| R0012043 |
PF-07202954 |
PF-07202954 is a weakly basic DGAT2 inhibitor with an IC50 of 10 nM for human DG
|
| R0012044 |
AZD1656 |
AZD1656 is a potent, selective and orally active glucokinase activator with an E
|
| R0012045 |
反式-4-[4-(4-氨基-7,7-二甲基-7H-嘧啶并[4,5-B][1,4]噁唑-6-基)苯基]-环己基乙酰胺 |
T863 is an orally active, selective and potent DGAT1 (acyl-CoA:diacylglycerol ac
|
| R0012046 |
反式-4-[4-(4-氨基-7,8-二氢-5-氧代嘧啶并[5,4-f][1,4]氧氮杂卓-6(5H)-基)苯基]环己烷乙酸 |
PF-04620110 is a potent, selective and orally bioavailable diglyceride acyltrans
|
| R0012047 |
Pradigastat(LCQ-908) |
Pradigastat (LCQ-908) is a potent, selective and orally active diacylglycerol ac
|
| R0012049 |
(R)-CR8(CR8, (R)-Isomer) |
(R)-CR8 (CR8), a second-generation analog of Roscovitine, is a potent CDK1/2/5
|
| R0012050 |
N5-(6-氨基己基)-N7-苄基-3-异丙基吡唑并[1,5-a]嘧啶-5,7-二胺 |
BS-181 is a potent and selective CDK7 inhibitor (IC50=21 nM) than Seliciclib (HY
|
| R0012051 |
CT7001盐酸盐 |
Samuraciclib hydrochloride (CT7001 hydrochloride) is a potent, selective, ATP-co
|
| R0012053 |
TVB-3166 |
TVB-3166 is an orally-available, reversible, and selective fatty acid synthase (
|
| R0012054 |
Denifanstat(TVB-2640) |
Denifanstat (TVB-2640) is an orally active and potent Fatty Acid Synthase (FASN)
|
| R0012055 |
diABZI STING agonist-1 |
diABZI STING agonist-1 is a selective stimulator of interferon genes (STING) rec
|
| R0012056 |
STING agonist-3 |
STING agonist-3, extracted from patent WO2017175147A1 (example 10), is a selecti
|
| R0012057 |
CC-885 |
CC-885 is a cereblon (CRBN) modulator with potent anti-tumour activity. CC-885 i
|
| R0012058 |
NVP-DKY709 |
NVP-DKY709 is a potent IKZF2 inhibitor for the research of cancers.
|
| R0012059 |
Migoprotafib(GDC-1971) |
Migoprotafib (GDC-1971) (compound 199) is a SHP2 inhibitor.
|
| R0012060 |
G150 |
G150 is a highly selective human cyclic GMP-AMP synthase (h-cGAS) inhibitor with
|
| R0012061 |
LSN3318839 |
LSN3318839 is an orally efficacious positive allosteric modulator of the glucago
|
| R0012062 |
(S,R)-LSN3318839 |
(S,R)-LSN3318839 is the stereoisomer of LSN3318839 (HY-142162). LSN3318839 is an
|
| R0012063 |
GLP-1受体激动剂1 |
Orforglipron (LY3502970) (Compound 67) is an orally active agonist for Glucagon-
|
| R0012064 |
AZD0780(PCSK9-IN-12) |
PCSK9-IN-12 is a heteroaryl compound. PCSK9-IN-12 has bind affinity for PCSK9 wi
|
| R0012065 |
Tri-GalNAc(OAc)3 TFA |
Tri-GalNAc(OAc)3 TFA is a tri-GalNAc ligand that can be used for the synthesis o
|
| R0012066 |
1426159-34-3 |
|
| R0012067 |
(3R,5S)-5-((双(4-甲氧基苯基)(苯基)甲氧基)甲基)吡咯烷-3-醇 |
|
| R0012068 |
Bexotegrast (PLN-74809) |
Bexotegrast (PLN-74809) is an orally active, potent dual αvβ6/αvβ1 integrin inhi
|
| R0016001 |
DPO-1 |
DPO-1 is a potent inhibitor of the voltage-gated potassium channel subtype Kv1.5
|