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产品数:86101
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已选条件
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T9118KEA1-97Apoptosis,KEA1 97,Proliferation,Apoptotic,Caspase,inhibit,KEA-1-97,DCTalkyne,KEA1-97,231MFP,I
Kea1-97 is a selective disruptor of interaction between thioredoxin and caspase-3 (IC50 = 10 μ M). Kea1-97 destroys the interaction between thioredoxin and caspase 3 and activates caspases without affecting the activity of thioredoxin.
价 格:¥电议型 号:T9118产 地:中国大陆
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T8881Dot1L-IN-4H3K79,Histone Methyltransferase,histone,methyltransferase,lysine,DOT1L,Dot1L IN 4,Inhibito
Dot1L-IN-4 is a potent disruptor of telomeric silencing 1-like protein (DOT1L) inhibitor.
价 格:¥电议型 号:T8881产 地:中国大陆
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T7055Bz-RS-ISer(3-Ph)-Ometumor,proliferation,BzRSISer(3Ph)Ome,cycle,Bz RS ISer(3 Ph) Ome,Inhibitor,inhibi
NA. Medical intermediate
价 格:¥电议型 号:T7055产 地:中国大陆
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TN1406DihydrokaempferolApoptosis,Dihydrokaempferol,Inhibitor,Bcl-2 Family,inhibit
Aromadendrin is a natural product. It induces apoptosis and inhibits Bcl-2 and Bcl-xL expression, possesses anti-inflammatory, antioxidant, and anti-diabetic properties, it exhibits anti-inflammatory activity
价 格:¥电议型 号:TN1406产 地:中国大陆
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T7052GnetolTGF-β,antidiabetic,Cyclooxygenase,anticancer,HDAC,antiproliferative,antinociceptive,Inhibitor,
Gnetol competitivity inhibits butyrylcholinesterase (IC50: 1.3 uM). Gnetol has a strong inhibitory effect on murine tyrosinase activity. Gnetol significantly suppresses melanin biosynthesis in murine B16 melanoma cells. It is active in the inhibition of arachidonic acid (AA)-induced platelet aggregation.
价 格:¥电议型 号:T7052产 地:中国大陆
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T7886Nidufexorinhibit,Inhibitor,Autophagy,NR1H4,FXR,Nidufexor,LMB-763,LMB763,LMB 763
Nidufexor is an agonist for the farnesoid X receptor (FXR).
价 格:¥电议型 号:T7886产 地:中国大陆
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TQ0242Fenebrutinibinhibit,Inhibitor,GDC0853,GDC 0853,Fenebrutinib,Btk,Bruton tyrosine kinase
Fenebrutinib is a selective and noncovalent Btk inhibitor (Ki: 0.91 nM).
价 格:¥电议型 号:TQ0242产 地:中国大陆
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TN1643Ferulamideinhibit,Ferulamide,nAChR,Inhibitor,Ferulic,Nicotinic acetylcholine receptors,anticholinest
Ferulamide, a Ferulic acid derivative, shows potent inhibitory activity against arachidonic acid-induced platelet aggregation.
价 格:¥电议型 号:TN1643产 地:中国大陆
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TN1091DehydronuciferineCholinesterase (ChE),Inhibitor,Dehydronuciferine,inhibit
Dehydronuciferine is isolated from the leaves of Nelumbo nucifera Gaertn. Dehydronuciferine shows inhibitory of acetylcholinesterase with the IC50 of 25 ug/mL.
价 格:¥电议型 号:TN1091产 地:中国大陆
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T6689T0070907PPAR,inhibit,T0070907,Inhibitor,T-0070907,T 0070907,Peroxisome proliferator-activated recept
T0070907(IC50=1 nM) , an effective and specific PPARγ inhibitor, with the >800-fold selectivity over PPARα and PPARδ.
价 格:¥电议型 号:T6689产 地:中国大陆
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THS1455DihydroarteMisinic acidInhibitor,DihydroarteMisinic acid,Parasite,Dihydroqinghao acid,inhibit,Ferrop
Dihydroartemisinic acid is a natural product from Artemisia annua and the main direct precursor of artemisinin, which is a medicinal herb that is widely used to treat Malaria.
价 格:¥电议型 号:THS1455产 地:中国大陆
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T9102WM-3835invasion,MYST2,HBO1,WM3835,MYLK-HOXA9,Histone Acetyltransferase,Apoptosis,inhibit,H4K12ac,HAT
WM-3835 is a novel and high-specific small molecule inhibitor of Lysine Acetyltransferase 7 (KAT7, MYST2, HBO1) , able to potently suppressed OS cell proliferation and migration, and leads to apoptosis activation.
价 格:¥电议型 号:T9102产 地:中国大陆
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T7138FB23-2FB23 2,AML,Apoptosis,leukemia,acute,anti-proliferation,Inhibitor,FB232,m6A,myeloid,mRNA,inhibi
FB23-2 is a potent and selective mRNA N6-methyladenosine (m6A) demethylase FTO inhibitor(IC50 : 2.6 μM).
价 格:¥电议型 号:T7138产 地:中国大陆
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T9137SN-011inflammatory,ERIS,inhibit,Inhibitor,Stimulator of Interferon Genes,CDN,SN-011,STING,MITA,autoi
GUN35901 is a STING inhibitor, which inhibited the activation of the STING signal pathway and to prevent or treat a STING- mediated disease. It is a demethyl analogue of DUN99845.
价 格:¥电议型 号:T9137产 地:中国大陆
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T7969DipyrithioneDipyrithione,dermatophytosis,G1 phase,antiproliferative,antifungal,Apoptosis,Bacterial,a
Dipyrithione appears to have novel cytotoxicity and potent broad-spectrum antitumor activity
价 格:¥电议型 号:T7969产 地:中国大陆
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T6941PI-1840cell proliferation,Proteasome,Caspase,proteasome substrates,poly ADP ribose polymerase,inhibi
PI-1840( IC50 = 27 nM)is a reversible and selective chymotrypsin-like (CT-L) inhibitor, with little proteasome proteolytic effects on trypsin-like (T-L) and postglutamyl-peptide-hydrolysis-like (PGPH-L).
价 格:¥电议型 号:T6941产 地:中国大陆
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T6420BMS-707035BMS 707035,HIV-1 integrase strand transfer,HIV,Human immunodeficiency virus,antiviral,BMS7
BMS-707035 is a specific HIV-I integrase (IN) inhibitor with IC50 of 15 nM. Phase 2.
价 格:¥电议型 号:T6420产 地:中国大陆
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TN1078SeneciphyllineP-450,hydrase,Inhibitor,Gutathione S-transferase,Cytochrome P450,Toxic,alkaloid,cytoch
Seneciphylline, one of the hepatotoxic pyrolizidine alkaloids, has mutagenic activity in Drosophila and their transfer into rat milk.Seneciphylline can significantly increased the activities of epoxide hydrase and glutathione-S-transferase but cause reduction of cytochrome P-450 and related monooxygenase activities.
价 格:¥电议型 号:TN1078产 地:中国大陆
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T21012DiflufenicanDiflufenican
Diflufenican increases the production of phytoene in carrot cell cultures by inducing the inhibition of phytoene desaturase gene expression.
价 格:¥电议型 号:T21012产 地:中国大陆
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T20103Isoxadifen-ethyl
Isoxadifen-ethyl is herbicide safener and an agrochemical. Isoxadifen-ethyl can effectively alleviate nicosulfuron injury in the maize.
价 格:¥电议型 号:T20103产 地:中国大陆