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+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
Angiogenesis
Anti-infection
Apoptosis
Autophagy
Cell Cycle
Cytoskeleton
DNA Damage
Epigenetics
GPCR & G Protein
Immunology & Inflammation
JAK/STAT
MAPK
Membrane Transporter/Ion Channel
Metabolism
Neuronal Signaling
NF-κB
Protein Tyrosine Kinase
Proteases
PI3K/Akt/mTOR
Stem Cells & Wnt
TGF-beta/Smad
Ubiquitin
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Cas号索引 1
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Cas号索引 1
1211441-98-3 | Ribociclib (LEE011)
(Catalog# : 51911)
Ribociclib (LEE011) is an orally available, and highly specificCDK4/6inhibitor. Phase
1020634-41-6 | Soclenicant (BNC-210 ; IW-2143)
(Catalog# : 25195)
Soclenicant (BNC-210;IW-2143)是一种新型的α7烟碱型乙酰胆碱受体负
1898206-17-1 | Safusidenib
(Catalog# : 25149)
Safusidenib,也称为DS-1001,是一种口服异柠檬酸脱氢酶[NADP]细胞质(
17094-01-8 | Sepiapterin
(Catalog# : 25117)
Sepiapterin is a tetrahydrobiopterin (BH4) precursor.
1415792-84-5 | Sovleplenib
(Catalog# : 25107)
Sovleplenib is a tyrosine kinase inhibitor. It is also an antineoplastic agent.
1394808-20-8 | SUVN-G3031 HCl
(Catalog# : 25087)
SUVN-G3031 is a Histamine H3 receptor antagonist, which is potentially useful for tre
160162-42-5 | SR-11302
(Catalog# : 24153)
SR 11302 is an activator protein-1 (AP-1) transcription factor inhibitor.
1150153-86-8 | SR 16584
(Catalog# : 24137)
SR 16584 is an antagonist of the α3β4 nAChR subtype (IC50 = 10.2 μM).
1262873-06-2 | Sepetaprost
(Catalog# : 24119)
Sepetaprost is a prodrug of ONO-AG-367. It has been used in trials studying the treat
152121-30-7 | SB-202190
(Catalog# : 24106)
SB-202190 is a highly selective, potent and cell-permeable inhibitor of p38 MAP kinas
1648843-04-2 | SX-682
(Catalog# : 24082)
SX-682 is a potent and selective Cxcr1/2 inhibitor potentially useful for castration-
1933514-13-6 | Sebetralstat free base
(Catalog# : 24048)
Sebetralstat(KVD-900),一种口服血浆激肽释放酶抑制剂。
1878218-66-6 | SY-008 乙酸盐
(Catalog# : 24016)
SY-008 是一种钠葡萄糖转运蛋白 1 (SGLT1) 抑制剂。
1480443-32-0 | SY-008
(Catalog# : 24021)
SY-008 是一种钠葡萄糖转运蛋白 1 (SGLT1) 抑制剂。
194032-32-1 | (S)-1-BOC-2-甲基-[1,4]二氮杂环庚烷
(Catalog# : 20541)
131690-60-3 | (S)-3-氨基-3-(4-氯苯基)-丙酸
(Catalog# : 20516)
1980023-96-8 | (S)-1-(6-(4-氟-1H-吡唑-1-甲基)吡啶-3-甲基)乙胺
(Catalog# : 20396)
100874-08-6 | SB-4 agonist
(Catalog# : G20378)
SB 4 is a potent BMP4 agonist.
1310422-41-3 (HCl) | SEP-363856 盐酸盐
(Catalog# : 822222)
SEP-363856 是一种新型微量胺受体 1 (TAAR1) 激动剂,具有血清素 5-HT1
1629138-41-5 | SRI-011381
(Catalog# : L20355)
SRI-011381 is an agonist of the TGF-beta signaling pathway for treatment of Alzheimer
1449597-34-5 | SMN-C3 抑制剂
(Catalog# : 20344)
SMN-C3 是一种口服活性 SMN2 剪接调节剂。可用于脊椎肌肉萎缩 (SMA)
1619931-27-9 | Seralutinib
(Catalog# : 21238)
Seralutinib,也称为 PK-10571 和 GB002,是一种新型吸入性 Pdgfr 激酶抑
1446712-19-1 | SNG-1153
(Catalog# : 21228)
SNG-1153 is a modulator of estrogen receptor ER-alpha36.
