Halophenols
Tetrabromobisphenol A 98.0+%, TCI America™
CAS: 79-94-7 Molecular Formula: C15H12Br4O2 Molecular Weight (g/mol): 543.875 MDL Number: MFCD00013962 InChI Key: VEORPZCZECFIRK-UHFFFAOYSA-N Synonym: tetrabromobisphenol a,3,3',5,5'-tetrabromobisphenol a,bromdian,4,4'-propane-2,2-diyl bis 2,6-dibromophenol,4,4'-isopropylidenebis 2,6-dibromophenol,firemaster bp 4a,tetrabromodian,2,2-bis 3,5-dibromo-4-hydroxyphenyl propane,fire guard 2000,great lakes ba-59p PubChem CID: 6618 ChEBI: CHEBI:33217 IUPAC Name: 2,6-dibromo-4-[2-(3,5-dibromo-4-hydroxyphenyl)propan-2-yl]phenol SMILES: CC(C)(C1=CC(=C(C(=C1)Br)O)Br)C2=CC(=C(C(=C2)Br)O)Br
2,4,6-Tribromophenol 98.0+%, TCI America™
CAS: 118-79-6 Molecular Formula: C6H3Br3O Molecular Weight (g/mol): 330.80 MDL Number: MFCD00002150 InChI Key: BSWWXRFVMJHFBN-UHFFFAOYSA-N Synonym: tribromophenol,bromol,bromkal pur 3,xeroform,phenol, 2,4,6-tribromo,flammex 3bp,unii-ys6k3eu393,ccris 1658,great lakes ph-73,5175-83-7 bismuth 3+ salt PubChem CID: 1483 ChEBI: CHEBI:47696 IUPAC Name: 2,4,6-tribromophenol SMILES: OC1=C(Br)C=C(Br)C=C1Br
Medchemexpress LLC Salicylaldoxime | 94-67-7 | 99.8% | 100 G
Salicylaldoxime is an organic compound that serves as a reagent for the gravimetric determination and separation of various heavy metals such as copper, nickel, palladium, lead, bismuth, and zinc. Its copper complex has also been shown to exhibit anticancer activity, specifically inhibiting topoisomerase II and L1210 leukemia cell proliferation.
- Used as a reagent for gravimetric determination and separation of heavy metals.
- Copper complex exhibits anticancer activity.
- Inhibits topoisomerase II relaxation activity when complexed with copper.
- Inhibits L1210 leukemia cell proliferation.
Medchemexpress LLC Salicylaldoxime | 94-67-7 | 99.8% | 25 G
Salicylaldoxime is an organic compound that has been used as a reagent for the gravimetric determination and separation of Copper, Nickel, Palladium, Lead, Bismuth, and Zinc. The copper complex of Salicylaldoxime exhibits anticancer activity, completely inhibiting the relaxation activity of topoisomerase II when forming a complex with copper, and also inhibiting L1210 leukemia cell proliferation.
- Used as a reagent for gravimetric determination
- Separates various heavy metals including Copper, Nickel, and Lead
- Copper complex shows anticancer activity
- Inhibits topoisomerase II activity when complexed with copper
- Inhibits L1210 leukemia cell proliferation
Medchemexpress LLC Milnacipran hydrochloride | 101152-94-7 | 99.7% | 25 MG
Milnacipran hydrochloride is an orally active Serotonin and Norepinephrine reuptake inhibitor. It inhibits monoamine transporters, specifically the norepinephrine transporter and the serotonin transporter, with Ki values of 31 and 8.5 nM, respectively. It also inhibits pERK1/2 activation. Milnacipran hydrochloride exhibits antidepressant, anxiolytic, and analgesic properties and can inhibit biting behavior in mice. It is used in the study of major depressive disorder, anxiety disorders, and neuropathic pain, such as fibromyalgia.
- Orally active serotonin and norepinephrine reuptake inhibitor
- Inhibits monoamine transporters with Ki values of 31 and 8.5 nM
- Inhibits pERK1/2 activation
- Exhibits antidepressant, anxiolytic, and analgesic properties
- Can inhibit biting behavior in mice
- Used in studies for major depressive disorder, anxiety disorders, and neuropathic pain
Medchemexpress LLC Milnacipran hydrochloride | 101152-94-7 | 99.7% | 5 MG
Milnacipran hydrochloride is an orally active serotonin and norepinephrine reuptake inhibitor. It specifically inhibits monoamine transporters with Ki values of 31 nM for the norepinephrine transporter and 8.5 nM for the serotonin transporter. This compound also inhibits pERK1/2 activation and exhibits antidepressant, anxiolytic, and analgesic properties. It is used in the study of major depressive disorder, anxiety disorders, and neuropathic pain, including fibromyalgia.
