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Janagliflozin

From Wikipedia, the free encyclopedia
Chemical compound
Pharmaceutical compound
Janagliflozin
Legal status
Legal status
  • Rx in China; investigational elsewhere
Identifiers
  • (2S,3R,4R,5S,6R)-2-[3-[[4-[[(1R,5S)-3-bicyclo[3.1.0]hexanyl]oxy]phenyl]methyl]-4-chlorophenyl]-6-(hydroxymethyl)oxane-3,4,5-triol
CAS Number
PubChemCID
DrugBank
UNII
Chemical and physical data
FormulaC25H29ClO6
Molar mass460.95 g·mol−1
3D model (JSmol)
  • C1[C@H]2[C@@H]1CC(C2)OC3=CC=C(C=C3)CC4=C(C=CC(=C4)[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)Cl
  • InChI=1S/C25H29ClO6/c26-20-6-3-14(25-24(30)23(29)22(28)21(12-27)32-25)8-17(20)7-13-1-4-18(5-2-13)31-19-10-15-9-16(15)11-19/h1-6,8,15-16,19,21-25,27-30H,7,9-12H2/t15-,16+,19?,21-,22-,23+,24-,25+/m1/s1
  • Key:WDBIPGHUEJEKTC-VWQPKTIXSA-N

Janagliflozin is anSGLT2 inhibitor developed bySihuan Pharmaceutical.[1][2][3][4][5][6] It is approved in China for the treatment oftype 2 diabetes.[7]

References

[edit]
  1. ^Song, Ling; Yao, Xueting; Liu, Yang; Zhong, Wen; Jiang, Ji; Liu, Hongzhong; Zhou, Huimin; Shi, Chongtie; Zong, Kaiqi; Wang, Chong; Ma, Chuanxiang; Liu, Dongyang; Hu, Pei (April 2020). "Translational prediction of first-in-human pharmacokinetics and pharmacodynamics of janagliflozin, a selective SGLT2 inhibitor, using allometric scaling, dedrick and PK/PD modeling methods".European Journal of Pharmaceutical Sciences.147: 105281.doi:10.1016/j.ejps.2020.105281.S2CID 212405270.
  2. ^Liu, Dongyang; Song, Ling; Wang, Xiaoxu; Liu, Xu; Cao, Fangrui; Liu, Hongzhong; Ding, Yanhua; Xiao, Xinhua; Jiang, Ji; Hu, Pei (1 June 2019). "154-LB: Accelerating Clinical Development of Janagliflozin, a Novel Antidiabetic Drug, Using Model-Informed Drug Development Strategy".Diabetes.68 (Supplement_1).doi:10.2337/db19-154-LB.S2CID 195440798.
  3. ^Zhao, Hengli; Wei, Yilin; He, Kun; Zhao, Xiaoyu; Mu, Hongli; Wen, Qing (December 2022). "Prediction of janagliflozin pharmacokinetics in type 2 diabetes mellitus patients with liver cirrhosis or renal impairment using a physiologically based pharmacokinetic model".European Journal of Pharmaceutical Sciences.179: 106298.doi:10.1016/j.ejps.2022.106298.PMID 36162752.S2CID 252505056.
  4. ^Zhao, Hengli; Zhao, Zhirui; He, Kun; Mi, Nianrong; Lou, Kai; Dong, Xiaolin; Zhang, Wenyu; Sun, Jingfang; Hu, Xinyu; Pang, Shuguang; Cheng, Hong; Wen, Qing (August 2023). "Pharmacokinetics, Pharmacodynamics and Safety of Janagliflozin in Chinese Type 2 Diabetes Mellitus Patients with Renal Impairment".Clinical Pharmacokinetics.62 (8):1093–1103.doi:10.1007/s40262-023-01256-0.PMID 37284974.S2CID 259097798.
  5. ^Gao, Leili; Cheng, Zhifeng; Su, Benli; Su, Xiuhai; Song, Weihong; Guo, Yushan; Liao, Lin; Chen, Xiaowen; Li, Jiarui; Tan, Xingrong; Xu, Fangjiang; Pang, Shuguang; Wang, Kun; Ye, Jun; Wang, Yuan; Chen, Lili; Sun, Jingfang; Ji, Linong (March 2023). "Efficacy and safety of janagliflozin as add‐on therapy to metformin in Chinese patients with type 2 diabetes inadequately controlled with metformin alone: A multicentre, randomized, double‐blind, placebo‐controlled, phase 3 trial".Diabetes, Obesity and Metabolism.25 (3):785–795.doi:10.1111/dom.14926.PMID 36433709.S2CID 253967474.
  6. ^Ji, Linong; Jiang, Xiaozhen; Hao, Qingshun; Cheng, Zhifeng; Wang, Kun; Pang, Shuguang; Liu, Meiying; Guo, Yushan; Chen, Xiaowen; Su, Xiuhai; Ning, Tao; Liu, Jie; Bian, Fang; Li, Yulan; Zhang, Zhinong; Song, Weihong; Sun, Jingfang (May 2023). "Efficacy and safety of janagliflozin monotherapy in Chinese patients with type 2 diabetes mellitus inadequately controlled on diet and exercise: A multicentre, randomized, double‐blind, placebo‐controlled, Phase 3 trial".Diabetes, Obesity and Metabolism.25 (5):1229–1240.doi:10.1111/dom.14971.PMID 36594724.S2CID 255474211.
  7. ^"NMPA approves China's second homegrown SGLT2 inhibitor janagliflozin".bioworld.com. January 23, 2024.
SGLT1Tooltip Sodium-glucose transporter 1
SGLT2Tooltip Sodium-glucose transporter 2
SGLT1Tooltip Sodium-glucose transporter 1 &SGLT2Tooltip Sodium-glucose transporter 2
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