Tricarboxylic acids and derivatives
eMolecules Oakwood Chemical Sodium citrate anhydrous 1kg 850217557 109898 0 000 68-04-2 MFCD00012462 258 068 C6H5Na3O7
Oakwood Chemical Sodium citrate anhydrous 1kg 850217557 109898 0 000 68-04-2 MFCD00012462 258 068 C6H5Na3O7
Electron Microscopy Sciences Ammonium Alcohol 500 ML
Used in Alizarin Red S and Toluidine Blue O for distinction of bone and cartilage in mammalian embryos. See Dawson A.B., Stain Techn., 1:123-4, 1926, Williams, T.W., Stain Techn., 16:23-5, 1941, or Clark, G., (ed), Staining Procedures, 3rd Ed., Williams & Wilkins Baltimore, p. 139, c. 1973
Sigma Aldrich Fine Chemicals Biosciences Ammonium citrate dibasic BioXtra, >=99.0% (T) | 3012-65-5 | MFCD00013068 | 500G
Ammonium citrate dibasic BioXtra, >=99.0% (T) | Purity: >=99.0% (T) | Mol Wt: 226.18 | 3012-65-5 | MFCD00013068 | 500G
Sigma Aldrich Fine Chemicals Biosciences Trisodium citrate dihydrate meets USP testing specifications | 6132-04-3 | MFCD00150031 | 5kg
Trisodium citrate dihydrate meets USP testing specificationsPurity: | MW: 294.1 | 6132-04-3 | MFCD00150031 | 5kg
Medchemexpress LLC KDOAM-25 citrate | 2448475-08-7 | MFCD00865590 | >98.0% | 499.51 g/mol | C21H33N5O9 | 1 ML
KDOAM-25 citrate is the citrate salt of a potent, selective inhibitor of KDM5 family histone lysine demethylases. It is supplied as a solid or as a 10 mM solution in DMSO (1 mL) and is intended for use in biochemical and cellular research probing KDM5 activity and epigenetic regulation.
- Potent, selective KDM5 inhibitor with low-nanomolar IC50 values.
- Available as solid or 10 mM solution in DMSO (1 mL).
- High purity (>98% by HPLC/LCMS).
- Molecular weight 499.51 g/mol; formula C21H33N5O9.
- Suitable for biochemical assays and cellular studies.
- Soluble in DMSO for convenient stock preparation.
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
Medchemexpress LLC Mangafodipir trisodium | 140678-14-4 | 99.7% | 5 MG
Mangafodipir trisodium (MnDPDP) is a hepatocellular-specific contrast agent and an efficacious inhibitor of chemotherapy-induced peripheral neuropathy (CIPN) and other conditions caused by cellular oxidative stress. It shows no negative interference with the tumoricidal activity of chemotherapy.
- Hepatocellular-specific contrast agent
- Efficacious inhibitor of chemotherapy-induced peripheral neuropathy
- Attenuates apoptosis caused by cisplatin in HGrC cells
- Protects against ovarian damage caused by cisplatin and paclitaxel in mice
Medchemexpress LLC Tos-PEG3-CH2COOH | 1581248-63-6 | 25 MG
Tos-PEG3-CH2COOH is a PEG-based PROTAC linker. It can be used in the synthesis of PROTACs, which are compounds designed to exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins. PROTACs typically contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein.
- PEG-based linker for PROTAC synthesis
- Utilizes the ubiquitin-proteasome system
- Designed to selectively degrade target proteins
- Composed of two ligands connected by a linker
Medchemexpress LLC Acetic acid, 2-[2-(2-azidoethoxy)ethoxy]- | 882518-90-3 | 99.0% | 189.17 | 100 MG
Azido-PEG2-CH2COOH is a PEG-based PROTAC linker utilized in the synthesis of PROTACs. It functions as a click chemistry reagent, containing an Azide group that can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with alkyne-containing molecules. It can also engage in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules possessing DBCO or BCN groups.
- Functions as a click chemistry reagent
- Contains an azide group
- Participates in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions
- Engages in strain-promoted alkyne-azide cycloaddition (SPAAC) reactions
Medchemexpress LLC 5,8,11,14,17,20-hexaoxa-2-azadocosanedioic acid, 1-(9H-fluoren-9-ylmethyl) ester | 437655-96-4 | MFCD26142983 | 99.4% | 561.62 g/mol | C29H39NO10 | 50 MG
Fmoc-NH-PEG6-CH2COOH is an Fmoc-protected PEG6 linker bearing a terminal carboxylic acid and an Fmoc-protected amine. It is used as a hydrophilic spacer in the synthesis of proteolysis targeting chimeras (PROTACs) and antibody-drug conjugates (ADCs), providing solubility and a reactive handle for amide coupling.
- Fmoc-protected amine for orthogonal protection in synthesis.
- Terminal carboxylic acid suitable for amide coupling.
- PEG6 spacer increases hydrophilicity and solubility.
- High reported purity (≈99.4%).
- Available in multiple package sizes for milligram to gram scale work.
Medchemexpress LLC IACS-8803 diammonium | 00-00-0 | 96.7% | C20H29FN12O9P2S2 | 10MG
IACS-8803 (diammonium) is a cyclic dinucleotide STING agonist supplied as a diammonium salt for research use. It potently activates the STING pathway and has demonstrated robust systemic antitumor efficacy in preclinical studies. The diammonium salt improves handling and stability compared with the free form and is intended for in vitro and in vivo immuno-oncology research.
- Potent STING pathway agonist for immune activation.
- Demonstrated systemic antitumor efficacy in preclinical models.
- Suitable for in vitro and in vivo research applications.
- Diammonium salt formulation for improved stability and handling.
- Requires cold-chain storage; research use only.
Apexbio Technology LLC Tandospirone citrate 112457-95-1 5mg
Tandospirone citrate (CAS 112457-95-1) is a selective partial agonist of the 5-HT1A receptor exhibiting high affinity for this target (Ki 27 nM) while demonstrating markedly lower affinity for other receptors such as 5-HT2 5-HT1C 1 2 D1 and D2 (Ki 1300 41000 nM) In vitro tandospirone citrate shows the strongest binding to 5-HT1A receptors In vivo studies indicate it reduces premature responses in a dose-dependent manner suggesting an inhibitory effect on impulsive behavior Tandospirone citrate is utilized as a pharmacological tool in research on depression anxiety and other neuropsychiatric conditions
Medchemexpress LLC Triammonium phosphate trihydrate | 25447-33-0 | MFCD00151223 | ≥98.0% | 203.13 | H18N3O7P | 100g
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]
Sigma Aldrich Fine Chemicals Biosciences Sodium Citrate Dihydrate | 6132-04-3 | MFCD00150031 | 10kg
Sodium Citrate Dihydrate | Purity: 99% | Mol Wt: 294.1 | 6132-04-3 | MFCD00150031 | 10kg
eMolecules Ambeed / Tris(4-methoxyphenyl)amine / 250mg / 627733411 / A218053 / / 13050-56-1 / MFCD00854211 / 335.403 / C21H21NO3
Ambeed / Tris(4-methoxyphenyl)amine / 250mg / 627733411 / A218053 / / 13050-56-1 / MFCD00854211 / 335.403 / C21H21NO3