142 Results for "

P388/ADM

" in MedChemExpress (MCE) Product Catalog:
Products (142)

142 Results for "P388/ADM" in MCE Product Catalog:

4
4 Cited Publications
Art. -Nr.: HY-N0876
CAS. Nr.: 464-74-4
Arenobufagin is a natural bufadienolide that can be extracted from toad venom. Arenobufagin can induce apoptosis and autophagy in human hepatocellular carcinoma cells through inhibition of PI3K/Akt/mTOR pathway. Arenobufagin has potent antineoplastic activity against HCC HepG2 cells as well as corresponding multidrug-resistant HepG2/ADM cells. Arenobufagin can inhibit VEGF-mediated angiogenesis through suppression of VEGFR-2 signaling pathway .
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3
3 Cited Publications
Art. -Nr.: HY-N3308
CAS. Nr.: 32383-76-9
Medicarpin is a flavonoid isolated from Medicago sativa. Medicarpin induces apoptosis and overcome multidrug resistance in leukemia P388 cells by modulating P-gp-mediated efflux of agents .
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3
3 Cited Publications
Art. -Nr.: HY-N0128
CAS. Nr.: 515-03-7
Sclareol is isolated from Salvia sclarea with anticarcinogenic activity. Sclareol shows strong cytotoxic activity against mouse leukemia (P-388), human epidermal carcinoma (KB) cells and human leukemia cell lines. Sclareol induces cell apoptosis .
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2
2 Cited Publications
Art. -Nr.: HY-14769
CAS. Nr.: 3432-99-3
Reinheit:  86.60%
Synonyms: 5,10-Methylenetetrafolate; ANX-510 free acid
Folitixorin (5,10-Methylenetetrafolate; ANX-510 free acid) is a reduced form of Folic acid (HY-16637) and a cofactor of thymidylate synthase . Folitixorin acts as an essential cofactor to promote the formation of a tight ternary complex between thymidylate synthase and FdUMP, thereby enhancing the inhibitory effect of FdUMP on thymidylate synthase. Folitixorin in combination with 5-fluorouracil and αVEGF reduces tumor volume in colorectal tumor models of nude mice. Folitixorin is used in related research on Yoshida sarcoma, P-388 leukemia, and colorectal cancer .
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1
1 Cited Publications
Art. -Nr.: HY-120504
CAS. Nr.: 1202-66-0
Reinheit:  98.90%
Target:  

Bacterial

Forschungsgebiete:  

Infection Cancer

N-Acetyltyramine is a quorum-sensing inhibitor (QSI) compound produced by V. alginolyticus M3-10. N-Acetyltyramine is capable of inhibiting the QS of C. violaceum ATCC 12472. N-acetyltyramine reverses resistance in Doxorubicin-resistant leukemia P388 cells .
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1
1 Cited Publications
Art. -Nr.: HY-P99177
CAS. Nr.: 2305638-98-4

Target:  

Inhibitory Antibodies

Forschungsgebiete:  

Cardiovascular Disease Infection

Enibarcimab is a humanized, non-neutralizing monoclonal antibody targeting adrenomedullin (ADM). Enibarcimab binds to the N-terminus of ADM, retains ADM in the circulation, and mobilizes interstitial ADM to increase the level of active bio-ADM, ultimately stabilizing blood vessels. Enibarcimab can be used in research related to septic shock and acute heart failure .
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1
1 Cited Publications
Art. -Nr.: HY-P74426
Reinheit:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ADM; Proadrenomedullin N-20 Terminal Peptide; Adrenomedullin; Preproadrenomedullin; AM; PAMP; Pro-Adrenomedullin
Species:  
Human
Source:  
HEK293
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Art. -Nr.: HY-18351
CAS. Nr.: 915303-09-2
Synonyms: LMP-400; NSC-724998
Target:  

Topoisomerase

Forschungsgebiete:  

Infection Cancer

Indotecan (LMP-400), an indenoisoquinoline derivative, is a potent Topoisomerase I inhibitor, with IC50s of 300, 1200, 560 nM for P388, HCT116, MCF-7 cell lines, respectively. Indotecan prevents the relaxation of supercoiled DNA and can be used for the research of visceral leishmaniasis .
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Art. -Nr.: HY-18351A
CAS. Nr.: 1228035-68-4
Synonyms: LMP-400 hydrochloride; NSC-724998 hydrochloride
Target:  

Topoisomerase

Forschungsgebiete:  

Infection Cancer

Indotecan hydrochloride, an indenoisoquinoline derivative, is a potent Topoisomerase I inhibitor, with IC50s of 300, 1200, 560 nM for P388, HCT116, MCF-7 cell lines, respectively. Indotecan hydrochloride prevents the relaxation of supercoiled DNA and can be used for the research of visceral leishmaniasis .
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Art. -Nr.: HY-P3116
CAS. Nr.: 173046-02-1
Target:  

Bacterial

Forschungsgebiete:  

