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T15470Heparastatin；化合物 T15470Heparastatin
Heparastatin is an inhibitor of heparanase.
价 格：￥电议型 号：T15470产 地：中国大陆
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T1547L-Cysteine methyl ester hydrochloride；L-半胱氨酸甲酯盐酸盐L-Cysteine methyl ester hydrochloride(Acdrile)；L-半胱
L-Cysteine methyl ester hydrochloride (L-Cysteine methyl ester hydrochloride (Acdrile)) is an antitussive and an expectorant agent, used to relieve breathing difficulties caused by mucus.
价 格：￥电议型 号：T1547产 地：中国大陆
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T15453GW7647化合物GW76472-[[4-[2-[[环己基氨基)羰基](4-环己基丁基)氨基]乙基]苯基]硫基]-2-甲基丙酸
GW7647 is a potent agonist of PPARα (EC50s: 6 nM, 1.1 μM, and 6.2 μM for human PPARα, PPARγ, and PPARδ, respectively).
价 格：￥电议型 号：T15453产 地：中国大陆
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T15447Guacetisal；呱西替柳Guacetisal
Guacetisal is extracted from the esterification reaction of acetylsalicylic acid with guaiacol which can be used for research on the treatment of chronic bronchitis.
价 格：￥电议型 号：T15447产 地：中国大陆
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T15347FR167344 free base；化合物 T15347FR167344 free base
FR167344 free base is an orally active and nonpeptide antagonist of bradykinin receptor B2. FR167344 free base displays a high-affinity binding to the B2 receptor (IC50: 65 nM). It has no binding affinity for the B1 receptor.
价 格：￥电议型 号：T15347产 地：中国大陆
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T15247ESI-05；化合物ESI-05NSC 116966；NSC 116966
ESI-05 (NSC-116966) is a specific EPAC2 (exchange protein directly activated by cAMP 2) antagonist (IC50: 0.4 μM). ESI-05 inhibits cAMP-mediated activation of EPAC2, as well as EAPC2, mediated Rap1 activation.
价 格：￥电议型 号：T15247产 地：中国大陆
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T15241ER-000444793；化合物ER-000444793ER-000444793
ER-000444793 is a potent mitochondrial permeability transition pore (mPTP) opening inhibitor and it also inhibits mPTP (IC50: 2.8 μM).
价 格：￥电议型 号：T15241产 地：中国大陆
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T15147DNMDP；化合物 T15147DNMDP
DNMDP is a phosphodiesterase 3A inhibitor with clear cell-selective cytotoxicity. DNMDP binding to PDE3A promotes interaction between PDE3A and Schlafen 12.
价 格：￥电议型 号：T15147产 地：中国大陆
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T15093Dehydro-ZINC39395747；化合物 T15093Dehydro-ZINC39395747
Dehydro-ZINC39395747 is a ZINC39395747 derivative. ZINC39395747 can increase NO bioavailability in vascular cells. ZINC39395747 is a potent cytochrome b5 reductase 3 inhibitor (IC50 : 9.14 μM and Kd: 1.11 μM).
价 格：￥电议型 号：T15093产 地：中国大陆
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T15055DB04760；化合物 DB04760MMP-13 Inhibitor；MMP-13 Inhibitor
DB04760 is a highly selective, non-zinc-chelating inhibitor of MMP-13 (IC50: 8 nM). DB04760 obviously decreases paclitaxel neurotoxicity and has anticancer activity.
价 格：￥电议型 号：T15055产 地：中国大陆
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T15047Dacisteine；达西司坦N,S-Diacetyl-L-cysteine；N,S-Diacetyl-L-cysteine|||达西司坦
Dacisteine (N,S-Diacetyl-L-cysteine) is an inhibitor of New Delhi metallo-beta-lactamase-1 (NDM-1, IC50 = 1000 μM).
价 格：￥电议型 号：T15047产 地：中国大陆
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T15013CS476；化合物 T15013NSC302998；NSC302998
CS476 is a potent drug of hypoglycaemic.
价 格：￥电议型 号：T15013产 地：中国大陆
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T14947CHDI-390576；化合物 CHDI-390576CHDI-390576
CHDI-390576 is a CNS-permeable, selective and potent dibenzoyl isohydroxamic acid class IIa histone deacetylase (HDAC) inhibitor that inhibits class IIa HDAC 4, HDAC 5, HDAC 7, HDAC 9, and can be used in cancer research.
价 格：￥电议型 号：T14947产 地：中国大陆
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T14943CGP60474；化合物CGP60474CGP60474
CGP60474 is an inhibitor of VEGFR-2 (IC50 = 84 nM) and an inhibitor of ATP-competitive PKC. CGP60474 is also a highly potent anti-endotoxemic agent and inhibits cyclin-dependent kinase (CDK) potently.
价 格：￥电议型 号：T14943产 地：中国大陆
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T14904CCT244747；化合物 T14904CCT244747
CCT244747 is a CHK1 inhibitor (IC50: 7.7 nM) and also abrogates G2 checkpoint (IC50: 29 nM).
价 格：￥电议型 号：T14904产 地：中国大陆
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T14847B I09；化合物B I09B I09
B I09, an IRE-1 RNase inhibitor with an IC50 of 1230 nM, inhibits splicing of XBP1 mRNA in human WaC3 cells and expression of xbp-1 in LPS-stimulated B cells. B I09 can be used to simulate the defects of XBP-1 in CLL cells., an IRE-1 RNase inhibitor with an IC50 of 1230 nM, inhibits splicing of XBP1 mRNA in human WaC3 cells and expression of xbp-1 in LPS-stimulated B cells. B I09 can be used to simulate the defects of XBP-1 in CLL cells., an IRE-1 RNase inhibitor with an IC50 of 1230 nM, inhibit
价 格：￥电议型 号：T14847产 地：中国大陆
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T14845BX471 hydrochloride化合物 T14845ZK-811752 hydrochloride
BX471 hydrochloride (ZK-811752 hydrochloride) is a potent, selective non-peptide CCR1 antagonist (Ki: 1 nM for human CCR1). It shows 250-fold selectivity for CCR1 over CCR2, CCR5, and CXCR4.
价 格：￥电议型 号：T14845产 地：中国大陆
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T14799Bromo-PEG3-CH2-Boc；化合物 T14799Bromo-PEG3-CH2-Boc
Bromo-PEG3-CH2-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：T14799产 地：中国大陆
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T14796Bromo-PEG3-bromide；化合物 T14796Bromo-PEG3-bromide
Bromo-PEG3-bromide 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：T14796产 地：中国大陆
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T14795Bromo-PEG3-azide；化合物 T14795Bromo-PEG3-azide
Bromo-PEG3-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：T14795产 地：中国大陆
