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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T29097 | VAS 3947 | VA-S3947,VA S3947,VAS3947 | Apoptosis , NADPH-oxidase |
VAS 3947 is a specific inhibitor of NADPH oxidase (NOX).VAS 3947 has a potent anti-platelet effect, inducing apoptosis through UPR activation, mainly due to protein aggregation and misfolding, independent of anti-NOX act... | |||
T4359 | VAS2870 | NADPH | |
VAS2870 is an inhibitor of NADPH oxidase (NOX). | |||
T69945 | MPT0L145 | ||
MPT0L145 is a first-in-class PIK3C3/FGFR inhibitor. | |||
T0229 | Rivastigmine | SDZ-ENA 713,S-Rivastigmine,Exelon | AChE |
Rivastigmine (Exelon) is a Cholinesterase Inhibitor, used for therapy of Alzheimer disease. | |||
T20765 | Atorvastatin | HMG-CoA Reductase , Autophagy | |
Atorvastatin is an orally active HMG-CoA reductase inhibitor that has the ability to effectively lower blood lipids by activating liver cytochrome p450 to accelerate metabolism. Atorvastatin inhibited proliferation and i... | |||
T12652 | (Rac)-5-Keto Fluvastatin | 5-Ketofluvastatin,3-Hydroxy-5-Keto Fluvastatin,rac 5-Keto Fluvastatin | Others |
(Rac)-5-Keto Fluvastatin (rac 5-Keto Fluvastatin) is an impurity of Fluvastatin which is an inhibitor of HMG-CoA reductase. | |||
T12490 | Pitavastatin lactone | Others | |
Pitavastatin lactone is a major Pitavastatin metabolite in humans. Pitavastatin is a potent competitive inhibitor of HMG-CoA reductase little metabolized in hepatic microsomes. | |||
T21405 | Fluvastatin | Canef,XU-62320,Vastin,Cranoc,Lescol | HMG-CoA Reductase |
Fluvastatin (XU-62320) is a potent and competitive HMG-CoA reductase inhibitor (IC50: 8 nM) that inhibits oxidative stress in vascular smooth muscle cells through an Nrf2-dependent pathway, and is used for the reduction ... | |||
T4551 | Acrivastine | Acrivastin,BW825C,Semprex | Histamine Receptor |
Acrivastine (Acrivastin) is a short-acting histamine 1 receptor antagonist. | |||
T3116 | Atorvastatin hemicalcium salt | Lipitor,Atorvastatin hemicalcium,Atorvastatin Calcium,CI-981,Sortis | Ferroptosis , HMG-CoA Reductase , Autophagy |
Atorvastatin hemicalcium salt (Atorvastatin Calcium), an effective HMG-CoA reductase inhibitor (IC50 = 8 nM), is utilized as a cholesterol-lowering medication. | |||
T1487 | Fluvastatin sodium | XU 62320 sodium,XU-62-320,Fluvastatin sodium salt | Ferroptosis , HMG-CoA Reductase , Autophagy |
Fluvastatin sodium (Fluvastatin sodium salt), a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), is a commonly used cholesterol lowering agent. | |||
T24865 | Tenivastatin | L-654969,L654969,Simvastatin acid,L 654969,Simvastatin hydroxy acid | ROS , HMG-CoA Reductase |
Tenivastatin (Simvastatin acid) is an anti-hyperlipidemic HMG-CoA reductase inhibitor that inhibits the production of reactive oxygen species (ROS) and can be used in the study of primary hyperlipidemia. | |||
T13131 | Tert-Buthyl Pitavastatin | HMG-CoA Reductase | |
tert-Buthyl Pitavastatin is Pitavastatin metabolite. Pitavastatin is a potent inhibitor of HMG-CoA reductase. | |||
T14342 | Atorvastatin lactone | HMG-CoA Reductase | |
Atorvastatin lactone is a prodrug form of atorvastatin. Which is an orally active 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitor. | |||
T2753 | Avasimibe | PD-148515,CI-1011 | P450 , Acyltransferase |
Avasimibe (PD-148515) is an orally bioavailable inhibitor of acyl-Coenzyme A: cholesterol acyltransferase (ACAT, IC50: 3.3 μM) that prevents cholesterol deposition in the arterial wall. It also inhibits human P450 isoenz... | |||
T5600 | Darovasertib | LXS196 | PKC |
Darovasertib (LXS196) is a potent, selective and orally active protein kinase C (PKC) inhibitor(IC50 values of 1.9 nM, 0.4 nM and 3.1 μM for PKCα, PKCθ and GSK3β, respectively). | |||
