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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T2118 | SC-514 | GK 01140 | IκB/IKK , p38 MAPK , Serine Protease , CDK , Aurora Kinase |
SC-514 (GK 01140) is a selective, orally active, ATP-competitive IKK-2 inhibitor (IC50=11.2±4.7 μM), obstructs NF-κB-dependent gene expression. | |||
T13780 | MS1943 | Apoptosis , Histone Methyltransferase | |
MS1943 is a orally bioavailable EZH2 selective degrader(IC50 of 120 nM). | |||
T1905 | EPZ005687 | Histone Methyltransferase | |
EPZ005687 is a potent and selective inhibitor of EZH2. | |||
T13189 | TP-10 | PDE | |
TP-10 is a selective inhibitor of PDE10A against other PDEs with IC50 of 0.8 nM. | |||
T28367L | (R)-PF-04822163 | Others | |
(R)-PF-04822163 is a biochemical reagent that can be used to synthesize other compounds. | |||
T50058 | 1-(cyclohexylmethyl)guanidine hydroiodide | Others | |
1-(cyclohexylmethyl)guanidine hydroiodide is a guanidine derivative that has been used as a reagent in the synthesis of a variety of compounds, including peptides, peptoids, and other bioactive molecules, and as a cataly... | |||
T12115 | MSC2360844 | PI3K | |
MSC2360844 is a potent, orally active and selective inhibitor of PI3Kδ(IC50 of 145 nM). | |||
T77744 | Maleic acid disodium salt | Others | |
Maleic acid disodium salt is a pharmaceutical intermediate used in the synthesis of other active compounds. | |||
T5432 | Eganelisib | IPI-549 | PI3K |
Eganelisib (IPI-549) is an inhibitor of PI3Kγ (IC50 = 16, 3,200, 3,500, and >8,400 nM for PI3Kγ, PI3Kα, PI3Kβ, and PI3Kδ, respectively) | |||
T7420 | Valifenalate | Valiphenal,IR5885 | Antibacterial |
Valifenalate (IR5885) is antifungal agent, effective against various types of mildew | |||
T9152 | 2-(2-Hydroxyphenyl)-1H-benzimidazole | Others | |
2-(2-Hydroxyphenyl)-1H-benzimidazole has been used as a catalyst for the synthesis of polymers and other materials. | |||
T9357 | Ro 5212773 | Epptb | Others |
Ro 5212773 (Epptb) is a selective TAAR1 antagonist. | |||
T7160 | Lofexidine | Adrenergic Receptor | |
Lofexidine is a selective α2-receptor agonist, Lofexidine reduces narcotic withdrawal symptoms. | |||
T2430 | HPOB | Apoptosis , HDAC | |
HPOB is an effective and specific HDAC6 inhibitor (IC50: 56 nM), >30-fold selectivity over other HDACs. | |||
T4296 | MTX-211 | MTX 211 | EGFR , PI3K |
MTX-211, an inhibitor of EGFR and PI3K, is used for the therapy of cancer and other diseases. | |||
T8370 | GSK5182 | Estrogen Receptor/ERR , Estrogen/progestogen Receptor , Reactive Oxygen Species | |
GSK5182 is a highly selective inverse estrogen-related receptor γ agonist (IC50 : 79 nM) | |||
T9446 | KB-0742 dihydrochloride | CDK | |
KB-0742 dihydrochloride is a potent, selective and orally inhibitor of CDK9. | |||
TNU1431 | (S)-GNA-T-phosphoramidite | Nucleoside Antimetabolite/Analog | |
(S)-GNA-T-phosphoramidite is a nucleoside analog commonly used in the synthesis of other active compounds. | |||
T76766 | Mirvetuximab | M9346A | Antifolate |
Mirvetuximab (M9346A) is a novel folate receptor α (FRα) monoclonal antibody targeting anti-FOLR1 (folate receptor 1). Mirvetuximab soravtansine is often conjugated with platinum compounds or other compounds to form anti... | |||
T17159 | Treosulfan | NSC 39069,Treosulphan | DNA Alkylator/Crosslinker , DNA Alkylation |
