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Filtered Search Results
Medchemexpress LLC Propyl pyrazole triol | 263717-53-9 | 386.44 g/mol | C24H22N2O3 | 50 MG
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Propyl pyrazole triol (PPT) is a synthetic, nonsteroidal selective estrogen receptor alpha (ERα) agonist used as a research reagent to probe ERα-mediated signaling in vitro and in vivo. It is supplied as a powder and includes manufacturer guidance for storage and formulation.
- Selective estrogen receptor alpha (ERα) agonist with reported high ERα selectivity.
- Intended for research use in vitro and in vivo studies.
- Supplied as a powder, suitable for formulation into standard dosing vehicles.
- Stable when stored as powder at -20°C for up to 3 years.
- Soluble in DMSO (≥100 mg/mL) and in recommended in vivo formulation vehicles.
- Molecular weight 386.44 g/mol; CAS number 263717-53-9.
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eMolecules 28456-54-4 | 2-Mercapto-5,6-dimethylpyrimidin-4-ol | MFCD00269435 | 1g
Ambeed | 1-Fluoro-2-iodo-3-methoxybenzene | 250mg | 572829030 | A389275 | 7079-54-1 | MFCD03788539 | 252.027 | C7H6FIO
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Medchemexpress LLC 1,3-Dimethylpyrazole | 694-48-4 | 96.13 | 25 G
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1,3-Dimethylpyrazole is a bioactive compound isolated from Moso Bamboo Root. It is an active small molecule that can be used as a building block for the synthesis of multiple compounds. Intended for research use only, this substance is a colorless to light yellow liquid.
- Isolated from Moso Bamboo Root
- Active small molecule for chemical synthesis
- Research use only
- Highly flammable liquid and vapor
- Causes skin irritation
- Causes serious eye irritation
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Medchemexpress LLC SU 5402 10mM 1mL | 215543-92-3 | 10MM 1ML
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SU 5402 is a potent multi-targeted receptor tyrosine kinase inhibitor with IC50 of 20 nM 30 nM and 510 nM for VEGFR2 FGFR1 and PDGFR respectively
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Apexbio Technology LLC SU 5402 215543-92-3 10mM (in 1mL DMSO)
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SU 5402 (CAS 215543-92-3) is a selective receptor tyrosine kinase inhibitor targeting VEGFR2 FGFR1 and PDGFR with respective IC50 values of 0 02 M 0 03 M and 0 51 M It exhibits minimal inhibitory activity against EGFR ( 100 M IC50) SU 5402 inhibits FGFR-mediated phosphorylation events impacting downstream signaling pathways including ERK1/2 STAT3 and MAP kinases leading to cell cycle arrest and induction of apoptosis particularly in FGFR3-dependent multiple myeloma cell lines This compound serves as a relevant tool for exploring receptor tyrosine kinase signaling in cancer research
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eMolecules 1153041-98-5 | 1-benzylpyrazole-4-sulfonyl chloride | Synthonix | MFCD12192693 | 256.700 | C10H9ClN2O2S | 95.000 | ClS(=O)(=O)c1cnn(Cc2ccccc2)c1 | 100mg | 784551974
1-benzylpyrazole-4-sulfonyl chloride | Synthonix | 1153041-98-5 | MFCD12192693 | 256.700 | C10H9ClN2O2S | 95.000 | ClS(=O)(=O)c1cnn(Cc2ccccc2)c1 | 100mg | 784551974
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Medchemexpress LLC APOC3 Human His-SU 20ug
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Recombinant human apolipoprotein C-III supplied as a lyophilized His-SUMO-tagged fusion protein for research use. The construct corresponds to UniProt accession P02656 (residues S21-A99), is produced in E. coli, and is offered in microgram-scale sizes. Consult the provided datasheet, COA, and SDS for handling, reconstitution, and storage details.
- Recombinant human apolipoprotein C-III with N-terminal 6xHis and SUMO tags.
- Expressed in E. coli for efficient production.
- Lyophilized powder format for convenient handling and storage.
- Molecular weight approximately 22-24.8 kDa.
- Corresponds to UniProt accession P02656 (S21-A99).
