NEU-1953
NEU-1953 is a parasite inhibitor. NEU-1953 inhibits Abl, EGFR, and KDR tyrosine kinases. NEU-1953 inhibits Aurora A, MNK2, and MAP4K4 serine/threonine kinases. NEU-1953 can be used for research on malaria, human African trypanosomiasis, schistosomiasis, Chagas disease, and leishmaniasis.
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- CAS No.: 2218480-85-2
- 화학식: C22H22N8
- 분자량:398.47
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보관:
Please store the product under the recommended conditions in the Certificate of Analysis.
All EGFR Isoforms
MoreAll VEGFR Isoforms
MoreAll Aurora Kinase Isoforms
MoreAll MAP4K Isoforms
MoreAll Parasite Isoforms
More
Biological Activity
제품 설명
IC50 & Target
[1]|
Abl |
EGFR |
KDR |
Aurora A |
MNK2 |
MAP4K4 |
In Vitro
NEU-1953 (compound 40) is a potent inhibitor of P. falciparum D6 (EC50: 0.026 μM) with low toxicity against HepG2 cells (TC50: >4 μM)[1].
NEU-1953 (compound 1) (50 μM; 48 h) exhibits moderate anti-trypanosome potency against T. b. brucei strain 427 with an EC50 of 0.43 μM[2].
NEU-1953 (5 μM) significantly inhibits seven human kinases (Aurora A, MNK2, MAP4K4, EGFR, Abl, and KDR) at 5 μM[1].
NEU-1953 (compound 3) has 87.0% human plasma protein binding[3].
NEU-1953 has an intrinsic clearance of 180 μL/min/mg protein in human liver microsomes[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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CAS No. 2218480-85-2
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분자량 398.47
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화학식 C22H22N8
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SMILES
N=1C=CN=C(C1)NC=2C=CN=C3C=C(C=CC32)C=4C=NC(=NC4)N5CCN(C)CC5
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선적
Room temperature in continental US; may vary elsewhere.
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보관
Please store the product under the recommended conditions in the Certificate of Analysis.
순도&문서
References
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)