Treosulfan (Treosulphan) is a bifunctional alkylating agent. It also has activity in ovarian cancer and other solid tumor types. | |||
T6082 | SSR128129E | SSR | FGFR |
SSR128129E (SSR) is an allosteric and orally-active FGFR1 inhibitor (IC50: 1.9 μM), but not affecting other related RTKs. | |||
T8310 | MMP-9-IN-1 | MMP | |
MMP-9-IN-1 is an inhibitor of specific matrix metalloproteinase-9 (MMP-9). | |||
T3995 | Amcasertib | BBI503 | Stemness kinase |
Amcasertib (BBI503) is an orally administered investigational agent designed to inhibit cancer stem cell pathways via targeting stemness kinases. | |||
T1440 | Ethacridine lactate monohydrate | Antibacterial , Antibiotic | |
Ethacridine lactate hydrate is a topically applied anti-infective agent. | |||
T77602 | WAY-324208 | Antifungal | |
WAY-324208 shows antifungal properties against S. dermatitidis (skin-infecting fungi), with activity against other fungi to be explored. | |||
T5533 | MC180295 | (rel)-MC180295 | CDK |
MC180295 ((rel)-MC180295) is a novel potent, highly selective CDK9 inhibitor (IC50: 5 nM), displays >22-fold selectivity over other CDKs. | |||
T13823 | Polyvinylpyrrolidone | PVP,Povidone,Polyvidone | Others |
Polyvinylpyrrolidone (Polyvidone) used in human and veterinary medicine as an effective wound healing accelerator. | |||
T5092 | AIM-100 | AIM100 | ACK |
AIM-100 is a Ack1 inhibitor (IC50: 24 nM). | |||
T67967 | EOB-DTPA | N-((2s)-2-(bis(carboxymethyl)amino)-3-(4-ethoxyphenyl)propyl)-n-(2-(bis(carboxymethyl)amino)ethyl)glycine | Others |
EOB-DTPA is a biochemical reagent that can be synthesized from other compounds and is commonly used in MRI. | |||
T6161 | Tubastatin A Hydrochloride | TSA HCl,Tubastatin A HCl | Apoptosis , HDAC , Autophagy |
Tubastatin A Hydrochloride (TSA HCl) is an effective and specific HDAC6 inhibitor (IC50: 15 nM). It has selectivity (>1000-fold) against all other isozymes except HDAC8 (>57-fold). | |||
T2452 | C646 | Apoptosis , Epigenetic Reader Domain , Histone Acetyltransferase , Autophagy | |
C646, a histone acetyltransferase inhibitor, inhibits p300 (Ki: 400 nM, in a cell-free assay). | |||
T5967 | Ethacridine lactate | Acrinol,6,9-DIAMINO-2-ETHOXYACRIDINE LACTATE | Others , Antibacterial |
Ethacridine lactate (Acrinol) is a poly(ADP-ribose) glycohydrolase (PARG) inhibitor. | |||
T1819 | Nexturastat A | HDAC | |
Nexturastat A is an effective and specific HDAC6 inhibitor (IC50: 5 nM). Its selectivity is >190-fold than other HDACs. | |||
T13951 | UCB-9260 | TNF | |
UCB-9260 inhibits TNF signaling by stabilizing an asymmetric form of the trimer. | |||
T16725 | RCM-1 | Others | |
RCM-1 is an inhibitor of FOXM1. | |||
T1841 | UNC0379 | Histone Methyltransferase | |
UNC0379 is a selective, substrate-competitive inhibitor of the lysine methyltransferase SETD8. | |||
T0684 | Ribavirin | Tribavirin,ICN-1229,NSC-163039,RTCA | Dehydrogenase , HCV Protease , DNA/RNA Synthesis , Antibiotic , AChR , RSV |
Ribavirin (Tribavirin) is a synthetic nucleoside analog of ribofuranose with activity against hepatitis C virus and other RNA viruses. | |||
T60196 | IHMT-PI3Kδ-372 S-isomer | PI3K | |
IHMT-PI3Kδ-372 S-isomer is a potent and selective PI3Kδ inhibitor with an IC50 of 14 nM. IHMT-PI3Kδ-372 S-isomer shows high selectivity over other class I PI3Ks (56∼83 fold) and other protein kinases. IHMT-PI3Kδ-372 can ... | |||
T33581 | Nafetolol | K 5407,K-5407 | Others |
Nafetolol (K 5407) is a biochemical reagent that can be used to synthesize other compounds. | |||
