Organoheterocyclic compounds
2-Phenylthiophene 95.0+%, TCI America™
CAS: 825-55-8 Molecular Formula: C10H8S Molecular Weight (g/mol): 160.234 MDL Number: MFCD00130080 InChI Key: PJRGDKFLFAYRBV-UHFFFAOYSA-N Synonym: thiophene, 2-phenyl,2-phenyl-thiophene,phenylthiophene,thiophene, phenyl,2-thienylbenzene,2-phenyithiophene,2-phenylthiofuran,2-phenylthiophene,acmc-209ppe PubChem CID: 69999 IUPAC Name: 2-phenylthiophene SMILES: C1=CC=C(C=C1)C2=CC=CS2
Atropine 99.0+%, TCI America™
CAS: 51-55-8 Molecular Formula: C17H23NO3 Molecular Weight (g/mol): 289.375 MDL Number: MFCD00022622 InChI Key: RKUNBYITZUJHSG-PJPHBNEVSA-N Synonym: r-atropine,+-atropine,+-hyoscyamine,hyoscyamine,tropan-3alpha-yl 2r-3-hydroxy-2-phenylpropanoate,3-endo-8-methyl-8-azabicyclo 3.2.1 oct-3-yl 2r-3-hydroxy-2-phenylpropanoate,atropine sulfate,unii-v3203si72m,1s,5r-8-methyl-8-azabicyclo 3.2.1 octan-3-yl 2r-3-hydroxy-2-phenylpropanoate,prestwick0_000233 PubChem CID: 174174 IUPAC Name: [(1R,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate SMILES: CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3
2-Isopropyl-4-(N-methylaminomethyl)thiazole Dihydrochloride 98.0+%, TCI America™
CAS: 1185167-55-8 Molecular Formula: C8H16Cl2N2S Molecular Weight (g/mol): 243.19 MDL Number: MFCD11841218 InChI Key: GNPOLJYMEXUGCG-UHFFFAOYSA-N PubChem CID: 45595264 IUPAC Name: N-methyl-1-(2-propan-2-yl-1,3-thiazol-4-yl)methanamine;dihydrochloride SMILES: CC(C)C1=NC(=CS1)CNC.Cl.Cl
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)aniline 98.0+%, TCI America™
CAS: 191171-55-8 Molecular Formula: C12H18BNO2 Molecular Weight (g/mol): 219.09 MDL Number: MFCD02179448 InChI Key: ZCJRWQDZPIIYLM-UHFFFAOYSA-N Synonym: 2-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl aniline,2-aminophenylboronic acid pinacol ester,2-aminophenylboronic acid, pinacol ester,2-aminophenylboronicacidpinacolester,2-aminophenylboronic acid pinacol cyclic ester,2-aminobenzeneboronic acid pinacol ester,2-aminophenyl boronic acid pinacol ester,2-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl benzenamine,2-tetramethyl-1,3,2-dioxaborolan-2-yl aniline,benzenamine, 2-4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl PubChem CID: 2734652 IUPAC Name: 2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline SMILES: CC1(C)OB(OC1(C)C)C1=CC=CC=C1N
Medchemexpress LLC Sophoranone | 23057-55-8 | 5 MG
Sophoranone is a flavonoid compound that can be isolated from the root of *Sophora subprostrata*. It exhibits anti-inflammatory activity in mouse RAW264.7 cells by inhibiting LPS-induced NO production.
- Flavonoid compound
- Isolated from the root of Sophora subprostrata
- Exhibits anti-inflammatory activity
- Molecular weight: 460.60
- Formula: C30H36O4
- Appearance: White to off-white solid
- Purity: 99.67%
- Soluble in DMSO (100 mg/mL)
Medchemexpress LLC ZB-R-55 | 2416593-55-8 | 99.4% | 441.48 | 1 MG
ZB-R-55 is an orally active RIPK1 inhibitor that can be used for sepsis study. It demonstrates anti-necroptotic activity in human U-937 cells, inhibiting LPS/Z-VAD-fmk induced necroptosis with an IC50 of 0.34 nM.
- Orally active RIPK1 inhibitor.
- Applicable for sepsis studies.
- Exhibits anti-necroptotic activity.
Apexbio Technology LLC Quinapril HCl 82586-55-8 50mg
Quinapril hydrochloride (CAS 82586-55-8) is an esterified precursor that undergoes hepatic conversion to quinaprilat an active inhibitor of angiotensin-converting enzyme (ACE) By impeding the conversion of angiotensin I to angiotensin II quinapril modulates the renin-angiotensin-aldosterone system resulting in decreased vasoconstriction and reduced aldosterone secretion This molecule is frequently utilized in cardiovascular research to investigate mechanisms underlying hypertension heart failure and the biological effects of ACE inhibition on vascular and renal systems
Apexbio Technology LLC Levothyroxine sodium 55-03-8 100mg
Levothyroxine sodium (55-03-8) is a synthetic thyroid hormone analogue It is designed to restore or modulate thyroid hormone levels thereby regulating metabolic and developmental processes Levothyroxine sodium exerts its biological activity primarily through enzymatic conversion to the active form triiodothyronine (T3) by deiodinases after which T3 interacts with nuclear thyroid hormone receptors to modulate gene expression and cellular metabolism Based on these pharmacological properties levothyroxine sodium holds research potential in studies of thyroid dysfunction particularly hypothyroidism and in investigations of thyroid-regulated physiological responses and endocrine interactions
Medchemexpress LLC PCS1055 | 357173-55-8 | 98.0% | 5 MG
PCS1055 is a selective and competitive antagonist of the muscarinic M4 receptor (mAChR4) with low-nanomolar potency and additional cholinesterase inhibitory activity. It is intended for research use in receptor pharmacology and enzymology studies.
