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产品数:86101
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T62360AChE-IN-26
AChE-IN-26 is an AChE (acetylcholinesterase) inhibitor (IC50= 0.42 μM). AChE-IN-26 has research value in Alzheimer’s disease.
价 格:¥电议型 号:T62360产 地:中国大陆
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TP2051LCTCE 9908 acetateCTCE 9908 acetate
CTCE 9908 acetate is an antagonist of CXCR4 and inhibits migration in CXCR4-expressing ovarian cancer cells.
价 格:¥电议型 号:TP2051L产 地:中国大陆
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TN1128Bruceine Ehypoglycemia,quassinoid,Bruceine E,effect,Inhibitor,antidiabetic,inhibit
Bruceine E is isolated from B. javanica seeds with hypoglycemia effects. Bruceine E can be used for studies about acting as an insulin secretagogue.
价 格:¥电议型 号:TN1128产 地:中国大陆
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TN6708ETHYL 3,5-DIHYDROXYBENZOATEETHYL 3,5 DIHYDROXYBENZOATE,ETHYL 3,5DIHYDROXYBENZOATE
ETHYL 3,5-DIHYDROXYBENZOATE is a natural product. It inhibits human carbonic anhydrase 2.
价 格:¥电议型 号:TN6708产 地:中国大陆
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TP1422Interleukin (IL)-6 ReceptorInterleukin (IL) 6 Receptor,Interleukin (IL)6 Receptor
Interleukin (IL)-6 Receptor is a peptide.
价 格:¥电议型 号:TP1422产 地:中国大陆
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T21818Pregnenolone CarbonitrileCYPs,Cytochrome P450,P4503A,orally,Pregnenolone Carbonitrile,Pregnenolone 1
Pregnenolone Carbonitrile is an activator of rodent-PXR and induces the expression of CYP3A.
价 格:¥电议型 号:T21818产 地:中国大陆
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T101083-Bromocytisine
3-Bromocytisine is an effective agonist of nAChR (IC50s: 0.28, 0.30 and 31.6 nM for hα4β4, hα4β2, and hα7).
价 格:¥电议型 号:T10108产 地:中国大陆
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T6740Bafilomycin A1Autophagy,Proton Pump,Bafilomycin A 1,Bafilomycin A1,Bafilomycin A-1,Antibiotic,BafA1,
Bafilomycin A1 induces caspase-independent cell death in hepatocellular carcinoma cells via targeting of autophagy and MAPK pathways. Bafilomycin A1 is a vacuolar H+-ATPase inhibitor (IC50: 0.44 nM). It is also found to inhibit autophagy while induces apoptosis.Bafilomycin A1 triggers proliferative potential of senescent cancer cells in vitro and in NOD/SCID mice.
价 格:¥电议型 号:T6740产 地:中国大陆
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T8933JNJ-63576253 free baseJNJ 63576253 free base,resistant,TRC 253,JNJ63576253,TRC-253,CRPC,JNJ63576253
JNJ-63576253 is a potent and orally active full antagonist of androgen receptor (AR), with IC50s of 37 and 54 nM for F877L mutant AR and wild-type AR in LNCaP cells. JNJ-63576253 can be used for the research of castration-resistant prostate cancer (CRPC).
价 格:¥电议型 号:T8933产 地:中国大陆
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T7914Acenaphthylenearomatic,hydrocarbon,polycyclic,Acenaphthylene,Inhibitor,inhibit
Acenaphthylene is environmental polycyclic aromatic hydrocarbon (PAH)pollutants
价 格:¥电议型 号:T7914产 地:中国大陆
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T9352hydrocotarnineE3 ligating enzyme,IL-18,NLRP3,E1/E2/E3 Enzyme,hydrocotarnine,inflammasome activation,
hydrocotarnine?is an inhibitor of Cbl.
价 格:¥电议型 号:T9352产 地:中国大陆
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Fr14145Compound Fr14145Compound Fr14145
价 格:¥电议型 号:Fr14145产 地:中国大陆
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T8684SotorasibAMG 510,Ras,KRAS,covalent,Sotorasib,regression,mutation,Inhibitor,G12C,anti-tumour,inhibit,
AMG-510 is a selective and orally bioavailable KRAS G12C covalent inhibitor.
价 格:¥电议型 号:T8684产 地:中国大陆
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T7631LEledoisin Related Peptide 2TFAEledoisin Related Peptide 2TFA
Eledoisin Related Peptide(2TFA) is a tachykinin receptor ligand.
价 格:¥电议型 号:T7631L产 地:中国大陆
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T17006TC-I 2014TCI 2014,TC I 2014
TC-I 2014 shows antiallodynic properties in pain models. TC-I 2014 is a potent and orally active Benzimidazole-containing transient receptor potential melastatin 8 antagonist (IC50: 0.8 nM, 3.0 nM, and 4.4 nM for canine, human and rat channels respectively).
价 格:¥电议型 号:T17006产 地:中国大陆
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T7667R1487R1487,R-1487
R1487 is an orally bioavailable and highly selective p38α mitogen-activated protein kinase inhibitor.
价 格:¥电议型 号:T7667产 地:中国大陆
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TP1104LMelanin Concentrating Hormone, salmon acetateMelanin Concentrating Hormone, salmon acetate
Melanin Concentrating Hormone, salmon acetate is a 19 amino acid cyclic peptide, is largely expressed in the hypothalamus.
价 格:¥电议型 号:TP1104L产 地:中国大陆
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T12589PI3Kα/mTOR-IN-1PI3Kα/mTORIN1,PI3Kα/mTOR IN 1,PI-3Kα/mTOR-IN-1
PI3Kα/mTOR-IN-1 is a potent dual inhibitor of PI3Kα/mTOR. PI3Kα/mTOR-IN-1 shows an IC50 of 7 nM for PI3Kα in a cell assay, and Kis of 12.5 nM and 10.6 nM for mTOR and PI3Kα in a cell free assay , respectively.
价 格:¥电议型 号:T12589产 地:中国大陆
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TN4618N-trans-SinapoyltyramineN trans Sinapoyltyramine,NtransSinapoyltyramine
N-trans-Sinapoyltyramine exhibited strong and selective cytotoxicity on the HeLa human cancer cell line with IC50 values of 9.77 ± 1.25 Μm.
价 格:¥电议型 号:TN4618产 地:中国大陆