SCHEMBL1048643

SCHEMBL1048643

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

nearest known ligand 0.44

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
LMNA P02545 6/20 0.44
SMN1; SMN2 Q16637 1/20 0.42
CYP2C19 P33261 1/20 0.40
HIF1A Q16665 1/20 0.40

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
SCHEMBL9189736 0.93 LMNA (0.41) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL9171058 0.88 LMNA (0.53) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL7607980 0.87 LMNA (0.47) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL5162293 0.87 LMNA (0.47) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL5033195 0.85 LMNA (0.45) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL16801766 0.84 LMNA (0.60) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL10318442 0.84 LMNA (0.44) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL619808 0.83 LMNA (0.60) LMNASMN1; SMN2CYP2C19HIF1A
SCHEMBL2763433 0.82 LMNA (0.38) LMNACYP2C19HIF1A
SCHEMBL9009288 0.82 LMNA (0.49) 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 22 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2022106715-A1 PROCEDURE FOR OBTAINING HIGH PURITY IOHEXOL JUSTESA IMAGEN S.A.U. (ES) 2022-05-27 WO claimed
CN-110590591-B Preparation method of iodixanol and iohexol impurities 浙江海洲制药有限公司 2022-05-17 CN claimed
US-20120184773-A1 REDUCTION OF FUSED BICYCLIC IMPURITIES IN TRIIODINATED X-RAY CONTRAST MEDIA MALLINCKRODT LLC (US) 2012-07-19 US claimed
US-5948940-A OXYALKYLATION OF5-ACETAMIDO-N,N-BIS(2,3-DIHYDROXYPROPYL)-2,4,6-TRIIODOPHTHAL IMIDE NYCOMED IMAGING AS (NO) 1999-09-07 US claimed
CN-116332787-B Preparation method of contrast agent intermediate acetyl iodide 安庆朗坤药业有限公司 2023-10-27 CN disclosed
CN-116332787-A Preparation method of contrast agent intermediate acetyl iodide 安庆朗坤药业有限公司 2023-06-27 CN disclosed
WO-2022106715-A1 PROCEDURE FOR OBTAINING HIGH PURITY IOHEXOL JUSTESA IMAGEN S.A.U. (ES) 2022-05-27 WO disclosed
CN-110590591-B Preparation method of iodixanol and iohexol impurities 浙江海洲制药有限公司 2022-05-17 CN disclosed
CN-110590591-B Preparation method of iodixanol and iohexol impurities 浙江海洲制药有限公司 2022-05-17 CN disclosed
EP-2935204-B1 PURIFICATION OF X-RAY CONTRAST AGENTS GE HEALTHCARE AS (NO) 2018-09-05 EP disclosed
US-9938233-B2 Purification of X-ray contrast agents GE HEALTHCARE AS (NO) 2018-04-10 US disclosed
US-20160304440-A1 PURIFICATION OF X-RAY CONTRAST AGENTS GE HEALTHCARE AS (NO) 2016-10-20 US disclosed
US-20110021823-A1 PROCESSING CRUDE IODIXANOL MIXTURE BY NANOFILTRATION GE HEALTHCARE AS (NO) 2011-01-27 US disclosed
US-20110021823-A1 PROCESSING CRUDE IODIXANOL MIXTURE BY NANOFILTRATION GE HEALTHCARE AS (NO) 2011-01-27 US disclosed
US-20110021828-A1 RECOVERING UNREACTED INTERMEDIATE FROM DESALINATED AND DESOLVENTIZED DIMERISATION REACTION MIXTURE BY ULTRAFILTRATION GE HEALTHCARE AS (NO) 2011-01-27 US disclosed
US-20110021828-A1 RECOVERING UNREACTED INTERMEDIATE FROM DESALINATED AND DESOLVENTIZED DIMERISATION REACTION MIXTURE BY ULTRAFILTRATION GE HEALTHCARE AS (NO) 2011-01-27 US disclosed
US-7754920-B1 Solvent reduction in crystallisation of intermediate for non-ionic X-ray contrast agents GE HEALTHCARE AS (NO) 2010-07-13 US disclosed
EP-0642492-B1 5,5'-/(1,3-PROPANEDIYL) BIS-/IMINO(2-OXO-2,1-ETHANEDIYL)ACETYLIMINO/BIS(2,4,6-TRIIODO-1,3-BENZENEDICARBOXYAMIDES), AND CONTRAST MEDIA CONTAINING THEM BRACCO SPA (IT) 1996-09-11 EP disclosed
EP-0642492-A1 5,5'-/(1,3-PROPANEDIYL) BIS-/IMINO(2-OXO-2,1-ETHANEDIYL)ACETYLIMINO/BIS(2,4,6-TRIIODO-1,3-BENZENEDICARBOXYAMIDES), AND CONTRAST MEDIA CONTAINING THEM. DIBRA SPA (IT) 1995-03-15 EP disclosed
US-5210300-A PURIFICATION OF CRUDE IOVERSOL USING CONTINUOUS DEIONIZATION MALINCKRODT MEDICAL, INC. (US) 1993-05-11 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 (4 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-20160304440-A1 PURIFICATION OF X-RAY CONTRAST AGENTS TMEM97, OGFR, TMEM120A LMNA 721/4885SMN1; SMN2 4009/4885CYP2C19 3870/4885
US-20110021823-A1 PROCESSING CRUDE IODIXANOL MIXTURE BY NANOFILTRATION ADH1A, ADH1C, NISCH LMNA 2242/4885SMN1; SMN2 4790/4885CYP2C19 3420/4885
US-20110021828-A1 RECOVERING UNREACTED INTERMEDIATE FROM DESALINATED AND DESOLVENTIZED DIMERISATION REACTION MIXTURE BY ULTRAFILTRATION REN, RCC2, AVPR2 LMNA 1966/4885SMN1; SMN2 4843/4885CYP2C19 3710/4885
US-20120184773-A1 REDUCTION OF FUSED BICYCLIC IMPURITIES IN TRIIODINATED X-RAY CONTRAST MEDIA GBA2, XRCC5, PAICS LMNA 866/4885SMN1; SMN2 4171/4885CYP2C19 1818/4885

“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.