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T18053Ipatasertib-NH2；化合物 T18053RG7440-NH2|||GDC-0068-NH2；RG7440-NH2|||GDC-0068-NH2
Ipatasertib-NH2 (GDC-0068-NH2;RG7440-NH2) is a ligand for target protein AKT for PROTAC, binds to lenalidomide, a ligand of ubiquitin E3 ligase cereblon (CRBN), via a ten-hydrocarbon linker to form INY-03-041 to degrade AKT[1].
价 格：￥电议型 号：T18053产 地：中国大陆
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T18052Iodoacetamide-PEG3-azide；化合物 T18052Iodoacetamide-PEG3-azide
Iodoacetamide-PEG3-azide is a PEG-derived PROTAC linker utilized for synthesizing PROTACs. [1]
价 格：￥电议型 号：T18052产 地：中国大陆
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T18051Iodo-PEG12-NHS ester；化合物 T18051Iodo-PEG12-NHS ester
Iodo-PEG12-NHS ester 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：T18051产 地：中国大陆
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T18050Iodo-PEG12-acid；化合物 T18050Iodo-PEG12-acid
Iodo-PEG12-acid 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：T18050产 地：中国大陆
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T1805Ataluren；化合物AtalurenPTC124；PTC124
Ataluren (PTC124) is a novel, orally administered drug that targets nonsense mutations. Ataluren is approved for use by the European Medicines Agency to treat Duchenne Muscular Dystrophy in patients aged 5 years and older who are able to walk.
价 格：￥电议型 号：T1805产 地：中国大陆
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T17805DBCO-PEG6-amine；化合物 T17805DBCO-PEG6-amine
DBCO-PEG6-amine 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：T17805产 地：中国大陆
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T16805RTS-V5；化合物 T16805RTS-V5
RTS-V5 is a dual inhibitor of HDAC/proteasome (IC50s: 6.9, 18, 15, 0.27, 0.53 μM for HDAC1, HDAC2, HDAC3, HDAC6, HDAC8, respectively).
价 格：￥电议型 号：T16805产 地：中国大陆
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T16444PD-118057；化合物PD-118057PD-118057
PD-118057 is a potent ether associated (hERG) potassium channel activator that shows no activity against hERG. PD-118057 inhibits the excitability of the membrane by activating the hERG channel. PD-118057 is a potential compound for the treatment of delayed repolarization in inherited or acquired long QT syndrome and congestive heart failure.
价 格：￥电议型 号：T16444产 地：中国大陆
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T15805LLY2510924 acetate(1088715-84-7 free base)；化合物LY2510924 acetateLY2510924 acetate(1088715-84-7 free ba
Ly2510924 acetate is an potent and selective CXCR4 antagonist. It prevents the binding of SDF-1 to CXCR4 with an IC50 of 0.079 nM.
价 格：￥电议型 号：T15805L产 地：中国大陆
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T15805LY2510924；化合物 T15805LY2510924
LY2510924 is an effective and selective CXCR4 antagonist. It blocks SDF-1 binding to CXCR4 (IC50: 0.079 nM).
价 格：￥电议型 号：T15805产 地：中国大陆
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T1492Gemifloxacin mesylate；甲磺酸吉米沙星LB-20304a|||SB-265805S|||Gemifloxacinu00A0mesylate；LB-20304a|||甲磺酸吉米沙星|
Gemifloxacin mesylate (Gemifloxacin?mesylate) inhibits activities of DNA gyrase and topoisomerase IV, thereby inhibiting DNA replication and eventually bacterial growth. Gemifloxacin Mesylate is the mesylate salt form of gemifloxacin, a synthetic broad-spectrum fluoroquinolone with antibacterial activity. This fluoroquinolone exerts an enhanced spectrum of activity against gram-positive bacteria such as Streptococcus pneumonia and Staphylococcus aureus, in addition to its activity against gram-n
价 格：￥电议型 号：T1492产 地：中国大陆
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T14805Bromo-PEG5-azide；化合物 T14805Bromo-PEG5-azide
Bromo-PEG5-azide 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：T14805产 地：中国大陆
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T13805Ophiopogonin C；麦冬胶原蛋白 COphiopogonin C；Ophiopogonin C|||麦冬胶原蛋白 C
Acetic Acid is a natural product isolated from the tubers of Ophiopogon japonicus, is a rare naturally occurring C29 steroidal glycoside.
价 格：￥电议型 号：T13805产 地：中国大陆
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T13400Ziprasidone D8；化合物 T13400CP-88059 D8；CP-88059 D8
Ziprasidone D8 is deuterium labeled Ziprasidone, which is a antagonist of combined 5-HT (serotonin) and dopamine receptor and exhibits potent effects of antipsychotic activity.
价 格：￥电议型 号：T13400产 地：中国大陆
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T12805S-methyl DM1；化合物 T12805S-methyl DM1
S-methyl DM1 is a thiomethyl derivative of Maytansine. S-methyl DM1 binds to tubulin(Kd of 0.93 μM) and inhibts microtubule polymerization.
价 格：￥电议型 号：T12805产 地：中国大陆
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T1255Tobramycin；妥布霉素NSC 180514|||Nebramycin Factor 6|||Deoxykanamycin B；NSC 180514|||妥布霉素|||Nebramycin Fa
Tobramycin (NSC-180514) is an aminoglycoside, broad-spectrum antibiotic produced by Streptomyces tenebrarius.
价 格：￥电议型 号：T1255产 地：中国大陆
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T124805Zopfiellamide A；化合物 Zopfiellamide AZopfiellamide A
Zopfiellamide A is a useful organic compound for research related to life sciences and the catalog number is T124805.
价 格：￥电议型 号：T124805产 地：中国大陆
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T12267NSP-805；化合物NSP-805NSP-805
NSP-805 is a potent and selective guinea pig cardiac phosphodiesterase 3 (PDE3) inhibitor.
价 格：￥电议型 号：T12267产 地：中国大陆
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T11805L-NIL；化合物 L-NILL-NIL
L-NIL is a selective nitric oxide synthase (iNOS) inhibitor that reverses burn-induced activation of glycogen synthase kinase-3β in rat skeletal muscle and may slow the progression of squamous cell carcinoma lung.
价 格：￥电议型 号：T11805产 地：中国大陆
