当前位置：易推广 > 上海陶术生物科技有限公司 > 产品展示
企业档案
会员类型：会员
已获得易推广信誉 等级评定
(0 -40)基础信誉积累，可浏览访问
(41-90)良好信誉积累，可接洽商谈
(91+ )优质信誉积累，可持续信赖
易推广会员：5年
工商认证 【已认证】
最后认证时间：
注册号： 【已认证】
法人代表： 【已认证】
企业类型：生产商 【已认证】
注册资金：人民币万 【已认证】
产品数：86101
参观次数：3739946
自主品牌
已选条件
-
T2306BrexpiprazoleBrexpiprazole,OPC-34712,
Brexpiprazole is a partial agonist of human 5-hydroxytryptamine (5-HT) 5-HT1A and dopamine D2 receptors.
价 格：￥电议型 号：T2306产 地：美洲
-
T48502-Picolinic acid2-Picolinic acid,PCL 016,
PCL 016 is a topical antiviral agent, which inhibits adenovirus replication in rabbit.
价 格：￥电议型 号：T4850产 地：美洲
-
T49491,2-Didecanoyl-sn-glycero-3-phosphocholi1,2-Didecanoyl-sn-glycero-3-phosphocholi,1,2-Didecanoyl PC,1
1,2-Didecanoyl-sn-glycero-3-phosphocholi is a synthetic, less hydrophobic phospholipid that has been found to be useful for enhancing the absorption of peptide drugs and hormones such as insulin.
价 格：￥电议型 号：T4949产 地：美洲
-
T5782BevirimatBevirimat,PA-457,MPC-4326
Bevirimat(PA-457) is a first-in-class inhibitor of HIV-1 maturation, blocking the cleavage of the Gag capsid (CA) precursor, CA-SPI, to mature CA protein during virion maturation.
价 格：￥电议型 号：T5782产 地：美洲
-
T5843R-flurbiprofenR-flurbiprofen,(R)-Flurbiprofen,MPC7869
R-flurbiprofen is the non-cyclooxygenase inhibiting R-enantiomer of the non-steroidal anti-inflammatory drug flurbiprofen, which was assessed as a remedy for Alzheimer´s disease.
价 格：￥电议型 号：T5843产 地：美洲
-
T6325PCI-34051PCI-34051,PCI34051,PCI 34051
PCI-34051 is an effective and selective HDAC8 inhibitor (IC50: 10 nM).
价 格：￥电议型 号：T6325产 地：美洲
-
T8690Brexpiprazole HCl；化合物Brexpiprazole HClOPC 34712 dihydrochloride；OPC 34712 dihydrochloride
Brexpiprazole HCl (OPC 34712 dihydrochloride) is a new antipsychotic drug.
价 格：￥电议型 号：T8690产 地：中国大陆
-
T8638NPC 15199；Fmoc-L-亮氨酸FMOC-L-Leucine；FMOC-L-Leucine|||Fmoc-L-亮氨酸
NPC 15199 (FMOC-L-Leucine) is an anti-inflammatory agent.
价 格：￥电议型 号：T8638产 地：中国大陆
-
T8561Apcin；化合物ApcinApcin
Apcin is a potent and competitive inhibitor of anaphase-promoting complex/cyclosome (APC/C(Cdc20)) E3 ligase activity. Apcin competitively inhibits APC/C-dependent ubiquitylation by binding to Cdc20 and preventing substrate recognition. It acts by blocking mitotic exit and being synergistically amplified by co-addition of Ts-Arg-OMe.
价 格：￥电议型 号：T8561产 地：中国大陆
-
T8527CPYPP；化合物CPYPPCPYPP
CPYPP is an inhibitor of DOCK2-Rac1 interaction. CPYPP binds to DOCK2 DHR-2 domain and inhibits the guanine nucleotide exchange factor (GEF) activity of DOCK2DHR-2 for Rac1 in a dose-dependent manner(IC50 : 22.8 μM). CPYPP also inhibits DOCK180, DOCK5 and less DOCK9
价 格：￥电议型 号：T8527产 地：中国大陆
-
T8412(S,R,S)-AHPC；化合物MDK7526VH032-NH2|||MDK7526|||VHL ligand 1；VH032-NH2|||MDK7526|||VHL ligand 1
(S,R,S)-AHPC (VH032-NH2) is the VH032-based VHL ligand used in the recruitment of the von Hippel-Lindau (VHL) protein. (S,R,S)-AHPC is potential useful for the targeted degradation of the androgen receptor.
