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T21548PF-4981517;化合物PF-4981517CYP3cide;CYP3cide
PF-4981517 (CYP3cide) is a efficient, specific and time-dependent inhibitor of cytochrome P4503A4 (CYP3A4). The IC 50 values for CYP3A activity are 0.03 μM,17 μM, and 71 μM for CYP3A4, CYP3A5, and CYP3A7, respectively. PF-4981517 is able to be used to distinguish the contributions of CYP3A4 versus CYP3A5 on drug Metabolism.
价 格:¥电议型 号:T21548产 地:中国大陆
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T21547PAF (C16);化合物PAF (C16)C16-PAF;C16-PAF
PAF (C16) is a potent MAPK and MEK/ERK activator that induces increased vascular permeability. PAF (C16) (PAF (C16)) is a platelet-activating factor, a phospholipid-derived mediator and a ligand for PAF G protein-coupled receptor (PAFR). PAF (C16) has shown anti-apoptotic and anti-inflammatory activity in vitro, inhibiting Caspase-dependent apoptosis by interacting with its receptor (PAF-R) to perform cell signaling.
价 格:¥电议型 号:T21547产 地:中国大陆
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T21546NG,NG-dimethyl-L-Arginine dihydrochloride;不对称二甲基精氨酸二盐酸盐NG,NG-dimethyl-L-Arginine dihydrochloride
NG,NG-dimethyl-L-Arginine dihydrochloride is an endogenous nitric oxide synthase inhibitor. Nitric oxide (NO) that is synthesised from L-arginine contributes to the regulation of blood pressure and to host defence[1].
价 格:¥电议型 号:T21546产 地:中国大陆
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T21544AZD-5597;化合物AZD-5597(S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)
AZD-5597 ((S)-(4-((5-Fluoro-4-(1-isopropyl-2-methyl-1H-imidazol-5-yl)pyrimidin-2-yl)amino)phenyl)(3-(methylamino)pyrrolidin-1-yl)methanone) is a potent imidazole pyrimidine amide CDK inhibitor.
价 格:¥电议型 号:T21544产 地:中国大陆
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T21543AP 18;化合物AP 18AP 18
AP-18 is a potent and selective TRPA1 inhibitor. AP-18 inhibits activation of TRPA1 induced by 50 μM Cinnamaldehyde with an IC50 of 3.1 μM and 4.5 μM for human and mouse TRPA1, respectively. AP-18 could reverse complete Freund´s adjuvant (CFA)-induced mechanical hyperalgesia in mice. AP-18 could attenuate Yo-Pro uptake induced by 30 μM AITC in a concentration-dependent manner (IC50= 10.3 μM).
价 格:¥电议型 号:T21543产 地:中国大陆
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T21540ZM323881;化合物 T21540ZM323881
ZM323881 is a potent and selective inhibitor of VEGFR2 with an IC 50 of less than 2 nM.
价 格:¥电议型 号:T21540产 地:中国大陆
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T2154MG-132;化合物MG-132Z-LLL-al|||Z-Leu-Leu-Leu-CHO;Z-LLL-al|||Z-Leu-Leu-Leu-CHO
MG-132 (Z-Leu-Leu-Leu-al) is a 26S proteasome inhibitor (IC50=100 nM) that is cell-permeable and reversible. MG-132 acts as an autophagy activator and also induces apoptosis.
价 格:¥电议型 号:T2154产 地:中国大陆
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T21452Anecortave Acetate;化合物Anecortave AcetateRetaane|||Al 3789|||NSC 24345|||NSC 15475|||Anecortave;Retaa
Anecortave Acetate (NSC-24345), an angiostatic steroid, is used for proteomics research.
价 格:¥电议型 号:T21452产 地:中国大陆
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T21154Chlorfluazuron;化合物 T21154IKI 7899|||AI3-29785|||CCRIS 2680|||CGA 112913|||Atabron;IKI 7899|||AI3-297
Chlorfluazuron, a chitin synthesis inhibitor, is commonly used as an insect growth regulator for controlling the major insect pests in crops.
价 格:¥电议型 号:T21154产 地:中国大陆
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T208154-Chloroloratadine;化合物 T208154-Chloro loratadine|||Loratadine specified impurity C;4-Chloro loratadi
4-Chloroloratadine is an impurity of Loratadine, a nonsedating-type histamine H1-receptor.
价 格:¥电议型 号:T20815产 地:中国大陆
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T20438(p-Acetylphenoxy)acetic acid;化合物 T20438AI3 15464|||AI315464|||AI3-15464;AI3 15464|||AI315464|||AI3-1
(p-Acetylphenoxy)acetic acid is an agent of biochemical.
价 格:¥电议型 号:T20438产 地:中国大陆
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T20437Tetrahydrofurfuryl propionate四氢糠醇丙酸酯四氢糠醇丙酸酯|||AI315415|||AI3-15415|||AI3 15415
Tetrahydrofurfuryl propionate (AI3 15415) is a carboxylate fragrance.
价 格:¥电议型 号:T20437产 地:中国大陆
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T20154Geranyl butyrate;化合物 T20154NSC 46146|||NSC46146|||NSC-46146;NSC 46146|||NSC46146|||NSC-46146
Geranyl butyrate is an agent of biochemical.
价 格:¥电议型 号:T20154产 地:中国大陆
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T1985WHI-P154;化合物WHI-P154Jak3 inhibitor ii;Jak3 inhibitor ii
WHI-P154 (Jak3 inhibitor ii) is a potent JAK3 inhibitor.
价 格:¥电议型 号:T1985产 地:中国大陆
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T191545-Methyl-2-thiophenecarboxaldehyde;5-甲基-2-噻吩甲醛5-Methyl-2-thiophenecarboxaldehyde
5-Methyl-2-thiophenecarboxaldehyde is a candidate microscopic third-order nonlinear optical (NLO) material.5-Methyl-2-thiophenecarboxaldehyde possesses a wide range of biological activities, such as anticancer activity.
价 格:¥电议型 号:T19154产 地:中国大陆
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T18154m-PEG16-Mal;化合物 T18154m-PEG16-Mal
m-PEG16-Mal is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T18154产 地:中国大陆
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T1726SB-431542;化合物SB 431542SB 431542;4-[4-(1,3-苯并二唑-5-基)-5-(2-吡啶基)-1H-咪唑-2-基]-苯酰胺水合物|||SB 431542
SB-431542 is an inhibitor of ALK5/TGF-β type I Receptor (IC50=94 nM) and is selective. SB 431542 also has inhibitory activity against ALK4 and ALK7 but not other proteins. SB 431542 can be used for induced differentiation of stem cells.
价 格:¥电议型 号:T1726产 地:中国大陆
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T17244VU0467154;化合物VU0467154VU0467154
VU0467154 is a positive allosteric modulator of the M4 muscarinic acetylcholine receptor.
价 格:¥电议型 号:T17244产 地:中国大陆
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T17154Tr-PEG8-OH;化合物 T17154Tr-PEG8-OH
Tr-PEG8-OH is a non-cleavable 8 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
价 格:¥电议型 号:T17154产 地:中国大陆
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T16844Sarmazenil;沙马西尼R-154513|||Ro 15-3505;R-154513|||Ro 15-3505
Sarmazenil (Ro 15-3505) is a partial inverse agonist at the benzodiazepine receptor with pro-convulsant properties and is used in the study of chronic hepatic encephalopathy (HE).
价 格:¥电议型 号:T16844产 地:中国大陆