Iodide

Iodide

SCHEMBL1361736

I.O=S(=O)(O)Oc1ccccc1.O=S(=O)(O)Oc1ccccc1.O=S(=O)(O)Oc1ccccc1

nearest known ligand 0.56

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
CA1 P00915 5/20 0.56
CA2 P00918 5/20 0.56
CA9 Q16790 5/20 0.56
KMT2A Q03164 2/20 0.48
MEN1 O00255 1/20 0.48
LMNA P02545 1/20 0.45
PPARG P37231 1/20 0.45
NFE2L2 Q16236 1/20 0.45
TDP1 Q9NUW8 1/20 0.45
TSHR P16473 2/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
GLA P06280 1/20 0.43
GAA P10253 1/20 0.43
STS P08842 2/20 0.42
SLC22A6 Q4U2R8 1/20 0.41
MAPT P10636 1/20 0.41
CISD1 Q9NZ45 1/20 0.40
CA12 O43570 2/20 0.40
SRC P12931 1/20 0.39
LTA4H P09960 1/20 0.39

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
SCHEMBL138895 0.97 CA2 (0.58) CA1CA2CA9KMT2AMEN1
SCHEMBL17456405 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1
SCHEMBL8058040 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1
SCHEMBL10359279 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1
SCHEMBL28760627 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1
Ammonia Solution, Strong SCHEMBL1115426 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1
SCHEMBL944250 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1
Water SCHEMBL2134977 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1
SCHEMBL17456525 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1
SCHEMBL11427595 0.95 CA1 (0.56) CA1CA2CA9KMT2AMEN1

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
US-8067462-B2 Processes of making sesquiterpenoid tashironin, its analogs and their uses THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF NEW YORK (US) 2011-11-29 US disclosed
US-20090105332-A1 PROCESSES OF MAKING SESQUITERPENOID TASHIRONIN, ITS ANALOGS AND THEIR USES THE TRUSTEES OF COLUMBIA UNIVERSITY IN THE CITY OF (US) 2009-04-23 US disclosed
US-7186854-B2 Process for making bicalutamide and intermediates thereof SYNTHON IP INC. (US) 2007-03-06 US disclosed
EP-1546093-A1 PROCESS FOR MAKING BICALUTAMIDE AND INTERMEDIATES THEREOF Synthon B.V. (NL) 2005-06-29 EP disclosed
US-6818766-B2 USING P-FLUOROBENZENESULFINIC ACID SYNTHON BV (NL) 2004-11-16 US disclosed
WO-2004031136-A1 PROCESS FOR MAKING BICALUTAMIDE AND INTERMEDIATES THEREOF SYNTHON B.V. (NL) 2004-04-15 WO disclosed
US-20030073742-A1 Process for making bicalutamide and intermediates thereof SYNTHON B.V. (NL) 2003-04-17 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 (2 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-20030073742-A1 Process for making bicalutamide and intermediates thereof BLVRB, BRDT, OTUB1 CA1 251/4885CA2 757/4885CA9 94/4885
US-20090105332-A1 PROCESSES OF MAKING SESQUITERPENOID TASHIRONIN, ITS ANALOGS AND THEIR USES OXER1, OXSR1, BRS3 CA1 1059/4885CA2 1277/4885CA9 849/4885

“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.