T25285 | Dalvastatin | RG-12561,RG 12561,RG12561 | HMG-CoA Reductase |
Dalvastatin (RG-12561) is an orally available inhibitor of HMG-CoA reductase and cholesterol-lowering synthesis.Dalvastatin competitively inhibits rat hepatic HMG-CoA reductase with an IC50 value of 3.4 nmol / l. Dalvast... | |||
T1510 | Rosuvastatin calcium | ZD 4522 Calcium,ZD4522,Rosuvastatin hemicalcium | Potassium Channel , HMG-CoA Reductase , Autophagy |
Rosuvastatin calcium (ZD4522) , a selective and competitive inhibitor of hepatic hydroxymethyl-glutaryl coenzyme A (HMG-CoA) reductase, has antilipidemic activity. | |||
T2534 | Pitavastatin calcium | P-872441,nisvastatin,itavastatin,Pitavastatin hemicalcium,NK-104 | Apoptosis , Mitophagy , Endogenous Metabolite , HMG-CoA Reductase , Autophagy |
Pitavastatin calcium (NK-104) is a potent inhibitor of HMG-CoA reductase (Ki: 1.7 nM). It lowers both total cholesterol and low-density lipoprotein cholesterol in animals and humans. Metabolism of pitavastatin by the cyt... | |||
T1628 | Rivastigmine tartrate | SDZ-ENA 713,ENA 713 | AChR , AChE |
Rivastigmine tartrate (SDZ-ENA 713) is a carbamate-derived reversible CHOLINESTERASE INHIBITOR that is selective for the CENTRAL NERVOUS SYSTEM and is used for the treatment of DEMENTIA in ALZHEIMER DISEASE and PARKINSON... | |||
T9857L | Vasopressin acetate | Vasopressin acetate (11000-17-2 Free base) | Endogenous Metabolite |
Vasopressin acetate, a cyclic nonapeptide, is synthesized centrally in the hypothalamus. Vasopressin acetate acts as a neurotransmitter, exerting its action by binding to specific G protein-coupled receptors. | |||
TP1400L | [Arg8]-Vasotocin acetate(113-80-4 free base) | Others | |
[Arg8]-Vasotocin acetate is a hormone present in the neurohypophysis of nonmammalian vertebrates that is related to vasopressin and oxytocin. | |||
T10324 | Anhydrosimvastatin | Dehydro simvastatin | HMG-CoA Reductase |
Anhydrosimvastatin (Dehydro simvastatin) is an impurity of Simvastatin. Simvastatin is an HMG-CoA reductase inhibitor. | |||
T9857 | Vasopressin | antidiuretic hormone (ADH),argipressin,arginine vasopressin (AVP) | Endogenous Metabolite |
Vasopressin (argipressin), a cyclic nine-peptide synthesized by hypothalamic neurons, is one of the hormones involved in peptide prohormone synthesis. Vasopressin is involved in the regulation process of hypothalamic-pit... | |||
T1676 | Rosuvastatin | ZD 4522 | Potassium Channel , HMG-CoA Reductase , Autophagy |
Rosuvastatin (ZD 4522) is an antilipemic agent that competitively inhibits hydroxymethyl-glutaryl-coenzyme A (HMG-CoA) reductase. HMG-CoA reductase catalyzes the conversion of HMG-CoA to mevalonic acid, the rate-limiting... | |||
T1920 | Capivasertib | AZD5363 | Akt , PKA , mTOR , Autophagy |
Capivasertib (AZD5363) is a broad-spectrum AKT inhibitor with inhibitory activity against Akt1, Akt2, and Akt3 (IC50=3/7/7 nM) with oral activity. Capivasertib has antitumor activity for the treatment of breast cancer. | |||
T20887 | Atorvastatin Sodium | Lipitor | LDL , Aquaporin , HMG-CoA Reductase |
Atorvastatin Sodium (Lipitor) is a competitive inhibitor of HMG-CoA reductase and increases the expression of low density lipoprotein (LDL) receptors on hepatocytes. Atorvastatin Sodium treatment inhibits aquaporin 4 to ... | |||
T25276 | Crilvastatin | PMD387,PMD 387,PMD-387 | HMG-CoA Reductase |
Crilvastatin (PMD 387) is a novel non-competitive hydroxymethylglutaryl coenzyme A reductase inhibitor with cholesterol-lowering activity that inhibits cholesterol uptake in rats with hereditary hypercholesterolemia. | |||
TQ0045 | 2-Hydroxy atorvastatin calcium salt | Drug Metabolite | |
2-Hydroxy atorvastatin calcium salt is a hydroxy metabolite of Atorvastatin calcium salt which is a potent HMG-CoA reductase inhibitor (IC50 = 8 nM). | |||
