Iodide

Iodide

SCHEMBL4355027

C/C(=C\c1cccnc1)[C@H](CC[P+](c1ccccc1)(c1ccccc1)c1ccccc1)O[Si](c1ccccc1)(c1ccccc1)C(C)(C)C.[I-]

nearest known ligand 0.36

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
CYP11B2 P19099 2/20 0.36
CYP19A1 P11511 1/20 0.36
MAPT P10636 3/20 0.33
LMNA P02545 2/20 0.33
SMN1; SMN2 Q16637 1/20 0.33
RAB9A P51151 2/20 0.32
KDM4E B2RXH2 1/20 0.32
NPC1 O15118 1/20 0.32
POLB P06746 1/20 0.32
CYP11B1 P15538 1/20 0.32
ALDH1A1 P00352 3/20 0.31
TBXAS1 P24557 2/20 0.31
MAPK1 P28482 1/20 0.31
KMT2A Q03164 1/20 0.31
HSP90AA1 P07900 1/20 0.31
GAA P10253 1/20 0.31
HPGD P15428 1/20 0.31
HTT P42858 1/20 0.31
NPSR1 Q6W5P4 1/20 0.31
GPR55 Q9Y2T6 1/20 0.31

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 SCHEMBL4355025 1.00 CYP11B2 (0.36) CYP11B2CYP19A1MAPTLMNASMN1; SMN2
Iodide SCHEMBL4355036 1.00 CYP11B2 (0.36) CYP11B2CYP19A1MAPTLMNASMN1; SMN2
Iodide SCHEMBL4355033 1.00 CYP11B2 (0.36) CYP11B2CYP19A1MAPTLMNASMN1; SMN2
Iodide SCHEMBL4189831 0.89 CYP19A1 (0.32) CYP11B2CYP19A1HIF1A
Iodide SCHEMBL4189835 0.89 CYP19A1 (0.32) CYP11B2CYP19A1HIF1A
Iodide SCHEMBL4189826 0.89 CYP19A1 (0.32) CYP11B2CYP19A1HIF1A
Iodide SCHEMBL4189822 0.89 CYP19A1 (0.32) CYP11B2CYP19A1HIF1A
SCHEMBL4190495 0.88 CYP11B2 (0.39) CYP11B2CYP19A1MAPTLMNASMN1; SMN2
SCHEMBL4190490 0.88 CYP11B2 (0.39) CYP11B2CYP19A1MAPTLMNASMN1; SMN2
SCHEMBL4197077 0.87 CYP11B2 (0.38) CYP11B2CYP19A1MAPTLMNASMN1; SMN2

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
US-20090018342-A1 NEW EPOTHIOLONE DERIVATIVES, PROCESS FOR THEIR PRODUCTION, AND THEIR PHARMACEUTICAL USE KLAR ULRICH 2009-01-15 US disclosed
US-7407975-B2 Epothilone derivatives, method for producing same and their pharmaceutical use BAYER SCHERING PHARMA AG (DE) 2008-08-05 US disclosed
US-20030144523-A1 EPOTHILONE DERIVATIVES, METHOD FOR PRODUCING SAME AND THEIR PHARMACEUTICAL USE BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2003-07-31 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-20030144523-A1 EPOTHILONE DERIVATIVES, METHOD FOR PRODUCING SAME AND THEIR PHARMACEUTICAL USE TUBB1, TUBA1C, TUBB4A CYP11B2 67/4885CYP19A1 300/4885MAPT 285/4885
US-20090018342-A1 NEW EPOTHIOLONE DERIVATIVES, PROCESS FOR THEIR PRODUCTION, AND THEIR PHARMACEUTICAL USE TUBB4A, TUBA1B, TUBB CYP11B2 62/4885CYP19A1 89/4885MAPT 715/4885

“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.