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Filtered Search Results
eMolecules 139504-50-0 | Medchem Express | Mertansine | 2mg | 446270342 | HY-19792 | 738.29 | C35H48ClN3O10S
Medchem Express | CJJ300 | 5mg | 788478320 | HY-146693 | 1807631-83-9 | 435.615 | C30H33N3
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eMolecules 1790895-25-8 | Medchem Express | CeMMEC13 | 5mg | 446256421 | HY-101088 | MFCD30742989 | 336.347 | C19H16N2O4
Medchem Express | GNE-1858 | 5mg | 533802486 | HY-135892 | 2680616-96-8 | 428.492 | C21H26F2N8
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Medchemexpress LLC HY-50098 5mg Medchemexpress, Mardepodect CAS:898562-94-2 Purity:>98%
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Medchemexpress, HY-50098 5mg Mardepodect CAS:898562-94-2 Mardepodect (PF-2545920) is a potent, orally active and selective PDE10A inhibitor with an IC50 of 0.37 nM, with >1000-fold selectivity over other PDEs. Mardepodect can cross the blood-brain barrier. 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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Medchemexpress LLC HY-124960 5mg Medchemexpress, CTPB CAS:586976-24-1 Purity:>98%
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Medchemexpress, HY-124960 5mg CTPB CAS:586976-24-1 CTPB is a good activator of p300 histone acetyl transferase (HAT) enzyme. 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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Medchemexpress LLC HY-18555 5mg Medchemexpress, TMPA CAS:1258275-73-8 Purity:>98%
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Medchemexpress, HY-18555 5mg TMPA CAS:1258275-73-8 TMPA is an antagonist of nuclear receptor Nur77 and LKB1 interaction. 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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Medchemexpress LLC HY-B0549A 100mg Medchemexpress, Flavoxate (hydrochloride) CAS:3717-88-2 Purity:>98%
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Medchemexpress, HY-B0549A 100mg Flavoxate (hydrochloride) CAS:3717-88-2 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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Medchemexpress LLC HY-70003 50mg Medchemexpress, Carboxypeptidase G2 (CPG2) Inhibitor CAS:192203-60-4 Purity:>98%
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Medchemexpress, HY-70003 50mg Carboxypeptidase G2 (CPG2) Inhibitor CAS:192203-60-4 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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Medchemexpress LLC HY-A0022A 100mg Medchemexpress, Azaphen (dihydrochloride monohydrate) CAS:63302-99-8 Purity:>98%
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Medchemexpress, HY-A0022A 100mg Azaphen (dihydrochloride monohydrate) CAS:63302-99-8 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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eMolecules 2366260-33-3 | Medchem Express | Tubulin inhibitor 11 | 5mg | 788478508 | HY-152156 | 409.5 | C22H23N3O3S
Medchem Express | Boc-D-norleucine | 1g | 721434795 | HY-41912B | 55674-63-0 | MFCD00063168 | 231.292 | C11H21NO4
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eMolecules 16139-79-0 | Diphenylphosphonoacetic acid ethyl ester | Combi-Blocks | MFCD01321165 | 320.281 | C16H17O5P | 95.000 | CCOC(=O)CP(=O)(Oc1ccccc1)Oc1ccccc1 | 1g | 267210979
Diphenylphosphonoacetic acid ethyl ester | Combi-Blocks | 16139-79-0 | MFCD01321165 | 320.281 | C16H17O5P | 95.000 | CCOC(=O)CP(=O)(Oc1ccccc1)Oc1ccccc1 | 1g | 267210979
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eMolecules 142229-74-1 | 4-(Trifluoromethoxy)phenylthiourea | Apollo Scientific | MFCD00052992 | 236.210 | C8H7F3N2OS | 97.000 | NC(=S)Nc1ccc(OC(F)(F)F)cc1 | 1g | 562441180
4-(Trifluoromethoxy)phenylthiourea | Apollo Scientific | 142229-74-1 | MFCD00052992 | 236.210 | C8H7F3N2OS | 97.000 | NC(=S)Nc1ccc(OC(F)(F)F)cc1 | 1g | 562441180
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Medchemexpress LLC XST-14 | 2607143-50-8 | 99.3% | 291.34 | 50 MG
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XST-14 is a potent, competitive, and highly selective ULK1 inhibitor with an IC50 of 26.6 nM. It induces autophagy inhibition by reducing the phosphorylation of the ULK1 downstream substrate. XST-14 also induces apoptosis in hepatocellular carcinoma (HCC) cells and exhibits antitumor effects.
- Potent, competitive, and highly selective ULK1 inhibitor
- Induces autophagy inhibition
- Reduces phosphorylation of ULK1 downstream substrate
- Induces apoptosis in hepatocellular carcinoma (HCC) cells
- Exhibits antitumor effects
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eMolecules 2095432-71-4 | GSK269962 hydrochloride | MFCD31536773 | 50mg
Medchem Express | Valerylcarnitine | 5mg | 446276299 | HY-113266 | 40225-14-7 | 245.319 | C12H23NO4
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Medchemexpress LLC HY-17507B 500mg Medchemexpress, Pantoprazole (sodium hydrate) CAS:164579-32-2 Purity:>98%
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Medchemexpress, HY-17507B 500mg Pantoprazole (sodium hydrate) CAS:164579-32-2 Pantoprazole sodium hydrate (BY10232 sodium hydrate) is an orally active and potent proton pump inhibitor (PPI). Pantoprazole sodium hydrate, a substituted benzimidazole, is a potent H+/K+-ATPase inhibitor with an IC50 of 6.8 μM. Pantoprazole sodium hydrate improves pH stability and has anti-secretory, anti-ulcer activities. Pantoprazole sodium hydrate significantly increased tumor growth delay combined with Doxorubicin (HY-15142)[4]. 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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Medchemexpress LLC (S)-UFR2709 hydrochloride | 2934318-93-9 | 98.1% | 255.74 | 100 MG
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(S)-UFR2709 hydrochloride is a competitive nAChR antagonist that displays higher affinity for α4β2 nAChRs than for α7 nAChRs. It decreases anxiety and reduces ethanol consumption and ethanol preference in alcohol-preferring rats. It acts as an anxiolytic agent and can be used for the study of nicotine addiction.
- Competitive nAChR antagonist
- Exhibits higher affinity for α4β2 nAChRs than for α7 nAChRs
- Decreases anxiety
- Reduces ethanol consumption and ethanol preference
- Acts as an anxiolytic agent
- Used for the study of nicotine addiction
- Molecular target for the treatment of alcohol abuse and dependence
- Does not affect the weight or locomotor activity of rats
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