Tricarboxylic acids and derivatives
Selleck Chemical LLC Amfenac Sodium Monohydrate S4149-1g
Amfenac Sodium monohydrate is a non-steroidal analgesic anti-inflammatory drug with acetic acid moiety The IC50 values for COX1 and COX2 is 250 nM and 150 nM respectively
Sigma Aldrich Fine Chemicals Biosciences Citric acid trisodium salt anhydrous, >=98% (GC) | 68-04-2 | MFCD00012462 | 1KG
Citric acid trisodium salt anhydrous, >=98% (GC) | Purity: >=98% (GC) | Mol Wt: 258.07 | 68-04-2 | MFCD00012462 | 1KG
Sigma Aldrich Fine Chemicals Biosciences Trisodium citrate dihydrate meets USP testing specifications | 6132-04-3 | MFCD00150031 | 25KG
Trisodium citrate dihydrate meets USP testing specifications | Purity: 99.0-100.5% anhydrous basis | Mol Wt: 294.1 | 6132-04-3 | MFCD00150031 | 25KG
Medchemexpress LLC Azido-PEG6-CH2COOH | 880129-82-8 | ≥98.0% | 365.38 | 5 G
Azido-PEG6-CH2COOH is a PEG-based PROTAC linker used in the synthesis of PROTACs. It functions as a click chemistry reagent, enabling copper-catalyzed azide-alkyne cycloaddition (CuAAc) with alkyne-containing molecules and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- PEG-based PROTAC linker
- Suitable for synthesizing PROTACs
- Click chemistry reagent due to azide group
- Enables CuAAc reactions
- Participates in SPAAC reactions with DBCO or BCN groups
Medchemexpress LLC m-PEG10-CH2COOH | 908258-58-2 | ≥98.0% | 530.60 | 1 G
m-PEG10-CH2COOH is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins by connecting two different ligands, one for an E3 ubiquitin ligase and the other for the target protein.
- PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- Exploits intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
- Contains two different ligands connected by a linker
- One ligand for E3 ubiquitin ligase, the other for target protein
eMolecules AstaTech / NN-DIETHYLPROPARGYLAMINE / 5g / 454893684 / 28713 / 95.000 / 4079-68-9 / MFCD00039881 / 111.188 / C7H13N
AstaTech / NN-DIETHYLPROPARGYLAMINE / 5g / 454893684 / 28713 / 95.000 / 4079-68-9 / MFCD00039881 / 111.188 / C7H13N
Chem-Impex International, Inc. Tris-(carboxyethyl)phosphine hydrochloride | 51805-45-9 | MFCD00145469 | 1G
Tris-(carboxyethyl)phosphine hydrochloride , 51805-45-9, MFCD00145469, 1G
Medchemexpress LLC Triammonium phosphate trihydrate | 25447-33-0 | MFCD00151223 | ≥98.0% | 203.13 | H18N3O7P | 500g
Triammonium phosphate trihydrate interacts with the magnesium ions to form a precipitate which can be used for magnesium separation from lithium in salt-lake brines[1]
Medchemexpress LLC Icerguastat (Sephin1) | 951441-04-6 | 99.93% | 196.64 | 10 MG
Icerguastat (Sephin1) is a Guanabenz derivative that selectively inhibits the phosphatase regulatory subunit PPP1R15A (R15A). It functions by inhibiting eIF2α dephosphorylation, which prolongs the protective cellular response and demonstrates an anti-prion effect.
- Selectively inhibits the phosphatase regulatory subunit PPP1R15A (R15A).
- Inhibits eIF2α dephosphorylation, extending protective cellular responses.
- Demonstrates anti-prion effects in models.
- Prolongs eIF2α phosphorylation in stressed oligodendrocytes.
- Delays the onset of experimental autoimmune encephalomyelitis (EAE) in animal models.
- Prolongs survival in prion-infected mice.
![eMolecules Ambeed / (3aS3aS8aR8aR)-22-(13-diphenylpropane-22-diyl)bis(3a8a-dihydro-8H-indeno[12-d]oxazole) / 100mg / 600827831 / A1147876 / / 195703-68-5 / [null] / 510.637 / C35H30N2O2](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502463151.JPG-250.jpg)
eMolecules Ambeed / (3aS3aS8aR8aR)-22-(13-diphenylpropane-22-diyl)bis(3a8a-dihydro-8H-indeno[12-d]oxazole) / 100mg / 600827831 / A1147876 / / 195703-68-5 / [null] / 510.637 / C35H30N2O2
Ambeed / (3aS3aS8aR8aR)-22-(13-diphenylpropane-22-diyl)bis(3a8a-dihydro-8H-indeno[12-d]oxazole) / 100mg / 600827831 / A1147876 / / 195703-68-5 / [null] / 510.637 / C35H30N2O2
Sigma Aldrich Fine Chemicals Biosciences Propyl 4-hydroxybenzoate BioXtra | 94-13-3 | MFCD00002354 | 500G
Propyl 4-hydroxybenzoate BioXtra | Mol Wt: 180.2 | 94-13-3 | MFCD00002354 | 500G
Medchemexpress LLC Dicresulene diammoni 5mg | 5MG
Dicresulene diammonium is an impurity of Policresulen an organic acid with hemostatic antimicrobial and antiviral activities[1 [2
Medchemexpress LLC Amino-PEG5-CH2COOH | 141282-35-1 | ≥97.0% | 500 MG
Amino-PEG5-CH2COOH is a PEG-based PROTAC linker used in the synthesis of PROTACs. PROTACs contain two distinct ligands connected by a linker; one targets an E3 ubiquitin ligase and the other targets the protein. They function by exploiting the intracellular ubiquitin-proteasome system to selectively degrade target proteins.
- PEG-based PROTAC linker
- Targets PROTAC linkers within the PROTAC pathway
- Solid appearance
- White to off-white color
- Store at 4°C, protected from light
- In solvent, store at -80°C for 6 months or -20°C for 1 month, protected from light
Medchemexpress LLC Acetic acid, 2-[2-(2-azidoethoxy)ethoxy]- | 882518-90-3 | 99.03% | 189.17 | 50 MG
Azido-PEG2-CH2COOH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. It is also a click chemistry reagent, containing an Azide group that can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups. This product is for research use only.
- Peg-based PROTAC linker
- Click chemistry reagent
- Contains an Azide group for CuAAc and SPAAC reactions
Apexbio Technology LLC Enclomiphene citrate 7599-79-3 5mg
Enclomiphene citrate (CAS 7599-79-3) is a small-molecule antagonist targeting estrogen receptors It is designed to competitively bind to estrogen receptors thereby inhibiting receptor-mediated estrogen signaling and attenuating estrogen-induced negative feedback on the hypothalamic-pituitary axis Enclomiphene citrate exerts its biological activity primarily by increasing endogenous secretion of gonadotropins including luteinizing hormone (LH) and follicle stimulating hormone (FSH) which promotes endogenous testosterone biosynthesis in gonadal tissues Based on these pharmacological properties enclomiphene citrate holds research potential in studies of male hypogonadism fertility disorders and regulation of male gonadal function