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T17629Bis-PEG29-acid；化合物 T17629Bis-PEG29-acid
Bis-PEG29-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：T17629产 地：中国大陆
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T1667Tandutinib；坦度替尼MLN518|||CT53518|||NSC726292；MLN518|||CT53518|||NSC726292|||坦度替尼
Tandutinib (CT53518) (MLN518, CT53518), an effective FLT3 antagonist (IC50: 0.22 μM), can also inhibit c-Kit and PDGFR, 15-20 fold higher potency for FLT3 versus CSF-1R and >100-fold selectivity for the same target versus FGFR, EGFR, and KDR.
价 格：￥电议型 号：T1667产 地：中国大陆
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T16629Propargyl-PEG4-O-C1-Boc；化合物 T16629Propargyl-PEG4-O-C1-Boc
Propargyl-PEG4-O-C1-Boc 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：T16629产 地：中国大陆
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T16299NH-bis(PEG2-C2-Boc)；化合物 T16299NH-bis(PEG2-C2-Boc)
NH-bis(PEG2-C2-Boc) is an alkyl/ether-based linker, utilized for the synthesis of PROTACs[1].
价 格：￥电议型 号：T16299产 地：中国大陆
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T16298NH-bis(m-PEG8)；化合物 T16298NH-bis(m-PEG8)
NH-bis(m-PEG8) 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：T16298产 地：中国大陆
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T16297NH-bis(m-PEG4)；化合物 T16297NH-bis(m-PEG4)
NH-bis(m-PEG4) 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：T16297产 地：中国大陆
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T16296NH-bis(C2-PEG2-NH-Boc)；化合物 T16296NH-bis(C2-PEG2-NH-Boc)
NH-bis(C2-PEG2-NH-Boc) 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：T16296产 地：中国大陆
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T16295NH-bis(C2-PEG1-azide)；化合物 T16295NH-bis(C2-PEG1-azide)
NH-bis(C2-PEG1-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：T16295产 地：中国大陆
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T16293NGD-4715；化合物 T16293NGD-4715
NGD-4715 is a selective and orally active antagonist of melanin-concentrating hormone receptor 1.
价 格：￥电议型 号：T16293产 地：中国大陆
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T16292NFPS；化合物 T16292NFPS
NFPS exerts neuroprotection via glyR alpha1 subunit in the rat model of transient focal cerebral ischaemia and reperfusion. NFPS is a selective and non-competitive glycine transporter-1 (GlyT1) inhibitor (IC50s: 2.8 nM and 9.8 nM for hGlyT1 and rGlyT1, respectively).
价 格：￥电议型 号：T16292产 地：中国大陆
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T16291NF157；化合物 T16291NF157
NF157 significantly decreases the expression of metalloproteinase (MMP)-3, MMP-13, which can be used in the treatment of osteoarthritis (OA). NF157 is a highly selective nanomolar P2Y11 antagonist (pKi: 7.35). The IC50s are 463 nM, 1811 μM, 170 μM for P2Y11 (Ki=44.3 nM), P2Y1 (Ki=187 μM), P2Y2 (Ki=28.9 μM), respectively.
价 格：￥电议型 号：T16291产 地：中国大陆
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T16290NIK SMI1；化合物NIK SMI1NIK SMI1
NIK SMI1 is an effective and selective NF-κB inducing kinase (NIK) inhibitor. It also inhibits NIK-catalyzed hydrolysis of ATP to ADP (IC50: 0.23±0.17 nM).
价 格：￥电议型 号：T16290产 地：中国大陆
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T1629Rifapentine；利福喷丁MDL473|||Rifapentina|||Rifapentinum|||DL 473|||Priftin|||Cyclopentylrifampicin；MDL47
Rifapentine (Rifapentinum) is a long-acting, cyclopentyl-substituted derivative of rifamycin used to treat mycobacterium infections.
价 格：￥电议型 号：T1629产 地：中国大陆
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T1615LIrbesartan HCl；化合物 T1615LIrbesartan hydrochloride|||BMS186295|||BMS 186295|||BMS-186295；Irbesartan h
Irbesartan is an angiotensin II receptor antagonist used mainly for the treatment of hypertension. It selectively and competitively blocks the binding of angiotensin II to the angiotensin I receptor.
价 格：￥电议型 号：T1615L产 地：中国大陆
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T1615Irbesartan；厄贝沙坦SR-47436|||BMS-186295；厄贝沙坦|||SR-47436|||BMS-186295
Irbesartan (SR-47436) is an Angiotensin 2 Receptor Blocker. The mechanism of action of irbesartan is as an Angiotensin 2 Receptor Antagonist.
价 格：￥电议型 号：T1615产 地：中国大陆
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T15629JTE-013；化合物JTE-013JTE-013
JTE-013 is an effective and specific antagonist of S1P2. JTE-013 suppresses the specific binding of radiolabeled S1P to human and rat S1P2 (IC50s: 17 nM and 22 nM, respectively).
价 格：￥电议型 号：T15629产 地：中国大陆
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T15430GSK2256294A；化合物GSK2256294AGSK 2256294；GSK 2256294
GSK2256294A (GSK 2256294) is potent, selective inhibitor of recombinant human, rat and mouse sEH with IC50 of 27 pM, 61 pM and 189 pM, respectively.
价 格：￥电议型 号：T15430产 地：中国大陆
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T14629Bis-PEG10-acid；化合物 T14629Bis-PEG10-acid
Bis-PEG10-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：T14629产 地：中国大陆
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T1419Azithromycin hydrate；阿奇霉素二水合物CP-62993 dihydrate|||Azithromycin dihydrate；CP-62993 dihydrate|||阿奇霉素二水
Azithromycin hydrate (CP-62993 dihydrate) is a semi-synthetic macrolide antibiotic structurally related to ERYTHROMYCIN. It has been used in the treatment of Mycobacterium avium intracellulare infections, toxoplasmosis, and cryptosporidiosis.
价 格：￥电议型 号：T1419产 地：中国大陆
