33 Results for "

Hybrid compound

" in MedChemExpress (MCE) Product Catalog:
Products (33)

33 Results for "Hybrid compound" in MCE Product Catalog:

Cat. No.: HY-N7093
CAS No.: 3658-77-3
Synonyms: Strawberry furanone
Furaneol is mainly isolated from American grape (Vitis labrusca) and its hybrid grape. Furaneol is an important aroma compound in fruits and contribute to the strawberry-like note in some wines .
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Cat. No.: HY-107987
CAS No.: 2231812-31-8
Purity:  99.50%
Target:  

CXCR

Research Areas:  

Endocrinology

CXCR7 modulator 1 (compound 25) is a potent and orally bioavailable peptoid hybrid CXCR7 modulator, with a Ki of 9 nM .
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Cat. No.: HY-N7093R
CAS No.: 3658-77-3
Synonyms: Strawberry furanone (Standard)
Furaneol (Standard) is the analytical standard of Furaneol. This product is intended for research and analytical applications. Furaneol is mainly isolated from American grape (Vitis labrusca) and its hybrid grape. Furaneol is an important aroma compound in fruits and contribute to the strawberry-like note in some wines .
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Cat. No.: HY-149958
CAS No.: 2934738-40-4
Target:  

Parasite

Research Areas:  

Infection

Antileishmanial agent-17 is a coumarin hybrid compound with antileishmanial effects (IC50 <0.78 μM). Antileishmanial agent-17 is safe to normal VERO cells. Antileishmanial agent-17 binds to folate pathway enzymes pteridine reductase and DHFR-TS. And Antileishmanial agent-17 shows the most potent with IC50 value of 0.40 μM against promastigote and 0.68 μM against amastigote, respectivley.
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Cat. No.: HY-145294
CAS No.: 3031515-48-4
Target:  

ROCK

Research Areas:  

Neurological Disease

ROCK2-IN-5 (compound 1d) is a hybrid compound containing structural fragments of the Rho kinase inhibitor fasudil and the NRF2 inducers caffeic and ferulic acids. ROCK2-IN-5 has good multitarget profile and good tolerability. ROCK2-IN-5 has the potential for thr research of Amyotrophic lateral sclerosis (ALS) with a SOD1 mutation .
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Cat. No.: HY-118295
CAS No.: 441742-93-4
Target:  

Endogenous Metabolite

Research Areas:  

Cancer

Pyrimidine-indole hybrid is a compound that inhibits ciliogenesis and has the activity of antagonizing the Hedgehog signaling pathway by destabilizing microtubules. Pyrimidine-indole hybrid exerts its biological effects by inhibiting ciliogenesis and deconstructing the stable form of α-tubulin. Pyrimidine-indole hybrid has shown its unique mechanism of action in in vitro cell experiments and zebrafish embryo models, interfering with microtubule dynamics .
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Cat. No.: HY-119673
CAS No.: 148077-13-8
Target:  

Antibiotic

Research Areas:  

Others

Lincophenicol is a hybrid antibiotic that has the activity of inhibiting the puromycin reaction catalyzed by Escherichia coli ribosomal peptidyl transferase and also inhibits the binding of specific compounds to the Escherichia coli ribosome.
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Cat. No.: HY-161340
CAS No.: 2361522-62-3
Target:  

Apoptosis

Research Areas:  

Cancer

Anti-melanoma agent 2 (Compound IId) is a steroid hybrid that effectively induces endoplasmic reticulum stress (ERS) and causes apoptosis. Anti-melanoma agent 2 shows anti-melanoma effects .
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Cat. No.: HY-128346
CAS No.: 2089415-51-8
Purity:  99.17%
Target:  

Amyloid-β

Research Areas:  

Neurological Disease

PQM130, a Feruloyl-Donepezil Hybrid compound with brain penatration, is a multitarget agent candidate against the neurotoxicity induced by Aβ1-42 oligomer (AβO) and shows anti-inflammatory activity. PQM130 acts as a neuroprotective compound for anti-AD agent development .
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Cat. No.: HY-156188
CAS No.: 3038811-77-4
Target:  

Cholinesterase (ChE)

Research Areas:  

