Iodide

Iodide

SCHEMBL5014654

CO[Si](CCC[n+]1ccc(-c2cc[n+](CCC[Si](OC)(OC)OC)cc2)cc1)(OC)OC.[I-].[I-]

nearest known ligand 0.50

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
ACHE known ✓ P22303 11/20 0.35
HTT P42858 2/20 0.50
KDM4E B2RXH2 1/20 0.50
NPC1 O15118 1/20 0.50
LMNA P02545 1/20 0.50
RAB9A P51151 1/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
MEN1 O00255 1/20 0.47
TP53 P04637 1/20 0.47
CYP1A2 P05177 1/20 0.47
CYP2D6 P10635 1/20 0.47
MAPT P10636 1/20 0.47
CYP2C9 P11712 1/20 0.47
CYP2C19 P33261 1/20 0.47
KMT2A Q03164 1/20 0.47
BCHE P06276 11/20 0.35
CHRNA7 P36544 2/20 0.35
CHRNA10 Q9GZZ6 2/20 0.35
CHRNA9 Q9UGM1 2/20 0.35
CHKA P35790 2/20 0.33

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
SCHEMBL1316266 0.98 MEN1 (0.48) HTTKDM4ENPC1LMNARAB9A
Bromide SCHEMBL8598361 0.96 MEN1 (0.47) HTTKDM4ENPC1LMNARAB9A
SCHEMBL1316129 0.90 PABPC1 (0.43) HTTKDM4ENPC1LMNARAB9A
Bromide SCHEMBL8622785 0.87 PABPC1 (0.41) HTTKDM4ENPC1LMNARAB9A
Hydrochloric Acid SCHEMBL9618165 0.80 CHKA (0.42) HTTKDM4ENPC1LMNARAB9A
SCHEMBL10332332 0.80 BCHE (0.50) BCHEACHE
Hydrochloric Acid SCHEMBL8959775 0.79 CHKA (0.58) HTTNPC1LMNARAB9ASMN1; SMN2
Hydrochloric Acid SCHEMBL1973961 0.78 MEN1 (0.48) SMN1; SMN2MEN1MAPTKMT2ABCHE
SCHEMBL14364681 0.74 SMN1; SMN2 (0.50) KDM4ENPC1LMNARAB9ASMN1; SMN2
Bromide SCHEMBL7743409 0.74 MEN1 (0.41) HTTKDM4ENPC1LMNARAB9A

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 2 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8247680-B2 Light energy conversion material KABUSHIKI KAISHA TOYOTA CHUO KENKYUSHO (JP) 2012-08-21 US disclosed
US-20080057420-A1 Silica porous material including an electron donor in skeleton; and an electron acceptor; efficiency, durability KABUSHIKI KAISHA TOYOTA CHUO KENKYUSHO (JP) 2008-03-06 US disclosed