Iodide

Iodide

SCHEMBL4930438

CSCC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccc2c(c1)CCCN(C(=O)[O-])C2.C[S+](C)CC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccc2c(c1)CCCN(C(=O)OC(C)(C)C)C2.C[S+](C)CC[C@H](NC(=O)OCc1ccccc1)C(=O)Nc1ccc2c(c1)CCCN(C(=O)OC(C)(C)C)C2.[I-]

nearest known ligand 0.42

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 19)

geneUniProtsupporting neighboursconfidence
CTSL P07711 1/20 0.42
CTSB P07858 1/20 0.42
CTSK P43235 1/20 0.42
MMP8 P22894 1/20 0.41
TMEM97 Q5BJF2 2/20 0.39
SIGMAR1 Q99720 2/20 0.39
P2RX7 Q99572 7/20 0.39
CA1 P00915 2/20 0.38
CA12 O43570 1/20 0.38
CA2 P00918 1/20 0.38
CA4 P22748 1/20 0.38
CA9 Q16790 1/20 0.38
KLK5 Q9Y337 1/20 0.37
KLK7 P49862 1/20 0.37
FNTA P49354 1/20 0.37
FNTB P49356 1/20 0.37
BACE1 P56817 2/20 0.36
NPC1 O15118 1/20 0.36
RAB9A P51151 1/20 0.36

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 SCHEMBL4639203 0.93 TMEM97 (0.44) CTSLCTSKMMP8TMEM97SIGMAR1
SCHEMBL4930098 0.92 CTSL (0.47) CTSLCTSBCTSKMMP8TMEM97
SCHEMBL4169157 0.88 CTSL (0.47) CTSLCTSBCTSKMMP8TMEM97
Iodide SCHEMBL4931537 0.83 TMEM97 (0.41) CTSLCTSBCTSKMMP8TMEM97
Iodide SCHEMBL4927029 0.80 P2RX7 (0.42) CTSLCTSBCTSKP2RX7BACE1
SCHEMBL4929374 0.80 CTSL (0.43) CTSLCTSBCTSKP2RX7CA1
SCHEMBL3007646 0.79 KDM1A (0.49) MMP8P2RX7
SCHEMBL3007640 0.79 KDM1A (0.49) MMP8P2RX7
SCHEMBL17797697 0.78 TMEM97 (0.55) TMEM97SIGMAR1NPC1RAB9A
SCHEMBL17797552 0.75 TMEM97 (0.55) TMEM97SIGMAR1NPC1RAB9A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20080306045-A1 1-Benzazepine-3-Sulfonylamino-2-Pyrroridones as Factor Xa Inhibitors CAMUS LAURE 2008-12-11 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-20080306045-A1 1-Benzazepine-3-Sulfonylamino-2-Pyrroridones as Factor Xa Inhibitors TFPI, TPSAB1, TFPI2 CTSL 522/4885CTSB 819/4885CTSK 406/4885

“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.