Alkyl Halides
Medchemexpress LLC RN-1665 | 1803003-65-7 | 99.93% | 513.54 | 50 MG
RN-1665 is an orally active TRPV4 antagonist that exhibits excellent selectivity for related TRP receptors such as TRPV1, TRPV3 and TRPM8. RN-1665 is a TRPV4 probe for focus screens, with IC50s of 0.26 μM and 0.39 μM for hTRPV4 and rTRPV4 from human and rat, respectively.
- Orally active TRPV4 antagonist.
- Excellent selectivity for related TRP receptors (TRPV1, TRPV3, TRPM8).
- TRPV4 probe for focus screens.
- IC50s: 0.26 μM for hTRPV4, 0.39 μM for rTRPV4.
Medchemexpress LLC Thymol iodide | 552-22-7 | 500 MG
Thymol iodide is an iodine derivative of thymol, functioning as a mild preservative and fungicide. It is frequently employed as an iodine source in the intensive cultivation of rotifers, enabling *Brachionus "Cayman"* rotifers to achieve iodine levels comparable to those found in copepods and maintaining a high iodine content during storage.
- Iodine derivative of thymol.
- Serves as a mild preservative and fungicide.
- Commonly used as an iodine source in the intensive culture of rotifers.
- Enables *Brachionus "Cayman"* rotifers to reach iodine levels similar to copepods.
- Maintains high iodine content in rotifers during storage.
- Does not enhance the efficacy of inducing pleurodesis in rabbits.
- Efficiently enriches iodine content of rotifers with low dietary replacement.
- Maintains stable iodine retention in rotifers during storage at room or low temperature.
Medchemexpress LLC TEPP-46-based aggregation-induced emission (AIE) probe | 2621957-88-6 | 99.4% | 544.6 g/mol | C27H20N4O5S2 | 10 MG
TEPC466 is an aggregation-induced emission (AIE) fluorescent probe based on TEPP-46, designed for selective detection and imaging of pyruvate kinase M2 (PKM2) in biological samples. It is used for cellular imaging applications and is supplied as a high-purity research chemical.
- Selective detection of PKM2 via the AIE effect.
- Suitable for cellular imaging applications.
- High purity (99.43%) for reliable experimental results.
- Molecular weight 544.6 g/mol; formula C27H20N4O5S2.
- Multiple pack sizes available for experimental flexibility.
- Accompanied by analytical documents such as COA, HNMR, LCMS, and RP-HPLC.
Cambridge Isotope Laboratories Chloroiodomethane (D2 98%) copper 1 g
Chloroiodomethane (D2 98%) copper 1 g
Medchemexpress LLC Thymol iodide | 552-22-7 | 1 G
Thymol iodide is an iodine derivative of thymol, functioning as a mild preservative and fungicide. It serves as an iodine source for intensive rotifer culture, enabling rotifers to achieve and maintain high iodine content similar to copepods during storage. Research shows it does not enhance pleurodesis efficacy in rabbits after intrapleural injection.
- Iodine derivative of thymol.
- Acts as a mild preservative.
- Functions as a fungicide.
- Used as an iodine source in the intensive culture of rotifers.
- Enables rotifers to reach iodine levels similar to copepods.
- Maintains a high iodine content in rotifers during storage.
- Does not enhance pleurodesis efficacy in rabbits.
- Enriches rotifer iodine content to copepod levels with low dietary replacement (0.36-2.03%).
- Maintains stable iodine retention in rotifers for up to 18 hours.
Medchemexpress LLC 1H,5H-Imidazo[1,2-a]pyrrolo[1,2-d]pyrazin-5-one, 2,3,10,10a-tetrahydro-1-[(3-methyl-4-isoxazolyl)carbonyl]-10a-(6-methyl-3-pyridinyl)-, (10aS)- | 1323077-88-8 | 99.7% | 377.40 | 1 MG
Enzaplatovir (BTA-C585) is an orally bioavailable inhibitor for respiratory syncytial virus (RSV) infection and is described as a small-molecule RSV entry inhibitor. It is used for respiratory syncytial virus (RSV) infection and is relevant for RSV-associated lower respiratory tract infection (LRTI).
- Orally bioavailable
- Inhibitor for respiratory syncytial virus (RSV) infection
- Small-molecule RSV entry inhibitor
- Used for respiratory syncytial virus infection
- Relevant for RSV-associated lower respiratory tract infection (LRTI)
Medchemexpress LLC Pralidoxime (iodide) | 94-63-3 | 98.0% | 250 MG
Pralidoxime iodide is a potent reactivator of acetylcholinesterase (AChE). It reactivates nerve agent-inhibited AChE through direct nucleophilic attack by the oxime moiety on the phosphorus center of the bound nerve agent. It is also an antidote for organophosphate poisoning.
- Potent reactivator of acetylcholinesterase (AChE).
- Reactivates nerve agent-inhibited AChE.
- Antidote for organophosphate poisoning.
Medchemexpress LLC 2-cyclohexen-1-one, 3-(15-hydroxypentadecyl)-2,4,4-trimethyl- | 220757-88-0 | 99.1% | 364.60 | C24H44O2 | 5 MG
tCFA15 is a trimethyl cyclohexenonic long-chain fatty alcohol reported to promote neuronal differentiation and modulate Notch signaling. It is supplied as a pure-form research reagent with molecular formula C24H44O2 and molecular weight 364.60, and has documented analytical purity and storage stability.
- Promotes neuronal differentiation and modulates Notch signaling.