1293281-49-8 | Seltorexant
(Catalog# : 81498)
Seltorexant, also known as JNJ-42847922 and MIN-202, is a selective orexin-2 receptor
1415792-84-5 | Samelisant
(Catalog# : 20123101)
Samelisantis a novel, highly selective and potent small molecule oral inhibitor targe
1401682-78-7 | Senaparib
(Catalog# : 20103002)
Senaparib (IMP4297) is a novel agent targeting PARP (poly-ADP ribose polymerase) with
1433953-83-3 | SAR131675
(Catalog# : 2091901)
SAR131675 is a potent and selective VEGFR-3 inhibitor. It inhibited VEGFR-3 tyrosine
18298-32-4 | SB 225002
(Catalog# : 2071510)
1369767-20-3 | ((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2-diyl)dimethanol
(Catalog# : 202331)
我们可以提供公斤级定制合成。((1S,2R)-1-(3-fluorophenyl)cyclopropane-1,2
1393477-72-9 (free base) | Selinexor free base
(Catalog# : 2051501)
Selinexor, also known as KPT-330, is an orally bioavailable, potent and selective XPO
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产品分类
信号通路
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Src
----
ALK
----
Syk
----
HIF
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
----
Eukaryotic Initiation Factor (eIF)
----
NEKs
-- Cytoskeleton
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
----
Gap Junction Protein
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- GPCR & G Protein
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
Endothelin Receptor
----
SGLT
----
OX Receptor
----
CaSR
----
CXCR
----
Vasopressin Receptor
----
Glucagon Receptor
----
Prostaglandin Receptor
----
5-HT Receptor
----
Adrenergic Receptor
----
Cannabinoid Receptor
----
Sphingosine 1 Phosphate Receptor
----
PKA
----
Adenosine Receptor
----
GnRH
----
LPL Receptor
----
Ras
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
----
Bradykinin Receptor
----
GLP Receptor
-- Immunology & Inflammation
----
PD-1
----
PD-L1
----
COX
----
CCR
----
Histamine Receptor
----
TLR
----
CXCR
----
MALT
----
TDO
----
NOS
----
NADPH-oxidase
----
IDO
----
Thrombopoietin Receptor(TPO)
----
NLR inhibitor
----
Interleukin Related
----
CD73
----
Complement System
----
Aryl Hydrocarbon Receptor
----
Kallikrein
----
IRAK
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Membrane Transporter/Ion Channel
----
BCRP
----
CFTR
----
EAAT2
----
GABA Receptor
----
HCN Channel
----
Monoamine Transporter
----
Na+/Ca2+ Exchanger
----
Na+/K+ ATPase
----
nAChR
----
Calcium Channel
----
Chloride Channel
----
CRAC Channel
----
GlyT1
----
iGluR
----
P2X Receptor
----
P-glycoprotein
----
Amino acid transporter
----
Monocarboxylate Transporter
----
Potassium Channel
----
Proton Pump
----
Potassium Channel
-- Metabolism
----
PPAR
----
P450
----
HSP
----
PDE
----
Factor Xa
----
Phospholipase
----
FAAH
----
CETP
----
Lipoxygenase
----
HMG-CoA Reductase
----
Fatty Acid Synthase
----
FXR
----
NAMPT
----
TDO
----
Carbonic Anhydrase