T38740 | Rivastigmine carbamate impurity | 3-Nitrophenyl ethyl(methyl)carbamate | |
Rivastigmine carbamate impurity (3-Nitrophenyl ethyl(methyl)carbamate) is a byproduct found in Rivastigmine, which is recognized as a powerful and orally active inhibitor of cholinesterase (ChE). Specifically, Rivastigmi... | |||
T10136 | 4-Acetylsimvastatin | Others | |
4-Acetylsimvastatin is acetylated simvastatin. Simvastatin is a competitive inhibitor of HMG-CoA reductase (Ki: 0.2 nM). | |||
T10129 | (3S,5R)-Fluvastatin sodium | (3S,5R)-XU 62-320 | Others |
(3S,5R)-Fluvastatin sodium is the (3S,5R)-enantiomer of Fluvastatin. Fluvastatin is a first fully synthetic, competitive HMG-CoA reductase inhibitor (IC50: 8 nM). Fluvastatin protects vascular smooth muscle cells against... | |||
T19551 | Rosuvastatin D6 Calcium | Others | |
Rosuvastatin D6 Calcium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
T12757 | Rosuvastatin D3 Sodium | Others | |
Rosuvastatin D3 Sodium is deuterium labeled Rosuvastatin, which is a competitive HMG-CoA reductase inhibitor(IC50 of 11 nM). | |||
T11306 | Fluvastatin D6 sodium | XU 62-320 (D6) | Others |
Fluvastatin sodium is a first fully synthetic, competitive HMG-CoA reductase inhibitor with an IC50 of 8 nM.Fluvastatin D6 sodium is deuterium labeled Fluvastatin sodium. | |||
T10132 | (3S,5S)-Pitavastatin calcium | Others | |
(3S,5S)-Pitavastatin calcium is the 3-epimer of Pitavastatin which is a potent HMG-CoA reductase inhibitor. | |||
T19918 | Lovastatin hydroxy acid sodium | 6-α-Methylcompactin sodium,Lovastatin Na,Lovastatin Sodium,Mevinolin sodium | |
Lovastatin Sodium is an HMG-CoA reductase inhibitor. | |||
T76509 | Desamino(D-3-(3′-pyridyl)-Ala2,Arg8)-Vasopressin | ||
Desamino(D-3-(3′-pyridyl)-Ala2,Arg8)-Vasopressin, a synthetic analog of vasopressin (AVP), acts as a weak agonist at the antidiuretic receptor but is a potent agonist at the pituitary corticotrope receptor [1]. | |||
T25902 | Ota-vasotocin | OVTA | |
Ota-vasotocin is a ligand utilized in quantitative receptor autoradiography for oxytocin receptors. | |||
T39036 | (3R,5S)-Fluvastatin | (3R,5S)-Fluvastatin,(3R,5S)-XU 62-320 free acid | |
(3R,5S)-Fluvastatin, the 3R,5S-isomer of Fluvastatin (XU 62-320 free acid), stands as the inaugural fully synthetic, competitive inhibitor of HMG-CoA reductase, exhibiting an IC50 value of 8 nM. It safeguards vascular sm... | |||
TP1400 | [Arg8]-Vasotocin | ||
[Arg8]-Vasotocin is a hormone present in the neurohypophysis of nonmammalian vertebrates that is related to vasopressin and oxytocin. | |||
T76510 | [Asu1,6-Arg8]Vasopressin | ||
[Asu1,6-Arg8]Vasopressin is a vasopressin agonist that enhances cyclic AMP accumulation and adrenocorticotropic hormone (ACTH) release triggered by corticotropin-releasing factor (CRF) in cultured rat anterior pituitary ... | |||
TP2136 | (d(CH2)51,Tyr(Me)2,Arg8)-Vasopressin | ||
Selective vasopressin V1A receptor antagonist. Inhibits vasopressin and oxytocin-induced increases in intracellular calcium concentrations in vitro (IC50 values are 5 and 30 nM respectively). Exhibits potent and prolonge... | |||
T83488 | [Lys8] Vasopressin Desglycinamide | ||
[Lys8] Vasopressin Desglycinamide, a vasopressin analog, supports the maintenance of active and passive avoidance behavior and aids in the facilitation of memory consolidation processes [1]. | |||
T76633 | (Phenylac1,D-Tyr(Et)2,Lys6,Arg8,des-Gly9)-Vasopressin | ||
(Phenylac1,D-Tyr(Et)2,Lys6,Arg8,des-Gly9)-Vasopressin, a potent vasopressin V1 receptor (VP V1R) antagonist, significantly lowers mean arterial pressure (MAP) in rats [1]. | |||
T37642 | Pravastatin lactone | ||