T77351 | Tert-Butyl5-bromo-1H-indole-1-carboxylate | N-Boc-5-bromoindole | |
Tert-Butyl5-bromo-1H-indole-1-carboxylate (N-Boc-5-bromoindole) is an indole derivative with therapeutic potential for pain, inflammation, and other conditions. | |||
T4504 | Triclocarban | Solubacter,Cutisan,Procutene,3,4,4′-Trichlorocarbanilide | Antibacterial |
Triclocarban (Cutisan), an antimicrobial agent, is used in personal cleaning products. | |||
T8916 | WEE1-IN-3 | JUN76288 | Wee1 |
WEE1-IN-3 (JUN76288) is a potent Wee1 kinase inhibitor with an IC50 of <10 nM. It treatment of cancer and other proliferative diseases. | |||
T8708 | Paroxetine | Serotonin Transporter | |
Paroxetine is a inhibitor of serotonin uptake that is effective in the treatment of depression. | |||
T69753 | HDAC6 degrader 9c | HDAC | |
HDAC6 degrader 9c is a small molecule histone deacetylase 6 (HDAC6) degrader that can be used to study cancer or other diseases. | |||
T7653 | JNJ 303 | Potassium Channel | |
JNJ 303 is a potent blocker of IKs (IC50 : 64 nM). | |||
T21965 | MBCQ | PDE | |
MBCQ is an inhibitor of cGMP-specific phosphodiesterase PDE5. | |||
T9082 | 1,3-Benzoxazole-6-carboxylic acid | Others | |
1,3-Benzoxazole-6-carboxylic acid is used as a catalyst in drug synthesis, and a building block in the synthesis of other compounds. | |||
T19724 | 5NAA | 5-NAA,5 NAA | Others |
5NAA is a molecule secreted by Streptomyces scabies and is a raw material for the synthesis of dyes and other nitroaromatic compounds. | |||
T4393 | MS049 2HCl (1502816-23-0(free base)) | Histone Methyltransferase | |
MS049 is a potent and selective inhibitor of PRMT4 (IC50 = 34 nM) and PRMT6 (IC50 = 43 nM). It is less active against additional type I PRMTs (IC50s = >130, >220, and 1.6 μM for PRMT1, PRMT3, and PRMT8, respectively) and... | |||
T1745 | Balipodect | TAK063,TAK-063,TAK 063 | PDE |
Balipodect (TAK063) is a highly effective and selective PDE10A inhibitor (IC50: 0.30 nM); Its selectivity is >15000-fold over other PDEs. |
Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T8011 | 1,2-dioleoyl-sn-glycero-3-phosphocholine | DOPC | Others |
1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) is a phospholipid containing the unsaturated long-chain (18:1) oleic acid inserted at the sn-1 and sn-2 positions. | |||
TQ0160 | Hydrastine | (-)-β-Hydrastine,(1R,9S)-β-Hydrastine | Others |
Hydrastine ((-)-β-Hydrastine) is a natural alkaloid that is present in Hydrastis Canadensis. | |||
T19231 | Cellulase | Others | |
Cellulase is an enzyme that catalyzes the hydrolysis of certain linkages in cellulose. | |||
T6377 | Aloperine | Apoptosis , Virus Protease , HIV Protease , Antibiotic , Autophagy | |
Aloperine exhibits anti-inflammatory, antibacterial, antiviral, and anti-tumor properties. | |||
TN7027 | Benzoylalbiflorin | Paeonivayin | Others |
Benzoylalbiflorin (Paeonivayin) is a monoterpenoid isolated from Radix Paeoniae Alba. | |||
T7977 | Benzofuroxan | Others | |
Benzofuroxan is used as a starting material for the synthesis of other compounds, such as drugs and other chemicals; it is also used in the synthesis of polymers; it is also used in the synthesis of fluorescent dyes and ... | |||
TN7223 | 3,5-Dibromo-4-methoxybenzoic acid | Others | |
3,5-Dibromo-4-methoxybenzoic acid was isolated from the Malagasy sponge Amphimedon sp. | |||
TN1582 | Compound TN1582(SC) | Antiviral | |
