Alcohols and polyols
1,1,1-Trifluoroacetone cyanohydrin, 95%
CAS: 335-08-0 Molecular Formula: C4H4F3NO Molecular Weight (g/mol): 139.077 MDL Number: MFCD00040885 InChI Key: XDCMNDCKYSQKAX-UHFFFAOYSA-N Synonym: 1,1,1-trifluoroacetone cyanohydrin,2-cyano-1,1,1-trifluoro-2-propanol,2-hydroxy-2-trifluoromethyl propionitrile,propanenitrile, 3,3,3-trifluoro-2-hydroxy-2-methyl,2-trifluoromethyl lactonitrile,trifluoroacetone cyanohydrin,lactonitrile, 2-trifluoromethyl,3-trifluoro-a-hydroxyisobutyronitrile,lactonitrile,3,3-trifluoro-2-methyl,2-cyano-1,1,1-trifluoropropan-2-ol PubChem CID: 274400 IUPAC Name: 3,3,3-trifluoro-2-hydroxy-2-methylpropanenitrile SMILES: CC(C#N)(C(F)(F)F)O
2-(2,4-Dichlorophenyl)ethanol 97.0+%, TCI America™
CAS: 81156-68-5 Molecular Formula: C8H8Cl2O Molecular Weight (g/mol): 191.051 MDL Number: MFCD00192010 InChI Key: JIJGKPVJAALUQQ-UHFFFAOYSA-N Synonym: 2,4-dichlorophenethyl alcohol,2-2,4-dichlorophenyl ethanol,2,4-dichlorophenethylalcohol,2-2,4-dichlorophenyl ethan-1-ol,2,4-dichlorobenzeneethanol,acmc-209pku,ksc450o3l,2,4-dichlorophenylmethyl-carbinol,2-2,4-dichlorophenyl-ethanol PubChem CID: 2734099 IUPAC Name: 2-(2,4-dichlorophenyl)ethanol SMILES: C1=CC(=C(C=C1Cl)Cl)CCO
Ancymidol 98.0+%, TCI America™
CAS: 12771-68-5 Molecular Formula: C15H16N2O2 Molecular Weight (g/mol): 256.31 MDL Number: MFCD00072501 InChI Key: HUTDUHSNJYTCAR-UHFFFAOYNA-N Synonym: alpha-Cyclopropyl-alpha-(4-methoxyphenyl)-5-pyrimidinemethanol PubChem CID: 25572 ChEBI: CHEBI:73171 IUPAC Name: cyclopropyl(4-methoxyphenyl)(pyrimidin-5-yl)methanol SMILES: COC1=CC=C(C=C1)C(O)(C1CC1)C1=CN=CN=C1
Medchemexpress LLC Asiaticoside B | 125265-68-1 | 5 MG
Asiaticoside B is a 9,19-cycloartane triterpene glycoside found in Actaea asiatica. It exhibits cytotoxicity against HepG2 and MCF-7 cancer cells with IC50 values of 9.74 μM and 8.32 μM, respectively.
- Purity: 99.46%
- Molecular weight: 975.12
- Formula: C48H78O20
- Appearance: Solid
- Color: White to off-white
- Structure classification: Terpenoids, triterpenes
- Initial source: Plants (Compositae, Tagetes lucida Cav., Umbelliferae)
- Storage: 4°C, protect from light. In solvent: -80°C for 6 months; -20°C for 1 month (protect from light)
- Solubility (in vitro): DMSO: 100 mg/mL (102.55 mM; requires ultrasonic; hygroscopic DMSO has a significant impact on solubility, use newly opened DMSO)
Medchemexpress LLC Alfuzosin hydrochloride | 81403-68-1 | 99.7% | 5 MG
Alfuzosin hydrochloride (SL 77499-10) is an orally active, selective, and competitive α1-adrenoceptor antagonist. It relaxes the muscles of the prostate and bladder neck, aiding in urination, and can be used in the study of benign prostatic hyperplasia (BPH).
- Orally active, selective, and competitive α1-adrenoceptor antagonist.
- Relaxes the muscles of the prostate and bladder neck, aiding in urination.
- Used in the study of benign prostatic hyperplasia (BPH).
Medchemexpress LLC Lecozotan hydrochloride | 433282-68-9 | 98.7% | 520.02 | 5 MG
Lecozotan hydrochloride (SRA-333) hydrochloride is an orally active and selective antagonist of 5-HT1A with a Ki of 4.5 nM for cloned human 5-HT1A receptor. It enhances the stimulated release of glutamate and acetylcholine in the hippocampus and possesses cognitive-enhancing properties. This product has the potential for mild-to-moderate Alzheimer's disease (AD) research.
- Orally active and selective 5-HT1A antagonist.
- Enhances the release of glutamate and acetylcholine in the hippocampus.
- Possesses cognitive-enhancing properties.
- Potential for mild-to-moderate Alzheimer's disease research.
Medchemexpress LLC Indotecan hydrochloride | 1228035-68-4 | 99.8% | 514.95 | 5 MG
Indotecan hydrochloride, an indenoisoquinoline derivative, is a potent Topoisomerase I inhibitor. It prevents the relaxation of supercoiled DNA and can be used for the research of visceral leishmaniasis.
- Potent Topoisomerase I inhibitor.
- Can be used for the research of visceral leishmaniasis.
Medchemexpress LLC Prx-07034 hydrochloride | 903580-39-2 | 99.0% | C21H29Cl2N3O4S | 25 MG
PRX-07034 hydrochloride is a highly selective and potent 5-HT6 receptor antagonist with a Ki of 4-8 nM and IC50 of 19 nM. Intended for research on enhancing working memory and cognitive flexibility, it shows significant 5-HT6 receptor selectivity (>100-fold over 68 other GPCRs, ion channels, and transporters). It also inhibits 5-HT1A, 5-HT1B, 5-HT1D, Dopamine D3, Histamine H2, and Opioid μ receptors. In vivo studies in rats demonstrated enhanced delayed spontaneous alternation and improved cognitive strategy switching.
- Highly selective and potent 5-HT6 receptor antagonist
- Ki of 4-8 nM and IC50 of 19 nM for 5-HT6 receptor
- Enhances working memory and cognitive flexibility
- >100-fold selectivity over 68 other GPCRs, ion channels, and transporters
- Inhibits 5-HT1A, 5-HT1B, 5-HT1D, Dopamine D3, Histamine H2, and Opioid μ receptors