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

General Information of DTT (ID: TT3OT40)

• DTT Name: Multidrug resistance protein 1 (ABCB1) DTT Info
• Gene Name: ABCB1

Molecule-Related Drug & Molecule List

2 Clinical Trial Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
EDP-322	DMWTVM1	Bacterial infection	1A00-1C4Z	Phase 1	[1]
W-198	DMJ2R69	Solid tumour/cancer	2A00-2F9Z	Phase 1	[2]

8 Discontinued Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
CBT-1	DM097UP	Non-small-cell lung cancer	2C25.Y	Discontinued in Phase 3	[3]
LY335979	DM2KITF	Acute myeloid leukaemia	2A60	Discontinued in Phase 3	[4]
Biricodar	DM65JCM	Ovarian cancer	2C73	Discontinued in Phase 2	[5]
S-9788	DMER3I9	Solid tumour/cancer	2A00-2F9Z	Discontinued in Phase 2	[6]
Tariquidar	DMJG7VP	Adrenocortical carcinoma	2D11.Z	Discontinued in Phase 2	[7]
Elacridar	DMURVE8	Solid tumour/cancer	2A00-2F9Z	Discontinued in Phase 1	[8]
ONT-093	DMB8T5U	Solid tumour/cancer	2A00-2F9Z	Discontinued in Phase 1	[9]
XR-9051	DMCK210	Solid tumour/cancer	2A00-2F9Z	Discontinued in Phase 1	[10]

8 Investigative Drug(s) Transported by This DTP

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
4,3'',5''-trimethoxy-[1,1':2',1'']-terphenyl	DMBN4G6	Discovery agent	N.A.	Investigative	[11]
6-(3,5-dimethoxy-phenyl)-naphthalen-2-ol	DMIXT2L	Discovery agent	N.A.	Investigative	[11]
TRISMETHOXYRESVERATROL	DM6USPC	Discovery agent	N.A.	Investigative	[11]
XR-9456	DMTUFI1	Discovery agent	N.A.	Investigative	[12]
XR-9504	DMIQP69	Discovery agent	N.A.	Investigative	[12]
XR-9544	DM1OZPN	Discovery agent	N.A.	Investigative	[12]
XR-9577	DMIZV6T	Discovery agent	N.A.	Investigative	[12]
[1,1':2',1'']-terphenyl-4,3'',5''-triol	DMVOY4D	Discovery agent	N.A.	Investigative	[11]

References

• [1] In vitro activities of the novel bicyclolides modithromycin (EDP-420, EP-013420, S-013420) and EDP-322 against MDR clinical Neisseria gonorrhoeae isolates and international reference strains. J Antimicrob Chemother. 2015 Jan;70(1):173-7.
• [2] Mechanisms of tetrandrine and 5-bromotetrandrine in reversing multidrug resistance may relate to down-regulation of multidrug resistance associated protein 7 expression. Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2012 Jun;20(3):558-63.
• [3] A pharmacodynamic study of the P-glycoprotein antagonist CBT-1 in combination with paclitaxel in solid tumors. Oncologist.2012;17(4):512.
• [4] A Phase I trial of a potent P-glycoprotein inhibitor, zosuquidar trihydrochloride (LY335979), administered intravenously in combination with doxoru... Clin Cancer Res. 2004 May 15;10(10):3265-72.
• [5] ClinicalTrials.gov (NCT00003847) VX-710, Doxorubicin, and Vincristine for the Treatment of Patients With Recurrent Small Cell Lung Cancer. U.S. National Institutes of Health.
• [6] In vitro activity of S 9788 on a multidrug-resistant leukemic cell line and on normal hematopoietic cells-reversal of multidrug resistance by sera from phase I-treated patients. Cancer Chemother Pharmacol. 1995;36(3):195-203.
• [7] Inhibition of P-glycoprotein (ABCB1)- and multidrug resistance-associated protein 1 (ABCC1)-mediated transport by the orally administered inhibitor, CBT-1((R)).Biochem Pharmacol.2008 Mar 15;75(6):1302-12.
• [8] 2-[(3-Methoxyphenylethyl)phenoxy]-based ABCB1 inhibitors: effect of different basic side-chains on their biological properties. J Med Chem. 2008 Dec 11;51(23):7602-13.
• [9] A phase I pharmacokinetic study of the P-glycoprotein inhibitor, ONT-093, in combination with paclitaxel in patients with advanced cancer. Invest New Drugs. 2005 Aug;23(4):311-5.
• [10] Communication between multiple drug binding sites on P-glycoprotein. Mol Pharmacol. 2000 Sep;58(3):624-32.
• [11] Identification of a terphenyl derivative that blocks the cell cycle in the G0-G1 phase and induces differentiation in leukemia cells. J Med Chem. 2006 May 18;49(10):3012-8.
• [12] Functional assay and structure-activity relationships of new third-generation P-glycoprotein inhibitors. Bioorg Med Chem. 2008 Mar 1;16(5):2448-62.