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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
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DNA Damage
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Cas号索引 1
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Cas号索引 1
164658-13-3 | CGP60474
(Catalog# : 185171)
CGP60474是一种有效的双cdk1/cdk2抑制剂(IC50值分别为20和50 nM)。
1190932-38-7 | COH29
(Catalog# : 184127)
COH29是一种可口服的、芳香的取代噻唑和人核糖核苷酸还原酶(RNR)
1039455-84-9 | COTI-2
(Catalog# : 184320)
COTI-2是P53基因调制器和AKT2抑制剂。OTI-2在体外和体内都对多种人类
1202402-40-1 | CPI-444
(Catalog# : 18439)
CPI-444,又名V81444,是一种腺苷A2A受体的口服拮抗剂。
1443437-74-8 | CCG-203971
(Catalog# : 18437)
CCG-203971是前列腺癌细胞系PC-3中SRE活化的抑制剂(IC50 = 6.4 μM),能够
175140-00-8 | CP-376395 free base
(Catalog# : 184213)
CP-376395 is a CRF1-selective antagonist. CRF1 receptor signaling regulates food and
1402152-13-9 | Copanlisib HCl
(Catalog# : 18351)
Copanlisib也称为BAY 80 - 6946,是一个强有力的磷酸肌醇3-激酶(PI3K)抑制
19608-29-8 | CB-03-01
(Catalog# : 1712153)
CB-03-01, also known as cortexolone 17alpha-propionate, is a topical and peripherally
1797989-42-4 | CHIR99021 HCl
(Catalog# : 179825)
CHIR99021,又被称为 CT99021,是糖原合成酶激酶3β(GSK3β)抑制剂,
1005334-57-5 | CVT-10216
(Catalog# : 179818)
CVT-10216是强有力的和有选择性的,乙醛脱氢酶2(ALDH2)的可逆性抑
14513-15-6 | Cambinol
(Catalog# : 178313)
Cambinol是一种SIRT抑制剂。它能抑制促炎性细胞因子的表达,提高模
119671-47-5 | 2-吗啉-4-基-6-噻蒽-1-基吡喃-4-酮
(Catalog# : 1781504)
2-吗啉-4-基-6-噻蒽-1-基吡喃-4-酮;2-Chloro-6-morpholinopyran-4-one
1163719-56-9 | CCT196969
(Catalog# : 178913)
CCT196969,是一种pan-RAF / SFK抑制剂对治疗单纯的BRAF和NRAS突变型黑色
1846570-40-8 | CM-579
(Catalog# : 2017874)
CM-579是一种生物活性化学药品 。
1072946-52-1 | 5-氯-2-氰基苯硼酸
(Catalog# : 20178120)
5-氯-2-氰基苯硼酸
113359-04-9 | 头孢唑兰
(Catalog# : 17032402)
头孢唑兰(SCE 2787)是第四代头孢菌素。
122841-10-5 | 头孢噻利
(Catalog# : 17032401)
头孢噻利是一种广泛使用于β-内酰胺的抗生素。
1015474-32-4 | CC-122
(Catalog# : 17030313)
CC-122是一种具有潜在抗肿瘤活性的多向性通路调制器。
125314-13-8 | CP21R7
(Catalog# : 17022715)
CP21R7,也称CP21,是一个强有力的和选择性GSK-3β抑制剂。
1316215-12-9 | Citarinostat
(Catalog# : 17022701)
Citarinostat是一种HDAC6特异性抑制剂,HDAC6和HDAC3的IC50分别为4nM和76
147859-80-1 | CA-074 methyl ester (CA-074 Me)
(Catalog# : 17011104)
CA-074 Me是CA- 074的一种膜-渗透性衍生物,作为一种不可逆转的蛋白
1429639-50-8 | CZ415
(Catalog# : 17011101)
CZ415,是一种有效的ATP-竞争性mTOR抑制剂,拥有非常好的细胞渗透率
1628208-23-0 | CPI-455
(Catalog# : 17109005)
CPI-455是一种特殊的KDM5抑制剂,提高了H3K4三甲基化(H3K4me3)的全球水
199986-75-9 | CVT-313
(Catalog# : 16122923)
CVT-313 is a potent and selective inhibitor of CDK2 that prevents neointimal prolifer
1213669-91-0 | CTP354
(Catalog# : 16122922)
CTP354, also known as C-21191, a novel deuterated subtype-selective GABA(A) modulator
1198300-79-6 | Cerdulatinib (PRT062070)
(Catalog# : 16122917)
Cerdulatinib, also known as PRT2070 and PRT062070, is a n ovel, oral, dual spleen tyr
178946-89-9 | C-DIM12
(Catalog# : 16122915)
C-DIM12 is a novel synthetic activator of Nurr1. C-DIM12 induces dopaminergic gene ex
1813527-81-9 | CCG215022
(Catalog# : 16122914)
CCG215022 is a potent GRK2 and GRK5 inhibitor. CCG215022 exhibited nanomolar IC50 val
1439399-58-2 | CB-839
(Catalog# : 16122913)
CB-839 an is orally bioavailable inhibitor of glutaminase, with potential antineoplas
1477949-42-0 | CAY10683
(Catalog# : 16122912)
CAY10683, also known as Santacruzamate A, is a potent and selective histone deacetyla
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产品分类
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-- Angiogenesis
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
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----
Parasite
-- Apoptosis
----
PD-1
----
PD-L1
----
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----
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----
TNF-alpha
----
Survivin
----
IAP
----
PERK
----
p53
----
Mdm2
----
E1/E2/E3 Enzyme
-- Autophagy
----
LRRK2
----
CXCR
----
Autophagy
-- Cell Cycle
----
CDK
----
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----
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----
Chk
----
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----
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----
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----
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----
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----
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----
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----
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----
Eukaryotic Initiation Factor (eIF)
-- Cytoskeleton
----
HSP
----
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----
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----
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----
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----
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----
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-- DNA Damage
----
PARP
----
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----
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----
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----
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----
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----
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-- Epigenetics
----
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----
