SCHEMBL8978151

SCHEMBL8978151

CC(=O)Nc1c(I)c(C(=O)NC(CO)CO)c(I)c(C(=O)NC(CO)CO)c1I

nearest known ligand 0.71

Predicted protein targets (top 7)

geneUniProtsupporting neighboursconfidence
LMNA P02545 6/20 0.71
SMN1; SMN2 Q16637 1/20 0.46
CYP2C19 P33261 1/20 0.35
HIF1A Q16665 1/20 0.35
MAP2K1 Q02750 1/20 0.30
PCNA P12004 1/20 0.30
TACR3 P29371 1/20 0.30

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
SCHEMBL8373498 0.95 LMNA (0.66) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL10875551 0.93 LMNA (0.63) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL619948 0.90 LMNA (0.60) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL8978033 0.89 LMNA (0.58) LMNASMN1; SMN2
SCHEMBL9189587 0.89 LMNA (0.61) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL17264622 0.86 LMNA (0.83) LMNASMN1; SMN2CYP2C19HIF1AMAP2K1
SCHEMBL15760478 0.84 LMNA (0.67) LMNASMN1; SMN2CYP2C19HIF1AMAP2K1
Iopamidol SCHEMBL471484 0.83 LMNA (1.00) LMNASMN1; SMN2CYP2C19HIF1A
Iopamidol SCHEMBL7101453 0.83 LMNA (1.00) LMNASMN1; SMN2CYP2C19HIF1A
Iopamidol SCHEMBL27781 0.83 LMNA (1.00) LMNASMN1; SMN2CYP2C19HIF1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3300499-B1 PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL IN THE PREPARATION OF NON-IONIC CONTRAST AGENTS HOVIONE SCIENTIA LTD (IE) 2023-10-04 EP disclosed
CN-116730858-A Method for preparing intermediate for preparing non-ionic contrast agent 好利安科技有限公司 2023-09-12 CN disclosed
US-11059021-B2 Process for the preparation of intermediates useful in the preparation of non-ionic contrast agents HOVIONE SCIENTIA LIMITED (IE) 2021-07-13 US disclosed
US-20180169607-A1 Process for the Preparation of Intermediates Useful in the Preparation of Non-ionic Contrast Agents HOVIONE SCIENTIA LIMITED (IE) 2018-06-21 US disclosed
EP-3300499-A1 PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL IN THE PREPARATION OF NON-IONIC CONTRAST AGENTS Hovione Scientia Limited (IE) 2018-04-04 EP disclosed
WO-2016193740-A1 PROCESS FOR THE PREPARATION OF INTERMEDIATES USEFUL IN THE PREPARATION OF NON-IONIC CONTRAST AGENTS HOVIONE SCIENTIA LIMITED (IE) 2016-12-08 WO disclosed
US-8835672-B2 Manufacture of a triiodinated contrast agent HOVIONE INTER LIMITED (CH) 2014-09-16 US disclosed
US-8835672-B2 Manufacture of a triiodinated contrast agent HOVIONE INTER LIMITED (CH) 2014-09-16 US disclosed
US-20140155648-A1 Manufacture of a Triiodinated Contrast Agent HOVIONE INTER LIMITED (CH) 2014-06-05 US disclosed
US-20140155648-A1 Manufacture of a Triiodinated Contrast Agent HOVIONE INTER LIMITED (CH) 2014-06-05 US disclosed
EP-0707572-A1 IODINATED OLIGOMERIC COMPOUNDS AND DIAGNOSTIC COMPOSITIONS CONTAINING THE SAME BRACCO S.p.A. (IT) 1996-04-24 EP disclosed
WO-1995001966-A1 IODINATED OLIGOMERIC COMPOUNDS AND DIAGNOSTIC COMPOSITIONS CONTAINING THE SAME BRACCO S.P.A. (IT) 1995-01-19 WO disclosed
US-5349085-A IODIXANOL; 1,3-bis(acetylamino)-N,N'-bis(3,5-bis(2,3dihydroxypropylaminocarbonyl)-2,4,6-triiodophenyl)-2-hydroxypropane NYCOMED IMAGING AS (NO) 1994-09-20 US disclosed
US-5204086-A 2,4,6-triiodoisophthalamide derivatives NYCOMED IMAGING AS (NO) 1993-04-20 US disclosed
EP-0108638-B1 X-RAY CONTRAST AGENTS NYEGAARD & CO. A/S (NO) 1986-07-16 EP disclosed
EP-0105752-B1 X-RAY CONTRAST AGENTS NYEGAARD & CO. A/S (NO) 1986-05-07 EP disclosed
EP-0108638-A1 X-ray contrast agents NYEGAARD & CO. A/S (NO) 1984-05-16 EP disclosed
EP-0105752-A1 X-ray contrast agents NYEGAARD & CO. A/S (NO) 1984-04-18 EP 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-11059021-B2 Process for the preparation of intermediates useful in the preparation of non-ionic contrast agents PPIP5K2, IPO4, ITPA LMNA 651/4885SMN1; SMN2 3123/4885CYP2C19 2333/4885
US-20140155648-A1 Manufacture of a Triiodinated Contrast Agent SAT1, LYPLA2, AGPAT5 LMNA 2871/4885SMN1; SMN2 4778/4885CYP2C19 2660/4885

“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.