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ChemicalBook >> CAS DataBase List >>INX-315

INX-315

CAS No.
2745060-92-6
Chemical Name:
INX-315
Synonyms
INX-315
CBNumber:
CB113837881
Molecular Formula:
C19H21N7O3S
Molecular Weight:
427.48
MDL Number:
MOL File:
2745060-92-6.mol
Last updated:2025-04-18 09:51:36

INX-315 Properties

Density 1.712±0.14 g/cm3(Temp: 25 °C; Press: 760 Torr)(predicted)
pka 9.847±0.12(predicted)
form Solid
color White to off-white

INX-315 Chemical Properties,Uses,Production

Uses

INX-315 is an orally active and selective CDK2 inhibitor that induces cell cycle arrest in the G1 phase. INX-315 reduces CDK2 substrate phosphorylation and inhibits tumor growth in a dose-dependent manner in xenograft mouse models. INX-315 may be used in cancer research[1].

in vivo

INX-315 (100 mg/kg, p.o., twice daily for 56 days) effectively inhibits tumor growth in a gastric adenocarcinoma BALB/c nude mouse model[1]. INX-315 (100 mg/kg twice daily or 200 mg/kg once daily, i.p.) demonstrates significant tumor inhibition in the OVCAR3 ovarian cancer CDX model with good tolerance[2]. INX-315 (100 mg/kg twice daily, i.p.) demonstrates significant antitumor activity in the GA0103 gastric cancer PDX model with good tolerance[2].

Animal Model:OVCAR3 ovarian cancer CDX model constructed by injecting OVCAR3 ovarian cancer cell line into immunodeficient mice[2]
Dosage:100 or 200 mg/kg
Administration:Intraperitoneal injection (i.p.), 100 mg/kg twice daily or 200 mg/kg once daily for up to 42 days
Result:Resulted in tumor stasis (100 mg/kg twice daily), achieved 89% tumor growth inhibition (TGI), and did not cause significant weight loss (200 mg/kg once daily).
Animal Model:GA0103 gastric cancer PDX model constructed by injecting patient-derived GA0103 gastric cancer tumor into immunodeficient mice[2]
Dosage:100 mg/kg
Administration:Intraperitoneal injection (i.p.), twice daily for 56 days
Result:Resulted in tumor stasis and did not cause significant weight loss.
Animal Model:CCNE1-amplified gastric adenocarcinoma PDX (GA0103) in BALB/c nude mice model[1]
Dosage:25, 50 或 100 mg/kg
Administration:Oral gavage (p.o.), twice daily, for 56 days
Result:inhibited the growth of tumor in a dose-dependent manner, with 100 mg/kg group showing tumor regression.

References

[1] Dietrich C, et al. INX-315, a selective CDK2 inhibitor, induces cell cycle arrest and senescence in solid tumors. Cancer Discov. 2023 Dec 4. DOI:10.1158/2159-8290.CD-23-0954
[2] Trub A G, et al. INX-315, a potent and selective CDK2 inhibitor, demonstrates robust antitumor activity in CCNE1-amplified cancers[J]. Cancer Research, 2023, 83(7_Supplement): 5994-5994.

INX-315 Preparation Products And Raw materials

Raw materials

Preparation Products

INX-315 Suppliers

Global( 7)Suppliers
Supplier Tel Email Country ProdList Advantage
Suzhou youruike Chemical Pharmaceutical Technology Co., Ltd 15317229551 15151849396@163.com China 997 58
Changzhou Borl Biotechnology Co.,LTD 13606124132;13656121842 luyan0021@163.com China 219 58
Shanghai Tachizaki Biomedical Research Center 18014399201 sales@chemlab-tachizaki.com China 2672 58
Nantong QuanYi Biotechnology Co., Ltd 0513-66337626 18051384581 sales@chemhifuture.com China 5519 58
Jiangsu Aikon Biopharmaceutical R&D Co.,Ltd. 025-66061636 18013972705 qqyang@aikonchem.com China 10152 58
Selleck Chemicals 400-668-6834 info@selleck.cn China 12071 58
Suzhou Jinglige Technology Co., Ltd 18551175068 jinglige888@163.com China 232 58
INX-315 2745060-92-6