Iodide

Iodide

SCHEMBL964663

COc1cc(N=C(N)SC)ccc1-c1cnnc(C)c1.I

nearest known ligand 0.39

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
HTR3E A5X5Y0 1/20 0.39
HTR3B O95264 1/20 0.39
HTR3A P46098 1/20 0.39
HTR3D Q70Z44 1/20 0.39
HTR3C Q8WXA8 1/20 0.39
NOS3 P29474 7/20 0.38
NOS1 P29475 7/20 0.38
NOS2 P35228 4/20 0.38
IMPDH2 P12268 5/20 0.36
PSEN1 P49768 2/20 0.35
PSEN2 P49810 2/20 0.35
APH1B Q8WW43 2/20 0.35
NCSTN Q92542 2/20 0.35
APH1A Q96BI3 2/20 0.35
PSENEN Q9NZ42 2/20 0.35
PDE10A Q9Y233 2/20 0.33
MKNK1 Q9BUB5 1/20 0.33
MKNK2 Q9HBH9 1/20 0.33
AAK1 Q2M2I8 1/20 0.32
POLQ O75417 1/20 0.32

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
SCHEMBL12918156 0.99 HTR3E (0.40) HTR3EHTR3BHTR3AHTR3DHTR3C
Iodide SCHEMBL3708570 0.86 HTR3E (0.40) HTR3EHTR3BHTR3AHTR3DHTR3C
Iodide SCHEMBL964573 0.77 AAK1 (0.45) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL12918153 0.76 AAK1 (0.46) HTR3EHTR3BHTR3AHTR3DHTR3C
Iodide SCHEMBL964547 0.76 IMPDH2 (0.43) HTR3EHTR3BHTR3AHTR3DHTR3C
SCHEMBL962710 0.75 PSEN1 (0.37) IMPDH2PSEN1PSEN2APH1BNCSTN
SCHEMBL12918145 0.74 IMPDH2 (0.44) HTR3EHTR3BHTR3AHTR3DHTR3C
Iodide SCHEMBL2539138 0.74 AAK1 (0.33) HTR3EHTR3BHTR3AHTR3DHTR3C
Iodide SCHEMBL964231 0.74 PSEN1 (0.42) IMPDH2PSEN1PSEN2APH1BNCSTN
SCHEMBL16398210 0.73 IMPDH2 (0.48) IMPDH2PSEN1PSEN2APH1BNCSTN

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2379553-B1 BICYCLIC COMPOUNDS FOR THE REDUCTION OF BETA-AMYLOID PRODUCTION BRISTOL MYERS SQUIBB CO (US) 2013-06-26 EP disclosed
US-8349880-B2 Bicyclic compounds for the reduction of beta-amyloid production BRISTOL-MYERS SQUIBB COMPANY (US) 2013-01-08 US disclosed
US-20110015175-A1 Bicyclic Compounds for the Reduction of Beta-Amyloid Production BRISTOL-MYERS SQUIBB COMPANY 2011-01-20 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20110015175-A1 Bicyclic Compounds for the Reduction of Beta-Amyloid Production APP, BACE1, APBA1 HTR3E 3947/4885HTR3B 2529/4885HTR3A 3099/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.