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T15663Kinesore化合物 T15663Kinesore
Kinesore is a KLC2-SKIP Interaction inhibitor.
价 格:¥电议型 号:T15663产 地:中国大陆
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T15662KIN1408;化合物 T15662KIN1408
KIN1408 is an antiviral small molecule compound. KIN1408 also is an agonist of the RLR pathway.
价 格:¥电议型 号:T15662产 地:中国大陆
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T15661Kif15-IN-1;化合物 T15661Kif15-IN-1
Kif15-IN-1, a mitotic Kinesin family member 15 (Kif15) inhibitor, is utilized in the study of cellular proliferative diseases.
价 格:¥电议型 号:T15661产 地:中国大陆
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T15660KHK-IN-1;化合物KHK-IN-1KHK-IN-8|||Ketohexokinase inhibitor 8;KHK-IN-8|||Ketohexokinase inhibitor 8
KHK-IN-1 (KHK-IN-8) is a selective and cell membrane permeable inhibitor of ketohexokinase (KHK, IC50=12 nM; F=34%). KHK-IN-1 inhibits F1P production in HepG2 cell lysates with IC50 of 400 nM. KHK-IN-1 has potential for the study of obesity and diabetes.
价 格:¥电议型 号:T15660产 地:中国大陆
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T1566Aripiprazole;阿立哌唑OPC-14597;阿立哌唑|||OPC-14597
Aripiprazole (OPC-14597) is an antipsychotic agent that is structurally related to piperazines and quinolones. It is a partial agonist of SEROTONIN RECEPTOR, 5-HT1A and DOPAMINE D2 RECEPTORS, where it also functions as a post-synaptic antagonist, and an antagonist of SEROTONIN RECEPTOR, 5-HT2A.
价 格:¥电议型 号:T1566产 地:中国大陆
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T15594MKC8866;化合物MKC8866MKC8866
MKC8866 is a selective IRE1 RNase inhibitor (IC50: 0.29 μM in human vitro). MKC8866 inhibits IRE1 RNase in breast cancer cells leading to the decreased production of pro-tumorigenic factors and it can inhibit prostate cancer (PCa) tumor growth.
价 格:¥电议型 号:T15594产 地:中国大陆
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T15585IRBP(668-687) (TFA);化合物 T15585Interphotoreceptor retinoid-binding protein(668-687) TFA;Interphotorec
Interphotoreceptor retinoid-binding protein TFA is the amino acid residue 668 to 687 of human interphotoreceptor retinoid-binding protein (IRBP). It also induces uveitis.
价 格:¥电议型 号:T15585产 地:中国大陆
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T15566Imexon;亚美克松BM 06002;BM 06002|||亚美克松
Imexon is an iminopyrrolidone aziridine. It has anti-cancer activity.
价 格:¥电议型 号:T15566产 地:中国大陆
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T15422GSK-626616;化合物GSK-626616GSK-626616
GSK-626616 is a potent and orally bioavailable DYRK3 inhibitor (IC50: 0.7 nM). It inhibits other members of the DYRK family with similar potency. GSK-626616 is a potential therapy for the treatment of anemia.
价 格:¥电议型 号:T15422产 地:中国大陆
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T15368LGalantide acetate;化合物Galantide醋酸盐Galantide acetate(138579-66-5 Free base);Galantide acetate(138579-6
Galantide acetate, a non-specific galanin receptor antagonist, is a peptide consisting of fragments of galanin and substance P. Galantide acetate recognizes two classes of galanin binding sites (KD<0.1 nM and ~6 nM) in the rat hypothalamus. Galantide acetate dose dependently (IC50=1.0 nM) antagonizes the galanin-mediated inhibition of the glucose-induced insulin secretion from mouse pancreatic islets. Galantide acetate appears to bind to a single population of SP receptors (KD~40 nM).
价 格:¥电议型 号:T15368L产 地:中国大陆
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T15366Gabapentin enacarbil加巴喷丁酯XP-13512|||加巴喷丁酯
Gabapentin enacarbil (XP-13512) is a prodrug for the anticonvulsant and analgesic drug gabapentin. Gabapentin enacarbil provides sustained dose-proportional exposure to gabapentin and predictable bioavailability.
价 格:¥电议型 号:T15366产 地:中国大陆
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T15266F16;化合物F16(E)-4-(3-indolylvinyl)-N-methylpyridinium iodide;(E)-4-(3-indolylvinyl)-N-methylpyridinium
F16 ((E)-4-(3-indolylvinyl)-N-methylpyridinium iodide) inhibits the growth of neu-overexpressing cells and the proliferation of mammary epithelial.
价 格:¥电议型 号:T15266产 地:中国大陆
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T15247ESI-05;化合物ESI-05NSC 116966;NSC 116966
ESI-05 (NSC-116966) is a specific EPAC2 (exchange protein directly activated by cAMP 2) antagonist (IC50: 0.4 μM). ESI-05 inhibits cAMP-mediated activation of EPAC2, as well as EAPC2, mediated Rap1 activation.
价 格:¥电议型 号:T15247产 地:中国大陆
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T15207Eleclazine hydrochloride;化合物Eleclazine hydrochlorideGS 6615 hydrochloride;GS 6615 hydrochloride
Eleclazine hydrochloride (GS 6615 hydrochloride) is a novel inhibitor of late Na+ current (IC50: 0.7 uM).
价 格:¥电议型 号:T15207产 地:中国大陆
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T1518Olmesartan Medoxomil;奥美沙坦酯CS 866|||Benicar;奥美沙坦酯|||CS 866|||Benicar
Olmesartan Medoxomil (Benicar) is an angiotensin II type 1 receptor blocker that is used to manage hypertension.
价 格:¥电议型 号:T1518产 地:中国大陆
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T15166DPM-1001;化合物 T15166DPM-1001
DPM-1001 is an orally bioavailable and non-competitive protein-tyrosine phosphatase (PTP1B) inhibitor (IC50: 100 nM) with the anti-diabetic property.
价 格:¥电议型 号:T15166产 地:中国大陆
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T15142Vebufloxacin;化合物 T15142OPC7241|||Flumenique|||DM8966;OPC7241|||Flumenique|||DM8966
Vebufloxacin (OPC-7251) shows potent antibacterial activity against gram-positive and -negative bacteria, including Staphylococcus aureus and Pseudomonas aeruginosa. It has potent activity characteristically against Propionibacterium acnes.
价 格:¥电议型 号:T15142产 地:中国大陆
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T15113Diazepinomicin;化合物 T15113TLN-4601|||BU 4664L|||ECO-4601;TLN-4601|||BU 4664L|||ECO-4601
Diazepinomicin is a secondary metabolite produced by Micromonospora sp. It inhibits the EGF-induced Ras-ERK MAPK signaling pathway and induces apoptosis. Diazepinomicin also is an anti-tumor agent for K-Ras mutant models.
价 格:¥电议型 号:T15113产 地:中国大陆
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T15066DBCO-NHS ester 2;化合物 T15066DBCO-NHS ester 2
DBCO-NHS ester 2 is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs). It is a Dibenzylcyclooctyne (DBCO) derivative specifically designed for application in copper-free click chemistry [1].
价 格:¥电议型 号:T15066产 地:中国大陆
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T15005CP-66948;化合物CP-66948CP-66948
CP-66948 is a potent histamine H2 receptor antagonist with inhibitory effect on gastric acid secretion and can be used to protect gastric and intestinal mucosa.
价 格:¥电议型 号:T15005产 地:中国大陆