Details of the Drug-Related molecule(s) Interaction Atlas

General Information of DTT (ID: TT2UE56)

• DTT Name: Sodium/glucose cotransporter 1 (SGLT1) DTT Info
• Gene Name: SLC5A1

Molecule-Related Drug & Molecule List

1 Approved Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
Sotagliflozin	DMMLXA9	Heart failure	BD10-BD13	Approved	[1]

5 Clinical Trial Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
LIK-066	DM32NWD	Heart failure	BD10-BD13	Phase 2	[2]
YG1699	DM1NR1J	Type-1 diabetes	5A10	Phase 2	[3]
1614235 + 2330672	DMD751X	Type-2 diabetes	5A11	Phase 1	[2]
GSK1614235	DM7I1AQ	Type-2 diabetes	5A11	Phase 1	[4]
LX2761	DM8ZS7T	Type 2 diabetes	5A11	Phase 1	[5]

1 Discontinued Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
T-1095	DMGFS51	Diabetic complication	5A2Y	Discontinued in Phase 2	[6]

18 Investigative Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
10-methoxy-N(1)-methylburnamine-17-O-veratrate	DMJW25X	Discovery agent	N.A.	Investigative	[7]
Acerogenin A	DM4BWMO	Discovery agent	N.A.	Investigative	[8]
ACEROGENIN B	DMVQ30P	Discovery agent	N.A.	Investigative	[8]
Alstiphyllanine D	DM2FLDJ	Discovery agent	N.A.	Investigative	[7]
Alstiphyllanine E	DMTNQ5E	Discovery agent	N.A.	Investigative	[7]
Alstiphyllanine F	DMKRAEW	Discovery agent	N.A.	Investigative	[7]
Burnamine-17-O-3',4',5'-trimethoxybenzoate	DMBO0WI	Discovery agent	N.A.	Investigative	[7]
KURAIDIN	DMLDUJ1	Discovery agent	N.A.	Investigative	[9]
KURARINONE	DMH0G8W	Discovery agent	N.A.	Investigative	[9]
Kushenol N	DMY13UR	Discovery agent	N.A.	Investigative	[9]
O-spiroketal glucoside	DM3FS62	Discovery agent	N.A.	Investigative	[10]
Phlorizin	DMNARGO	Discovery agent	N.A.	Investigative	[11]
QCP	DM62PI8	Discovery agent	N.A.	Investigative	[12]
QCPac	DMSMQXZ	Discovery agent	N.A.	Investigative	[12]
QNEQCPQVSac	DMTY5HP	Discovery agent	N.A.	Investigative	[12]
QSPac	DMJHTUG	Discovery agent	N.A.	Investigative	[12]
sergliflozin	DMF8GAX	Discovery agent	N.A.	Investigative	[13]
Sophoraflavanone G	DMBTMN5	Discovery agent	N.A.	Investigative	[9]

References

• [1] LX4211, a dual SGLT1/SGLT2 inhibitor, improved glycemic control in patients with type 2 diabetes in a randomized, placebo-controlled trial. Clin Pharmacol Ther. 2012 Aug;92(2):158-69.
• [2] URL: http://www.guidetopharmacology.org Nucleic Acids Res. 2015 Oct 12. pii: gkv1037. The IUPHAR/BPS Guide to PHARMACOLOGY in 2016: towards curated quantitative interactions between 1300 protein targets and 6000 ligands. (Target id: 915).
• [3] ClinicalTrials.gov (NCT04956263) A Comparison of Postprandial Glucose After a Mixed Meal Tolerance Test, and the Metabolic Effects of Insulin Withdrawal in a Crossover Study of the Dual Systemic SGLT1 and SGLT2 Inhibitor YG1699, and the Selective SGLT2 Inhibitor Dapagliflozin in Subjects With Type 1 Diabetes. U.S.National Institutes of Health.
• [4] Clinical pipeline report, company report or official report of GlaxoSmithKline (2009).
• [5] Clinical pipeline report, company report or official report of Lexicon Pharmaceuticals.
• [6] T-1095, an inhibitor of renal Na+-glucose cotransporters, may provide a novel approach to treating diabetes. Diabetes. 1999 Sep;48(9):1794-800.
• [7] Alstiphyllanines E-H, picraline and ajmaline-type alkaloids from Alstonia macrophylla inhibiting sodium glucose cotransporter. Bioorg Med Chem. 2010 Mar 15;18(6):2152-2158.
• [8] Cyclic diarylheptanoids as Na+-glucose cotransporter (SGLT) inhibitors from Acer nikoense. Bioorg Med Chem Lett. 2010 Feb 1;20(3):1070-4.
• [9] Na+-glucose cotransporter (SGLT) inhibitory flavonoids from the roots of Sophora flavescens. Bioorg Med Chem. 2007 May 15;15(10):3445-9.
• [10] ortho-Substituted C-aryl glucosides as highly potent and selective renal sodium-dependent glucose co-transporter 2 (SGLT2) inhibitors. Bioorg Med Chem. 2010 Jun 15;18(12):4422-32.
• [11] J Biol Chem. 1988 Jan 5;263(1):187-92.High affinity phlorizin binding to the LLC-PK1 cells exhibits a sodium:phlorizin stoichiometry of 2:1.
• [12] Tripeptides of RS1 (RSC1A1) inhibit a monosaccharide-dependent exocytotic pathway of Na+-D-glucose cotransporter SGLT1 with high affinity. J Biol Chem. 2007 Sep 28;282(39):28501-13.
• [13] Sergliflozin, a novel selective inhibitor of low-affinity sodium glucose cotransporter (SGLT2), validates the critical role of SGLT2 in renal gluco... J Pharmacol Exp Ther. 2007 Jan;320(1):323-30.