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+86-17702719238
sales@sun-shinechem.com
首页
抑制剂/受体激动剂
PI3K/Akt/mTOR
Epigenetics
Protein Tyrosine Kinase
Angiogenesis
Apoptosis
Autophagy
JAK/STAT
MAPK
Cytoskeletal Signaling
Cell Cycle
TGF-beta/Smad
DNA Damage
Stem Cells & Wnt
Ubiquitin
Neuronal Signaling
NF-κB
GPCR & G Protein
Metabolism
Anti-infection
Proteases
Immunology & Inflammation
Vitamin D Related
Membrane Transporter/Ion Channel
others
PROTAC
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Amines
Amino Acids
Anilines
Boronic Acids
Bromides
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Cas号索引 1
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Cas号索引 1
1399715-48-0 | Setafrastat
(Catalog# : 192146)
Setafrastat是一种转胺酶抑制剂和血管内皮生长因子(VEGF)促进剂。
1037210-93-7 | Saridegib
(Catalog# : 1812251)
Saridegib,又称IPI-926,是一种口服生物利用的环帕胺衍生物,是Hed
1260612-13-2 | SAR260301
(Catalog# : 1812134)
SAR260301是强有力的和选择性组 I 磷脂酰肌醇-3-激酶(PI3K)β特定抑制
1613695-14-9 | SGC-CBP30
(Catalog# : 1810244)
SGC-CBP30是CREBBP (CBP)和EP300的有效选择性抑制剂;它们是一般的转录共
1362850-20-1 | Seletalisib
(Catalog# : 1810221)
Seletalisib,也被称为UCB-5857,是一种有效的选择性PI3激酶抑制剂,
188817-13-2 | SC-560
(Catalog# : 185113)
SC-560是一种有效的具有口服活性和选择性的COX-1抑制剂。
1609452-30-3 | SEL120-34A盐酸盐
(Catalog# : 18574)
SEL120-34A是一种高效、选择性的CDK8抑制剂,活跃于AML细胞中,具有
1816294-67-3 | SR-4370
(Catalog# : 1842814)
SR-4370是一种HDAC抑制剂。
1821908-49-9 | SGC2085盐酸盐
(Catalog# : 184287)
SGC2085是一种强效的选择性共激活剂,它可以使精氨酸甲基转移酶
1222097-72-4 | S38093盐酸盐
(Catalog# : 184176)
S38093是组胺H3受体的反向激动剂。
1173022-21-3 | STO-609醋酸盐
(Catalog# : 184123)
STO-609是一种细胞渗透性抑制剂,钙/钙调蛋白依赖性激酶激酶(CaMK
1599441-71-0 | Super-TDU
(Catalog# : 18495)
Super-TDU是靶向YAP-TEADs interaction的抑制性多肽。
1253955-19-9 | (S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)methyl 2,4-dimethylbenzoate
(Catalog# : 183219)
(S)-(4-(3-(tert-butoxycarbonyl)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)phenyl)met
132513-51-0 | (S)-2-羟基丁酸正丁酯
(Catalog# : 1712291)
(S)-2-羟基丁酸正丁酯是一种分子砌块。
14892-97-8 | SCR7 pyrazine
(Catalog# : 1712261)
SCR7吡嗪是DNA连接酶IV的小分子抑制剂,防止非同源端连接通过干扰
1333207-63-8 | SAR-7334盐酸
(Catalog# : 17101610)
SAR-7334是一种新颖的、高效的、生物可利用的TRPC6通道,打开了新
1160833-51-1 | SEN-826
(Catalog# : 1710168)
SEN-826是一种潜在抗癌剂。
1366002-50-7 | Senexin A
(Catalog# : 1710136)
Senexin A是一种强效的选择性与抑制剂(IC50 = 280 nm)。Senexin A结合
1799633-27-4 | S63845
(Catalog# : 171071)
s63845是专门结合MCL1的BH3结合槽高亲和力的小分子。s63845有效杀死
1105698-15-4 | Salermide
(Catalog# : 1791511)
salermide是一个强大的肿瘤特异性凋亡的影响长寿基因蛋白质抑制剂
1308672-74-3 | Sulfatinib
(Catalog# : 179135)
Sulfatinib是一种口服的血管内皮生长因子受体(VEGFR)1, 2,3,和成
101526-62-9 | 司美利特盐酸盐
(Catalog# : 179830)
司美利特,也称为CK-1752,是III类抗心律失常药。它是一种选择性
168835-82-3 | SU-1498
(Catalog# : 17984)
SU-1498是一种选择性的受体酪氨酸激酶抑制剂,血管内皮生长因子
1174428-47-7 | SF2523
(Catalog# : 17918)
SF2523是一种高效、选择行的日常pan-PI3K/BRD4抑制剂。具有明显的选
1450881-55-6 | SAR-20347
(Catalog# : 1781101)
SAR-20347是一种强力JAK1和酪氨酸激酶2的双抑制剂 (TYK2).
