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T25450LGGTI 2147 FA;GGTI 2147甲酸盐GGTI2147 FA|||GGTI-2147 FA|||GGTI 2147 FA(191102-87-1 Free base);GGTI2147 F
GGTI 2147 FA, a selective GGT inhibitor, abolishes bicuculline-induced increase in dendritic spine density in hippocampal experiments and may reduce learning and memory abilities in mice.
价 格:¥电议型 号:T25450L产 地:中国大陆
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T25358EC-17 free acid;化合物 T25358EC17|||EC 17|||EC-17|||FTIC-Folate|||Folate-FTIC;EC17|||EC 17|||EC-17|||FT
EC17 is a FITC conjugated folic acid, also known as Folate-FITC. It also acts as an FRα-targeting agent that fluoresces at 500nm. EC17 is a conjugate consisting of fluorescein isothiocyanate (FITC) conjugated with folate with potential antineoplastic activity.
价 格:¥电议型 号:T25358产 地:中国大陆
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T25355LDurlobactam Triethylamine;杜洛巴坦三乙胺盐Durlobactam Triethylamine(1467829-71-5 Free base)|||ETX 2514 Triet
Durlobactam Triethylamine (ETX2514 Triethylamine) is a diazabicyclooctane β-lactamase inhibitor that inhibits classes A, C, and D β-lactams.Durlobactam Triethylamine has antifungal infection activity.
价 格:¥电议型 号:T25355L产 地:中国大陆
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T25354LDuP 747 HCl;DuP 747 盐酸盐DuP 747 HCl(142515-44-4 Free base);DuP 747 HCl(142515-44-4 Free base)
DuP 747 HCl is a selective kappa agonist with analgesic activity.DuP 747 consists of two conformations.
价 格:¥电议型 号:T25354L产 地:中国大陆
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T2531LEprosartan;依普沙坦KF-108566J free base|||Teveten;KF-108566J free base|||Teveten
Eprosartan (SKF-108566J free base) is a selective and competitive nonpeptide angiotensin II receptor antagonist with high affinity for AT1 receptor subtypes and can be used as an antihypertensive agent.Eprosartan has an inhibitory effect on angiotensin II receptor, with IC50 values of 9.2 nM and 3.9 nM in rat and human adrenocortical membranes, respectively. The IC50 values of Eprosartan in rat and human adrenocortical membranes were 9.2 nM and 3.9 nM, respectively.
价 格:¥电议型 号:T2531L产 地:中国大陆
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T25282CYM 50358 hydrochloride (1314212-39-9 free base);化合物 T25282CYM50358 hydrochloride|||CYM 50358 hydroc
CYM50358 HCl is an S1P4 antagonist.
价 格:¥电议型 号:T25282产 地:中国大陆
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T24924Umibecestat HCl (1387560-01-1 free base);化合物 T24924CNP 520|||Umibecestat HCl|||Umibecestat hydrochlo
Umibecestat is a beta-secretase inhibitor. CNP520 has a selectivity, pharmacodynamics, and distribution profile suitable for AD prevention studies.
价 格:¥电议型 号:T24924产 地:中国大陆
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T24885LTiaspirone hydrochloride;噻螺酮 盐酸盐BMY-13859 hydrochloride|||Tiaspirone hydrochloride(87691-91-6 Free b
Tiaspirone hydrochloride (BMY-13859 hydrochloride) exhibits antipsychotic activity. Tiaspirone hydrochloride influences the electrophysiological activity of dopaminergic neurons in the substantia nigra zona compacta (A9 DA cells) and ventral tegmental area (A10 DA cells) in the brain of the rat.
价 格:¥电议型 号:T24885L产 地:中国大陆
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T24747Sisunatovir;化合物 T24747RV-521|||RV521|||RV 521|||RV521 free base;RV-521|||RV521|||RV 521|||RV521 free
RV521 is a highly effective fusion inhibitor. It designed to treat RSV disease by the target of a surface protein that mediates RSV binding to cellular receptors.