Others

AChE-IN-41 (Compound 2) is a compound of the Galantamine Memantine hybrid. AChE-IN-41 has the inhibition ability of cholinesterase. AChE-IN-41 shows higher plasma stability and comparable microsomal stability in vitro, while showing lower half-life and faster clearance in vivo .
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Cat. No.: HY-N11880
2-O-Sinapoyl makisterone A (compound 2), a sinapinic acid-ecdysterone hybrid, is a selective inhibitor of COX-2. 2-O-Sinapoyl makisterone A significantly inhibits the expression of COX-2 protein .
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Cat. No.: HY-173213
Target:  

Parasite

Research Areas:  

Infection Inflammation/Immunology

Antileishmanial agent-33 (4e), a hybrid compound of grandisin and machilin G, shows moderate activity on promastigotes (IC50 of 38.1 μM). Antileishmanial agent-33 (4e) shows potential as an antileishmanial agent for the research of cutaneous leishmaniasis (CL) .
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Cat. No.: HY-146174
Target:  

Potassium Channel

Research Areas:  

Cardiovascular Disease

KCa1.1 channel activator-2 (compound 3F), a Quercetin hybrid derivative, is a selective vascular KCa1.1 channel stimulator. KCa1.1 channel activator-2 exhibits potent myorelaxant activity .
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Cat. No.: HY-162170
CAS No.: 3036299-85-8
Target:  

NF-κB Keap1-Nrf2 p38 MAPK

Research Areas:  

Inflammation/Immunology

Anti-inflammatory agent 72 (compound 5) is a novel resveratrol derivative hybrid with benzoylhydrazine. Anti-inflammatory agent 72 shows anti-inflammatory and antioxidant activities by activating Nrf2 and inhibiting NF-κB p65/iNOS and MAPKs signaling pathways .
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Cat. No.: HY-115970
Target:  

Microtubule/Tubulin

Research Areas:  

Cancer

Tubulin inhibitor 21 (compound 6f), a chalcone- and melatonin- based hybrid, is a potent tubulin inhibitor. Tubulin inhibitor 21 induces a remarkable cytotoxic activity toward SW480 cells (IC50=0.26 μM) with lower effect against nonmalignant cells .
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Cat. No.: HY-W598230A
m-PEG2000-NH2 hydrochloride is a barrier permeation compound involved in the preparation of hybrid gels with adsorption and size exclusion chromatography (AdSEC) properties. m-PEG-NH2 helps AdSEC gels separate from complex biological mixtures such as blood, urine, sweat, and tears.
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Cat. No.: HY-145908
CAS No.: 2763914-21-0
Target:  

NO Synthase

Research Areas:  

Cancer

Antitumor agent-49 (Compound 10) is a Harmine derivative-furoxan hybrids containing NO donor, with antitumor activities. Antitumor agent-49 shows cytotoxic activity against HepG2 cells with an IC50 of 1.79 µM. Antitumor agent-49 produces high levels of NO in vitro .
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Cat. No.: HY-163899
(+)-Crinatusin A1 (Compound (+)- 4) is a chalcone-monoterpene hybrid, which can be isolated from Cleistocalyx operculatus. (+)-Crinatusin A1 is an inhibitor for protein tyrosine phosphatase 1B (PTP1B) with IC50 of 0.9 μM. (+)-Crinatusin A1 exhibits potential as an antidiabetic agent .
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Cat. No.: HY-124499
CAS No.: 796886-30-1
Target:  

Integrin

Research Areas:  

Cardiovascular Disease

RUC-1 (Compound 1) is an inhibitor for αIIbβ3 integrin. RUC-1 inhibits fibrin deposition and platelet aggregation in hybrid hαIIb/mβ3 receptors expressing mice. RUC-1 exhibits antithrombotic effect in hαIIb/mβ3 receptor expressing mice .
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Cat. No.: HY-146173
Research Areas:  

Cardiovascular Disease

KCa1.1 channel activator-1 (compound 1E), a Quercetin hybrid derivative, is a selective vascular KCa1.1 channel channel stimulator. KCa1.1 channel activator-1 also displays CaV1.2 channel blocking activity. KCa1.1 channel activator-1 exhibits weak myorelaxant activity .
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