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ChemicalBook--->CAS DataBase List--->908112-37-8

908112-37-8

908112-37-8 Structure

908112-37-8 Structure
IdentificationBack Directory
[Name]

Benzamide, 2-[(trans-4-hydroxycyclohexyl)amino]-4-(4,5,6,7-tetrahydro-3,6,6-trimethyl-4-oxo-1H-indazol-1-yl)-
[CAS]

908112-37-8
[Synonyms]

AT-533
Benzamide, 2-[(trans-4-hydroxycyclohexyl)amino]-4-(4,5,6,7-tetrahydro-3,6,6-trimethyl-4-oxo-1H-indazol-1-yl)-
[Molecular Formula]

C23H30N4O3
[MOL File]

908112-37-8.mol
[Molecular Weight]

410.51
Chemical PropertiesBack Directory
[Melting point ]

133.8-136.1 °C
[Boiling point ]

631.0±55.0 °C(Predicted)
[density ]

1.36±0.1 g/cm3(Predicted)
[form ]

Solid
[pka]

15.09±0.40(Predicted)
[color ]

Off-white to light yellow
Hazard InformationBack Directory
[Uses]

AT-533 is a potent Hsp90 and HSV inhibitor. AT-533 suppresses tumor growth and angiogenesis by blocking the HIF-1α/VEGF/VEGFR-2 signaling pathway. AT-533 also inhibits the activation of the downstream pathways, including Akt/mTOR/p70S6K, Erk1/2 and FAK. AT-533 inhibits the tube formation, cell migration, and invasion of human umbilical vein endothelial cells (HUVECs)[1][2][3].
[in vivo]

AT-533 (10 mg/kg; i.p.; once daily for 21 d) suppresses the expression of the HIF-1α/VEGF signaling pathway-related proteins in MDA-MB-231 breast cancer xenografts tumor model in mouse[1].
AT-533 (1, 2 and 4 mg/kg; i.p.; once daily for 30 d) has no mortality, loss of appetite and body weight, adverse reactions in Sprague-Dawley rats in subacute toxicity test[3].

Animal Model:Male C57BL/6 mice with MDA-MB-231 breast cancer xenografts[1]
Dosage:10 mg/kg;
Administration:Intraperitoneal injection; once daily for 21 days
Result:Significantly downregulated HIF-1α and VEGF expression.
[IC 50]

HSP90; HSV-1; ERK1; ERK2; NF-κB; Akt; HIF-1α; VEGF/VEGFR-2
[References]

[1] Zhang PC, et al. AT-533, a novel Hsp90 inhibitor, inhibits breast cancer growth and HIF-1α/VEGF/VEGFR-2-mediated angiogenesis in vitro and in vivo. Biochem Pharmacol. 2020 Feb;172:113771. DOI:10.1016/j.bcp.2019.113771
[2] Li F, et al. AT-533, a Hsp90 inhibitor, attenuates HSV-1-induced inflammation. Biochem Pharmacol. 2019 Aug;166:82-92. DOI:10.1016/j.bcp.2019.05.003
[3] Wu Y, et al. Subacute toxicological evaluation of AT-533 and AT-533 gel in Sprague-Dawley rats. Exp Ther Med. 2021 Jun;21(6):632. DOI:10.3892/etm.2021.10064
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