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T3692GNE-477GNE 477
GNE-477 is a potent and efficacious dual PI3K/mTOR inhibitor.
价 格:¥电议型 号:T3692产 地:中国大陆
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T3647HTHQ1-O-hexyl-2,3,5-trimethylhydroquinone;HTHQ(1-O-Hexyl-2,3,5-trimethylhydroquinone);HX 1171
HTHQ, a hydroquinone monoalkyl ether, is an effective anti-oxidative agent. HTHQ is a potent anti-lipid-peroxidative compound and its antioxidation activity to be extremely elevated in biological systems, such as that of liver microsomes via the generatio
价 格:¥电议型 号:T3647产 地:中国大陆
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T3633CrenigacestatLY3039478
LY3039478 is an orally bioavailable Notch inhibitor with an IC50 of ~1 nM in most of the tumor cell lines tested. LY3039478 effectively inhibits mutant Notch receptor activity. In a xenograft tumor model, LY3039478 inhibited expression of Notch-regulated
价 格:¥电议型 号:T3633产 地:中国大陆
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T3547SotagliflozinLP-802034;LX-4211
LX-4211 is an orally bioavailable inhibitor of the sodium-glucose co-transporter subtype 1 (SGLT1) and 2 (SGLT2), with potential antihyperglycemic activity.
价 格:¥电议型 号:T3547产 地:中国大陆
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T3495TasimelteonVEC-162;BMS-214778;他司美琼
Tasimelteon is a melatonin receptor agonist that is used for the treatment of non-24 hour sleep-wake disorder in blind individuals.
价 格:¥电议型 号:T3495产 地:中国大陆
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T3479(RS)-MCPG(±)-MCPG;alpha-MCPG
(RS)-MCPG is a non-selective group I/II metabotropic glutamate receptor antagonist.
价 格:¥电议型 号:T3479产 地:中国大陆
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T3478Ro 67-7476
Ro 67-7476 is a positive allosteric modulator of mGlu1 receptors. No activity at human mGlu1 receptors. Potentiates glutamate-induced calcium release with EC 50 of 60.1 nM.
价 格:¥电议型 号:T3478产 地:中国大陆
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T3477E4CPG
E4CPG is a novel group I/II metabotropic glutamate receptor antagonist, more potent than (RS)-MCPG.
价 格:¥电议型 号:T3477产 地:中国大陆
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T34760SYR127063SYR-127063;BDBM92454;BDBM 92454;SYR 127063;BDBM-92454
SYR127063 (BDBM92454) is a potent and selective HER2 inhibitor, binds to HER2 in a reactive conformation.
价 格:¥电议型 号:T34760产 地:中国大陆
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T3476JI-101JI 101;JI101;CGI-1842
JI-101 is an oral multi-kinase inhibitor that targets vascular endothelial growth factor receptor type 2 (VEGFR-2), platelet derived growth factor receptor β (PDGFR-β), and ephrin type-B receptor 4 (EphB4).
价 格:¥电议型 号:T3476产 地:中国大陆
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T3475MD 39-AM
Anticytokinin activity was evaluated by 50% of the callus growth on the medium with kinetin but without anti-cytokinin
价 格:¥电议型 号:T3475产 地:中国大陆
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T34746Sulfo-SANPAH Crosslinker6-[(4-叠氮-2-硝基苯基)氨基]己酸磺酸基琥珀酰亚胺酯;Sulfo-SANPAH Cross linker;Sulfo-SANPAH Cross-
Sulfo-SANPAH Crosslinker is a water-soluble isobisfunctional protein crosslinker.
价 格:¥电议型 号:T34746产 地:中国大陆
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T3474RO 46-8443
RO 46-8443 is the first non-peptide endothelin ETB receptor selective antagonist. RO 46-8443 displays up to 2000-fold selectivity for ETB receptors both in terms of binding inhibitory potency and functional inhibition.
价 格:¥电议型 号:T3474产 地:中国大陆
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T3473(S)-ATPOATPO
ATPO is Competitive antagonist at GluR1-4 (AMPA-preferring) receptors.
价 格:¥电议型 号:T3473产 地:中国大陆
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T3472CGS 27023A
CGS 27023A is a non-peptidic, potent, and orally active stromelysin inhibitor.
价 格:¥电议型 号:T3472产 地:中国大陆
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T3471Trans-ACBD氨基二羧酸;Trans-1-aminocyclobutane-1,3-dicarboxylic acid
1-Aminocyclobutane-1, 3-dicarboxylic acid is an effective and specific N-methyl-D-aspartate receptor agonist.
价 格:¥电议型 号:T3471产 地:中国大陆
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T3470Cis-ACBD氨基二羧酸;cis-1-aminocyclobutane-1,3-dicarboxylic acid
2, 4-methanoglutamate is a potent and selective N-methyl-D-aspartate receptor agonist.
价 格:¥电议型 号:T3470产 地:中国大陆
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T3447Thiomyristoyl
Thiomyristoyl is an effective and selective SIRT2 inhibitor (IC50: 28 nM). It inhibits SIRT1 (IC50: 98 μM) but no effect on SIRT3 even at 200 μM.
价 格:¥电议型 号:T3447产 地:中国大陆
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T3354BIA 10-2474BIA10-2474
BIA10-2474 is a long-acting reversible inhibitor of fatty acid amide hydrolase (FAAH) that increases levels of the neurotransmitter anandamide in the central nervous system and in peripheral tissues (that is, the rest of the body other than the brain and
价 格:¥电议型 号:T3354产 地:中国大陆