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T7695PNU-282987 S enantiomer free baseInhibitor,Nicotinic acetylcholine receptors,PNU 282987 S enantiomer
PNU-282987 S enantiomer free base is an agonist of α7 nicotinic acetylcholine receptor (α7 nAChR).
价 格:¥电议型 号:T7695产 地:中国大陆
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T9989WAY-298592neurological diseases,alzheimer’s disease,WAY 298592,Inhibitor,dementia,myasthenia gravis,
WAY-298592 is a small molecule used for high-throughput assays.
价 格:¥电议型 号:T9989产 地:中国大陆
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T9298D-ValineDValine,inhibit,Inhibitor,D-Valine,Endogenous Metabolite,D Valine
D-Valine is the enantiomer of L-Valine.
价 格:¥电议型 号:T9298产 地:中国大陆
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T7298FT011Inhibitor,FT011,FT 011,inhibit,FT-011
FT011, a direct anti-fibrotic agent,attenuates cardiac remodelling and dysfunction in experimental diabetic cardiomyopathy.
价 格:¥电议型 号:T7298产 地:中国大陆
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T11492GSK2983559 free acidinhibit,THP-1 cell,RIP kinase,GSK 2983559,GSK2983559 free acid,Inhibitor,GSK-298
GSK2983559 free acid is an effective and selective inhibitor of receptor-interacting protein 2 (RIP2). GSK2983559 free acid shows excellent activity in blocking many proinflammatory cytokine responses in human inflammatory bowel disease explant samples an
价 格:¥电议型 号:T11492产 地:中国大陆
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T9194UMB298UMB-298,UMB298,inhibit,MOLM13,Inhibitor,bromodomain,UMB 298,selective,potent,Epigenetic Reader
UMB298 is a potent and selective CBP/P300 bromodomain inhibitor. UMB298 inhibits BRD4 with IC50 of 5193nM.
价 格:¥电议型 号:T9194产 地:中国大陆
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T8298Vasicine hydrochloridePeganine,Vasicine hydrochloride,Vasicine,inhibit,Inhibitor,Bacterial
Vasicine hydrochloride (peganine hydrochloride) is an alkaloid isolated from Justicia adhatoda. It possesses an anti-tuberculosis activity.
价 格:¥电议型 号:T8298产 地:中国大陆
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T8966ML-298ML-298,Inhibitor,ML 298,Phospholipase,inhibit
ML298 is a potent, specific inhibitor of Phospholipase D2 (PLD2, IC50 of 355 nM).
价 格:¥电议型 号:T8966产 地:中国大陆
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TQ0121VH-298E3 ligase-recruiting Moiety,VH-298,Inhibitor,VH298,Ligands for E3 Ligase,VH 298,inhibit
VH-298 is a potent inhibitor of VHL that stabilizes HIF-α and elicits a hypoxic response via a different mechanism, that is the blockade of the VHL:HIF-α protein-protein interaction downstream of HIF-α hydroxylation by PHD enzymes.
价 格:¥电议型 号:TQ0121产 地:中国大陆
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T7151GSK2982772inhibit,Receptor-interacting protein kinases,GSK2982772,RIPK,Inhibitor,RIP kinase,GSK 2982
GSK2982772 is an inhibitor of receptor interacting serine/threonine kinase 1 (RIPK1)with IC50 values of 16 nM and 20 nM for human and monkey RIP1, respectively.
价 格:¥电议型 号:T7151产 地:中国大陆
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T6066SCH772984
SCH 772984 is a potent inhibitor of ERK1/ERK2 (IC50: 4/1 nM) and has only weak inhibitory for other 300 tested kinases.
价 格:¥电议型 号:T6066产 地:中国大陆
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T5401GSK2983559 active metaboliteRIPK2 inhibitor 1;RIPK2-IN-1;GSK2983559
GSK 2983559 (RIP2 kinase inhibitor 1) is a potent, selective receptor-interacting protein-2 (RIP2) kinase inhibitor.
价 格:¥电议型 号:T5401产 地:中国大陆
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T5324BI 01383298
BI 01383298 is a selective inhibitor of the sodium-citrate co-transporter (SLC13A5).
价 格:¥电议型 号:T5324产 地:中国大陆
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T52984-hydroxy-3-methylbenzoic acid4,3-Cresotic acid;4-羟基-3-甲基苯甲酸
4-Hydroxy-3-methylbenzoic acid is a normal organic acid identified in urine specimens from a healthy population.
价 格:¥电议型 号:T5298产 地:中国大陆
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T4419UNC2025 2HCl (1429881-91-3(free base))
UNC2025 is a potent and orally bioavailable Mer/Flt3 dual inhibitor with IC50 of 0.8/0.74 nM for Mer/Flt3.
价 格:¥电议型 号:T4419产 地:中国大陆
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T4298JNJ-47965567JNJ-479655
JNJ-47965567 is a selective antagonist of the purinergic receptor P2X subtype 7 (P2X7), a ligand-gated ion channel(with pKis of 7.9 and 8.7 for human and rat P2X7, respectively).
价 格:¥电议型 号:T4298产 地:中国大陆
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T4282S-methyl-KE-298
S-methyl-KE-298 is the second main metabolite in plasma,is a methyl conjugate of deacetyl-KE-298.KE-298 inhibits matrix metalloproteinase (MMP-1) production from ?rheumatoid arthritis (RA) synovial cells.
价 格:¥电议型 号:T4282产 地:中国大陆
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T41298LMPTP INHIBITOR 1 dihydrochloride
LMPTP INHIBITOR 1 dihydrochloride is a selective inhibitor of low molecular weight protein tyrosine phosphatase (LMPTP), with an?IC50?of 0.8 μM LMPTP-A.
价 格:¥电议型 号:T41298产 地:中国大陆
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T4050GSK2981278ROR gama modulator 1
GSK2981278 is a highly potent and selective inverse agonist of retinoic acid receptor-related orphan receptor gamma (ROR gamma).
价 格:¥电议型 号:T4050产 地:中国大陆