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Search Results for " 泛素化 "

Targets

138

Compounds

15

Natural Products

20

Libraries

Cat No. Product Name Synonyms Targets
T9884 EN523 Others
EN523 targets non-catalytic allosteric cysteine C23 in K48 ubiquitin-specific deuquitinase OTUB1.
T12579 RAMB4 PTP1B-IN-9 Proteasome
RAMB4 (PTP1B-IN-9) is a ubiquitin-proteasome system (UPS)-stressor,with anticancer activity.
T16974 TAK-243 MLN7243 Apoptosis , E1/E2/E3 Enzyme , NF-κB
TAK-243 (MLN7243) is a selective inhibitor of the ubiquitin-activating enzyme UAE (IC50=1 nM). TAK-243 blocks ubiquitin binding and disrupts mono-ubiquitin signaling as well as overall protein ubiquitination. TAK-243 exh...
T22922 Lenalidomide hemihydrate TNF , Ligand for E3 Ligase , Molecular Glues
Lenalidomide hemihydrate is a TNF-α secretion inhibitor (IC50 = 13 nM). Lenalidomide hemihydrate could bound endogenous CRBN and recombinant CRBN-DNA damage binding protein-1 (DDB1) complexes.
T1642 Lenalidomide CC-5013 Apoptosis , TNF , Ligand for E3 Ligase , Molecular Glues
Lenalidomide (CC-5013) is a potent inhibitor of TNF-α that, at 10 μM, alters gene expression and cell viability in a range of cancer cell lines.
T1932 B-AP15 NSC 687852 Apoptosis , DUB
B-AP15 (NSC-687852)(NSC-687852) is a selective inhibitor of the deubiquitinating enzymes Usp14 and UCHL5 of the 26S proteasome. It blocks the deubiquitinating activity of the 26S proteasome.
T3110 PRT4165 NSC600157,PRT 4165 BMI-1 , Others , E1/E2/E3 Enzyme
PRT4165 (NSC600157) is a potent PRC1-mediated H2A ubiquitylation inhibitor.
T16904 Smurf1-IN-A01 A01 Others
Smurf1-IN-A01 (A01) is a ubiquitin ligase Smad ubiquitination regulatory factor-1 inhibitor (kd: 3.664 nM). It increases BMP-2 responsiveness by inhibiting Smurf1-mediated Smad1/5 degradation.
T25465 GS143 GS-143,GS 143 IκB/IKK , E1/E2/E3 Enzyme , NF-κB
GS143 is a selec­tive IκBα ubiquitination inhibitor with an IC50 of 5.2 μM for SCFβTrCP1-mediated IκBα ubiquitylation. GS143 sup­presses NF-κB acti­va­tion and tran­scrip­tion of tar­get genes and does not inhibit protea...
T6697 TCID UCH-L3 Inhibitor DUB
TCID (UCH-L3 Inhibitor)(IC50=0.6 μM) is a DUB inhibitor of ubiquitin C-terminal hydrolase L3. It has the 125-fold selectivity to L1.
T17879 E3 ligase Ligand 8 Others , Ligand for E3 Ligase
E3 ligase Ligand 8 is a ligand for E3 ubiquitin ligase. The E3 ligase Ligand 8 can be linked to protein ligands through linkers to form PROTACs, which are inducers of ubiquitination-mediated degradation of cancer-promoti...
T21773 SP-141 SP 141 Mdm2
SP 141 is a MDM2 inhibitor.SP-141 promotes MDM2 auto-ubiquitination and degradation, with anticancer activity.
T12024 MF-094 DUB
MF-094 is a potent and selective inhibitor of USP30 (IC50 of 120 nM).
T21527 HBX 41108 HBX-41108 DUB , p53