- Selective mAChR4 antagonist with IC50 18.1 nM.
- High affinity in radioligand binding (Ki 6.5 nM; Kd 5.72 nM).
- Cholinesterase inhibitor activity (electric eel AChE IC50 22 nM; human AChE IC50 120 nM).
- Molecular formula C27H32N4; molecular weight 412.57 g/mol.
- Supplied in small research quantities with recommended storage conditions for powder and solutions.
Medchemexpress LLC Hydroquinidine | 1435-55-8 | 100.0% | 25 G
Hydroquinidine, also known as Dihydroquinidine, is a potent ion channel blocker with demonstrated anti-cancer activity against colon, pancreatic, and hepatocellular cancer cells. It is also known to prolong the QT interval and exhibit antiarrhythmic efficacy.
- Potent ion channel blocker
- Demonstrates strong anti-cancer activity on colon, pancreatic, and hepatocellular cancer cells
- Prolongs the QT interval
- Exhibits antiarrhythmic efficacy
- Molecular formula: C20H26N2O2
- Molecular weight: 326.44
- Appearance: White to off-white solid
- For research use only
Medchemexpress LLC Atropine | 51-55-8 | 99.85% | 500 MG
Atropine is a competitive antagonist of muscarinic acetylcholine receptors (mAChR), demonstrating IC50 values of 0.39 and 0.71 nM for human mAChR M4 and chicken mAChR M4, respectively. It works by inhibiting acetylcholine-induced relaxations in human pulmonary veins.
- Acts as a competitive muscarinic acetylcholine receptor antagonist.
- Inhibits acetylcholine-induced relaxations in human pulmonary veins.
- Can be used for research related to anti-myopia.
- Can be used for research related to bradycardia.
Medchemexpress LLC Hydroquinidine | 1435-55-8 | 99.9% | 1 ML
Hydroquinidine (Dihydroquinidine) is a potent ion channel blocker that demonstrates strong anti-cancer activity against colon, pancreatic, and hepatocellular cancer cells. It also prolongs the QT interval and possesses antiarrhythmic efficacy.
- Potent ion channel blocker
- Exhibits strong anti-cancer activity on colon, pancreatic, and hepatocellular cancer cells
- Prolongs the QT interval
- Possesses antiarrhythmic efficacy
- For research use only
Medchemexpress LLC Interiorin | 119139-55-8 | 482.52 | 1 MG
Interiorin is a chemical compound isolated from Kadsura heteroclita, known for its moderate anti-HIV activity. This product is intended for research use by qualified scientists in appropriately equipped and authorized facilities. The information provided is based on current knowledge, but the chemical, physical, and toxicological properties have not been completely investigated. The burden of safe use of this material rests entirely with the user.
- Isolated from Kadsura heteroclita
- Exhibits moderate anti-HIV activity with an EC50 value of 1.6 μg/mL
- Intended for research use only
- Requires handling by suitably qualified and experienced scientists
Medchemexpress LLC Atropine | 51-55-8 | 99.9% | 1 ML
Atropine (Tropine tropate) is a competitive muscarinic acetylcholine receptor (mAChR) antagonist. It inhibits ACh-induced relaxations in human pulmonary veins and can be used for research on anti-myopia and bradycardia.
- Competitive muscarinic acetylcholine receptor (mAChR) antagonist.
- IC50 values of 0.39 and 0.71 nM for human mAChR M4 and chicken mAChR M4.
- Inhibits ACh-induced relaxations in human pulmonary veins.
- Used for research of anti-myopia and bradycardia.
Apexbio Technology LLC Levothyroxine sodium 55-03-8 25mg
Levothyroxine sodium (55-03-8) is a synthetic thyroid hormone analogue It is designed to restore or modulate thyroid hormone levels thereby regulating metabolic and developmental processes Levothyroxine sodium exerts its biological activity primarily through enzymatic conversion to the active form triiodothyronine (T3) by deiodinases after which T3 interacts with nuclear thyroid hormone receptors to modulate gene expression and cellular metabolism Based on these pharmacological properties levothyroxine sodium holds research potential in studies of thyroid dysfunction particularly hypothyroidism and in investigations of thyroid-regulated physiological responses and endocrine interactions