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----
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----
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----
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----
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----
HDAC
----
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----
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----
METTL3
----
Epigenetic Reader Domain
-- GPCR & G Protein
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Histamine Receptor
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-- MAPK
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----
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----
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----
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MAP4K
-- Membrane Transporter/Ion Channel
----
BCRP
----
CFTR
----
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----
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----
HCN Channel
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----
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Na+/K+ ATPase
----
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Calcium Channel
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CRAC Channel
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GlyT1
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P2X Receptor
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-- Metabolism
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PPAR
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----
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----
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----
HMG-CoA Reductase
----
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----
FXR
----
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----
TDO
----
Carbonic Anhydrase
----
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----
IDO
----
Mitochondrial Metabolism
----
MAGL
----
Epoxide Hydrolase
----
LXR
----
Myeloperoxidase (MPO)
----
RAR/RXR
----
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----
UGT
----
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----
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----
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-- Neuronal Signaling
----
COX
----
Histamine Receptor
----
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----
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----
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-- NF-κB
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-- Protein Tyrosine Kinase
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----
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----
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----
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----
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-- PI3K/Akt/mTOR
----
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----
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----
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----
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----
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----
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----
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----
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----
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----
mTOR
----
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----
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----
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-- Stem Cells & Wnt
----
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----
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----
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----
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----
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----
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----
smo
-- TGF-beta/Smad
----
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----
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----
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-- Ubiquitin
----
Proteasome
----
p97
----
Deubiquitinase
----
DUB
-- Vitamin D Related
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Newest added products
抑制剂/受体激动剂
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On Sale
新产品
天然化合物
最新产品
85622-93-1 | Temozolomide
(Catalog# : 25209)
替莫唑胺是一种烷化剂。
2035010-37-6 | ALT-007
(Catalog# : 25157)
ALT-007 是一种口服生物可利用的 SPT 抑制剂,比多球菌素更有效,
2376397-93-0 | Opakalim
(Catalog# : 25193)
Opakalim(BHV-7000)是Kv7.2/7.3钾通道(KCNQ2/3)的口服小分子激活剂,
2102501-84-6 | PF-06835919 ( MDK-1846 )
(Catalog# : 193264)
MDK1846是一种强效的酮己糖激酶(KHK)抑制剂。
2271348-04-8 | MK256
(Catalog# : 25208)
MK256是一种新型CDK8抑制剂,通过下调STAT通路在急性髓系白血病(
2351225-46-0 | NSD1 抑制剂 BT5
(Catalog# : 25207)
BT5可有效抑制NSD1,与细胞中的SET结构域结合,并降低H3K36me2水平。
1049704-18-8 | MA242 TFA
(Catalog# : 25206)
MA242是一种MDM2和NFAT1双重抑制剂,可诱导MDM2自泛素化及降解,并抑
2800223-30-5 | Dabogratinib ( TYRA-300 )
(Catalog# : 24073)
Dabogratinib ( TYRA-300 )是一种口服选择性成纤维细胞生长因子受体3(
N/A | AF710B
(Catalog# : 25205)
AF710B 是一种高效、选择性变构 M1 毒蕈碱和 σ1 受体激动剂。 AF710
2957874-18-7 | MAT2A inhibitor 5
(Catalog# : 25204)
MAT2A抑制剂5具有抑制MAT2A的高效力和对MTAP缺失的癌症细胞系的显著