Alkyl Halides
Medchemexpress LLC Aryl Hydrocarbon Receptor Antibody (YA610) | Predicted: 96 kDa; Observed: 105 kDa | 100 UL
Aryl Hydrocarbon Receptor Antibody (YA610) is a rabbit-derived, non-conjugated IgG monoclonal antibody. It targets the Aryl Hydrocarbon Receptor and is protein A affinity purified. This antibody is for research use only.
- Rabbit-derived
- IgG monoclonal antibody
- Targets Aryl Hydrocarbon Receptor
- Protein A affinity purified
- Non-conjugated
- Reactive with human samples
- Suitable for Western Blot (WB) and Immunocytochemistry/Immunofluorescence (ICC/IF) applications
Medchemexpress LLC Sodium 2-bromoethanesulfonate | 4263-52-9 | MFCD00007530 | 97.0% | 211.01 g·mol⁻¹ | C2H4BrNaO3S | 1 ML
Sodium 2-bromoethanesulfonate is an organosulfonate reagent supplied as a 10 mM solution in DMSO for biochemical and life-science research. The compound has CAS 4263-52-9, formula C2H4BrNaO3S, and a molecular weight of 211.01 g·mol⁻¹. The solid is described as white to off-white; listed purity is 97.0% (assay 99.7%). Certificates and safety data are available.
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 (7S)-BAY-593 | 2413068-25-2 | 99.6% | 476.53 | 100 MG
(7S)-BAY-593 is the S-enantiomer of BAY-593, an orally active GGTase-I inhibitor. It effectively blocks YAP1/TAZ signaling in animals and demonstrates significant antitumor activity.
- S-enantiomer of BAY-593
- Orally active GGTase-I inhibitor
- Blocks YAP1/TAZ signaling
- Exhibits antitumor activity
- Targets YAP/TAZ-TEAD and GGTase I
- Soluble in DMSO
Medchemexpress LLC 2-cyclohexen-1-one, 3-(15-hydroxypentadecyl)-2,4,4-trimethyl- | 220757-88-0 | 99.1% | 364.60 | C24H44O2 | 10 MG
tCFA15 is a trimethyl cyclohexenonic long-chain fatty alcohol (C24H44O2, MW 364.60) that promotes neuronal differentiation and modulates Notch1 signaling. It is supplied as a high-purity research standard intended for in vitro studies of neural stem cell differentiation and neuronal signaling pathways.
- Promotes differentiation of neural stem cell-derived neurospheres toward neurons.
- Modulates Notch1 expression and signaling.
- High purity suitable for in vitro research applications.
- Soluble in DMSO for solution-based assays.
- Shown to stimulate arginine vasopressin secretion in neurohypophysis preparations.
Sigma Aldrich Fine Chemicals Biosciences 3-Bromocyclohexene technical grade, 90% | Purity: 90% | Mol Wt: 161.04 | 1521-51-3 | MFCD00013775 | 250ML
3-Bromocyclohexene technical grade, 90% | Purity: 90% | Mol Wt: 161.04 | 1521-51-3 | MFCD00013775 | 250ML
Medchemexpress LLC Rapastinel Trifluoroacetate | 1435786-04-1 | 98.0% | 527.49 | 100 MG
Rapastinel Trifluoroacetate (GLYX-13 Trifluoroacetate) is an NMDA receptor modulator with glycine-site partial agonist properties. It has potential for treating major depressive disorder and is currently in phase II clinical development as an adjunctive therapy for this condition. Studies have shown that Rapastinel Trifluoroacetate produces an antidepressant-like effect and an anxiolytic effect in animal models, without altering locomotor activity.
- NMDA receptor modulator with glycine-site partial agonist properties
- Potential for treating major depressive disorder
- Phase II clinical development as an adjunctive therapy
- Produces antidepressant-like and anxiolytic effects in animal models
- Does not alter locomotor activity
Medchemexpress LLC CCL4 Human 10ug
CCL4 Protein Human is a small cytokine of the CC chemokine subfamily that binds to the CCR5 chemokine receptor on the cell surface promotes leukocyte aggregation under various inflammatory conditions and contributes to immune protection against human immunodeficiency virus type 1 CCL4 Protein Human is a recombinant human CCL4 (A24-N92) expressed by E coli[1]
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
Medchemexpress LLC 1-Bromooctane | 111-83-1 | MFCD00000276 | 99.9% | 193.12 | C8H17Br | 500 G
1-Bromooctane is a primary alkyl bromide (CAS 111-83-1) commonly used as an electrophile in nucleophilic substitution and alkylation reactions. It functions as a building block in organic synthesis and is supplied for laboratory research applications.
- Primary alkyl bromide suitable for SN2 reactions.
- Useful electrophile for alkylation and substitution steps.
- High purity for reliable reaction outcomes.
- Available in multiple pack sizes for bench-scale synthesis.
- Liquid at room temperature for easy handling and dosing.
Medchemexpress LLC CHI-KAT8i5 | 2839860-29-4 | 98.00% | 523.69 | 5 MG
CHI-KAT8i5 is a selective, 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 demonstrates high specificity and anti-proliferative effects in vitro and in vivo.
- Selective, orally active KAT8 inhibitor
- High specificity; does not bind to other HAT family proteins
- Induces cancer cell apoptosis
- Suppresses esophageal squamous cell carcinoma (ESCC) growth
- Targets KAT8/c-Myc signaling pathway
- Demonstrates in vitro anti-proliferative effects against KYSE 30 and KYSE 150 cells
- Represses NPM1 and PPAT transcript expression; decreases H4K16ace and c-Myc levels
- Effective in vivo in suppressing ESCC tumor growth
- Reduces Ki-67, c-Myc expression, and H4K16ace levels in vivo
![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/
eMolecules 1416444-88-6 | ChemScene | (R)-(66-Dimethylmorpholin-2-yl)methanol hydrochloride | 100mg | 569146498 | CS-0129999 | MFCD22690353 | 181.66 | C7H16ClNO2
ChemScene | 1-(3-Methoxyphenyl)butan-1-amine hydrochloride | 100mg | 714105315 | CS-0497690 | 1864057-25-9 | MFCD28126397 | 215.720 | C11H18ClNO
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