HBX 41108 (HBX-41108) is a non-competitive, reversible inhibitor of USP7 with an IC50 of 424nM. HBX 41108 inhibited deubiquitination of p53 mediated by USP7 in a dose-dependent manner with an IC50 of 0.8μM.
T6629 PYR-41 PYR41,PYR 41 Apoptosis , E1/E2/E3 Enzyme
PYR-41 is the first cell-permeable inhibitor of ubiquitin-activating enzyme E1, with no activity at E2.
T1919 Tenovin-1 Tenovin 1 Mdm2 , Dehydrogenase , Sirtuin , p53 , Autophagy
Tenovin-1 inhibits protein-deacetylating activities of SirT1 and SirT2 and protects against MDM2-mediated p53 degradation, which involves ubiquitination.
T1757 ML-323 ML323 DUB
ML323 is a reversible and effective USP1-UAF1 inhibitor in a Ub-Rho assay (IC50: 76 nM) and in orthogonal gel-based assays using K63-linked diubiquitin (di-Ub) (IC50: 174 nM 820 nM)and monoubiquitinated PCNA (Ub-PCNA) (I...
T27240 Eeyarestatin I Apoptosis
Eeyarestatin I is an inhibitor that inhibits the degradation and translocation of ER-associated proteins. Eeyarestatin I is associated with the p97 deubiquitination process and inhibits atx3 deubiquitination. Eeyarestati...
T6910 NSC59984 p53
NSC59984, a p53 pathway activator, induces mutant p53 protein degradation and p73 activation.
T3088 N-Ethylmaleimide 1-Ethyl-1H-pyrrole-2,5-dione,Ethylmaleimide,NEM Cysteine Protease , DUB
N-Ethylmaleimide (NEM) is a sulfhydryl reagent that is widely used in experimental biochemical studies.
T5199 COH000 E1/E2/E3 Enzyme
COH000 is a covalent and irreversible inhibitor of small ubiquitin-like modifier (SUMO)-activating enzyme and inhibited SUMOylation (IC50: ~ 0.2 μM in vitro).
T13349 WS-383 E1/E2/E3 Enzyme
WS-383 is a selective, potent and reversible DCN1-UBC12 interaction inhibitor(IC50 of 11 nM).
TP1186 Cyclo(Phe-Pro) A-64863,Cyclo(phenylalanylprolyl) Others
Cyclo(Phe-Pro) (A-64863) known as a secondary metabolite of some bacteria and fungi, is also produced by Vibrio vulnificus.
T11209 EOAI3402143 DUB
EOAI3402143 inhibits Usp9x and Usp24 activity, increases tumor cell apoptosis. EOAI3402143 phenocopies the FAS induction and apoptotic sensitization of Usp5 knockdown and fully blocks melanoma tumor growth.
T60130 USP5-IN-1 DUB
USP5-IN-1 (compound 64) is a potent deubiquitinase USP5 inhibitor, which binds to the USP5 ZnF-UBD with a KD of 2.8 μM and is selective over nine proteins containing structurally similar ZnF-UBD domains. USP5-IN-1 inhibi...
T11485 GSK2643943A DUB
GSK2643943A is a deubiquitylating enzyme (DUB) inhibitor, with an IC 50 of 160 nM for USP20/Ub-Rho. GSK2643943A has anti-tumor efficacy.
T13244 Ubiquitination-IN-1 Others
Ubiquitination-IN-1 is an inhibitor of ubiquitination and Cksl-Skp2 protein-protein interaction (IC50: 0.17 μM).
T22263 Bavdegalutamide ARV-110 Androgen Receptor
Bavdegalutamide (ARV-110) is a PROTAC degrader of androgen receptor (AR). Bavdegalutamide can be used in studies about prostate cancer. Bavdegalutamide shows oral activity and selectivity and facilitates the ubiquitinati...
