51 Results for "

Structural analogue

" in MedChemExpress (MCE) Product Catalog:
Products (51)

51 Results for "Structural analogue" in MCE Product Catalog:

5
5 Cited Publications
Cat. No.: HY-15643A
CAS No.: 2070014-90-1
Purity:  98.87%
Research Areas:  

Cancer

LY 303511 hydrochloride is a structural analogue of LY294002. LY303511 does not inhibit PI3K. LY303511 enhances TRAIL sensitivity of SHEP-1 neuroblastoma cells. LY303511 reversibly blocks K + currents (IC50=64.6±9.1 μM) in MIN6 insulinoma cells.
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4
4 Cited Publications
Cat. No.: HY-153723
CAS No.: 2937344-16-4
Purity:  99.79%
Target:  

Ras

Research Areas:  

Cancer

BI-2493 is a structural analogue of BI-2865 and a highly selective and orally active pan-KRAS inhibitor. BI-2493 can attenuate tumor growth. BI-2493 can be used for cancer iseases research .
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2
2 Cited Publications
Cat. No.: HY-W015764
CAS No.: 55321-99-8
Target:  

Flavivirus

Research Areas:  

Infection

T-1105, a structural analogue of T-705, is a novel broad-spectrum viral polymerase inhibitor. T-1105 inhibits the polymerases of RNA viruses after being converted to ribonucleoside triphosphate (RTP) metabolite. T-1105 has antiviral activity against various RNA viruses. T-1105 can be formed by nicotinamide mononucleotide adenylyltransferase .
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1
1 Cited Publications
Cat. No.: HY-100197
CAS No.: 162758-94-3
Purity:  99.30%
Synonyms: N-Docosahexaenoyl ethanolamine (DHEA); Docosahexaenoyl ethanolamide
Target:  

Cannabinoid Receptor

Research Areas:  

Neurological Disease

Synaptamide (Dehydroepiandrosteron; DHEA) is an endogenous metabolite and structural analogue of Anandamide. Synaptamide binds to both the cannabinoid-1 and 2 (CB1 and CB2) cannabinoid receptors and has anti-inflammatory properties. Synaptamide is the first small-molecule endogenous ligand of an adhesion G protein-coupled receptor (aGPCR) .
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1
1 Cited Publications
Cat. No.: HY-150102
CAS No.: 2139288-26-7
Purity:  99.86%
Target:  

Androgen Receptor

Research Areas:  

Cancer

EPI-7170, a ralaniten analogue, is a potent androgen receptor N-terminal structural domain antagonist that blocks the transcriptional activity of full-length AR (FL-AR) and AR splice variants (AR-Vs). EPI-7170 has antitumor effects against enzalutamide resistant castration-resistant prostate cancer (CRPC) .
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1
1 Cited Publications
Cat. No.: HY-131583
CAS No.: 544-47-8
Purity:  99.50%
Synonyms: 4-Chlorobenzyl carbamimidothioate hydrochloride
Target:  

Bacterial

Research Areas:  

Infection

MP265 (4-Chlorobenzyl carbamimidothioate hydrochloride) is a structural analogue of A22 but is less toxic. MP265 is a MreB inhibitor .
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1
1 Cited Publications
Cat. No.: HY-120954
CAS No.: 519038-92-7
Target:  

Endogenous Metabolite

Research Areas:  

Cardiovascular Disease

14,15-EE-5(Z)-E is a structural analogue of 14, 15-epoxide dicartrienoic acid (14,15-EET). 14,15-EE-5(Z)-E antagonizes the relaxation of vascular smooth muscle induced by EET .
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1
1 Cited Publications
Cat. No.: HY-Y1373S1
CAS No.: 93131-16-9
Synonyms: Hexahydrobenzoic acid-d11
Cyclohexanecarboxylic acid-d11 is the deuterium labeled Cyclohexanecarboxylic acid . Cyclohexanecarboxylic acid is a Valproate structural analogue with anticonvulsant action .
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Cat. No.: HY-W007656
CAS No.: 294-90-6
Cyclen is a macrocyclic tetraamine chelating agent. Cyclen is the aza analogue of crown ether, used as a precursor for MRI contrast agents, and is an intermediate for the preparation of effective macrocyclic chelates. Cyclen is employed as a structural regulator through interfacial polymerization of polyethleneimine (PEI) and trimesoyl chloride (TMC) to develop polyamide NF membrane with efficient Li +/Mg 2+ separation performance. Cyclen has specific cavity structure and exhibits selective coordination properties for Li + ions [1][2].
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Cat. No.: HY-W011517
CAS No.: 146-78-1
Synonyms: 2FA
2-Fluoroadenosine (2FA) is a nucleoside analogue. 2-Fluoroadenosine has antiparasite activity with EC50 value of 0.842 mM for Cryptosporidium parvum. 2-Fluoroadenosine has a highly specific structural basis for MtADK. 2-Fluoroadenosine is commonly used in the study of parasitic conditions .
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Cat. No.: HY-131606B
Research Areas:  