1523406-39-4 | SAR-405
(Catalog# : 2017882)
SAR-405是一种有效且选择性的PIK3C3/Vps34抑制剂,防止自噬和协同MTO
148554-65-8 | 雷帕霉素(钠盐)
(Catalog# : 20177313)
雷帕霉素是第一个体内open-ring代谢物,不影响mTOR的雷帕霉素抑制Ch
1184843-57-9 | SAR-020106
(Catalog# : 17031004)
SAR-020106是一种 ATP -竞争性、强效和选择性的CHK1抑制剂,其IC50为1
1456632-41-9 | SH5-07
(Catalog# : 17031002)
SH5-07是一种健壮的氧肟抗酸的STAT3抑制剂,它能在体外诱导抗肿瘤
138794-73-7 | Sardomozide HCl
(Catalog# : 17030306)
Sardomozide,又名SAM486A或CGP48664,是第二代多胺合成抑制剂,它抑制
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产品分类
信号通路
-- PI3K/Akt/mTOR
----
PI3K
----
Akt
----
GSK-3
----
S6 Kinase
----
AMPK
----
DNA-PK
----
MELK
----
PIKfyve
----
PI4K
----
PTEN
----
mTOR
----
ATM
----
PDK-1
----
ATR
-- Epigenetics
----
PARP
----
JAK
----
Pim
----
PKC
----
PKD
----
Sirtuin
----
Histone Demethylase
----
Histone Acetyltransferase
----
HDAC
----
HIF-PH
----
Aurora Kinase
----
Histone Methyltransferase
----
METTL3
----
Epigenetic Reader Domain
-- 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
-- Angiogenesis
----
VEGFR
----
JAK
----
EGFR
----
PDGFR
----
FLT3
----
FGFR
----
Bcr-Abl
----
Src
----
ALK
----
Syk
----
FAK
----
BTK
----
HIF
-- Apoptosis
----
PD-1
----
PD-L1
----
Bcl-2
----
Caspase
----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- JAK/STAT
----
JAK
----
STAT
----
Pim
----
EGFR
-- MAPK
----
MEK
----
Raf
----
p38 MAPK
----
ERK
----
MNK
----
Mixed Lineage Kinase
----
JNK
----
MAP4K
-- Cytoskeletal Signaling
----
Akt
----
Bcr-Abl
----
PKC
----
FAK
----
HSP
----
Kinesin
----
Integrin
----
Dynamin
----
Wnt
----
β-catenin
-- Cell Cycle
----
CDK
----
PD-1
----
PD-L1
----
Chk
----
ROCK
----
PLK
----
APC
----
Wee1
----
DYRK
----
c-Myc
----
Aurora Kinase
----
ROCK inhibitor
-- TGF-beta/Smad
----
Bcr-Abl
----
PKC
----
ROCK
----
TGF-beta/Smad
-- DNA Damage
----
PARP
----
DNA/RNA Synthesis
----
Sirtuin
----
Topoisomerase
----
DNA-PK
----
Telomerase
----
RAD51
----
HDAC
----
ATM
----
DNA alkylator
----
Mps1
-- Stem Cells & Wnt
----
GSK-3
----
JAK
----
STAT
----
ROCK
----
TGF-beta/Smad
----
Wnt
----
γ-secretase
----
β-catenin
----
smo
-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
-- 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
----
α-Synuclein
----
Tau Protein
----
Cannabinoid Receptor
----
Transthyretin (TTR)
-- NF-κB
----
NF-κB
----
HDAC
----
IKK
-- 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
----
Sigma Receptor
----
Ras
----
mAChR
----
Cholecystokinin Receptor
----
Melanocortin Receptor
----
RXFP Receptor
-- 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
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
Acyltransferase
----
UGT
----
MMP
----
ATP Citrate Lyase
-- Anti-infection
----
CMV
----
Filovirus
----
HBV
----
HCV
----
HIV
----
HSV
----
Influenza Virus
----
RSV
----
SARS-CoV
----
Antibacterial
----
Antifungal
----
Parasite
-- Proteases
----
Proteasome
----
Caspase
----
HIV Protease
----
MMP
----
γ-secretase
----
DPP4
----
Mitochondrial Metabolism
----
Isocitrate Dehydrogenase (IDH)
----
FPTase
----
Acetyl-CoA Carboxylase
----
Glutaminase
-- 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
-- Vitamin D Related
----
VD/VDR
-- 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
-- others
----
PKK
----
Others modulator
----
Estrogen Receptor/ERR
----
ChoKα
-- PROTAC
----
Molecular Glues
--
Antibody-drug Conjugate/ADC Related
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
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2375779-31-8 | GP130 modulator-1
(Catalog# : 25062)
GP130 modulator-1 (compound A33) 是一种GP130信号通路调节剂。GP130 modulato
877459-36-4 | TGN 073
(Catalog# : 25061)
TGN 073 is a facilitator of aquaporin-4 (AQP4), an astroglial water channel. The rats
2257492-95-6 | OPN expression inhibitor 1
(Catalog# : 25060)
OPN expression inhibitor 1 (Compound 11) is an osteopontin (OPN) expression inhibitor
3036109-10-8 | SDU-071
(Catalog# : 25059)
SDU-071 is a potent and orally active inhibitor of BRD4-p53 inhibitor. SDU-071 suppre
2644662-83-7 | BBC0403
(Catalog# : 25058)
BBC0403 is a selective BRD2 inhibitor. BBC0403 inhibits the progression of osteoarthr
694488-83-0 | MFI8
(Catalog# : 25057)
MFI8 is a Mitochondrial Fusion Inhibitor
146255-66-5 | DHPG
(Catalog# : 25056)
DHPG, also known as (RS)-3,5-DHPG, is a selective agonist for group I metabotropic gl
2413020-56-9 | BAY-593 free base
(Catalog# : 25055)
BAY-593 is an orally active inhibitor of geranylgeranyltransferase-I (GGTase-I) that
188425-85-6 | Boscalid
(Catalog# : 25054)
Boscalid is a broad spectrum fungicide used in agriculture to protect crops from fung
690681-65-3 | SABA1
(Catalog# : 25053)
SABA1 is an antibacterial agent against Pseudomonas aeruginosa and Escherichia coli.