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T19112LSacubitril Enantiomer;LCZ 696杂质A2R,4S-Sacubitril|||ahu377 isomer 2;2R,4S-Sacubitril|||LCZ 696杂质A|||a
Sacubitril Enantiomer (ahu377 isomer 2) is the enantiomer of Sacubitril which is a neprilysin inhibitor.
价 格:¥电议型 号:T19112L产 地:中国大陆
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T191122R,4S-Sacubitril;LCZ 696杂质ASacubitril Enantiomer|||ahu377 isomer 2;LCZ 696杂质A|||Sacubitril Enantiome
2R,4S-Sacubitril (Sacubitril Enantiomer) is the impurity of Sacubitril which is a neprilysin inhibitor.
价 格:¥电议型 号:T19112产 地:中国大陆
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T191112R,4R-Sacubitril;化合物 T191112R,4R-Sacubitril
2R,4R-Sacubitril is the impurity of Sacubitril. Sacubitril is used in combination with valsartan for the treatment of patients with heart failure.
价 格:¥电议型 号:T19111产 地:中国大陆
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T19110(2E,4E,6Z)-Methyl deca-2,4,6-trienoate;(2E,4E,6Z)-2,4,6-癸三烯酸甲酯Methyl (2E,4E,6Z)-decatrienoate;Methyl
(2E,4E,6Z)-Methyl deca-2,4,6-trienoate (Methyl (2E,4E,6Z)-decatrienoate) is a small molecule compound from the bed bug Thyanta pallidovirens. (Methyl (2E,4E,6Z)-decatrienoate), a small molecular compound from Thyanta pallidovirens, is a sexually attractive pheromone that is thermally unstable.
价 格:¥电议型 号:T19110产 地:中国大陆
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T1911Afuresertib;化合物AfuresertibGSK2110183C|||GSK2110183;GSK2110183C|||GSK2110183
Afuresertib (GSK2110183) is an orally bioavailable inhibitor of the serine/threonine protein kinase Akt (protein kinase B) with potential antineoplastic activity.
价 格:¥电议型 号:T1911产 地:中国大陆
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T18911Acriflavine;吖啶黄Acriflavinium chloride 3,6-Acridinediamine mix;Acriflavinium chloride 3,6-Acridinedia
Acriflavine (Acriflavinium chloride 3,6-Acridinediamine mix) is a papain-like protease (PL(pro)) inhibitor, a fluorescent dye for labeling high molecular weight RNAs, has antimicrobial and anticancer activity, inhibits SARS-CoV-2 and other β-coronaviruses, and can be used for research on leukemia. be used to study leukemia.
价 格:¥电议型 号:T18911产 地:中国大陆
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T17911(S,R,S)-AHPC-C6-PEG3-C4-Cl;化合物 T17911VH032-C6-PEG3-C4-Cl|||VHL Ligand-Linker Conjugates 12|||E3 liga
(S,R,S)-AHPC-C6-PEG3-C4-Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 3-unit PEG linker. (S,R,S)-AHPC-C6-PEG3-C4-Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
价 格:¥电议型 号:T17911产 地:中国大陆
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T17106TMC310911;化合物 T17106TMC310911
TMC310911 is an effective and orally active HIV type-1 protease inhibitor (EC50: ranged from 2.2 nM to 14.2 nM for wild-type HIV-1). TMC310911 has effective activity against a wide spectrum of recombinant HIV-1 isolates.
价 格:¥电议型 号:T17106产 地:中国大陆
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T16911Sorivudine;索立夫定BV-araU;BV-araU|||索立夫定
Sorivudine (BV-araU) has antiviral activity against several viruses including varicella zoster virus, herpes simplex type 1 virus, and Epstein-Barr virus by interfering with viral DNA synthesis.
价 格:¥电议型 号:T16911产 地:中国大陆
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T16879LSHU 9119 acetate;化合物SHU 9119 acetateSHU 9119 acetate (168482-23-3 free base);SHU 9119 acetate (16848
SHU 9119 acetate is a well-known antagonist of human melanocortin 3 and 4 (hMC3R, hMC4R) receptors and a partial hMC5R agonist. The IC50 values of human MC3R, MC4R and MC5R is 0.23, 0.06, and 0.09 nM respectively.
