Tricarboxylic acids and derivatives
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Filtered Search Results
eMolecules 6132-04-3 | Sodium citrate dihydrate, ACS reagent grade | Oakwood Chemical | MFCD00150031 | 294.098 | C6H9Na3O9 | 99.000 | O.O.[Na+].[Na+].[Na+].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O | 25g | 599151402
Sodium citrate dihydrate, ACS reagent grade | Oakwood Chemical | 6132-04-3 | MFCD00150031 | 294.098 | C6H9Na3O9 | 99.000 | O.O.[Na+].[Na+].[Na+].OC(CC([O-])=O)(CC([O-])=O)C([O-])=O | 25g | 599151402
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Apexbio Technology LLC Clomiphene citrate 50-41-9 10mM (in 1mL DMSO)
Clomiphene citrate (CAS 50-41-9) is a small-molecule modulator targeting estrogen receptors (ER) It is designed to selectively modulate ER-mediated signaling thereby influencing estrogen-dependent cellular pathways Clomiphene citrate exerts its biological activity primarily through competitive inhibition at estrogen receptors It demonstrates both antiestrogenic and estrogenic activities depending on tissue context Based on these pharmacological properties clomiphene citrate holds research potential in the investigation of estrogen receptor-mediated transcriptional regulation cellular proliferation and differentiation as well as hypothalamic-pituitary-gonadal axis regulation and ovarian follicular maturation in reproductive biology studies
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Medchemexpress LLC AZIDO-PEG6-CH2COOH 250 mg
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AZIDO-PEG6-CH2COOH 250MG
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Selleck Chemical LLC Pentoxyverine Citrate S4143-100mg
Pentoxyverine Citrate (Carbetapentane) is an antitussive (cough suppressant) commonly used for cough associated with illnesses like common cold
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Selleck Chemical LLC Orphenadrine Citrate S2054-50mg
Orphenadrine Citrate is a skeletal muscle relaxant it acts in the central nervous system to produce its muscle relaxant effects
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Medchemexpress LLC Sparfosic acid trisodium | 70962-66-2 | 98.0% | 321.06 | 50 MG
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Sparfosic acid trisodium is a DNA antimetabolite agent and a potent inhibitor of aspartate transcarbamoyl transferase, an enzyme that catalyzes the second step of de novo pyrimidine biosynthesis. It synergistically enhances the cytotoxicity of a combination of 5-fluorouracil (5-FU) and interferon-alpha (IFN) against human colon cancer cell lines. It is for research use only.
- DNA antimetabolite agent
- Potent inhibitor of aspartate transcarbamoyl transferase
- Synergistically enhances the cytotoxicity of 5-fluorouracil (5-FU) and interferon-alpha (IFN) against human colon cancer cell lines
- Causes apoptosis in resistant Br1 cells
- Leads to progressive accumulation of cells in S phase and activation of an apoptotic pathway at 300 μM
- Increases lifespan in mice bearing B16 melanoma
- Curative in 50% of mice with Lewis lung carcinoma when treated on days 1, 5, and 9 following s.c. implantation
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Medchemexpress LLC Sparfosic acid trisodium | 70962-66-2 | 98.0% | 321.06 | 100 MG
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Sparfosic acid trisodium is a DNA antimetabolite agent and a potent inhibitor of aspartate transcarbamoyl transferase, an enzyme that catalyzes the second step of de novo pyrimidine biosynthesis. It synergistically enhances the cytotoxicity of a combination of 5-fluorouracil (5-FU) and interferon-alpha (IFN) against human colon cancer cell lines. This product is for research use only and not intended for sale to patients.
- Potent inhibitor of aspartate transcarbamoyl transferase.
- Synergistically enhances cytotoxicity of 5-FU and IFN against human colon cancer cell lines.
- Causes apoptosis in resistant Br1 cells.
- Leads to progressive accumulation of cells in S phase and activation of an apoptotic pathway.
- Increases lifespan and is curative in mice models of B16 melanoma and Lewis lung carcinoma.
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Medchemexpress LLC Adenosine 5'-(α,β-methylene)diphosphate triammonium | 99.9% | 476.32 | 1 ML
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MethADP (Adenosine 5'-(α,β-methylene)diphosphate) triammonium is a CD73 inhibitor. It can be used for the research of the ATP-adenosine pathway. It inhibits 5'-AMP induced adenosine formation in A498 cells at concentrations of 20 and 100 μmol/L.
- CD73 inhibitor
- Used for research of ATP-adenosine pathway
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Accela Chembio Inc Triethyl Methanetricarboxylate | 25g | 6279-86-3 | MFCD00009150 | 95+% | D: 1.095 | Shelf Life: 1080 Days | Regular
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Triethyl Methanetricarboxylate | 25g | 6279-86-3 | MFCD00009150 | 95+% | D: 1.095 | Shelf Life: 1080 Days | Regular
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Crescent Chemical Co Inc TRIS-(2-CARBOXYETHYL)PHOSPHINE
Tris-(2-carboxyethyl)phosphine hydrochloride Water-soluble and odorless reagent for selective and fast reduction of disulfides. Does not react with other functional groups of proteins. Unreactive towards many common alkylating reagents, so reductions have been carried out simultaneously wit
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Selleck Chemical LLC D-()-Galacturonic acid monohydrate S3310-25mg
D-( )-Galacturonic acid monohydrate (D-Galacturonic acid hydrate d-GalA D-galUA) is an endogenous metabolite that can be used in engineering Saccharomyces cerevisiae
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eMolecules 189178-09-4 | Ambeed | Tris(4-ethynylphenyl)amine | 250mg | 624121628 | A693154 | MFCD09030768 | 317.391 | C24H15N
ChemScene | 4-Methyl-3-(methylsulfonyl)aniline | 100mg | 712840109 | CS-0434875 | 307989-41-9 | MFCD16809481 | 185.240 | C8H11NO2S
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TARGETMOL CHEMICALS INC Zoledronic acid monohydrate
Also available in 10 mg, 25 mg, 50 mg, 200 mg, 500 mg and bulk. Please contact Fisher for quotes. Zoledronic acid monohydrate (CGP 42446) is a synthetic imidazole bisphosphonate analog with anti-bone-resorption activity. Purity ≥95%
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Selleck Chemical LLC Sodium citrate dihydrate
Sodium citrate dehydrate (Trisodium citrate dihydrate Citric acid trisodium salt dihydrate) is the preferred anticoagulant
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Apexbio Technology LLC Amfenac Sodium Monohydrate 61618-27-7 10mM (in 1mL DMSO)
Amfenac Sodium Monohydrate (CAS 61618-27-7) is a synthetic non-steroidal anti-inflammatory compound structurally characterized by an acetic acid moiety It functions by inhibiting cyclooxygenase (COX) enzymes consequently suppressing prostaglandin synthesis and mitigating inflammatory processes and pain signaling Amfenac Sodium Monohydrate is utilized in biomedical research to investigate inflammatory pathways and to evaluate non-steroidal analgesic drug effects in cellular and animal models of inflammation Its well-defined inhibitory mechanism makes it a valuable tool for elucidating COX-mediated physiological and pathological responses
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