- High purity (99.12% by LCMS).
- Long-chain fatty alcohol structure with a 15-carbon side chain.
- Stable in pure form for extended storage at -20°C.
- Intended for research use in neuronal and stem cell pathway studies.
eMolecules AstaTech / 2-PHENYLOXAZOLE / 0.25g / 233627069 / 36029 / 95.000 / 20662-88-8 / MFCD00461764 / 145.161 / C9H7NO
AstaTech / 2-PHENYLOXAZOLE / 0.25g / 233627069 / 36029 / 95.000 / 20662-88-8 / MFCD00461764 / 145.161 / C9H7NO
Medchemexpress LLC Ethanaminium, 2-hydroxy-N-(iodomethyl)-N,N-dimethyl-, iodide (1:1) | 28508-22-7 | MFCD20489393 | 98.0% | 356.97 | C5H13I2NO | 100 MG
Iodocholine iodide is the iodide salt of choline used as a biochemical reagent and non-radioactive reference for radiolabeled choline. It is described as a metabolizable, non-toxic "green" catalyst useful for catalyzing free radical polymerization and is supplied for laboratory assay and research applications.
- High purity: 97.99%.
- Molecular formula C5H13I2NO and molecular weight 356.97 g/mol.
- Suitable as a non-radioactive reference for PET imaging research.
- Functions as a metabolizable, low-toxicity catalyst for free radical polymerization.
- Available in multiple pack sizes including 100 mg for laboratory use.
Medchemexpress LLC Methylene blue | 61-73-4 | 95.0% | C16H18ClN3S | 500 MG
Methylene blue is a chemical compound frequently used as a dye in medical procedures and functions as a vasopressor. It acts as an inhibitor for guanylyl cyclase (sGC), monoamine oxidase A (MAO-A), and NO synthase (NOS). Methylene blue influences the nitric oxide synthase/guanylate cyclase signaling pathway and is capable of crossing the blood-brain barrier. It also functions as a Tau aggregation inhibitor, demonstrating potential in reducing cerebral edema, attenuating microglial activation, and diminishing neuroinflammation.
- Inhibits sGC, MAO-A, and NOS pathways
- Used as a vasopressor and medical dye
- Influences nitric oxide synthase/guanylate cyclase signaling
- Crosses the blood-brain barrier
- Functions as a Tau aggregation inhibitor
- Reduces cerebral edema and neuroinflammation
Apexbio Technology LLC 360A iodide 737763-37-0 50mg
360A iodide (CAS 737763-37-0) is a 2 6-pyridine-dicarboxamide derivative that acts as a selective ligand for G-quadruplex DNA structures By stabilizing telomeric G-quadruplexes 360A inhibits telomerase activity and induces alterations in cell cycle progression notably causing S-phase accumulation in ATM-proficient EBV-lymphocytes Its mechanism of action involves promoting sister telomere fusions via DNA-PKcs-dependent non-homologous end joining (NHEJ) as well as triggering NHEJ and homologous recombination (HR) pathways at telomeres which disrupt mitotic progression 360A has been shown to preferentially bind telomeric G-quadruplex DNA over duplex DNA and to delay growth in HT1080 tumor cells This compound is valuable for investigating telomere biology DNA damage response and G-quadruplex-mediated genomic stability
Medchemexpress LLC Omzotirome | 1092551-88-6 | 99.9% | 328.41 | C19H24N2O3 | 100 MG
Omzotirome is a thyromimetic research compound used in preclinical and clinical studies of lipid metabolism and hyperlipidaemia. It is a functional analog of iodothyronines and is supplied with chemical and structural identifiers for laboratory research.
- Thyromimetic activity useful for lipid metabolism studies.
- Documented chemical identifiers (CAS 1092551-88-6, molecular formula C19H24N2O3).
- High reported purity suitable for analytical and biological assays.
- Available in multiple small pack sizes for research use.
- Provided with structural data and registry cross-references for traceability.
![Strem, An Ascensus Company CAS# 415918-91-1. 100mg. (S)-(+)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)bis[(1R)-1-phenylethyl]amine, dichloromethane adduct, min. 95%. MFCD04117687](https://assets.fishersci.com/TFS-Assets/CCG/product-images/15-1520.jpg-250.jpg)
Strem, An Ascensus Company CAS# 415918-91-1. 100mg. (S)-(+)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)bis[(1R)-1-phenylethyl]amine, dichloromethane adduct, min. 95%. MFCD04117687
CAS# 415918-91-1. 100mg. (S)-(+)-(3,5-Dioxa-4-phospha-cyclohepta[2,1-a;3,4-a']dinaphthalen-4-yl)bis[(1R)-1-phenylethyl]amine, dichloromethane adduct, min. 95%. MFCD04117687. Molecular Weight: 539.60. Molecular Formula: C36H30NO2P. Color/form: white pwdr. Strem# 15-1520. http://www.strem.com/catalog/v/15-1520/
Medchemexpress LLC CHI-KAT8i5 | 98.0% | 523.69 | 25 MG
CHI-KAT8i5 is a selective and orally active KAT8 inhibitor that induces cancer cell apoptosis and suppresses esophageal squamous cell carcinoma (ESCC) growth by targeting the KAT8/c-Myc signaling pathway. It is a white to off-white solid.
- Selective KAT8 inhibitor
- Induces cancer cell apoptosis
- Suppresses ESCC tumor growth
- Soluble in DMSO at 100 mg/mL
- Stable as powder for up to 3 years