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T500341-{1H-pyrrolo[2,3-d]pyrimidin-4-yl}piperazine 2HCl;1-{1H-pyrrolo[2,3-d]pyrimidin-4-yl}piperazine 盐酸盐
1-{1H-pyrrolo[2,3-d]pyrimidin-4-yl}piperazine dihydrochloride (1-PPZ-DHC) is a compound used as a molecular structural unit. It is an analog of the natural product piperazine and has a wide range of biological activities, including anti-inflammatory, anti-tumor and antibacterial activities. It has also been studied for the treatment of neurological disorders such as Alzheimer´s and Parkinson´s.
价 格:¥电议型 号:T50034产 地:中国大陆
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T500201-(1-phenyltetrazol-5-yl)piperazine HCl;1-(1-phenyltetrazol-5-yl)piperazine 盐酸盐1-(1-phenyl-1H-1,2,3,
1-(1-phenyltetrazol-5-yl)piperazine;hydrochloride (1-(1-phenyl-1H-1,2,3,4-tetrazol-5-yl)piperazine hydrochloride) is a chemical derivative of piperazine that has been used as a starting material for the synthesis of other compounds, such as anti-inflammatory agents. It modulates the activity of enzymes and proteins by binding to their active sites, and has been used in studies of enzyme inhibition and protein structure, as well as in drug metabolism.
价 格:¥电议型 号:T50020产 地:中国大陆
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T500181-(3-chloropyridin-2-yl)piperazine 2HCl;1-(3-chloropyridin-2-yl)piperazine 盐酸盐1-(3-chloropyridin-2-y
1-(3-chloropyridin-2-yl)piperazine dihydrochloride is a piperazine analog often used as a reagent in organic synthesis, as a ligand in coordination chemistry, and as a drug in pharmaceuticals. It is an inhibitor of DPP4, and DPP4 inhibition has been shown to have beneficial effects in the treatment of certain diseases such as type 2 diabetes and obesity.
价 格:¥电议型 号:T50018产 地:中国大陆
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T4967NPS-2143 hydrochloride;化合物NPS-2143 HCLNPS-2143 HCL;2-氯-6-[(2R)-3-[[1,1-二甲基-2-(2-萘基)乙基]氨基]-2-羟基丙氧基]苯腈
NPS-2143 hydrochloride (NPS-2143 HCL) is a selective potent calcium ion-sensing receptor antagonist.
价 格:¥电议型 号:T4967产 地:中国大陆
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T4965LTCS-OX2-29 HCl;化合物 T4965LTCSOX 229|||TCS-OX229|||TCS OX229|||TCS OX2 29|||TCSOX-229|||TCSOX229;TCSOX
TCS-OX2-29 is a selective orexin-2 receptor antagonist (IC50 = 40 nM), which plays an important role in pain modulation.
价 格:¥电议型 号:T4965L产 地:中国大陆
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T49529-Hydroxycamptothecin;9-羟基喜树碱9-HCPT|||10-Hydroxycampothecin;9-HCPT|||9-羟基喜树碱|||10-Hydroxycampothecin
9-Hydroxycampothecin is a camptothecin derivative with anticancer activity.
价 格:¥电议型 号:T4952产 地:中国大陆
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T49237-Dehydrocholesterol;7-去氢胆固醇Provitamin D3|||7-DHC;Provitamin D3|||7-DHC|||7-去氢胆固醇
7-Dehydrocholesterol (Provitamin D3) down-regulates cholesterol biosynthesis in cultured Smith-Lemi-Opitz syndrome skin fibroblasts.
价 格:¥电议型 号:T4923产 地:中国大陆
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T4866H-Trp-NH2.HCl;L-色氨酰胺盐酸盐L-Tryptophanamide hydrochloride|||(2S)-2-amino-3-(1H-indol-3-yl)propanamide h
H-Trp-NH2.HCl ((2S)-2-amino-3-(1H-indol-3-yl)propanamide hydrochloride) is an endogenous metabolite that has been detected in various biological fluids, e.g. Urine and blood.
价 格:¥电议型 号:T4866产 地:中国大陆
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T4680HC-067047;化合物HC-067047HC067047;HC067047
HC-067047 is a potent and selective TRPV4 antagonist.Also inhibits the endogenous TRPV4-mediated response to 4α-PDH .