T1372 2-Methoxybenzylamine Others
2-Methoxybenzylamine is widely used in the synthesis of other compounds such as dyes, fragrances and plastics; it can also be used in the synthesis of bioactive compounds such as antibiotics and antifungals.
T0922 Zoxazolamine NSC 24995,Contrazole Others
Zoxazolamine (NSC-24995) is a uricosuric and muscle relaxant. Zoxazolamine acts centrally as a muscle relaxant, but the mechanism of its action is not understood.
T36682 USP30 inhibitor 18 DUB
USP30 inhibitor 18 is a selective USP30 inhibitor with an IC50 of 0.02 μM. USP30 inhibitor 18 increases protein ubiquitination and accelerates mitophagy[1]. [1]. Arthur F Kluge, et al. Novel highly selective inhibitors o...
T61477 DCeMM2 Molecular Glues
dCeMM2 is a glue degrader. dCeMM2 prompts an interaction of CDK12-cyclin K with a CRL4B ligase complex, leading to the ubiquitination and degradation of cyclin K.
T6743 (E/Z)-4-Hydroxytamoxifen Afimoxifene,4-Hydroxytamoxifen Estrogen Receptor/ERR , Estrogen/progestogen Receptor
(E/Z)-4-Hydroxytamoxifen (Afimoxifene) is the active metabolite of tamoxifen and a selective estrogen receptor (ER) modulator that is widely used in the therapeutic and chemopreventive treatment of breast cancer.
T67876 USP8-IN-2 DUB
USP8-IN-2 is a potent inhibitor of the deubiquitinating enzymes USP7 and USP8, with an IC50 of 4.0 μM against USP8D. USP8-IN-2 is a potential compound for the treatment of cancer and viral infections.
T8951 JTP 0819958 - HOIPIN-1 IκB/IKK
JTP-0819958 is a selective linear ubiquitin chain assembly complex (LUBAC) inhibitor with an IC50 of 2.8 μM[1]. JTP-0819958 suppress LUBAC-mediated NF-kB activation in vitro[2].
T73560 I-138 DUB
I-138 is an orally active and potent reversible inhibitor of USP1-UAF1.I-138 induces mono-ubiquitination of FANCD2 and PCNA and inhibits USP1 auto-cleavage in cells.
T10765 Eragidomide CC-90009,Cereblon modulator 1 Apoptosis , Ligand for E3 Ligase , Molecular Glues
Eragidomide (CC-90009; Cereblon modulator 1) is a cereblon (CRBN) E3 ligase modulator. Eragidomide specifically binds to CRBN, thereby affecting the activity of the ubiquitin E3 ligase complex.
T6300 Degrasyn WP1130 Apoptosis , JAK , Bcr-Abl , DUB , Autophagy
Degrasyn (WP1130) (WP1130), a specific deubiquitinase (DUB: USP5, UCH-L1, USP9x, USP14, and UCH37) inhibitor, also inhibits Bcr/Abl, which is a JAK2 transducer (without affecting 20S proteasome) and activator of transcri...
T37042 SCH529074 SCH 529074 p53
SCH529074 is a selective activator of p53 (Ki = 1 μM) and can be used in studies about non-small-cell lung carcinoma. SCH529074 restores mutant p53 function and interrupts HDM2-mediated ubiquitination of wild Type p53.
T8773 MID-1 Others , IGF-1R