- Stable when stored at -20°C; aliquot and freeze at -20°C or -80°C after reconstitution.
- Not recommended to reconstitute below 100 μg/mL in ddH2O.
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eMolecules Key Organics/BIONET 3-Bromo-1H pyrazole 9mg 629239569 TS-01911 90 000 14521-80-3 MFCD01646049 146 975 C3H3BrN2
Key Organics/BIONET 3-Bromo-1H pyrazole 9mg 629239569 TS-01911 90 000 14521-80-3 MFCD01646049 146 975 C3H3BrN2
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Matrix Scientific 1-METHYL-1H-PYRAZOLE-25G
1-Methyl-1H-pyrazole, 98%; 25g,C4H6N2, MFCD00144943, mw 82.11, [930-36-9]
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eMolecules 1153042-50-2 | 1-(2-Bromophenyl)pyrazole-4-carbaldehyde | Combi-Blocks | MFCD09054741 | 251.083 | C10H7BrN2O | 97.000 | Brc1ccccc1-n1cc(C=O)cn1 | 1g | 290706029
1-(2-Bromophenyl)pyrazole-4-carbaldehyde | Combi-Blocks | 1153042-50-2 | MFCD09054741 | 251.083 | C10H7BrN2O | 97.000 | Brc1ccccc1-n1cc(C=O)cn1 | 1g | 290706029
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Medchemexpress LLC TEAD3 Human His-SU 50ug
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Recombinant human TEAD3 (residues M112-D435) is supplied as an N-terminal SUMO-6xHis tagged protein expressed in E. coli. The purified protein (~52.3 kDa) is provided at 90% purity for biochemical and structural studies and is suitable for binding assays, structural characterization, and in vitro functional assays.
- Expressed in E. coli
- N-terminal SUMO and 6xHis affinity tags
- Approximately 52.3 kDa molecular weight
- Purity approximately 90%
- Includes residues M112-D435 of the human sequence
- Supplied in microgram pack sizes for laboratory use
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eMolecules 885519-98-2 | 3-Formyl-1H-indazole-5-carboxylic acid | ChemScene | MFCD06656900 | 190.158 | C9H6N2O3 | 95.000 | OC(=O)c1ccc2[nH]nc(C=O)c2c1 | 250mg | 572176483
3-Formyl-1H-indazole-5-carboxylic acid | ChemScene | 885519-98-2 | MFCD06656900 | 190.158 | C9H6N2O3 | 95.000 | OC(=O)c1ccc2[nH]nc(C=O)c2c1 | 250mg | 572176483
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eMolecules 71501-10-5 | 4,4'-Diantipyrylmethane monohydrate | Combi-Blocks, Inc. | MFCD00149122 | 406.486 | C23H26N4O3 | 98.000 | O.Cc1c(Cc2c(C)n(C)n(-c3ccccc3)c2=O)c(=O)n(-c2ccccc2)n1C | 25g | 603146906
4,4'-Diantipyrylmethane monohydrate | Combi-Blocks, Inc. | 71501-10-5 | MFCD00149122 | 406.486 | C23H26N4O3 | 98.000 | O.Cc1c(Cc2c(C)n(C)n(-c3ccccc3)c2=O)c(=O)n(-c2ccccc2)n1C | 25g | 603146906
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eMolecules 885278-53-5 | Methyl 6-methoxy-1H-indazole-3-carboxylate | J & W PharmLab, LLC | MFCD07371587 | 206.201 | C10H10N2O3 | 96.000 | COC(=O)c1n[nH]c2cc(OC)ccc12 | 5g | 249979540
Methyl 6-methoxy-1H-indazole-3-carboxylate | J & W PharmLab, LLC | 885278-53-5 | MFCD07371587 | 206.201 | C10H10N2O3 | 96.000 | COC(=O)c1n[nH]c2cc(OC)ccc12 | 5g | 249979540
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Medchemexpress LLC 1H-Pyrazole-1-carbox 10mg | 1026682-51-8 | 10MG
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1H-Pyrazole-1-carboxylic acid 3-amino-5-cyclobutyl- 1 1-dimethylethyl ester (Protac cdk9-binding moiety 1) is a drug intermediate for synthesis of various active compounds
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