Pravastatin lactone is a metabolite of pravastatin , a hydroxymethylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor that is a ring-hydroxylated metabolite of mevastatin . Pravastatin lactone is formed when pravastatin ... | |||
T63430 | Rosuvastatin Sodium | ||
Rosuvastatin Sodium is a competitive HMG-CoA reductase (HMGCR) inhibitor (IC50: 11 nM) that effectively blocks hERG currents (IC50: 195 nM). Rosuvastatin Sodium reduces the expression of mature hERG and inhibits the inte... | |||
T38249 | 2-Hydroxy atorvastatin lactone | ||
2-Hydroxy atorvastatin lactone, a metabolite of Atorvastatin, is an orally active HMG-CoA reductase inhibitor that efficiently reduces blood lipids [1][2]. | |||
T69006 | Atorvastatin lysine | ||
Atorvastatin lysine is a selective and competitive HMGCR (HMG-CoA reductase) inhibitor. | |||
T68566 | Pitavastatin methyl ester | ||
Pitavastatin methyl ester is the methyl ester derivative of Pitavastatin -- a competitive inhibitor of HMG-CoA reductase and an anti-lipemic agent. |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T4960 | VASICINE | Anti-infection , AChR | |
Vasicine is oxytocic and abortifacient agents.Vasicine, a potential natural cholinesterase inhibitor, has been in development for treatment of Alzheimer's disease. Vasicine can regulate the inflammatory reaction, have gr... | |||
TC0039 | Vasicinone | Others | |
Vasicinone may act as a hepatoprotective agent. (±)-Vasicinone has significant antitussive, expectorant, and bronchodilating activities, which can be used to treat respiratory disease.(S)-Vasicinone exhibits antiprolifer... | |||
T8298 | Vasicine hydrochloride | Peganine hydrochloride | Antibacterial , Antibiotic |
Vasicine hydrochloride (Peganine hydrochloride) (peganine hydrochloride) is an alkaloid isolated from Justicia adhatoda. It possesses an anti-tuberculosis activity. | |||
T0672 | Pravastatin sodium | CS-514 Sodium,CS-514 (sodium) | Ferroptosis , HMG-CoA Reductase , Autophagy |
Pravastatin sodium (CS-514 (sodium)), an HMG-CoA reductase inhibitor, inhibits sterol synthesis with IC50 of 5.6 μM. | |||
T0687 | Simvastatin | MK-0733,MK 733 | Apoptosis , Mitophagy , Ferroptosis , HMG-CoA Reductase , Autophagy |
Simvastatin (MK 733) is an HMG-CoA reductase inhibitor (Ki=0.2 nM) with oral activity. Simvastatin has hypolipidemic activity, inhibits hepatic production of cholesterol, and is also used for the prevention of cardiovasc... | |||
T0683 | Mevastatin | Compactin,ML236B | Apoptosis , Antibacterial , Antibiotic , HMG-CoA Reductase , Autophagy , Lipid |
Mevastatin (ML236B) is an HMG-CoA reductase inhibitor that was initially isolated from the mold Pythium ultimum. Mevastatin was the first statin to enter clinical trials. | |||
T1207 | Lovastatin | MK-803,Mevinolin | Ferroptosis , HMG-CoA Reductase , Autophagy |
Lovastatin (MK-803) is an HMG-CoA Reductase Inhibitor, used for lowering cholesterol. | |||
T12681 | (±)-Vasicine | (±)-Peganine | Others |
(±)-Vasicine is the racemate of Vasicine. Vasicine isolated from Peganum harmala seeds, with anti-ulcer activity. | |||
TN1570 | Deoxyvasicinone | Others | |
Deoxyvasicinone derivatives can be considered as promising lead molecules for the development of more potent inhibitors of NEDD8-activating enzyme. | |||
T16885 | Simvastatin acid ammonium | Tenivastatin ammonium | Others |
Simvastatin ammonium is an active metabolite of simvastatin lactone mediated. Simvastatin ammonium reduces indoxyl sulfate-mediated reactive oxygen species and modulates OATP3A1 expression in cardiomyocytes and HEK293 ce... | |||
TN5222 | Vasicinol | Others | |
Vasicinol shows a high sucrase inhibitory activity, and the IC50 values was 250 μM.vasicinol could be an useful treatment for metabolic disorders.Vasicinol and vasicinone severe antifertility effects are exhibited by vas... | |||
TN5223 | Vasicinolone | Antifection | |
