| R2304198 |
SM-102 |
SM-102 is an ionizable amino lipid that can be used for the formation of lipid n
|
| R2304199 |
ALC-0315 |
ALC-0315 is an ionisable aminolipid that is responsible for mRNA compaction and
|
| R2304200 |
Triprolidine hydrochloride |
Triprolidine hydrochloride is an orally active histamine H1 antagonist. Triproli
|
| R2304201 |
PF-06260933 |
PF-06260933 is an orally active and highly selective inhibitor of MAP4K4 with IC
|
| R2304202 |
Longdaysin |
Longdaysin is a inhibitor of the Wnt/β-catenin signaling pathway, which exerts a
|
| R2304203 |
HA-100 hydrochloride |
HA-100 hydrochloride is a potent protein kinase inhibitor, with IC50s of 4 μM, 8
|
| R2304204 |
PF-06928215 |
PF-06928215 is a cGAS (cyclic GMP-AMP Synthase) inhibitor with an IC50 of 4.9 μΜ
|
| R2304206 |
LDC7559 |
LDC7559 is a gasdermin D (GSDMD) inhibitor via blocking neutrophil extracellular
|
| R2304207 |
NCATS-SM1441 |
|
| R2304208 |
ZN-c3 |
ZN-c3 is a potent and selective Wee1 inhibitor with balanced potency, ADME, and
|
| R2304209 |
GMB-475 |
GMB-475 is a degrader of BCR-ABL1 tyrosine kinase based on PROTAC, overcoming BC
|
| R2304210 |
Gefitinib hydrochloride |
Gefitinib hydrochloride (ZD1839 hydrochloride) is a potent, selective and orally
|
| R2304211 |
AZM475271 |
AZM475271 is a potent and selective Src kinase inhibitor with IC50 of 5 nM; no i
|
| R2304212 |
Taraxasterol |
Taraxasterol is a pentacyclic triterpenoid isolated from Taraxacum mongolicum. T
|
| R2304213 |
Bicyclol |
Bicyclol(SY 801) is a anti-hepatitis drug. Target: HBV Oral administration of bi
|
| R2304214 |
HQ461 |
HQ461 is a molecular glue that promotes CDK12-DDB1 interaction to trigger cyclin
|
| R2304215 |
JNJ-5207852 dihydrochloride |
JNJ-5207852 dihydrochloride is a selective and potent histamine H3 receptor (H3R
|
| R2304216 |
Melperone hydrochloride |
|
| R2304217 |
MRK 560 |
MRK-560 is an orally active, brain barrier-penetrating γ-Secretase inhibitor, ca
|
| R2304218 |
Bifemelane hydrochloride |
Bifemelane hydrochloride (MCI-2016) is a potent, selective and competitive inhib
|
| R2304219 |
MK1903 |
MK-1903 is a potent and selective hydroxycarboxylic acid receptor 2 (HCA2, GPR10
|
| R2304220 |
Compound 10 |
GPR35 agonist 3 is a synthetic GPR35 agonist with an EC50value of 1.4 μM. GPR35
|
| R2304221 |
Zolmitriptan |
Zolmitriptan (BW-311C90; 311C90) is a 5-HT1B/1D receptor partial agonist with Ki
|
| R2304222 |
SR11237 (BMS-649) |
SR11237 (BMS-649) is a potent retinoid X receptor (RXR)-selective agonist that i
|
| R2304223 |
R-10015 |
R-10015, a broad-spectrum antiviral compound for HIV infection, acts as a potent
|