumonji AT-rich interactive domain 1 (JARID1/KDM5) family of histone demethylases, showing activity against JARID1B (IC50 ≈ 3 μM). Supplied as a powder for laboratory use in epigenetics and chromatin biology research.

Selective inhibitor of JARID1/KDM5 histone demethylases.
Activity against JARID1B with IC50 ≈ 3 μM.
High purity (99.5%).
Powder form suitable for preparing solutions.
Recommended storage: powder -20°C; in solvent -80°C for long-term storage.
Includes datasheet with molecular formula and molecular weight.

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4,337

eMolecules 958852-01-2 | Medchem Express | GSK1059615 | 5mg | 446260589 | HY-12036 | MFCD18074517 | 333.37 | C18H11N3O2S

Medchem Express | GSK1059615 | 5mg | 446260589 | HY-12036 | 958852-01-2 | MFCD18074517 | 333.370 | C18H11N3O2S

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4,338

eMolecules 66215-27-8 | 2-N-Cyclopropyl-1,3,5-triazine-2,4,6-triamine | Combi-Blocks | MFCD00078650 | 166.188 | C6H10N6 | 95.000 | Nc1nc(N)nc(NC2CC2)n1 | 25g | 205386668

2-N-Cyclopropyl-1,3,5-triazine-2,4,6-triamine | Combi-Blocks | 66215-27-8 | MFCD00078650 | 166.188 | C6H10N6 | 95.000 | Nc1nc(N)nc(NC2CC2)n1 | 25g | 205386668

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4,339

eMolecules Medchem Express | PF-06380101-d8 | 5mg | 686240310 | HY-12522S | 751.07 | C39H62N6O6S

Medchem Express | PF-06380101-d8 | 5mg | 686240310 | HY-12522S | | 751.070 | C39H62N6O6S

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4,340

eMolecules 62013-04-1 | Medchem Express | Dirithromycin | 500mg | 491484563 | HY-B0643 | 835.086 | C42H78N2O14

Medchem Express | Dirithromycin | 500mg | 491484563 | HY-B0643 | 62013-04-1 | 835.086 | C42H78N2O14

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4,341

Sigma Aldrich Fine Chemicals Biosciences Tunicamycin from Streptomyces sp. | 11089-65-9 | MFCD00065709 | 1mg

Tunicamycin from Streptomyces sp.Purity: MW: | 11089-65-9 | MFCD00065709 | 1mg

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4,342

eMolecules 122547-49-3 | Faropenem sodium | MFCD01682061 | 5mg

ChemScene | Methyl 23-difluoroisonicotinate | 100mg | 572177200 | CS-0043759 | 1353102-03-0 | MFCD21090433 | 173.119 | C7H5F2NO2

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4,343

Abcam Tetracycline 10-O-ß-D-galactopyranoside, 2MG

MW 606.6 Da. Broad spectrum polyketide antibiotic. Produced by Streptomyces genus of Actinobacteria. Acts as a protein synthesis inhibitor and is commonly used to treat acne today, and, more recently, rosacea. Historically important in reducing the number of deaths from cholera. In this galactoside analog, upon enzymatic or chemical hydrolysis of the galactoside group, the active antibiotic tetracyline is produced.

The product is subject to the following: Abcam Restricted Use Statement

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4,344

Sigma Aldrich Fine Chemicals Biosciences Loratadine United States Pharmacopeia (USP) Reference Standard | 79794-75-5 | MFCD00672869 | 200MG

Loratadine United States Pharmacopeia (USP) Reference Standard | Mol Wt: 382.88 | 79794-75-5 | MFCD00672869 | 200MG

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4,345

Sigma Aldrich Fine Chemicals Biosciences Amantadine hydrochloride British Pharmacopoeia (BP) Reference Standard | 665-66-7 | MFCD00074723 |

Amantadine hydrochloride British Pharmacopoeia (BP) Reference Standard | Mol Wt: 187.71 | 665-66-7 | MFCD00074723 |

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4,346

Medchemexpress LLC SCD1 inhibitor-1 | 1069094-65-0 | 99.9% | 451.54 | 10 MG

SCD1 inhibitor-1 (Compound 48) is an orally active and liver-selective inhibitor of stearoyl-CoA desaturase 1 (SCD1) with an IC50 of 8.8 nM for recombinant human SCD1 enzyme. SCD1 inhibitor-1 can be used in the study of diseases such as diabetes, hepatic steatosis and obesity.