Infection

Cidofovir diphosphate tri triethylamine is an active intracellular metabolite of Cidofovir. Cidofovir diphosphate tri triethylamine is a selective inhibitor of viral DNA polymerases with Ki values of 6.6, 0.86 and 1.4 μM for HCMV, HSV-1 and HSV-2 DNA polymerase, respectively .
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Cat. No.: HY-101445B
CAS No.: 53174-06-4
Purity:  99.36%
Target:  

Drug Isomer

Research Areas:  

Neurological Disease

(S)-Trolox is an analogue of vitamin E, in which the phytyl chain is replaced with a carboxyl group. (S)-Trolox is frequently used as a model compound for studies of structural features, as well as a standard for evaluation of antioxidant activity. (S)-Trolox has potent and specific neuroprotective and antioxidant effects .
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Cat. No.: HY-103503
CAS No.: 56189-68-5
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

CGP13501 is a positive allosteric modulator of GABAB receptor. CGP13501 is a structural analogue of propofol .
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Cat. No.: HY-Y1373
CAS No.: 98-89-5
Synonyms: Hexahydrobenzoic acid
Cyclohexanecarboxylic acid is a Valproate structural analogue. Cyclohexanecarboxylic acid is an essential intermediate for the aromatization of Shikimic acid (HY-N0130) by mammals. Cyclohexanecarboxylic acid has anticonvulsant action .
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Cat. No.: HY-106662
CAS No.: 97919-22-7
Purity:  99.06%
Synonyms: Chloroquinoxaline; NSC-339004
Research Areas:  

Infection Cancer

Chloroquinoxaline sulfonamide (Chloroquinoxaline), a structural analogue of sulfaquinoxaline, is a topoisomerase II alpha/beta poison. Chloroquinoxaline sulfonamide is used to control coccidiosis in poultry, rabbit, sheep, and cattle . Antitumor activity .
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Cat. No.: HY-P3615
CAS No.: 138716-98-0
Target:  

Endothelin Receptor

Research Areas:  

Cardiovascular Disease

[Asn18] Endothelin-1 swine, human is a structural analogue of Endothelin 1 (swine, human) (HY-P0202), with the Asp amino acid at position 18 mutated to Asn. Endothelin 1 (swine, human) is a synthetic peptide with human and porcine endothelin 1 sequences and is a potent endogenous vasoconstrictor .
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Cat. No.: HY-50848
CAS No.: 118675-50-6
Research Areas:  

Cardiovascular Disease

BW A868C, a hydantoin compound, is a BW245C structural analogue. BW A868C is a selective and potent competitive prostaglandin D2 (PGD2) antagonist. BW A868C has no effect on other prostaglandin receptors (IP, EP1, EP2, TP and FP) .
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Cat. No.: HY-125062
CAS No.: 60129-60-4
Purity:  99.87%
Synonyms: Glucosilsteviol
Target:  

GLUT

Research Areas:  

Metabolic Disease

Steviolmonoside (Glucosilsteviol) is a structural analogue of steviol. Steviolmonoside decreases glucose production and inhibits oxygen uptake in rat renal cortical tubules .
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Cat. No.: HY-P3221
CAS No.: 4294-11-5
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

[Leu3]-Oxytocin, an oxytocin analogue, is derived by structural variation in sequence position 3 replaced by leucine (Leu) .
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Cat. No.: HY-112140
CAS No.: 1639422-97-1
Purity:  98.98%
Research Areas:  

Cancer

JH-VIII-157-02 is a structural analogue of alectinib, acts as an ALK inhibitor, and shows an IC50 of 2 nM for echinoderm microtubule-associated protein-like 4-ALK (EML4-ALK) G1202R in cells.
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