- Inhibits norepinephrine and serotonin transporters.
- Inhibits pERK1/2 activation.
- Possesses antidepressant, anxiolytic, and analgesic properties.
- Used in studies of major depressive disorder, anxiety disorders, and neuropathic pain.
Medchemexpress LLC Milnacipran hydrochloride | 101152-94-7 | 99.7% | 50 MG
Milnacipran hydrochloride is an orally active Serotonin and Norepinephrine reuptake inhibitor. It inhibits monoamine transporters, specifically the norepinephrine transporter and the serotonin transporter. It also inhibits pERK1/2 activation and possesses antidepressant, anxiolytic, and analgesic properties. Milnacipran hydrochloride has been shown to inhibit biting behavior in mice and is used in the study of major depressive disorder, anxiety disorders, and neuropathic pain, including fibromyalgia.
Medchemexpress LLC Milnacipran hydrochloride | 101152-94-7 | 99.7% | 100 MG
Milnacipran hydrochloride is an orally active serotonin and norepinephrine reuptake inhibitor. It inhibits monoamine transporters, specifically the norepinephrine transporter and the serotonin transporter, with Ki values of 31 nM and 8.5 nM, respectively. It also inhibits pERK1/2 activation. This compound possesses antidepressant, anxiolytic, and analgesic properties, and has been observed to inhibit biting behavior in mice.
- It is an orally active serotonin and norepinephrine reuptake inhibitor.
- It inhibits monoamine transporters, with notable activity on norepinephrine and serotonin transporters.
- The compound inhibits pERK1/2 activation.
- It demonstrates antidepressant, anxiolytic, and analgesic properties.
- It can be used in studies related to major depressive disorder, anxiety disorders, and neuropathic pain, including fibromyalgia.
Apexbio Technology LLC Milnacipran HCl 101152-94-7 10mM (in 1mL DMSO)
Milnacipran hydrochloride (CAS 101152-94-7) is a small molecule classified as a serotonin-norepinephrine reuptake inhibitor (SNRI) It acts by selectively inhibiting the reuptake of both serotonin and norepinephrine in the central nervous system thereby modulating synaptic neurotransmitter levels Milnacipran HCl has been investigated for its ability to influence neurochemical pathways implicated in pain processing and mood regulation It is utilized in biomedical research to study the pathophysiology of fibromyalgia and related disorders involving monoaminergic dysfunction
Medchemexpress LLC Milnacipran hydrochloride | 101152-94-7 | 99.7% | 10 MM x 1 ML
Milnacipran hydrochloride is an orally active Serotonin and Norepinephrine reuptake inhibitor. It inhibits monoamine transporters, specifically the norepinephrine transporter and the serotonin transporter (Ki values of 31 and 8.5 nM, respectively). It also inhibits pERK1/2 activation.
- Antidepressant, anxiolytic, and analgesic properties.
- Inhibits biting behavior in mice.
- Can be used in the study of major depressive disorder, anxiety disorders, and neuropathic pain (e.g., fibromyalgia).
Medchemexpress LLC Bromo-PEG2-phosphonic acid diethyl ester | 1226767-94-7 | C10H22BrO5P | 100 MG
Bromo-PEG2-phosphonic acid diethyl ester is a PEG-based PROTAC linker designed for the synthesis of PROTACs. This compound facilitates the creation of bifunctional molecules that leverage the ubiquitin-proteasome system to degrade target proteins.
- Used in the synthesis of PROTACs
- Contains two different ligands connected by a linker
- Exploits the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins
Medchemexpress LLC Bromo-PEG2-phosphonic acid diethyl ester | 1226767-94-7 | C10H22BrO5P | 1 G
Bromo-PEG2-phosphonic acid diethyl ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
- A PEG-based PROTAC linker
- Used in the synthesis of PROTACs
- PROTACs contain two different ligands connected by a linker
- PROTACs exploit the intracellular ubiquitin-proteasome system
- For research use only
Medchemexpress LLC Bromo-PEG2-phosphonic acid diethyl ester | 1226767-94-7 | 98% | C10H22BrO5P | 500 MG
Bromo-PEG2-phosphonic acid diethyl ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs. This linker is essential for creating PROTACs, which degrade target proteins by connecting a ligand for an E3 ubiquitin ligase and a ligand for the target protein.
- Used in the synthesis of PROTACs
- PROTACs exploit the intracellular ubiquitin-proteasome system
- Selectively degrades target proteins