| DC66393 |
WAY-221060
Featured
|
WAY-221060-A is an active molecule. |
|
| DC66394 |
Anti-inflammatory agent 63
Featured
|
Anti-inflammatory agent 63 is an anti-inflammatory agent that shows optimal inhibitory activity (EC50 = 5.33±0.57 μM) against the production of nitric oxide (NO) induced by lipopolysaccharide (LPS) in RAW264.7 cells. |
|
| DC66395 |
WAY-639872
Featured
|
WAY-639872 is an active molecule. |
|
| DC66396 |
WAY-215718
Featured
|
WAY-215718 is an active molecule. |
|
| DC66397 |
WAY-328127
Featured
|
WAY-328127 is an active molecule. |
|
| DC66398 |
WAY-616296
Featured
|
WAY-616296 is an active molecule. |
|
| DC66399 |
WAY-325811
Featured
|
WAY-325811 is an active molecule. |
|
| DC66400 |
WAY-649123
Featured
|
WAY-649123 is an active molecule. |
|
| DC66401 |
Tyrosinase-IN-17
Featured
|
Tyrosinase-IN-17 (Compound 5b) is a lipophilic, skin-permeable, and non-cytotoxic Tyrosinase inhibitor (pIC50=4.99). Tyrosinase-IN-17 can be used for research on melanin-related diseases, such as melanoma, melanogenesis, etc. |
|
| DC66402 |
Aβ42 agonist-1
Featured
|
Aβ42 agonist-1 (compound 7a) is a small molecule compound that can promote Aβ42 aggregation. Aβ42 agonist-1 can interact with Aβ42 oligomers and pentamers to promote nontoxic aggregate self-assembly and rapid fibril formation. Aβ42 agonist-1 prevents Aβ42-induced cytotoxicity in HT22 hippocampal neuronal cells. |
|
| DC66403 |
Aurora kinase inhibitor-11
Featured
|
Aurora kinase inhibitor-11 (compound 25) is an inhibitor of Aurora Kinase with an IC50 of 0.14 μM. Aurora kinase inhibitor-11 has anticancer activity. |
|
| DC66404 |
Aβ42 agonist-2
Featured
|
Aβ42 agonist-2 (compound 7b) is a small molecule compound that can promote Aβ42 aggregation. Aβ42 agonist-2 can interact with Aβ42 oligomers and pentamers to promote nontoxic aggregate self-assembly and rapid fibril formation. Aβ42 agonist-2 prevents Aβ42-induced cytotoxicity in HT22 hippocampal neuronal cells. |
|
| DC66405 |
ATG12-ATG3 inhibitor 1
Featured
|
ATG12-ATG3 inhibitor 1 (compound 189) is a potent inhibitor of autophage. |
|
| DC66406 |
hCAI/II-IN-7
Featured
|
hCAI/II-IN-7 (compound 1F) is a potent carbonic anhydrase (CA) inhibitor with Ki values of 23 nM, 44 nM and 20.57 µM for hCA-I, hCA-II and bovine CA, respectively. |
|
| DC66407 |
HDAC6-IN-27
Featured
|
HDAC6-IN-27 (compound 8C) is a HDAC inhibitor with IC50 vales of 15.9 nM 136.5 nM and 6180.2 nM for HDAC6, HDAC8 and HDAC1, respectively. HDAC6-IN-27 shows potent antiparasitic effects. |
|
| DC66408 |
AN-12-H5 intermediate-3
Featured
|
AN-12-H5 intermediate-3 is an intermediate of the viral inhibitor AN-12-H5 (HY-120900) and can be used to synthesize Antibody-Drug Conjugates (ADCs). |
|
| DC66409 |
Anti-osteoporosis agent-6
Featured
|
Anti-osteoporosis agent-6 (compound 174) is an anti-osteoporosis agent. Anti-osteoporosis agent-6 has 14.11% inhibition rate against osteoclast formation at 10 μM. |
|
| DC66410 |
Anti-osteoporosis agent-5
Featured
|
Anti-osteoporosis agent-5 (compound 189) is a potent inhibitor of the formation of osteoclasts. |
|
| DC66411 |