Vasicinolone has anti-inflammatory, and antimicrobial activities. |
Cat No. | Product Name | Species | Expression System |
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TMPK-00823 | VEGF165 Protein, Human, Recombinant (His & Avi) | Human | HEK293 |
Vascular endothelial growth factor (VEGF or VEGF-A), also known as vascular permeability factor (VPF), is a potent mediator of both angiogenesis and vasculogenesis in the fetus and adult. VEGF165 appears to be the most a... | |||
TMPK-00826 | VEGF121 Protein, Human, Recombinant (His & Avi), Biotinylated | Human | HEK293 |
Vascular endothelial growth factor (VEGF or VEGF-A), also known as vascular permeability factor (VPF), is a potent mediator of both angiogenesis and vasculogenesis in the fetus and adult. VEGF165 appears to be the most a... | |||
TMPK-00825 | VEGF121 Protein, Human, Recombinant (His & Avi) | Human | HEK293 |
Vascular endothelial growth factor (VEGF or VEGF-A), also known as vascular permeability factor (VPF), is a potent mediator of both angiogenesis and vasculogenesis in the fetus and adult. VEGF165 appears to be the most a... | |||
TMPK-00822 | VEGF165 Protein, Human, Recombinant (His & Avi), FITC-Labeled | Human | HEK293 |
Vascular endothelial growth factor (VEGF or VEGF-A), also known as vascular permeability factor (VPF), is a potent mediator of both angiogenesis and vasculogenesis in the fetus and adult. VEGF165 appears to be the most a... | |||
TMPY-03058 | SLITL2/VASN Protein, Human, Recombinant (His) | Human | HEK293 |
Vasorin is a typical type I membrane protein. It contains 1 EGF-like domain, 1 fibronectin type-III domain, 10 LRR (leucine-rich) repeats, 1 LRRCT domain and 1 LRRNT domain. Vasorin is predominantly expressed in vascular... | |||
TMPH-00028 | Adeno-associated virus 2 (isolate Srivastava/1982) Rep78 Protein (His & MBP) | AAV-2 | E. coli |
Plays an essential role in the initiation of viral DNA synthesis. Binds specifically to an inverted terminal repeat element (ITR) on the 3' and 5' ends of the viral DNA, where it cleaves a site specifically to generate a... | |||
TMPH-02263 | VASH1 Protein, Human, Recombinant (His) | Human | E. coli |
Tyrosine carboxypeptidase that removes the C-terminal tyrosine residue of alpha-tubulin, thereby regulating microtubule dynamics and function. Critical for spindle function and accurate chromosome segregation during mito... | |||
TMPH-03716 | Invasin Protein, Yersinia enterocolitica, Recombinant (His & SUMO) | Yersinia enterocolitica | E. coli |
Invasin is a protein that allows enteric bacteria to penetrate cultured mammalian cells. The entry of invasin in the cell is mediated by binding several beta-1 chain integrins. | |||
TMPH-02304 | Vasohibin-2/VASH2 Protein, Human, Recombinant (His & SUMO) | Human | E. coli |
Tyrosine carboxypeptidase that removes the C-terminal tyrosine residue of alpha-tubulin, thereby regulating microtubule dynamics and function. Critical for spindle function and accurate chromosome segregation during mito... | |||
TMPH-02303 | Vasculin Protein, Human, Recombinant (His & SUMO) | Human | E. coli |
Functions as a GC-rich promoter-specific transactivating transcription factor. | |||
TMPJ-00572 | Vasorin Protein, Human, Recombinant (His) | Human | Human Cells |
Vasorin is a Type I membrane protein, which is predominantly expressed in vascular smooth muscle cells in a developmentally regulated pattern. The expression level of Vasorin can be down regulated during vessel repair af... |
Cat No. | Product Name | ||
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L5400 | Anti-Cardiovascular Disease Compound Library | 1408 compounds | |
A unique collection of 1408 cardiovascular diseases related compounds for high throughput screening (HTS) and high content screening (HCS); |