MID-1 is an inhibitor of MG53-IRS-1 (Mitsugumin 53-Insulin Receptor Substrate-1) interaction. It disrupts molecular association of MG53 with IRS-1 and abolishes MG53-induced IRS-1 ubiquitination and degradation in skelet...
T0424 Bismuth Subsalicylate Bismuth subsalicylat,Bismuth(III) salicylate basic,Bismuth oxysalicylate COX , PGE Synthase
Bismuth Subsalicylate (Bismuth subsalicylat) is the active ingredient in the popular medication Pepto-Bismol that is used to treat nausea, heartburn, indigestion, upset stomach, diarrhea, and other temporary discomforts ...
T64339 Apcin A HCL APC
Apcin A HCL is an Apcin derivative. Apcin A HCL is an anaphase-promoting complex (APC) inhibitor. Apcin-A HCL interacts strongly with Cdc20, and inhibits the ubiquitination of Cdc20 substrates. Apcin-A HCL can be used to...
T1902 BAY 11-7082 BAY 11-7821 Apoptosis , Others , IκB/IKK , DUB , Autophagy
BAY 11-7082 (BAY 11-7821) is an NF-κB inhibitor that inhibits TNFα-induced IκBα phosphorylation (IC50=10 μM). BAY 11-7082 is also an inhibitor of the ubiquitin-specific proteases USP7 and USP21 (IC50=0.19/0.96 μM).
T63790 Cbl-b-IN-3 E1/E2/E3 Enzyme
Cbl-b-IN-3 is a potent proto-oncogene-B (CPL-B) inhibitor of casitas B-series lymphoma (ic50 < 1 nM). Cpl-b, a cyclic E3 ubiquitin protein ligase, is involved in the setting of T lymphocyte activation thresholds. Cpl-b n...
T5461 GNE-6640 DUB
GNE-6640 is a non-covalent inhibitor targeting ubiquitin specific peptidase 7 (USP7), exhibiting IC50 values of 0.75 μM for full-length USP7, 0.43 μM for the USP7 catalytic domain, 20.3 μM for full-length USP43, and 0.23...
T17187 TZ9 Apoptosis , E1/E2/E3 Enzyme
TZ9 is a selective and potent Rad6 inhibitor with anticancer and anti-tumor activity.TZ9 inhibits Rad6B-induced ubiquitination of histone H2A.TZ9 induces cell cycle arrest and apoptosis.
T8488 GMB-475 Bcr-Abl
GMB-475 is a BCR-ABL1 tyrosine kinase degrader based on PROTAC, overcoming BCR-ABL1-dependent drug resistance. GMB-475 targets BCR-ABL1 protein and recruits the E3 ligase Von Hippel Lindau (VHL).resulting in ubiquitinati...
T15069 DBCO-PEG4-Biotin ADIBO-NH-PEG2-Biotin Others
DBCO-PEG4-Biotin (ADIBO-NH-PEG2-Biotin) is an azadibenzocyclooctyne-biotin derivative containing a biotin moiety and 4 PEGs.DBCO-PEG4-Biotin is a versatile biotinylation reagent that introduces a portion of biotin into ...
T66491 4-(1-Phenylethyl)resorcinol 4-(1-Phenylethyl)benzene-1,3-diol,Phenylethyl resorcinol Others
4-(1-Phenylethyl)resorcinol (4-(1-Phenylethyl)benzene-1,3-diol) is a skin brightening agent that is a cosmetic additive. It works by inhibiting melanin production, reducing the appearance of dark spots, hyperpigmentation...
T67873 USP8-IN-3 DUB
USP8-IN-3 is a potent inhibitor of the deubiquitinating enzymes USP7 and USP8, with IC50 of 4.0 μM against USP8D. USP8-IN-3 inhibited the proliferation of GH3 and H1957 cells with GI50 values of 37.03 μM and 6.01 μM, res...