----
Monoamine Oxidase
----
IDO
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
----
Ketohexokinase(KHK)
----
Lactate dehydrogenase
----
Glyoxalase (GLO)
-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
Dopamine Receptor
----
Opioid Receptor
----
GABA Receptor
----
OX Receptor
----
Amyloid-β
----
5-HT Receptor
----
γ-secretase
----
Adrenergic Receptor
----
NMDA Receptor
----
GlyT1
----
Beta-secretase
----
Sigma Receptor
----
mAChR
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
----
Melanocortin Receptor
----
Glucosylceramide Synthase (GCS)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
----
Keap1-Nrf2
-- Protein Tyrosine Kinase
----
VEGFR
----
EGFR
----
PDGFR
----
IGF-1R
----
FLT3
----
FGFR
----
c-Kit
----
Src
----
ALK
----
Ephrin receptor
----
BTK
----
Trk receptor
----
c-Met/HGFR
----
Syk (Spleen tyrosine kinase)
----
TAM Receptor
----
ULK1
----
CSF-1R
----
TYK2
----
ROS Kinase
----
Bcr-Abl
----
FAK
----
RET
----
Phosphoglycerate Kinase (PGK)
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
----
Methionine Adenosyltransferase (MAT)
----
Lipase
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- TGF-beta/Smad
----
PKC
----
ROCK
----
TGF-beta/Smad
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
----
DUB
-- Vitamin D Related
----
VD/VDR
-- PROTAC
----
Molecular Glues
----
PROTACs
--
Antibody-drug Conjugate/ADC Related
--
Microbiology
-- Others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
----
Newest added products
抑制剂/受体激动剂
中间体
分子砌块
--
Aldehydes
--
Amines
--
Amino Acids
--
Anilines
--
Boronic Acids
--
Bromides
--
Carboxes
--
Catalysts
--
Chiral Compounds
--
Deuterated
--
Fluorides
--
Imidazoles
--
Indoles and Oxindoles
--
Iodos
--
Nitro Compounds
--
Oxazoles
--
Peg Linkers
--
Phenols
--
Piperidines
--
Pyridines
--
Pyrimidines
--
Quinolines
--
Sulfonamides
--
Thiazoles
--
Trifluoroborates
--
Other Azoles
--
Other Heterocycles
--
Other Building Blocks
--
On Sale
新产品
天然化合物
最新产品
1802632-22-9 | CT1812 ( Zervimesine )
(Catalog# : 193283)
CT-1812是一种同类首创的、可口服的sigma-2/PGRMC1拮抗剂(αβ寡聚体
3041025-10-6 | BLU-808
(Catalog# : 26A024)
BLU-808是一种针对肥大细胞疾病的野生型c-KIT的强效且具有选择性的
2243882-74-6 | Zedoresertib
(Catalog# : 26A023)
Zedoresertib(Debio 0123)是一种脑渗透剂,高选择性WEE1激酶抑制剂。
3033961-38-2 | BEN-28010
(Catalog# : 26A022)
BEN-28010是一种自由脑渗透剂,强效且具有选择性的CHK1抑制剂。
3107291-07-3 | 4-((2-(甲氨基)-6-(2,2,2-三氟乙基)噻吩并[2,3-d]嘧啶-4-基)氨基)哌啶-1-甲酸叔丁酯
(Catalog# : 26B007)
2565656-70-2 | Muvalaplin
(Catalog# : 20528)
Muvalaplin是一种小分子,通过干扰载脂蛋白(a)与载脂蛋白B100的结合
2925330-18-1 | MAT2A-IN-22
(Catalog# : 26A021)
MAT2A-IN-22 (Compound 29-1) 是一种可透过血脑屏障的和口服有效的 MAT2A
1497439-74-3 | AD-8007
(Catalog# : 26A018)
AD-8007是一种选择性且可穿透血脑屏障的乙酰辅酶A合成酶2(ACSS2)
1802650-31-2 | ZY-444
(Catalog# : 26A020)
ZY-444是一种通过抑制PC活性发挥抗癌作用的药物。
2306525-79-9 | AD-5584
(Catalog# : 26A019)
AD-5584是一种新型脑渗透性ACSS2抑制剂。