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

General Information of Drug (ID: DMY26JI)

Drug Name

3,6,9,12,15,18-HEXAOXAICOSANE Drug Info

Synonyms

3,6,9,12,15,18-Hexaoxaicosane; 3,6,9,12,15,18-Hexaoxaeicosane; 23601-39-0; 1-ethoxy-2-[2-[2-[2-(2-ethoxyethoxy)ethoxy]ethoxy]ethoxy]ethane; EINECS 245-774-2; AC1L3JHX; SCHEMBL987828; DTXSID1041473; CHEBI:39576; CTK1A3907; DB06867

Indication

Disease Entry	ICD 11	Status	REF
Discovery agent	N.A.	Investigative	[1]

Cross-matching ID

PubChem CID: 90206
ChEBI ID: CHEBI:39576
CAS Number: CAS 23601-39-0
TTD Drug ID: DMY26JI

Molecule-Related Drug Atlas

Molecule Type:

DTT

Drug Status:

Clinical Trial Drug(s)

Investigative Drug(s)

Download the Complete Related Drug List

Drug(s) Targeting Rotamase Pin1 (PIN1)

Drug Name	Drug ID	Indication	ICD 11	Highest Status	REF
Avastin+/-Tarceva	DMA86FL	Non-small-cell lung cancer	2C25.Y	Phase 3	[2]
Beta-(2-Naphthyl)-Alanine	DMP21ZO	Discovery agent	N.A.	Investigative	[1]
(R,)-2-(2-naphthamido)-5-phenylpent-4-enoic acid	DMCW5A9	Discovery agent	N.A.	Investigative	[3]
(R)-2-(2-naphthamido)-3-p-tolylpropanoic acid	DMXGCYZ	Discovery agent	N.A.	Investigative	[3]
(R)-3-(2-naphthamido)-4-m-tolylbutanoic acid	DM5TH2W	Discovery agent	N.A.	Investigative	[3]
(R)-2-(2-naphthamido)-3-m-tolylpropanoic acid	DMVEMNA	Discovery agent	N.A.	Investigative	[3]
(R)-2-(2-naphthamido)-5-phenylpent-4-ynoic acid	DM9WL6O	Discovery agent	N.A.	Investigative	[3]
Ac-Phe-D-Thr(PO3H2)-Pip-Nal-Gln-NH2	DM6ONY7	Discovery agent	N.A.	Investigative	[4]
Ac-Phe-Thr(PO3H2)-Pip-Nal-Gln-NH2	DMSWTPX	Discovery agent	N.A.	Investigative	[4]
Ac-Bth-Thr(PO3H2)-Pip-Nal-Gln-NH2	DMSE29N	Discovery agent	N.A.	Investigative	[4]
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Molecular Interaction Atlas of This Drug

Molecular Interaction Atlas

Download the Complete Interaction Atlas for Visualization in Cytoscape

Drug Therapeutic Target (DTT)

DTT Name	DTT ID	UniProt ID	MOA	REF
Rotamase Pin1 (PIN1)	TTJNTSI	PIN1_HUMAN	Inhibitor	[1]

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References

1	The Protein Data Bank. Nucleic Acids Res. 2000 Jan 1;28(1):235-42.
2	Overexpression of PIN1 Enhances Cancer Growth and Aggressiveness with Cyclin D1 Induction in EBV-Associated Nasopharyngeal Carcinoma.PLoS One. 2016 Jun 3;11(6):e0156833.
3	Structure-based design of novel human Pin1 inhibitors (II). Bioorg Med Chem Lett. 2010 Apr 1;20(7):2210-4.
4	Nanomolar inhibitors of the peptidyl prolyl cis/trans isomerase Pin1 from combinatorial peptide libraries. J Med Chem. 2006 Apr 6;49(7):2147-50.