所有产品分类
所有产品
信号通路
- Angiogenesis/Protein Tyrosine Kinase
- Apoptosis Pathway
- Cell Cycle/DNA Damage
- Epigenetics
-
GPCR/G Protein
- Urotensin Receptor
- Melatonin Receptor
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- Smoothened/Smo
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-
Neuro Signaling Pathway
- Imidazoline Receptor
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- FAAH
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- nAChR
- COX
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- mAChR
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-
Protease/Metabolic Enzyme
- COMT
- 11β HSD
- Carboxypeptidase
- ACC
- Xanthine Oxidase
- Pyruvate Kinase
- Mitochondrial Metabolism
- ALDH
- SCD
- Serine Protease
- MLR
- FTase
- CETP
- Neprilysin
- MAGL
- Carbonic Anhydrase
- E1 E2 E3 Enzyme
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- PAI1
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- Glucokinase
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- DGAT
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- Phosphatase
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- HCV Protease
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- Factor Xa
- DPP
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- Integrase
- Phosphodiesterase/PDE
- Phospholipase
- LXR
- Proteasome
- Cytochrome P450
- TGF beta/Smad
- Wnt/Stem Cell
- Others Pathway
研究领域
- Metabolic Disease
- Neurological Disease
- Endocrinology
- Diabetes
- Cardiovascular Disease
- Immunology
- Allergy
- Inflammation
- Infection
- Cancer
天然产物
抗体
多肽
催化剂
杂质对照品
医药中间体
基础原料
BCRP
结构式 | 货号 | 产品名称 | CAS号 |
---|
BCP33811 | Zamicastat 新 | 1080028-80-3 | |
Zamicastat is a dopamine β-hydroxylase (DBH) inhibitor that could cross the blood-brain barrier (BBB) and cause central as well as peripheral effects. Zamicastat is also a concentration-dependent dual P-gp and BCRP inhibitor with IC50 values of 73.8 μM and 17.0 μM, respectively. Reduces high blood pressure.
|
BCP25916 | ML753286 新 | 1699720-89-2 | |
ML753286 is a potent inhibitor for BCRP, ML753286 has low to medium clearance in rodent and human liver S9 fractions, and is stable in plasma cross species.
|
BCP24252 | Brevianamide F 新 | 38136-70-8 | |
Brevianamide F is a naturally occurring 2,5-diketopiperazine that possess interesting breast cancer resistance protein (BCRP) inhibitory activity.; also shows agonism towards Ca(2+)-channel activity at 100 uM, and has potentiation for use in the treatment of cardiovascular dysfunction.
|
BCP28922 | YHO-13177 | 912287-56-0 | |
YHO-13177 is a potent and specific inhibitor of breast cancer resistance protein (BCRP/ABCG2).
|
BCP17744 | KS 176 | 1253452-78-6 | |
KS176 is a potent and selective inhibitor of the breast cancer resistance protein (BCRP) multidrug transporter (IC50 values are 0.59 and 1.39 μM in Pheo A and Hoechst 33342 assays respectively). Displays no inhibitory activity against P-gp or MRP1.
|
BCP28919 | YHO-13351 (free base) 新 | 912288-64-3 | |
YHO-13351 (free base) is the water-soluble prodrug of YHO-13177, which is a potent and specific inhibitor of BCRP.
|
BCP28920 | YHO-13351 新 | 1346753-00-1 | |
YHO-13351 is the water-soluble prodrug of YHO-13177, which is a potent and specific inhibitor of BCRP.
|
BCP28921 | Fumitremorgin C 新 | 118974-02-0 | |
Fumitremorgin C is a potent and selective ABCG2/BRCP inhibitor.
|
BCP05709 | 依克立达 新 | 143664-11-3 | |
Elacridar is a P-glycoprotein and breast cancer resistance protein inhibitor that has been used to improve the brain distribution of drugs that are substrates of P-gp and BCRP.
|
BCP14056 | 依克立达盐酸盐 新 | 143851-98-3 | |
Elacridar hydrochloride (GF120918A) is a potent P-glycoprotein (Pgp) and BCRP inhibitor
|