Dihydromollugin is a naphthol ester found in Rubia cordifolia that may have anti-tumour, virus-inhibiting and other activities. | |||
TJS1159 | Chrysosplenetin | Chrysosptertin B | P450 , Ferroptosis , P-gp |
Chrysosplenetin is a metabolic inhibitor of artemisinin. | |||
T12095 | Monomethyl fumarate | GPR , Drug Metabolite | |
Monomethyl fumarate is a potent agonist of GPR109A . | |||
TN6786 | O-Desmethyl Galanthamine | Sanguinine | AChE |
O-Desmethyl Galanthamine (Sanguinine) is galanthamine-type alkaloid and it is an acetylcholinesterase (AChE) inhibitor, with an IC50 1.83 μM. | |||
T6S0535 | Pinoresinol diglucoside | Pinoresinol Diglucopyranoside | Glucosidase |
1. Pinoresinol diglucoside (Pinoresinol Diglucopyranoside) is a putative α-glucosidase inhibiting compound. 2. Pinoresinol diglucoside is a important antihypertensive compound. | |||
T13854 | Quininic acid | NMDAR | |
Quinic acid is an organic acid extracted from the bark of Eucalyptus, Cinchona and other plants in the Asteraceae family. | |||
T66911 | 1,3-Dimethoxybenzene | Resorcinol dimethyl ether | Others |
1,3-Dimethoxybenzene (Resorcinol dimethyl ether) is a dimethoxybenzene analog from German hazelnuts that is an intermediate in the synthesis of other compounds. | |||
T8083 | Pyridoxal 5'-phosphate monohydrate | Pyridoxal phosphate monohydrate,Pyridoxal 5-phosphate monohydrate | Others |
Pyridoxal 5'-phosphate monohydrate is an active vitamin B6 metabolite | |||
TN1333 | 7-O-Methylbiochanin A | 4',7-Dimethoxy-5-hydroxyisoflavone | |
7-O-Methylbiochanin A (4',7-Dimethoxy-5-hydroxyisoflavone) is an isoflavone derivative that can be isolated from the roots of Lotus polyphyllos and other plants of the water lily family. | |||
T5542 | Tiglic acid | Sabadillic acid,Tiglinic acid,Cevadic acid | Endogenous Metabolite , HSV |
Tiglic acid (Cevadic acid) is a thick, syrupy poisonous liquid, C5H8O2, derived from croton oil, having a spicy odor and used in making perfumes and flavoring agents | |||
T2140 | Parthenolide | (-)-Parthenolide | Apoptosis , Mitophagy , NF-κB , HDAC , Autophagy |
(-)-Parthenolide ((-)-Parthenolide), an inhibitor of the Nuclear Factor-κB Pathway, also promotes the ubiquitination of MDM2 and activates p53 cellular functions. | |||
T7933 | D(+)-LACTIDE | Others | |
D(+)-LACTIDE is a cyclic dimer of acetone used in the synthesis of a variety of drugs and other compounds, as well as in biochemical and physiological studies. | |||
TQ0211 | Brusatol | (+)-Brusatol,NSC 172924 | Others , Ferroptosis , Nrf2 |
Brusatol (NSC-172924) is a natural product isolated from the Brucea javanica plant. It inhibits Nrf2. | |||
T36390 | Sodium oleate | Oleic acid sodium salt,Sodium oleate,cis-9-Octadecenoic acid sodium salt | ATPase |
Sodium oleate (cis-9-Octadecenoic acid sodium salt) (Oleic acid sodium) is an abundant monounsaturated fatty acid sodium. Sodium oleate is a Na+/K+ ATPase activator. | |||
T6S1538 | Neochlorogenic acid | trans-5-O-Caffeoylquinic acid,Neochlorogenate,5-O-Caffeoylquinic acid | TNF , NF-κB , COX , Antibacterial , Interleukin |
Neochlorogenic acid (trans-5-O-Caffeoylquinic acid) is an antioxidant compound used in the treatment of oxidative stress and related afflictions. | |||
T8022 | Methyl 2-furoate | Methyl furan-2-carboxylate | Others , Endogenous Metabolite |
Methyl 2-furoate (Methyl furan-2-carboxylate) is a natural product that found in cocoa and cocoa products | |||