Compounds

EN523
T9884
Synonym:
Target: Others
RAMB4
T12579
Synonym: PTP1B-IN-9
Target: Proteasome
TAK-243
T16974
Synonym: MLN7243
Target: Apoptosis, E1/E2/E3 Enzyme, NF-κB
Lenalidomide hemihydrate
T22922
Synonym:
Target: TNF, Ligand for E3 Ligase, Molecular Glues
Lenalidomide
T1642
Synonym: CC-5013
Target: Apoptosis, TNF, Ligand for E3 Ligase, Molecular Glues
B-AP15
T1932
Synonym: NSC 687852
Target: Apoptosis, DUB
PRT4165
T3110
Synonym: NSC600157,PRT 4165
Target: BMI-1, Others, E1/E2/E3 Enzyme
Smurf1-IN-A01
T16904
Synonym: A01
Target: Others
GS143
T25465
Synonym: GS-143,GS 143
Target: IκB/IKK, E1/E2/E3 Enzyme, NF-κB
TCID
T6697
Synonym: UCH-L3 Inhibitor
Target: DUB
E3 ligase Ligand 8
T17879
Synonym:
Target: Others, Ligand for E3 Ligase
SP-141
T21773
Synonym: SP 141
Target: Mdm2
MF-094
T12024
Synonym:
Target: DUB
HBX 41108
T21527
Synonym: HBX-41108
Target: DUB, p53
PYR-41
T6629
Synonym: PYR41,PYR 41
Target: Apoptosis, E1/E2/E3 Enzyme
Tenovin-1
T1919
Synonym: Tenovin 1
Target: Mdm2, Dehydrogenase, Sirtuin, p53, Autophagy
ML-323
T1757
Synonym: ML323
Target: DUB
Eeyarestatin I
T27240
Synonym:
Target: Apoptosis
NSC59984
T6910
Synonym:
Target: p53
N-Ethylmaleimide
T3088
Synonym: 1-Ethyl-1H-pyrrole-2,5-dione,Ethylmaleimide,NEM
Target: Cysteine Protease, DUB
COH000
T5199
Synonym:
Target: E1/E2/E3 Enzyme
WS-383
T13349
Synonym:
Target: E1/E2/E3 Enzyme
Cyclo(Phe-Pro)
TP1186
Synonym: A-64863,Cyclo(phenylalanylprolyl)
Target: Others
EOAI3402143
T11209
Synonym:
Target: DUB
USP5-IN-1
T60130
Synonym:
Target: DUB
GSK2643943A
T11485
Synonym:
Target: DUB
Ubiquitination-IN-1
T13244
Synonym:
Target: Others
Bavdegalutamide
T22263
Synonym: ARV-110
Target: Androgen Receptor
2-Methoxybenzylamine
T1372
Synonym:
Target: Others
Zoxazolamine
T0922
Synonym: NSC 24995,Contrazole
Target: Others
USP30 inhibitor 18
T36682
Synonym:
Target: DUB
dCeMM2
T61477
Synonym:
Target: Molecular Glues
(E/Z)-4-Hydroxytamoxifen
T6743
Synonym: Afimoxifene,4-Hydroxytamoxifen
Target: Estrogen Receptor/ERR, Estrogen/progestogen Receptor
USP8-IN-2
T67876
Synonym:
Target: DUB
JTP 0819958 - HOIPIN-1
T8951
Synonym:
Target: IκB/IKK
I-138
T73560
Synonym:
Target: DUB
Eragidomide
T10765
Synonym: CC-90009,Cereblon modulator 1
Target: Apoptosis, Ligand for E3 Ligase, Molecular Glues
Degrasyn
T6300
Synonym: WP1130
Target: Apoptosis, JAK, Bcr-Abl, DUB, Autophagy
SCH529074
T37042
Synonym: SCH 529074
Target: p53
MID-1
T8773
Synonym:
Target: Others, IGF-1R
Bismuth Subsalicylate
T0424
Synonym: Bismuth subsalicylat,Bismuth(III) salicylate basic,Bismuth oxysalicylate
Target: COX, PGE Synthase
Apcin A HCL
T64339
Synonym:
Target: APC
BAY 11-7082
T1902
Synonym: BAY 11-7821
Target: Apoptosis, Others, IκB/IKK, DUB, Autophagy
Cbl-b-IN-3
T63790
Synonym:
Target: E1/E2/E3 Enzyme
GNE-6640
T5461
Synonym:
Target: DUB
TZ9
T17187
Synonym:
Target: Apoptosis, E1/E2/E3 Enzyme
GMB-475
T8488
Synonym:
Target: Bcr-Abl
DBCO-PEG4-Biotin
T15069
Synonym: ADIBO-NH-PEG2-Biotin
Target: Others
4-(1-Phenylethyl)resorcinol
T66491
Synonym: 4-(1-Phenylethyl)benzene-1,3-diol,Phenylethyl resorcinol
Target: Others
USP8-IN-3
T67873
Synonym:
Target: DUB
1 2 3
Cat No. Product Name Synonyms Targets
T1059 Retinyl palmitate Retinol palmitate,Vitamin A palmitate,Retinyl (Vitamin A) Palmitate Others , Endogenous Metabolite
Retinyl palmitate (Vitamin A palmitate) is a naturally-occurring phenyl analogue of retinol, with potential antineoplastic and chemopreventive activities.
T8201 Gambogenic acid Histone Methyltransferase
Gambogenic acid is a natural product,is an effective inhibitor of EZH2,with anticancer activity.