2',4',6',4-tetramethoxychalcone
Featured
|
4,2′,4′,6′-Tetramethoxychalcone is a flavonoids that can be isolated from Gnaphalium affine. |
|
| DC66412 |
Senexin A hydrochloride
Featured
|
Senexin A hydrochloride is an inhibitor of CDK8/19 (IC50: 280 nM, CDK8) and an inhibitor downstream of p21 transcription. It only inhibits p21-induced transcription but does not inhibit other biological effects of p21. Senexin A hydrochloride inhibits CMV-GFP induction as well as the p21 stimulatory activity of the consensus NF-κB-dependent promoters. |
|
| DC66413 |
TEAD-IN-8
Featured
|
TEAD-IN-8 is a novel TEAD inhibitor, which potently and specifically inhibits TEAD-YAP transcriptional activities. TM2, alone or in combination with MEK inhibitors, exhibits potent antiproliferative effects in YAP-dependent cancer cells. |
|
| DC66414 |
Antioxidant/anticancer agent 1
Featured
|
Antioxidant/anticancer agent 1 (compound 5) is a pyrimidine-derivatized Schiff base based on pyrimidine hydroxy-1-naphthaldehyde and has antibacterial, antioxidant, antifungal, and anticancer properties. Antioxidant/anticancer agent 1. |
|
| DC66415 |
HKI12134085
Featured
|
HKI12134085 (compound 3) is an orally available antibacterial nitrobenzothiazinone (BTZ) derivative with activity against Mycobacterium tuberculosis. HKI12134085 has in vivo inhibitory potency in a BALB/c mouse model of Mycobacterium tuberculosis infection. |
|
| DC66416 |
ATPase-IN-3
Featured
|
ATPase-IN-3 (compound 6) is a ATPase inhibitor. ATPase-IN-3 has Gastroprotective effect in ethanol-induced gastric ulcers by contribution of anti-apoptotic (BCL-2) and tumor suppressor (P53) proteins. |
|
| DC66417 |
CAY10512
Featured
|
CAY10512 is an inhibitor of NF-κB. CAY10512 can suppress the upregulation of NF-κB-sensitive proinflammatory miRNAs (miRNA-9, miRNA-125b, miRNA-146a, miRNA-155) in cerebrospinal fluid and extracellular fluid, and can be used for research on Alzheimer's disease. |
|
| DC66418 |
ZINC000028464438
Featured
|
ZINC000028464438 is a selective HDAC11 inhibitor with an IC50 of 3.5 µM. ZINC000028464438 shows almost no inhibition for other HDAC subtypes. |
|
| DC66419 |
AChE/Aβ-IN-5
Featured
|
AChE/Aβ-IN-5 (compound AV-2) is a bifunctional inhibitor that targets AChE and auto-induced Aβ (Amyloid-β) aggregation. AChE/Aβ-IN-5 can significantly improve scopolamine- and Aβ-induced cognitive impairment in mice. |
|
| DC66420 |
BFC1108
Featured
|
BFC1108 is a small molecule Bcl-2 functional converter. BFC1108 induces a conformational change in Bcl-2, resulting in the exposure of its BH3 domain both in vitro and in vivo. BFC1108 effectively induces apoptosis in Bcl-2 expressing cancers. |
|
| DC66421 |
p38-α MAPK-IN-6
Featured
|
p38-α MAPK-IN-6 (compound 3a) is a p38α mitogen-activated protein kinase inhibitor. |
|
| DC66422 |
Avenanthramide-C methyl ester
Featured
|
Avenanthramide-C methyl ester is an anti-inflammatory agent and NF-κB inhibitor that inhibits the secretion of pro-inflammatory factors. Avenanthramide-C methyl ester inhibits NF-κB activation by inhibiting IKK and IκB phosphorylation and inhibiting proteasome activity. |
|