TN1150 | Procyanidin B3 | Histone Acetyltransferase | |
Procyanidin B3(B3) is a procyanidin dimer that is widely studied due to its high abundance in the human diet and antioxidant activity. | |||
T0833 | Benzoic acid | Dracylic acid,FEMA 2131 | Others , Endogenous Metabolite , Antibacterial , Antifungal |
Benzoic acid (Dracylic acid) is a fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid. | |||
TN1725 | Hederacolchiside E | Beta Amyloid , ROS | |
Hederacolchiside E has antioxidant activity and shows neuroprotective effects in Alzheimer's disease (AD) models via modulating oxidative stress. Hederacolchiside E exhibits inhibition on lipid peroxidation of linoleic a... | |||
T9675 | α-Tocotrienol | Endogenous Metabolite | |
D-ALPHA-TOCOTRIENOL, an isoform of vitamin E, is found in vegetables, fruits, seeds, grains, oils and nuts. | |||
T22911 | β-N-methylamino-L-alanine hydrochloride | L-BMAA hydrochloride | Others |
β-N-methylamino-L-alanine hydrochloride (L-BMAA hydrochloride) is a neurotoxin produced by cyanobacteria. L-BMAA hydrochloride could cause amyotrophic lateral sclerosis (ALS) and possibly other neurodegenerative diseases... | |||
T14046 | Anandamide | (5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide | Cannabinoid Receptor , Endogenous Metabolite |
Anandamide ((5Z,8Z,11Z,14Z)-N-(2-Hydroxyethyl)icosa-5,8,11,14-tetraenamide), an immune modulator, acts via not only cannabinoid receptors (CB1 and CB2) but also other targets (e.g., GPR18/GPR55) in the central nervous sy... | |||
T2S0164 | Ethyl palmitate | Palmitic acid ethyl ester,Ethyl cetylate,Ethyl hexadecanoate | Others |
Ethyl palmate (palmitic acid ethyl ester) is a type of fatty acid ethyl ester (FAEE). After human subjects consumed alcohol, its synthesis was higher than other FAEEs. It can be used as a hair and skin conditioner. | |||
T0744 | 10-Undecenoic acid zinc salt | Zinc diundec-10-enoate,Zinc 10-undecenoate,Zinc undecylenate | Antibiotic , Antifungal |
10-Undecenoic acid zinc salt (Zinc undecylenate), a synthetic or natural fungistatic fatty acid, is used topically in creams against eczemas, fungal infections, ringworm, and other cutaneous conditions. The zinc offers a... | |||
T7916 | 4-Acetamidobenzenesulfonyl azide | Others | |
4-Acetamidobenzenesulfonyl azide is used in a variety of scientific research applications, including the synthesis of drugs, peptides and other biologically active molecules. It is also used as a catalyst in polymerizati... | |||
T5592 | Acetosyringone | Acetosyringenin | Others |
Acetosyringone (Acetosyringenin)(AS) is a phenol secreted by wounded plant tissues.Acetosyringone is a phenolic natural product with analgesic, antipyretic and anti-inflammatory actions. | |||
T1429 | 17α-Hydroxyprogesterone | Hydroxyprogesterone,17-OHP,17-Hydroxyprogesterone | Estrogen/progestogen Receptor , Progesterone Receptor , Endogenous Metabolite |
17α-Hydroxyprogesterone (17-OHP) is a physiological progestin that is produced during glucocorticoid and steroid hormone synthesis and is increased during the third trimester of pregnancy. Hydroxyprogesterone binds to th... | |||
TL0016 | Sulforaphene | Apoptosis , ERK , EGFR , NF-κB | |
Sulforaphene is a natural product isolated from radish seeds, exhibits an ED50 against velvetleaf seedlings approximately 2 x 10 -4 M. Sulforaphene promotes cancer cells apoptosis and inhibits migration via inhibiting EG... | |||