Orally active and liver-selective inhibitor of stearoyl-CoA desaturase 1 (SCD1).
IC50 of 8.8 nM for recombinant human SCD1 enzyme.
Improved effect in high-fat mice models (3-10 mg/kg; oral administration; 43 days), showing improved glucose tolerance in a dose-dependent manner and decreased body weight.
Improved effect in high-sucrose rat models (1-10 mg/kg; oral administration; single dose), inhibiting SCD1 inhibitory activity in a dose-dependent manner in epididymal adipose tissue and the liver 6 hours after oral administration.
Selective tissue distribution of liver/eyelid.

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4,347

Apexbio Technology LLC Napabucasin 83280-65-3 5mg

Napabucasin (CAS 83280-65-3) also known as BBI608 is an orally bioavailable small molecule that targets STAT3 (signal transducer and activator of transcription 3) a regulator of cancer cell pluripotency and survival Napabucasin inhibits STAT3 transcriptional activity with IC50 values of 0 395 M in bulk cancer cells and 0 142 M in cancer stem cells In vitro it reduces cell viability migration colony formation and stemness marker expression induces cell cycle arrest and apoptosis and sensitizes cells to chemotherapy In vivo napabucasin suppresses tumor growth and recurrence and limits self-renewal and metastasis of cancer stem cells in xenograft models This compound is widely utilized in studies of cancer stemness and STAT3-driven oncogenesis

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4,348

Medchemexpress LLC HY-100888A 5mg Medchemexpress, (R)-Simurosertib CAS:1330782-69-8 Purity:>98%

Medchemexpress, HY-100888A 5mg (R)-Simurosertib CAS:1330782-69-8 (R)-Simurosertib ((R)-TAK-931) is the (R)-enantiomer of Simurosertib, Simurosertib (TAK-931) is a selective cycle 7 (CDC7) kinase inhibitor, with an IC 50 <0.3 nM [1] . Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.

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4,349

Medchemexpress LLC 3α-Aminocholestane | 2206-20-4 | 98.0% | 387.68 | 5 MG

3α-Aminocholestane is a selective inhibitor of SH2 domain-containing inositol-5′-phosphatase 1 (SHIP1) with an IC50 of approximately 2.5 μM. It is intended for research use only. This compound effectively reduces multiple myeloma growth in vivo and blocks cell cycle progression.

Selectively inhibits SHIP1.
Effectively reduces OPM2 cell viability.
Blocks cell cycle progression in G0/G1 phase or reduces cells in S phase.
Reduces multiple myeloma (MM) growth in vivo.
Significantly enhances survival of mice after tumor challenge.

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4,350

eMolecules 1261590-48-0 | Medchem Express | Duvelisib (R enantiomer) | 5mg | 446268210 | HY-17044A | MFCD30187518 | 416.87 | C22H17ClN6O

Ambeed | 2-Ethylhexyl 3-(35-di-tert-butyl-4-hydroxyphenyl)propanoate | 250mg | 696731383 | A1364274 | 144429-84-5 | 390.608 | C25H42O3

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eMolecules Building Block Tool<|a>

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Antibiotics

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Medchemexpress LLC 2-(4-methylphenyl)-1,2-benzisothiazol-3(2H)-one | 2514-30-9 | MFCD05856231 | 99.5% | 241.31 g/mol | C14H11NOS | 25 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC SCD1 inhibitor-1 | 1069094-65-0 | 99.9% | 451.54 | 10 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Apexbio Technology LLC Napabucasin 83280-65-3 5mg Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC HY-100888A 5mg Medchemexpress, (R)-Simurosertib CAS:1330782-69-8 Purity:>98% Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC 3α-Aminocholestane | 2206-20-4 | 98.0% | 387.68 | 5 MG Small and Specialty Supplier PartnerSmall and/or specialty supplier based on Federal laws and SBA requirements.Learn More

Medchemexpress LLC 2-(4-methylphenyl)-1,2-benzisothiazol-3(2H)-one | 2514-30-9 | MFCD05856231 | 99.5% | 241.31 g/mol | C14H11NOS | 25 MG

Medchemexpress LLC SCD1 inhibitor-1 | 1069094-65-0 | 99.9% | 451.54 | 10 MG

Apexbio Technology LLC Napabucasin 83280-65-3 5mg

Medchemexpress LLC HY-100888A 5mg Medchemexpress, (R)-Simurosertib CAS:1330782-69-8 Purity:>98%

Medchemexpress LLC 3α-Aminocholestane | 2206-20-4 | 98.0% | 387.68 | 5 MG