Classified by application
All Products
Signaling Pathways
- Angiogenesis/Protein Tyrosine Kinase
- Apoptosis Pathway
- Cell Cycle/DNA Damage
- Epigenetics
-
GPCR/G Protein
- Urotensin Receptor
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- Neurotensin Receptor
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- Smoothened/Smo
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- Hormone Pathay
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- Microbiology/Virology
-
Neuro Signaling Pathway
- Imidazoline Receptor
- Monoamine Oxidase
- COMT
- Amyloid β
- NK Receptor
- Beta secretase
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- SSRI
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- P glycoprotein
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- nAChR
- CGRP Receptor
- FAAH
- P2 Receptor
- COX
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- mAChR
- NFκB
- PI3K/Akt/mTOR
-
Protease/Metabolic Enzyme
- COMT
- 11β HSD
- Carboxypeptidase
- Xanthine Oxidase
- ACC
- Mitochondrial Metabolism
- Pyruvate Kinase
- ALDH
- SCD
- Serine Protease
- Neprilysin
- CETP
- FTase
- MLR
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- Carbonic Anhydrase
- E1 E2 E3 Enzyme
- NOX
- Elastase
- PAI1
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- Glucokinase
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- Tyrosinase
- FAS
- DGAT
- Lipoxygenase
- Nampt
- IDO
- IDH
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- Phosphatase
- Thrombin
- FXR
- RAR/RXR
- HMGCR
- FAAH
- Gamma secretase
- RAAS/ACE
- Caspase
- HIV Protease
- Aminopeptidase
- HCV Protease
- HSP
- Tryptophan Hydroxylase/TPH
- DPP
- Factor Xa
- Procollagen C Proteinase
- Integrase
- Phospholipase
- Phosphodiesterase/PDE
- LXR
- Proteasome
- Cytochrome P450
- TGF beta/Smad
- Wnt/Stem Cell
- Others Pathway
Research Areas
- Metabolic Disease
- Neurological Disease
- Endocrinology
- Diabetes
- Cardiovascular Disease
- Immunology
- Allergy
- Inflammation
- Infection
- Cancer
Nature products
Antibodies
Peptides
Catalysts
Impurities
Intermediate
- Amino acid
- Ammonia Series
- Azaindazole
- Pyridazine Series
- Nucleoside Series
- Quinoline Series
- Quinazoline
- Pyrazole Series
- Pyrimidine Series
- Boric acid
- Saccharide
- Thiophene Series
- Pyrrole Series
- Indole Series
- Azaindole
- Piperidine Series
- Indazole Series
- Heterocyclic Series
- Pyridine Series
- Benzene Series
Raw Materials
HSP
Chemical Structure | Cat. No. | Product Name | CAS No. |
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BCP36508 | Retaspimycin hydrochloride New | 857402-63-2 |
Retaspimycin Hydrochloride is a potent and water-soluble inhibitor of Hsp90 with EC50s of 119 nM for both Hsp90 and Grp9.
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BCP33248 | Tamoxifen New | 10540-29-1 |
Tamoxifen is a selective estrogen receptor modulator (SERM) which blocks estrogen action in breast cells and can activate estrogen activity in other cells, such as bone, liver, and uterine cells. Tamoxifen is a potent Hsp90 activator and enhances the Hsp90 molecular chaperone ATPase activity. Tamoxifen activates autophagy and induces apoptosis.
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BCP31061 | JG98 New | 1456551-16-8 |
JG-98, an allosteric heat shock protein 70 (Hsp70) inhibitor, which binds tightly to a conserved site on Hsp70 and disrupts the Hsp70-Bag3 interaction.
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BCP22705 | Alvespimycin HCl New | 467214-21-7 |
Alvespimycin hydrochloride is a potent inhibitor of Hsp90, binding to Hsp90 with EC50 of 62±29 nM.
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BCP27980 | Debio 0932 New | 1061318-81-7 |
Debio 0932 is an orally active HSP90 inhibitor, with IC50s of 100 and 103 nM for HSP90α and HSP90β, respectively.
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BCP29281 | TRC 051384 New | 867164-40-7 |
TRC051384 is a heat shock protein 70 (HSP70) inducer.
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BCP25132 | TAS-116 New | 1260533-36-5 |
TAS-116 is an oral bioavailable, ATP-competitive, highly specific HSP90α/HSP90β inhibitor (Kis of 34.7 nM and 21.3 nM, respectively) without inhibiting other HSP90 family proteins such as GRP94. TAS-116 demonstrates less ocular toxicity.
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BCP30844 | 3-Methyltoxoflavin New | 32502-62-8 |
3-Methyltoxoflavin is a potent Protein disulfide isomerase (PDI) inhibitor, with an IC50 of 170 nM.
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BCP30211 | MKT-077 New | 147366-41-4 |
MKT-077 is an inhibitor of mitochondrial hsp70 family member mortalin (mot-2), causing the selective death of cancer cells.
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BCP28527 | KNK437 New | 218924-25-5 |
KNK437 is a HSP inhibitor, and inhibits the induction of HSP105, HSP70, and HSP40.
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