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产品数:86101
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T60094SU 4981
SU 4981 is an inhibitor of VEGFR and a modulator of tyrosine kinase activity.
价 格:¥电议型 号:T60094产 地:中国大陆
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T60095CCF0058981CCF0058981
CCF0058981 (CCF981) is a 3-chlorophenyl analogue which is a noncovalent SARS-CoV-2 3CL pro (SC2) inhibitor with an IC 50 of 68 nM. CCF0058981 inhibits SC1 (SARS-CoV-1 3CL pro ) with an IC 50 of 19 nM. CCF0058981 has antiviral efficacy and has the potential for COVID-19 research [1].
价 格:¥电议型 号:T60095产 地:中国大陆
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T60061RU-TRAAK-2RU TRAAK 2,inhibit,Inhibitor,channels,reversible,TRAAK non-K2P,Potassium Channel,RUTRAAK2,
RU-TRAAK-2 is a reversible inhibitor of TWIK-related arachidonic acid-stimulated K+ channel with no activity for non-K2P channels including Kv1.2, GIRK2, and Slo1.
价 格:¥电议型 号:T60061产 地:中国大陆
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T60009YS-370YS370,YS 370
YS-370 is an orally active inhibitor of P-gp and shows moderate inhibition against CYP3A4. YS-370 effectively reverses multidrug resistance to paclitaxel and colchicine and exhibits stronger antitumor activity in combination with paclitaxel.
价 格:¥电议型 号:T60009产 地:中国大陆
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T60063WAY-323975
WAY-323975 is a nonfluorescent inhibitors of Fluorogen–Fluorogen Activating Protein Binding Pairn.
价 格:¥电议型 号:T60063产 地:中国大陆
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T60008BCL6-IN-6BCL6 IN 6,BCL6IN6
BCL6-IN-6 is an inhibitor of Bcl-6 and can be used in studies about diffuse large B-cell lymphoma. BCL6-IN-6 blocks the interaction of Bcl-6 with its corepressors and dose-dependently reactivates Bcl-6 target genes.
价 格:¥电议型 号:T60008产 地:中国大陆
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T60096EN106
EN106 is a potent inhibitor of FEMIB and is a cysteine-reactive covalent ligand. EN106 disrupts recognition of the key reductive stress substrate of FEM1B, FNIP1.
价 格:¥电议型 号:T60096产 地:中国大陆
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T60036ML-SA5MLSA5,ML SA5
ML-SA5 is an MCOLN1 agonist and arrests autophagic flux by perturbing fusion between autophagosomes and lysosomes.
价 格:¥电议型 号:T60036产 地:中国大陆
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T60034TH1085Inhibitor,DNA glycosylase 1 (OGG1),TH-10785,TH 10785,DNA oxidative lesions,TH1085,enzyme,pheny
TH1085 is an enhancer of OGG1. TH1085 stimulates DNA repair and protects cells from the environmental hazard paraquat (PQ).
价 格:¥电议型 号:T60034产 地:中国大陆
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T60064WAY-270360WAY270360,WAY 270360
WAY-270360 is a sirtuin modulator and an epidermal growth factor receptor (EGFR) inhibitor.
价 格:¥电议型 号:T60064产 地:中国大陆
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T60022WAY-604116WAY604116,WAY 604116
WAY-604116 has anti-inflammatory, antitumor and antiasthmatic effects.
价 格:¥电议型 号:T60022产 地:中国大陆
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T63872KU-60019
KU-60019 is a specific inhibitor of ATM kinase (IC50: 6.3 nM).
价 格:¥电议型 号:T63872产 地:中国大陆
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T60056Benzonitrile, 4-[[5-cyclopropyl-3-methyl-1-[(methylsulfonyl)methyl]-1H-pyrazol-4-yl]oxy]-2,6-dimethy
Benzonitrile, 4-[[5-cyclopropyl-3-methyl-1-[(methylsulfonyl)methyl]-1H-pyrazol-4-yl]oxy]-2,6-dimethyl- is a progesterone receptor antagonist with antiprogestin effects.
价 格:¥电议型 号:T60056产 地:中国大陆
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T60026KIF18A-IN-2Inhibitor,Mitotic,Microtubule,Cancer,OVCAR-3,KIF18A,Microtubule/Tubulin,KIF18A IN 2,inhib
KIF18A-IN-2 is an inhibitor of mitotic kinesin Kif18A with IC50 of 28 nM and can be used in studies about chromosomal instability-associated vulnerabilities.
价 格:¥电议型 号:T60026产 地:中国大陆
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T60053HamalineHamaline
Hamaline is a substrate-selective cyclooxygenase-2 (COX-2) inhibitor.
价 格:¥电议型 号:T60053产 地:中国大陆
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TN1600Eclalbasaponin IEclalbasaponin I,inhibit,Inhibitor
Eclalbasaponin I has anti-oxidative, and antitumor activities, it reduces oxidative stress-induced neural cell death by autophagy activation, it can dose-dependently inhibit the proliferation of hepatoma cell smmc-7721 with the IC(50) value of 111.1703 ug/ml.
价 格:¥电议型 号:TN1600产 地:中国大陆
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T60077SCP1-IN-1SCP1 IN 1,SCP1IN1
SCP1-IN-1 (compound SH T-62) is a potent and selective covalent inhibitor against SCP1. SCP1-IN-1 promotes REST degradation and reduces transcriptional activity. In some glioblastoma cells, the high level of REST protein drives tumor growth. SCP1-IN-1 has the potential for the research of glioblastoma whose growth is driven by REST transcription activity [1].
价 格:¥电议型 号:T60077产 地:中国大陆
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T60012HS-243RA-FLSs,Inhibitor,immunology,autoimmune disease,inhibit,Interleukin-1 receptor associated kina
HS-243 is an inhibitor of IRAK-4 and IRAK-1 with IC50s of 20 and 24 nM. HS-243 shows anti-inflammatory and anticancer activity.
价 格:¥电议型 号:T60012产 地:中国大陆
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T12809(S)-PF-06873600(S)PF06873600,(S) PF 06873600
(S)-PF-06873600 is the S enantiomer of PF-06873600 which is an inhibitor of CDK.
价 格:¥电议型 号:T12809产 地:中国大陆
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T8463PF-06873600PF06873600,PF 06873600
PF-06873600 is a selective and orally bioavailable cyclin-dependent kinase (CDK) inhibitor(CDK2, CDK4 and CDK6 with Ki of 0.09 nM, 0.13 nM and 0.16 nM, respectively), has potential antineoplastic activity.
价 格:¥电议型 号:T8463产 地:中国大陆