Cancer

Thiocoraline is a depsipeptide that can be isolated by marine Micromonospora. Thiocoraline has antitumor activity with IC50s of 0.002, 0.002, 0.01 and 0.002 μg/mL in P388, A549, HT-29 and MEL-28 cells, respectively. Thiocoraline also a strong antimicrobial activity against Gram-positive microorganisms .
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Art. -Nr.: HY-108603
CAS. Nr.: 87745-28-6
Synonyms: (+)-Bryostatin 2
Target:  

PKC

Forschungsgebiete:  

Cancer

Bryostatin 2 ((+)-Bryostatin 2) is a 20-membered ring lactone that can be found in Bryozoan Eugufa neritina L. Bryostatin 2 has the potential for the research of P-388 lymphocytic leukemia .
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Art. -Nr.: HY-N6955
CAS. Nr.: 757202-08-7
Eupalinilide B is a guaiane type sesquiterpene lactone that can be found in Eupatorium lindleyanum. Eupalinilide B shows potent cytotoxicity against P-388 and A-549 tumor cell lines .
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Art. -Nr.: HY-124277
CAS. Nr.: 1644134-60-0
Target:  

TRP Channel

Forschungsgebiete:  

Neurological Disease

ADM 12 is a highly selective transient receptor potential ankyrin 1 (TRPA1) channel antagonist. ADM 12 blocks nitroglycerin (NTG)-induced trigeminal hyperalgesia in animal models, reducing expression of pain-related genes (c-Fos, TRPA1) and neuropeptides (CGRP, SP). ADM_12 is promising for research of migraine and neuropathic pain .
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Art. -Nr.: HY-N10208
CAS. Nr.: 1216840-17-3
Aspericin C is a pyran derivative found in the marine-derived fungus Rhizopus sp. 2-PDA-61. Aspericin C shows cytotoxic activities against P388, A549, HL-60, and BEL-7420 cell lines (IC50=14.6, 7.1, 61.4, and 24.2 μM, respectively) .
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Art. -Nr.: HY-12458
CAS. Nr.: 118292-36-7
Target:  

DNA/RNA Synthesis

Forschungsgebiete:  

Infection Cancer

Pyrindamycin A is an antibiotic that inhibits DNA synthesis. Pyrindamycin A shows antitumor activities against murine leukemia, exhibits stronger cytotoxic activities towards murine and human tumor cell lines and especially towards doxorubicin-resistant cells, inhibits P388 and P388/ADR cells with the same IC50 of 3.9 μg/ml .
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Art. -Nr.: HY-N1631
CAS. Nr.: 53600-24-1
Synonyms: 1-Hydroxyrutaecarpine
Target:  

Drug Derivative

Forschungsgebiete:  

Others

1-Hydroxyrutaecarpine (compound 1a) is a hydroxy-derivative of rutaecarpine. 1-Hydroxyrutaecarpine shows cytotoxicities with ED50s of 3.72, 7.44 µg/mL for P-388 and HT-29 cells, respectively. 1-Hydroxyrutaecarpine shows antiplatelet activity .
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Art. -Nr.: HY-125037
CAS. Nr.: 1190948-58-3
Diptoindonesin G is a 2-arylbenzofuran derivative and a modulator of estrogen receptor and HSP90 middle domain. Diptoindonesin G exhibits strong cytotoxicity against mouse leukemia P-388 cells with an IC50 of 13.2 μM. Diptoindonesin G has antitumor activity and can be used in the research of tumors such as breast cancer .
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Art. -Nr.: HY-23120
CAS. Nr.: 6345-29-5
Forschungsgebiete:  

Infection Cancer

1-Hydroxyguanidine sulfate is an antitumor agent that inhibits mast cell P815, leukaemia P388, leukaemia L1210 and carcinosarcoma Walker 256 cells growth. 1-Hydroxyguanidine sulfate also has antiviral activity .
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Art. -Nr.: HY-N1655
CAS. Nr.: 873999-88-3
2,3-Dihydroamentoflavone 7,4'-dimethyl ether is a biflavonoid, which can be isolated from the aerial parts of Selaginella delicatula. 2,3-Dihydroamentoflavone 7,4'-dimethyl ether exhibits cytotoxicities against P-388 and HT-29 cell lines, with ED50 (median effective dose) values of 3.50 and 5.25 µg/mL, respectively .
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Art. -Nr.: HY-121123
CAS. Nr.: 42381-05-5
Reinheit:  ≥97.0%
Synonyms: 2-Aminoadamantane-2-carboxylic acid
Target:  

Aminopeptidase

Forschungsgebiete:  

Cancer

Adamantanine (2-Aminoadamantane-2-carboxylic acid) inhibits the transport of methionine (Ki is 0.76 mM) and leucine into Ehrlich ascites carcinoma cells. Adamantanine inhibits proliferation of P388 lymphocytic leukemia cells with an IC50 of >1 mM. Adamantanine inhibits the leucine aminopeptidase with an I/S0.5 of 10.5 .
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