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Filtered Search Results
Ambeed AMBEED
5000895579 10-BROMODECYLBENZENE 250MG
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eMolecules 114616-27-2 | MMT-hexylaminolinker phosphoramidite | ChemScene | MFCD00036166 | 589.761 | C35H48N3O3P | 95.000 | COc1ccc(cc1)C(NCCCCCCOP(OCCC#N)N(C(C)C)C(C)C)(c1ccccc1)c1ccccc1 | 100mg | 801477451
MMT-hexylaminolinker phosphoramidite | ChemScene | 114616-27-2 | MFCD00036166 | 589.761 | C35H48N3O3P | 95.000 | COc1ccc(cc1)C(NCCCCCCOP(OCCC#N)N(C(C)C)C(C)C)(c1ccccc1)c1ccccc1 | 100mg | 801477451
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000757553 1 14-DIBROMOTETRADEC 250MG
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Medchemexpress LLC Methyl 5-formylsalicylate | 41489-76-3 | MFCD03840784 | 25g
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Methyl 5-formylsalicylate is a drug impurity
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eMolecules 5657-51-2 | 4-Azaphthalide | ChemScene | MFCD01860224 | 135.122 | C7H5NO2 | 98.000 | O=C1OCc2ncccc12 | 250mg | 536780060
4-Azaphthalide | ChemScene | 5657-51-2 | MFCD01860224 | 135.122 | C7H5NO2 | 98.000 | O=C1OCc2ncccc12 | 250mg | 536780060
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Medchemexpress LLC Alclofenac | 22131-79-9 | 99.4% | 226.66 | 250 MG
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Alclofenac (Allopydin) is a non-steroidal anti-inflammatory agent (NSAID). It acts as a prostaglandin H2 synthase inhibitor. It can be used for research related to rheumatoid arthritis, degenerative joint disease, and ankylosing spondylitis.
- Acts as a non-steroidal anti-inflammatory agent (NSAID)
- Functions as a prostaglandin H2 synthase inhibitor
- Suitable for research on rheumatoid arthritis, degenerative joint disease, and ankylosing spondylitis
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eMolecules 1046816-75-4 | (2-Chloropyrimidin-5-yl)methanol | Ambeed | MFCD16659172 | 144.560 | C5H5ClN2O | 97.000 | OCc1cnc(Cl)nc1 | 1g | 552652982
(2-Chloropyrimidin-5-yl)methanol | Ambeed | 1046816-75-4 | MFCD16659172 | 144.560 | C5H5ClN2O | 97.000 | OCc1cnc(Cl)nc1 | 1g | 552652982
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Medchemexpress LLC TTHA | 869-52-3 | 98.0% | 494.45 | 250 MG
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TTHA is a complexonate that exhibits high affinity for light rare earth elements (LREE), particularly for La3+ in ternary mixtures and Y3+ in quinary mixtures. It is intended for research use only.
- High affinity for light rare earth elements (LREE)
- Specifically effective for La3+ in ternary mixtures
- Specifically effective for Y3+ in quinary mixtures
- Intended for research use only
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eMolecules 94160-25-5 | Ethyl 3-hydroxycyclohexanecarboxylate | Ambeed | MFCD00205586 | 172.224 | C9H16O3 | 98.000 | CCOC(=O)C1CCCC(O)C1 | 5g | 596330806
Ethyl 3-hydroxycyclohexanecarboxylate | Ambeed | 94160-25-5 | MFCD00205586 | 172.224 | C9H16O3 | 98.000 | CCOC(=O)C1CCCC(O)C1 | 5g | 596330806
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Cambridge Isotope Laboratories Mono-(2-ethyl-5-carboxypentyl)phthalate (DEHP metabolite V) (13C4 99%) 100 ug/mL in MTBE 1 2 mL
Mono-(2-ethyl-5-carboxypentyl)phthalate (DEHP metabolite V) (13C4 99%) 100 ug/mL in MTBE 1 2 mL
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eMolecules 5680-79-5 | Methyl 2-aminoacetate hydrochloride | Synthonix | MFCD00012870 | 125.550 | C3H8ClNO2 | 95.000 | Cl.COC(=O)CN | 100g | 779539276
Methyl 2-aminoacetate hydrochloride | Synthonix | 5680-79-5 | MFCD00012870 | 125.550 | C3H8ClNO2 | 95.000 | Cl.COC(=O)CN | 100g | 779539276
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Apexbio Technology LLC HLCL-61 1158279-20-9 50mg
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HLCL-61 (CAS 1158279-20-9) is a selective inhibitor of protein arginine methyltransferase 5 (PRMT5) an enzyme implicated in the epigenetic regulation of gene expression through symmetric dimethylation of arginine residues on histones and other proteins HLCL-61 shows specificity for PRMT5 exhibiting no inhibitory activity against PRMT1 PRMT4 or other type II PRMT family members In cellular studies HLCL-61 suppresses symmetric dimethylation of histones H3 and H4 leading to reduced viability and enhanced differentiation of acute myeloid leukemia (AML) cell lines and primary blasts HLCL-61 is currently utilized in preclinical research to investigate PRMT5-mediated epigenetic mechanisms in cancer
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Ambeed AMBEED
5000868343 ETHYL 1-AMINOCYCLOBUTANECA 1GR
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Medchemexpress LLC TMP195 | 1314891-22-9 | 99.8% | 456.42 | 250 MG
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TMP195 is a selective class IIa histone deacetylase (HDAC) inhibitor. It has reported Ki values of 59, 60, 26, and 15 nM for HDAC4, HDAC5, HDAC7, and HDAC9, respectively. It is intended for research use only and not for sale to patients.
- Selective class IIa HDAC inhibitor.
- Blocks the accumulation of CCL2 protein in monocyte-derived macrophage differentiation cultures.
- Significantly increases CCL1 protein secretion by monocytes.
- Occupies the acetyllysine-binding site of class IIa HDACs.
- Alters the tumor microenvironment, reducing tumor burden and pulmonary metastases by modulating macrophage phenotypes in vivo.
- Induces recruitment and differentiation of highly phagocytic and stimulatory macrophages within tumors in vivo.
- Combining with chemotherapy regimens or T-cell checkpoint blockade enhances the durability of tumor reduction in vivo.
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Aobchem AOBCHEM
5000872043 ETHYL 2- 3-ETHYL-2-METHOXYPHEN
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