T5584 | Phytic acid sodium salt | Sodium phytate hydrate | Others |
Phytic acid sodium salt (Sodium phytate hydrate) is known to function as a [PO4]3- storage depot and a precursor for other inositol phosphates and pyrophosphates. It is a potent chelator of divalent and trivalent cations... | |||
T0070 | Pentoxifylline | Oxpentifylline,PTX,BL-191 | HIV Protease , PDE , Adenosine Receptor , Autophagy |
Pentoxifylline (PTX) modulates immunologic activity by stimulating cytokine production. Pentoxifylline is a methylxanthine derivative that inhibits phosphodiesterase and affects blood rheology. It also inhibits platelet ... | |||
T7998 | 1,7-Diaminoheptane | Others | |
1,7-Diaminoheptane is a compound of the aliphatic amine family. It is used in the synthesis of peptides, peptidomimetics, and other compounds, and has also been used as a substrate in enzyme reactions, as a ligand in met... | |||
T3S0717 | Thymol | 2-isopropyl-5-methylphenol,Pseudoaspidin,Thymic Acid,Thyme Camphor | Antibacterial |
Thymol, also known as Pseudoaspidin, is a principal monoterpene phenol found in the essential oils of plants from the Lamiaceae family, along with several other families including Verbenaceae, Scrophulariaceae, Ranuncula... | |||
T0461 | Berberine chloride | Berberine hydrochloride,Benzodioxide,Natural Yellow 18 | Reactive Oxygen Species , Topoisomerase , Antibacterial , Antibiotic , Autophagy |
Berberine chloride (Natural Yellow 18) is an alkaloid from Hydrastis canadensis L., Berberidaceae and also found in many other plants. It is relatively toxic to parenterally but has been used orally for various fungal an... | |||
T41358 | 2-Hydroxybenzylamine | Others | |
2-Hydroxybenzylamine, a potent small molecule scavenger of IsoLGs, sequesters the reactive species as inert adducts. 2-Hydroxybenzylamine may be used to decrease early recurrence of atrial fibrillation and other atrial a... | |||
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... | |||
T7989 | Trimethyl phosphate | Others | |
Trimethyl phosphate is an organophosphorus compound that is an inhibitor of enzymes that catalyze the hydrolysis of phosphorylated compounds. It has been used as a reactant in the synthesis of peptides and other proteins... | |||
T4703 | (2-Aminoethyl)phosphonic acid | 2-Aminoethylphosphonic acid,Ciliatine,2-AEP | Others , Endogenous Metabolite |
(2-Aminoethyl)phosphonic acid (2-Aminoethylphosphonic acid) is primarily detected in urine. (2-Aminoethyl)phosphonic acid participates in many enzymatic reactions and is also the parent compound of other transformation p... | |||
T3874 | Diosgenin glucoside | Disogluside,Trillin | Apoptosis , Others , Autophagy |
Diosgenin glucoside (Trillin) and other synthetic glycosides with similar activities may be of use in the management of hypercholesterolemia and atherosclerosis. Significant inhibition of Diosgenin glucoside synthesis an... | |||
T2864 | Lycopene | ψ,ψ-Carotene | Reactive Oxygen Species , ROS |
Lycopene (ψ,ψ-Carotene) is a linear, unsaturated hydrocarbon carotenoid, the major red pigment in fruits such as tomatoes, pink grapefruit, apricots, red oranges, watermelon, rosehips, and guava. As a class, carotenoids ... | |||
T4788 | L-Norvaline | Others , Endogenous Metabolite | |
L-Norvaline is an arginase inhibitor and a non-proteinogenic branched-chain amino acid. L-Norvaline has previously been reported to be a natural component of an antifungal peptide of Bacillus subtilis. L-Norvaline and ot... | |||