价 格：￥电议型 号：T8412产 地：中国大陆
-
T83978Safingol hydrochloride；沙芬戈盐酸盐SPC 100270 hydrochloride|||L-threo-dihydrosphingosine hydrochloride；SPC
Safingol hydrochloride (L-threo-dihydrosphingosine hydrochloride) is a specific inhibitor of protein kinase C. It induces autophagy in solid tumor cells and cancer cell death by inhibiting the PKC and PI3-kinase pathways.BIIB 722 Mesylate is a selective sodium-hydrogen exchange inhibitor. Safingol hydrochloride inhibits PKC and PI3k.
价 格：￥电议型 号：T83978产 地：中国大陆
-
T83974OPC18750 HCl；化合物 OPC18750 HClOPC18750 HCl
OPC18750 HCl is a potential phosphodiesterase inhibitor with positive inotropic effects that can be used to study asthma, cancer, diabetes, and psychiatric disorders.
价 格：￥电议型 号：T83974产 地：中国大陆
-
T83954VH 032 amide-alkylC7-acid；化合物 VH 032 amide-alkylC7-acid(S,R,S)-AHPC-amido-C7-acid；(S,R,S)-AHPC-amido
VH 032 amide-alkylC7-acid is a specialized compound designed for PROTAC research and development, serving as a functionalized von-Hippel-Lindau (VHL) protein ligand. It combines an E3 ligase ligand with an alkylC7 linker, ending in a terminal carboxylic acid for efficient conjugation to target protein ligands. This compound is among a series of functionalized tool molecules aimed at facilitating PROTAC R&D efforts.
价 格：￥电议型 号：T83954产 地：中国大陆
-
T8350TPCK；L-1,4’-甲基磺酰基-2-苯基乙基氯甲基酮TPCK
TPCK is an irreversible inhibitor of chymotrypsin-like proteases that affect cell proliferation, apoptosis, and tumorigenesis
价 格：￥电议型 号：T8350产 地：中国大陆
-
T82943AtPCO4-IN-1；化合物 AtPCO4-IN-1AtPCO4-IN-1
AtPCO4-IN-1 is a selective AtPCO4 inhibitor, exhibiting an IC50 value of 264.4 μM [1].
价 格：￥电议型 号：T82943产 地：中国大陆
-
T82888Bibapcitide；化合物 BibapcitideBibapcitide
Bibapcitide, a 26-amino-acid peptide, acts as a thrombosis inhibitor [1].
价 格：￥电议型 号：T82888产 地：中国大陆
-
T82632Cys-C-cGMP；化合物 Cys-C-cGMPCys-C-cGMP
Cys-C-cGMP serves as an autophagy tag for AUTACs (autophagy-targeting chimeras). It enhances K63-linked ubiquitination of mitochondria within HeLa cells [1].
价 格：￥电议型 号：T82632产 地：中国大陆
-
T81535PCSK9-IN-20；化合物 PCSK9-IN-20PCSK9-IN-20
PCSK9-IN-20 (Compound 3i) is a PCSK9 inhibitor exhibiting an IC50 value of 3.96 ?M, shown to reduce PCSK9 and enhance LDLR protein levels in vitro [1].
价 格：￥电议型 号：T81535产 地：中国大陆
-
T81480Phytochelatin 2 (PC2) (TFA)；化合物 Phytochelatin 2 (PC2) (TFA)Phytochelatin 2 (PC2) (TFA)
Phytochelatin 2 (PC2) TFA, a heavy metal-binding peptide, facilitates metal chelation, mitigates metal toxicity, and promotes metal homeostasis within internal environments [1].
价 格：￥电议型 号：T81480产 地：中国大陆