价 格:¥电议型 号:T24747产 地:中国大陆
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T2467R406 free base;化合物R406 free baseR406 (free base);R406 (free base)
R406 free base (R406 (free base)) is a potent Syk inhibitor.
价 格:¥电议型 号:T2467产 地:中国大陆
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T24661Pridefine;化合物 PridefineAHR-1118 free base|||Pridefina;AHR-1118 free base|||Pridefina
Pridefine (Pridefina) is a pyrrolidine derivative, a reuptake blocker of catecholamines and serotonin, with antidepressant activity.
价 格:¥电议型 号:T24661产 地:中国大陆
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T24642YH-306;化合物YH-306YH306|||TRV055 acetate (25849-90-5 Free base);YH306|||TRV055 acetate (25849-90-5 Fre
YH-306 (TRV055 acetate ) is a modulator of the FAK signaling pathway that acts by suppressing colorectal tumor growth and metastasis.
价 格:¥电议型 号:T24642产 地:中国大陆
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T24572OSI-7904L free acid;化合物 T24572OSI 7904|||OSI-7904L|||OSI7904|||OSI 7904L|||OSI7904L|||OSI-7904;OSI 7
OSI-7904L is a folate-based thymidylate synthase inhibitor. It also has antimalarial and antitumor properties.
价 格:¥电议型 号:T24572产 地:中国大陆
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T24466Milademetan free base;化合物 T24466DS3032B|||DS-3032|||DS3032|||DS 3032|||DS 3032B|||DS-3032B;DS3032B||
Milademetan (DS-3032b or DS-3032) is a potent and selective MDM2 inhibitor with potential antineoplastic activity. Milademetan (p.o.) binds to and prevents the binding of MDM2 protein to the transcriptional activation domain of the tumor suppressor protein p53.
价 格:¥电议型 号:T24466产 地:中国大陆
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T24400LEQ-506 HCl (1204975-42-7 free base);化合物 T24400LEQ-506|||LEQ-506 dihychloride|||NPVLEQ 506|||LEQ506|
LEQ506 is an orally bioavailable small-molecule Smoothened antagonist. It also has a potential antineoplastic activity.
价 格:¥电议型 号:T24400产 地:中国大陆
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T24380L-796568 free base;化合物 T24380L-796568 free base
L-796568 free base is a β3 adrenergic receptor agonist potentially for the treatment of obesity. L-796568 is a potent full beta(3) agonist (EC50: 3.6 nM). It has 600-fold selectivity over the human beta(1) and beta(2) receptors.
价 格:¥电议型 号:T24380产 地:中国大陆
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T24370L-368899 free base;化合物 T24370L 368899|||L 368,899|||L368,899|||L-368899|||L368899|||L-368,899;L 3688
L-368899 is a non-peptide and orally active antagonist of oxytocin receptor (IC50: 8.9 nM). It displays 40-fold selectivity over vasopressin V1a and V2 receptors (IC50: 370 and 570 nM respectively).
价 格:¥电议型 号:T24370产 地:中国大陆
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T2435LEPZ011989 HCl(1598383-40-4 Free base);化合物 EPZ011989 HClEPZ-011989 TFA|||EPZ011989 TFA salt|||EPZ 011
EPZ011989 is a highly potent and selective oral EZH2 inhibitor with Ki value <3 nM.
价 格:¥电议型 号:T2435L产 地:中国大陆
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T24358L 741742 (free base);化合物 T24358L-741,742|||L-741742|||L 741742|||L 741,742|||L741742;L-741,742|||L-7
L 741742 is an effective and highly selective antagonist of the D4 dopamine receptor (Ki: 1700, 770, and 3.5 nM at cloned human D2, D3, and D4 receptors).
价 格:¥电议型 号:T24358产 地:中国大陆
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T24220JTH-601 free base;化合物 T24220JTH-601;JTH-601
JTH-601 free base is an antagonist of alpha 1 adrenergic receptor.
价 格:¥电议型 号:T24220产 地:中国大陆