T7963 | 2,4-Dihydroxypyridine | Others | |
2,4-Dihydroxypyridine is a pyridine derivative that acts as a chelating agent binding to metal ions and forming complexes. It is used as a reagent for determining the concentration of various ions, such as calcium, magne... | |||
TMA2474 | δ-Tocotrienol | Delta-Tocotrienol | ERK , BCL , VEGFR , Akt , PI3K , PDK , p53 |
δ-Tocotrienol (Delta-Tocotrienol) is a potential angiogenic inhibitor. δ-Tocotrienol is also a nontoxic activator of mir-34a which can inhibit nonsmall cell lung cancer cells (NSC-LC) cell proliferation, induce apoptosis... | |||
T2563 | Acetyl-L-carnitine hydrochloride | Acetyl L-carnitine hydrochloride,O-Acetylcarnitine,O-acetyl-L-carnitine,O-Acetyl-L-carnitine hydrochloride | Others , Endogenous Metabolite |
Acetyl-L-carnitine hydrochloride (Acetyl L-carnitine hydrochloride) is a nutritional supplement composed of the hydrochloride salt form of the acetylated form of the endogenously produced L-carnitine, with potential neur... | |||
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Cat No. | Product Name | ||
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L2010 | Highly Selective Inhibitor Library | 580 compounds | |
A collection of xunm highly selective inhibitors | |||
L1120 | AMPK-Targeted Compound Library | 80 compounds | |
80 well-chosen unique AMPK-targeted small molecules; | |||
L3100 | Hematopoietic Toxicity Compound Library | 104 compounds | |
A unique collection of 104 compounds with defined hematopoietic toxicity for high throughput and high content drug screening; | |||
L2700 | Adrenergic Receptor-Targeted Compound Library | 219 compounds | |
A unique collection of 219 bioactive compounds specifically targeting adrenergic receptors, effective tool for screening new drugs or new target identification; | |||
L9820 | Beta-Lactam Compound Library | 105 compounds | |
A unique collection of 105 beta-lactam compounds, can be used in HTS and HCS; | |||
L1600 | Kinase Inhibitor Library | 2720 compounds | |
A unique collection of 2720 kinase inhibitors/regulators for high throughput screening and high content screening for drug discovery in kinase related diseases; | |||
L9001 | Food Additive Library | 430 compounds | |
430 food additives; | |||
L6001 | Mini Fungal Metabolite Natural Product Screening Library | Inquiry | |
L1800 | Anti-Infection Compound Library | 2977 compounds | |
A unique collection of 2977 anti-infective compounds including anti-bacterial, anti-fungi, anti-Human Cytomegalovirus (HCMV), anti-HIV, anti-SARS, anti-influenza, etc; | |||
L9610 | Cyclic Peptide Library | 58 compounds | |
58 species of cyclic peptide molecules for high-throughput and high-content screening; | |||
L1720 | Nucleotide Compound Library | 337 compounds | |
A unique collection of 337 nucleoside and nucleotide analogues, can be used for research and development of anti-viral, anti-tumor, anti-fungal, and anti-depressive drugs; | |||
L5500 | Toxic Compound Library | 277 compounds | |
A unique collection of 277 toxic substances for high throughput screening (HTS) and high content screening (HCS); | |||
L2196 | Anti-Ovarian Cancer Compound Library | 1888 compounds | |
A unique collection of 1888 compounds with anti-ovarian cancer therapeutic activity, can be used for anti-ovarian cancer drug discovery and pharmacological study; | |||