价 格:¥电议型 号:T4680产 地:中国大陆
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T4657LWHI-P97 HCl 211555-05-4(free base);化合物WHI-P97 HClWHI-P97 HCl 211555-05-4(free base)
WHI-P97 HCl is a potent and selective JAK-3 inhibitor. WHI-P97 had an estimated Ki value of 0.09 microM from modeling studies and a measured IC50 value of 2.5 microM in EGFR kinase inhibition assays. WHI-P97 effectively inhibited the in vitro invasiveness of EGFR-positive human cancer cells in a concentration-dependent manner.
价 格:¥电议型 号:T4657L产 地:中国大陆
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T4614Ellipticine hydrochloride;玫瑰树碱盐酸盐Ellipticine HCl|||NSC 71795 (hydrochloride);Ellipticine HCl|||NSC 7
Ellipticine hydrochloride (NSC-71795 (hydrochloride)) is a potent antineoplastic agent; inhibits DNA topoisomerase II activities.
价 格:¥电议型 号:T4614产 地:中国大陆
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T4604HC-056456;化合物HC-056456HC 056456|||3,4-Bis(2-thienoyl)-1,2,5-oxadiazole-N-oxide;HC 056456|||3,4-Bis(2
HC-056456 (3,4-Bis(2-thienoyl)-1,2,5-oxadiazole-N-oxide) is a CatSper channel modulator.
价 格:¥电议型 号:T4604产 地:中国大陆
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T4592TOMATIDINE HYDROCHLORIDE盐酸番茄碱Tomatidine|||Tomatidine HCl|||盐酸番茄碱
Tomatidine hydrochloride (Tomatidine HCl) is a steriodal alkaloid structurally similar to Cyclopamine but does not inhibit hedgehog pathway. May be used as a negative control for Cyclopamine and KAAD-Cyclopamine. Tomatidine protects against muscle atrophy and boosting muscle growth.
价 格:¥电议型 号:T4592产 地:中国大陆
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T4583PFI-2 hydrochloride;化合物(R)-PFI-2 hydrochloride(R)-PFI-2 hydrochloride|||PFI-2 HCl;(R)-PFI-2 hydrochl
PFI-2 hydrochloride ((R)-PFI-2 hydrochloride) is a potent, highly selective, and cell-active inhibitor of the methyltransferase activity of SETD7 (IC50: 2 nM), 500 fold active than (S)-PFI-2.
价 格:¥电议型 号:T4583产 地:中国大陆
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T4569LLucanthone hydrochloride;化合物 T4569LLucanthone HCl;Lucanthone HCl
Lucanthone hydrochloride is a novel acridine derivative which supresses autophagic degradation and triggers apoptosis in colon cancer cells.
价 格:¥电议型 号:T4569L产 地:中国大陆
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T4545Propacetamol Hydrochloride;盐酸丙帕他莫Propacetamol HCL;盐酸丙帕他莫|||Propacetamol HCL
Propacetamol Hydrochloride (Propacetamol HCL) is a prodrug of paracetamol (acetaminophen) with improved water solubility. Propacetamol Hydrochloride is an analgesic drug delivered by IV when the oral application of NSAID is not appropriate or contradicted.
价 格:¥电议型 号:T4545产 地:中国大陆
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T4522SSD114 HCl;化合物SSD114 hydrochlorideSSD114 HCl
SSD114 is a novel GABAB receptor positive allosteric modulator.
价 格:¥电议型 号:T4522产 地:中国大陆
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T4444A-674563 HCl (552325-73-2(free base));化合物A-674563 HClA-674563 HCl (552325-73-2(free base))
A-674563 is an orally available, ATP-competitive, and reversible inhibitor of Akt (Ki: 11 nM for Akt1) [1]. It exhibits inhibitory activity against PKA and Cdk2 (IC50: 16/46 nM) but is 10- to >1, 800-fold selective for Akt1 versus additional kinases in the CMGC, CAMK, and TK families [1].
价 格:¥电议型 号:T4444产 地:中国大陆
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T4419UNC2025 2HCl (1429881-91-3(free base));化合物UNC2025 2HClUNC2025 2HCl (1429881-91-3(free base))
UNC2025 is a potent and orally bioavailable Mer/Flt3 dual inhibitor with IC50 of 0.8/0.74 nM for Mer/Flt3.
价 格:¥电议型 号:T4419产 地:中国大陆
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T4418GSK2879552 2HCl (1401966-69-5(free base));化合物GSK2879552 2HClGSK2879552 2HCl (1401966-69-5(free base)
GSK2879552 is an orally available, irreversible inhibitor of lysine specific demethylase 1 (LSD1), with potential antineoplastic activity.
价 格:¥电议型 号:T4418产 地:中国大陆