SCHEMBL343443

SCHEMBL343443

O=C(Cl)OCCOCc1ccccc1

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.69
TSHR P16473 1/20 0.50
LMNA P02545 3/20 0.47
SMN1; SMN2 Q16637 2/20 0.47
TDP1 Q9NUW8 2/20 0.47
KMT2A Q03164 2/20 0.47
MAPK1 P28482 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
SLC6A2 P23975 1/20 0.47
SLC6A3 Q01959 1/20 0.47
HTT P42858 1/20 0.46
NAAA Q02083 1/20 0.44
ESR1 P03372 1/20 0.44
ESR2 Q92731 1/20 0.44
HCAR2 Q8TDS4 1/20 0.43
MEN1 O00255 1/20 0.43
GAA P10253 1/20 0.43
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
CA2 P00918 1/20 0.42

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
SCHEMBL342830 0.98 ALDH1A1 (0.67) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL28934013 0.89 ALDH1A1 (0.65) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL9871595 0.88 ALDH1A1 (0.62) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL8506264 0.85 TSHR (0.54) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL3543227 0.83 LMNA (0.53) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL3543222 0.83 LMNA (0.53) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL8454471 0.83 ALDH1A1 (0.71) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL3845851 0.82 ALDH1A1 (0.64) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL4644782 0.82 ALDH1A1 (0.55) ALDH1A1TSHRLMNASMN1; SMN2TDP1
SCHEMBL960 0.82 ALDH1A1 (1.00) ALDH1A1TSHRLMNASMN1; SMN2TDP1

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 81 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4556480-A1 COMPOUNDS CONSTITUTING C20-MODIFIED SALINOMYCIN DERIVATIVES, A METHOD FOR OBTAINING THE SAME, A COMPOSITION CONTAINING THE SAME AND A USE OF SAID COMPOUNDS Fileclo Spolka Z Ograniczona Odpowiedzialnoscia (PL) 2025-05-21 EP disclosed
US-20240294541-A1 COMPOUNDS CONSTITUTING C20-MODIFIED SALINOMYCIN DERIVATIVES, A METHOD FOR OBTAINING THE SAME, A COMPOSITION CONTAINING THE SAME AND A USE OF SAID COMPOUNDS FILECLO SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA (PL) 2024-09-05 US disclosed
CN-118103377-A Compounds constituting C20 modified salinomycin derivatives, process for obtaining the compounds, compositions containing the compounds and uses of said compounds 菲莱克洛有限责任公司 2024-05-28 CN disclosed
CN-115677718-A Methylmethylamine derivative preparation, pharmaceutical composition and application thereof 武汉思瓴生物科技有限公司 2023-02-03 CN disclosed
CN-108779082-B Contrast agents 伯拉考成像股份公司 2022-08-02 CN disclosed
EP-3442949-B1 CONTRAST AGENTS BRACCO IMAGING SPA (IT) 2022-06-08 EP disclosed
EP-3442949-B1 CONTRAST AGENTS BRACCO IMAGING SPA (IT) 2022-06-08 EP disclosed
US-11007283-B2 Contrast agents BRACCO IMAGING S.P.A. (IT) 2021-05-18 US disclosed
US-11007283-B2 Contrast agents BRACCO IMAGING S.P.A. (IT) 2021-05-18 US disclosed
US-20190167819-A1 CONTRAST AGENTS BRACCO IMAGING S.P.A. (IT) 2019-06-06 US disclosed
US-5547950-A FOR TREATING DRUG RESISTANT STAPHYLOCOCCUS AND STREPTOCOCCUS INFECTIONS THE UPJOHN COMPANY (US) 1996-08-20 US disclosed
EP-0640077-A1 OXAZOLIDINONES CONTAINING A SUBSTITUTED DIAZINE MOIETY AND THEIR USE AS ANTIMICROBIALS PHARMACIA & UPJOHN COMPANY (US) 1995-03-01 EP disclosed
WO-1993023384-A1 OXAZOLIDINONES CONTAINING A SUBSTITUTED DIAZINE MOIETY AND THEIR USE AS ANTIMICROBIALS THE UPJOHN COMPANY (US) 1993-11-25 WO disclosed
US-4958024-A REACTION OF CARBAMATE SUBSTITUTED ACRYLIC ESTER, VASODILATORS, HYPOTENSIVE AGENTS BANYU PHARMACEUTICAL COMPANY, LTD. (JP) 1990-09-18 US disclosed
US-4914227-A FOR VASODILATING AND HYPOTENSIVE AGENTS BANYU PHARMACEUTICAL COMPANY, LTD. (JP) 1990-04-03 US disclosed
US-4739106-A VASODILATION, HYPOTENSIVE AGENTS BANYU PHARMACEUTICAL CO., LTD. (JP) 1988-04-19 US disclosed
EP-0101023-B1 PROCESS FOR PREPARING 2-CARBAMOYLOXYALKYL-1,4-DIHYDROPYRIDINE DERIVATIVES AND INTERMEDIATES USEFUL FOR THE PROCESS BANYU PHARMACEUTICAL CO., LTD. (JP) 1987-07-29 EP disclosed
EP-0101023-A1 Process for preparing 2-carbamoyloxyalkyl-1,4-dihydropyridine derivatives and intermediates useful for the process BANYU PHARMACEUTICAL CO., LTD. (JP) 1984-02-22 EP disclosed
US-4017503-A Antifungal 1-substituted benzimidazoles MERCK & CO., INC. (US) 1977-04-12 US disclosed
US-3998816-A 7-[5-N-(n-Butoxyethoxy carbonyl and 2-chloroethoxy carbonyl)-amino] cephalosporins C MEIJI SEIKA KAISHA, LTD. (JA) 1976-12-21 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 (3 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-11007283-B2 Contrast agents PHOSPHO1, ITPA, PPIP5K2 ALDH1A1 4787/4885TSHR 3208/4885LMNA 2726/4885
US-20190167819-A1 CONTRAST AGENTS PHOSPHO1, ITPA, PPIP5K2 ALDH1A1 4787/4885TSHR 3208/4885LMNA 2726/4885
US-20240294541-A1 COMPOUNDS CONSTITUTING C20-MODIFIED SALINOMYCIN DERIVATIVES, A METHOD FOR OBTAINING THE SAME, A COMPOSITION CONTAINING THE SAME AND A USE OF SAID COMPOUNDS MRPS22, MRPS27, DHPS ALDH1A1 2884/4885TSHR 4476/4885LMNA 927/4885

“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.