Iodide

Iodide

SCHEMBL8723547

C[n+]1cccc(C(=O)O[C@H]2CCC3C4CCc5cc(OC(=O)c6ccccc6)ccc5C4CC[C@@]32C)c1.[I-]

nearest known ligand 0.67

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHRM1CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNG

The experimentally established mechanism targets of Iodide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CHRM1 known ✓ P11229 2/20 0.51
KMT2A Q03164 6/20 0.67
LMNA P02545 6/20 0.67
SMN1; SMN2 Q16637 5/20 0.67
ESR1 P03372 5/20 0.67
ADORA3 P0DMS8 4/20 0.67
ATM Q13315 3/20 0.67
NR3C1 P04150 1/20 0.67
SHBG P04278 1/20 0.67
FYN P06241 1/20 0.67
ADRA2C P18825 1/20 0.67
SLC6A2 P23975 1/20 0.67
SLC6A4 P31645 1/20 0.67
HTR2B P41595 1/20 0.67
HTT P42858 1/20 0.67
MAPT P10636 6/20 0.61
CYP3A4 P08684 5/20 0.61
TP53 P04637 3/20 0.61
MEN1 O00255 4/20 0.58
THRB P10828 1/20 0.58

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Iodide SCHEMBL8723544 1.00 KMT2A (0.67) KMT2ALMNASMN1; SMN2ESR1ADORA3
Iodide SCHEMBL8727187 0.98 MAPT (0.63) KMT2ALMNASMN1; SMN2ESR1ADORA3
Iodide SCHEMBL9011178 0.98 MAPT (0.63) KMT2ALMNASMN1; SMN2ESR1ADORA3
SCHEMBL3300046 0.91 LMNA (0.80) KMT2ALMNASMN1; SMN2ESR1ADORA3
SCHEMBL3299315 0.86 MAPT (0.81) KMT2ALMNASMN1; SMN2ESR1ADORA3
SCHEMBL8155723 0.86 MAPT (0.81) KMT2ALMNASMN1; SMN2ESR1ADORA3
SCHEMBL3864661 0.85 KMT2A (0.68) KMT2ALMNASMN1; SMN2ESR1ADORA3
SCHEMBL3870740 0.85 KMT2A (0.68) KMT2ALMNASMN1; SMN2ESR1ADORA3
SCHEMBL3864673 0.85 SMN1; SMN2 (0.67) KMT2ALMNASMN1; SMN2ESR1ADORA3
SCHEMBL8722555 0.84 KMT2A (0.69) KMT2ALMNASMN1; SMN2ESR1ADORA3

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 7 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0335545-B2 Pharmaceutical formulations for parenteral use UNIV FLORIDA (US) 1998-09-23 EP disclosed
EP-0327766-B1 Redox systems for brain-targeted drug delivery UNIV FLORIDA (US) 1998-04-08 EP disclosed
US-5024998-A Administering in aqueous solution with cyclodextrin derivative UNIVERSITY OF FLORIDA (US) 1991-06-18 US disclosed
US-5017566-A Redox systems for brain-targeted drug delivery UNIVERSITY OF FLORIDA (US) 1991-05-21 US disclosed
US-5002935-A Inclusion Complexing Hydroxypropylcyclodextrin with a Dihydropyridine-substituted Drug UNIVERSITY OF FLORIDA (US) 1991-03-26 US disclosed
US-4983586-A Decreasing precipitation at injection site or in lungs or other organs by combining with hydroxypropyl-beta-cyclodextrin UNIVERSITY OF FLORIDA (US) 1991-01-08 US disclosed
EP-0327766-A2 Redox systems for brain-targeted drug delivery UNIVERSITY OF FLORIDA (US) 1989-08-16 EP disclosed