价 格:¥电议型 号:T16879L产 地:中国大陆
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T16879SHU 9119;化合物 T16879SHU 9119
SHU 9119 is an effective human melanocortin 3 and 4 receptors (MC3/4R) antagonist and a partial MC5R agonist (IC50: 0.23, 0.06, and 0.09 nM for human MC3R, MC4R and MC5R, respectively).
价 格:¥电议型 号:T16879产 地:中国大陆
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T16783Rolziracetam;罗拉西坦CI-911;罗拉西坦|||CI-911
Rolziracetam (CI-911) is a nootropic drug of the racetam family. It can improve short-term memory in rats and monkeys.
价 格:¥电议型 号:T16783产 地:中国大陆
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T15911m-PEG7-CH2-OH;化合物 T15911m-PEG7-CH2-OH
m-PEG7-CH2-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格:¥电议型 号:T15911产 地:中国大陆
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T15565Imetit dihydrobromide化合物 T15565VUF 8325 dihydrobromide|||SKF 91105 dihydrobromide
Imetit dihydrobromide is a high affinity and effective agonist of histamine H3 and H4 receptors (Ki: 0.3 and 2.7 nM). Imetit mimics the histamine effect in triggering a shape change in eosinophils (EC50: 25 nM).
价 格:¥电议型 号:T15565产 地:中国大陆
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T14911CD2665;化合物CD2665CD2665
CD2665 is an orally active antagonist of retinoic acid receptor (RAR). For RARγ and RARβ, the Kis are 110 nM and 306 nM.
价 格:¥电议型 号:T14911产 地:中国大陆
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T14338Atabecestat;化合物 T14338JNJ-54861911;JNJ-54861911
Atabecestat (JNJ-54861911) is a potent brain-penetrant and orally active β-site amyloid precursor protein cleaving enzyme 1 (BACE1) inhibitor, achieves robust and high CSF Aβ reduction and it is tolerated and displays a sustained pharmacokinetic (PK) and pharmacodynamic (PD) characteristics. Atabecestat (JNJ-54861911) has the potential for Alzheimer´s Disease treatment[1].
价 格:¥电议型 号:T14338产 地:中国大陆
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T139911,7-Bis-Boc-1,4,7-triazaheptane;化合物 T139911,7-Bis-Boc-1,4,7-triazaheptane
1,7-Bis-Boc-1,4,7-triazaheptane is an alkyl/ether-based PROTAC linker utilized for the synthesis of PROTACs[1].
价 格:¥电议型 号:T13991产 地:中国大陆
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T13911Tacalcitol monohydrate;他卡西醇一水物Curatoderm monohydrate|||TV 02 monohydrate|||TV-02H monohydrate|||1,24
Tacalcitol monohydrate(Curatoderm monohydrate), a vitamin D3 analog that promotes bone development by regulating calcium ions, can be used to study psoriasis.
价 格:¥电议型 号:T13911产 地:中国大陆
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T12911Sigma-1 receptor antagonist 2;化合物Sigma-1 receptor antagonist 2Sigma-1 receptor antagonist 2
Sigma-1 receptor antagonist 2 is a more potent and selective antagonist of sigma 1 receptor (σ1 R, Ki = 3.88 nM) than σ2 receptor (Ki = 1288 nM).
价 格:¥电议型 号:T12911产 地:中国大陆
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T1288TTNPB化合物TTNPBAGN191183|||Arotinoid acid|||Ro 13-7410,AGN-191183|||Ro 13-7410
TTNPB (Ro 13-7410,AGN-191183), a potent RAR agonist, inhibits binding of [3H]tRA of human RARα (IC50: 5.1 nM), β (IC50: 4.5 nM), and γ (IC50: 9.3 nM), respectively.
价 格:¥电议型 号:T1288产 地:中国大陆