T1558 Resveratrol trans-Resveratrol,SRT 501 Apoptosis , Mitophagy , IκB/IKK , Lipoxygenase , Sirtuin , COX , NADPH , DNA/RNA Synthesis , Nrf2 , Antibacterial , Antibiotic , Autophagy , Antifungal
Resveratrol (SRT 501) is a polyphenolic natural product, a plant antitoxin with antioxidant and chemopreventive activities. Resveratrol has a wide range of targets including COX, SIRT, LOC, etc. Resveratrol induces autop...
T3S0137 Bavachalcone Antibacterial , Antibiotic
Bavachalcone is a major bioactive compounds isolated from Psoralea corylifolia L. it may be useful as a therapeutic drug for bone resorption-associated diseases.Bavachalcone can protect the endothelial function by increa...
T4970 LANOSTEROL 3β-Hydroxy-8,24-lanostadiene,8,24-Lanostadien-3β-ol Endogenous Metabolite
Lanosterol (3β-Hydroxy-8,24-lanostadiene) is a tetracyclic triterpenoid which is the compound from which all steroids are derived.
T22417 Rutin hydrate Rutoside,Sophorin,Quercetin-3-O-rutinoside Beta Amyloid , Others , Autophagy
Rutin hydrate (Sophorin), a kind of glycoside, widely exists in many plants including citrus fruit.
T5813 BYAKANGELICIN Reductase
BYAKANGELICIN,a main furanocoumarin constituent isolated and characterized as an aldose reductase inhibitor,and is effective for the treatment of sugar cataracts and diabetic neuropathy and hence might be useful as a lea...
T6S1780 Protosappanin B Q-100961,FT-0689654 Apoptosis
1. Protosappanin B (Q-100961) significantly increases cell viability, inhibits cell apoptosis and up-regulates the expression of growth-associated protein 43. 2. Protosappanin B induces the degradation of p53 protein, vi...
T3254 PHYTOL trans-Phytol,(E)-Phytol Antibacterial , PPAR , Parasite
PHYTOL (trans-Phytol) , a diterpene alcohol from chlorophyll widely used as a food additive and in medicinal fields, shows antinociceptive and antioxidant activities as well as anti-inflammatory and antiallergic effects....
T65269 L-Aspartic acid potasium salt Aspartic acid potasium salt,Potassium L-aspartate Others
L-aspartic acid potasium salt(VX-548) is an amino acid widely found in plants and animals.L-aspartic acid potasium salt drives the production of nitrogen oxides, which promotes phagocytosis and contributes to fish surviv...
T78486 Cis-Nerolidol
cis-Nerolidol, a sesquiterpene alcohol present in numerous plants, exhibits antioxidant and antibacterial properties. Additionally, it can potentiate the effects of antibiotics [1].
T75743 HA Peptide TFA
HA Peptide (TFA), a nine amino acid sequence derived from human influenza hemagglutinin (HA), is widely employed in cell biology and biochemistry for the isolation, purification, detection, and tracking of target protein...
T83437 18-O-Demethylpederin
18-O-Demethylpederin, a pederin analogue, is a natural polyketide first isolated from Paederus. This compound is a non-protein insect toxin and exhibits a range of biological activities, such as antibacterial, antiviral,...
T79941 Antimycin A2c Apoptosis
Anticancer Agent 141 (Compound AE), an antimycin alkaloid, exhibits inhibitory potential against HPV-infected cervical cancer. It impedes HeLa cell proliferation by arresting the cell cycle at the S phase and induces cas...
T78506 α-Lactose hydrate α-D-Lactose hydrate
α-Lactose (hydrate) (α-D-Lactose (hydrate)), the main carbohydrate in mammalian milk, comprises two sugar units: glucose and galactose, and occurs as two anomers, α and β. It serves multiple roles in the food and pharmac...
Cat No. Product Name
L8600 Ubiquitination Compound Library