L4400 | Antibiotics Library | 708 compounds | |
A unique collection of 708 compounds with antibiotic activity for new antibacterial drug screening; | |||
L1100 | Protease Inhibitor Library | 344 compounds | |
A unique collection of 344 protease and proteasome inhibitors for research in chemical genomics, and drug screening; | |||
L2110 | Anti-Cancer Approved Drug Library | 1825 compounds | |
A unique collection of 1825 approved anti-cancer drugs for high throughput screening (HTS) and high content screening (HCS); | |||
L6400 | Marine Natural Product Library | 148 compounds | |
A unique collection of 148 marine natural products for high throughput screening (HTS) and high content screening (HCS); | |||
L2200 | Tyrosine Kinase Inhibitor Library | 1033 compounds | |
A unique collection of 1033 tyrosine kinase inhibitors for high throughput screening and high content screening for drug discovery in tyrosine kinase related diseases; | |||
L7600 | Chemokine Inhibitor Library | 59 compounds | |
A unique collection of 59 chemokines or chemokine receptors targeted compounds for high throughput and high content screening; | |||
L2300 | Ion Channel Inhibitor Library | 946 compounds | |
A unique collection of 946 compounds targeting ion channels for research in ion channels-related diseases and ion channel drug discovery; | |||
L4600 | Selected Plant-Sourced Compound Library | 3076 compounds | |
A unique collection of 3076 plant-sourced compounds that derived from 277 plant species for high throughput screening (HTS) and high content screening (HCS); | |||
L7200 | Calcium Channel Compound Library | 143 compounds | |
A unique collection of 143 calcium channel blockers and agonists for high throughput and high content screening; | |||
L7000 | Bioactive Lipid Compound Library | 385 compounds | |
A unique collection of 385 bioactive lipids related compounds for high throughput screening (HTS) and high content screening (HCS), including Agonists & Antagonists, Endocannabinoids, Farnesyl/geranylgeranyl derivates, ... | |||
L4800 | Angiogenesis related Compound Library | 1370 compounds | |
A unique collection of 1370 proangiogenic and antiangiogenic compounds for new targets identification, research in mechanisms of angiogenesis, and high throughput screening (HTS) and high content screening (HCS); | |||
L4700 | Immunology/Inflammation Compound Library | 3483 compounds | |
A unique collection of 3483 anti-inflammation compounds effective for high throughput screening and high content screening. | |||
L8800 | Drug-Fragment Library | 1158 compounds | |
1158 drug fragments,a must-have tool for FBDD; | |||
L1710 | Anti-COVID-19 Compound Library | 1160 compounds | |
A unique collection of 1160 compounds with confirmed anti-SARS-CoV-2 activity or potential activity and part of them are broad-spectrum antiviral agents; | |||
L9840 | Anti-Alzheimer's Disease Compound Library | 1040 compounds | |
A unique collection of 1040 compounds with anti-AD activities or acting on main drug targets of AD can be used for HTS and HCS. | |||
L2550 | Glutamine Metabolism Compound Library | 580 compounds | |
A unique collection of 580 glutamine metabolism related compounds can be used for high throughput screening (HTS) and high content screening (HCS), and also is an effective tool for research in glutamine metabolism and ... |