214 compounds
A unique collection of 214 ubiquitination related small chemicals can be used for high throughput and high content screening;
L9820 Beta-Lactam Compound Library

105 compounds
A unique collection of 105 beta-lactam compounds, can be used in HTS and HCS;
L3300 Histamine & Melatonin Receptor-Targeted Compound Library

155 compounds
A unique collection of 155 compounds targeting histaminergic receptor and melatonin receptor for high throughput screening (HTS) and high content screening (HCS) for new drugs;
L7300 Potassium Channel Blocker Library

160 compounds
A unique collection of 160 potassium channel blockers and agonists for high throughput and high content screening;
L6140 Saccharide and Glycoside Natural Product Library

364 compounds
A unique collection of 364 saccharides and glycosides compounds can be used for HTS and HCS;
L4710 Nonsteroidal Anti-Inflammatory Compound Library

530 compounds
530 non-steroidal anti-inflammatory compounds for high-throughput and high-content screening.
L8200 Anti-Aging Compound Library

3324 compounds
A unique collection of 3324 anti-aging compounds for high throughput screening (HTS) and high content screening (HCS);
L4020 NO PAINS Compound Library

9555 compounds
TargetMol created the L4020 NO-PAINS Compound Library that applied the PAINS filter, remaining 9555 small molecules that are suitable for new drug development, signaling pathway research, drug repurposing and other resea...
L3500 Histone Modification Compound Library

480 compounds
A unique collection of 480 histone modification related compounds for high throughput screening (HTS) and high content screening (HCS);
L6750 PBCRBS Traditional Chinese Medicine Compound Library

588 compounds
A unique collection of 588 compounds derived from traditional Chinese medicines (TCMs) for promoting blood circulation and removing blood stasis.
L2800 Serotonin Receptor-Targeted Compound Library

275 compounds
A unique collection of 275 compounds targeting serotonin receptors for high throughput screening and high content screening;
L8300 Chromatin Modification Compound Library

256 compounds
A unique collection of 256 compounds targeting chromatin remodeling pathway for high throughput screening (HTS) and high content screening (HCS);
L9300 Macrocyclic Compound Library

216 compounds
216 macrocyclic compounds of known activity for high-throughput, high-content screening;
DO1200 SmartTM Library

53200 compounds
L1300 PI3K-AKT-mTOR Compound Library

425 compounds
A unique collection of 425 compounds targeting PI3K/Akt/mTOR signaling for research in PI3K/Akt/mTOR signaling, and drug discovery in diseases involved with PI3K/Akt/mTOR signaling;
L6110 Alkaloid Natural Product Library

468 compounds
A unique collection of 468 natural alkaloids can be used for high throughput and high content screening;
L7200 Calcium Channel Compound Library

143 compounds
A unique collection of 143 calcium channel blockers and agonists for high throughput and high content screening;
L9600 Peptide Compound Library

800 compounds
800 peptides can be used in peptide drug development and signaling transduction and mechanism study;
L5510 Drug-induced Liver Injury (DILI) Compound Library

1040 compounds
A unique collection of 1040 hepatotoxicity causing compounds, a powerful tool for drug toxicity study, can be used for HTS and HCS screening;
L6820 Tobacco Monomer Library

750 compounds
A unique collection of 750 tobacco monomer compounds for high throughput screening and high content screening;
TargetMol