SCHEMBL633303

SCHEMBL633303

O=C(NCC1CO1)OCc1ccccc1

nearest known ligand 0.55

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.55
SMN1; SMN2 Q16637 1/20 0.55
CYP1A2 P05177 1/20 0.54
HTT P42858 1/20 0.52
ALDH1A1 P00352 2/20 0.52
GAA P10253 1/20 0.52
TSHR P16473 1/20 0.50
CCKBR P32239 1/20 0.49
MEN1 O00255 1/20 0.49
KMT2A Q03164 1/20 0.49
L3MBTL1 Q9Y468 1/20 0.49
NPC1 O15118 1/20 0.49
RAB9A P51151 1/20 0.49

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
SCHEMBL6154117 1.00 LMNA (0.55) LMNASMN1; SMN2CYP1A2HTTALDH1A1
SCHEMBL633304 1.00 LMNA (0.55) LMNASMN1; SMN2CYP1A2HTTALDH1A1
SCHEMBL13897189 0.88 CYP1A2 (0.50) LMNASMN1; SMN2CYP1A2HTTALDH1A1
SCHEMBL5542852 0.85 SMN1; SMN2 (0.47) SMN1; SMN2CYP1A2ALDH1A1GAATSHR
SCHEMBL5546401 0.85 POLB (0.47) LMNASMN1; SMN2CYP1A2ALDH1A1CCKBR
SCHEMBL591373 0.85 LMNA (0.60) LMNASMN1; SMN2HTTALDH1A1GAA
SCHEMBL30772550 0.84 CYP1A2 (0.52) LMNASMN1; SMN2CYP1A2HTTALDH1A1
SCHEMBL31310017 0.84 LMNA (0.51) LMNASMN1; SMN2CYP1A2HTTALDH1A1
SCHEMBL11537938 0.84 CYP1A2 (0.48) LMNASMN1; SMN2CYP1A2HTTALDH1A1
SCHEMBL6154554 0.83 SMN1; SMN2 (0.47) LMNASMN1; SMN2CYP1A2HTTALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024200838-A1 NEW ODILORHABDINS ANALOGUES AS ANTIBIOTICS AGAINST MULTI-RESISTANT BACTERIA NOSOPHARM (FR) 2024-10-03 WO 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-20190167819-A1 CONTRAST AGENTS BRACCO IMAGING S.P.A. (IT) 2019-06-06 US disclosed
EP-2531221-B1 POLYANIONIC MULTIVALENT MACROMOLECULES FOR INTRACELLULAR TARGETING OF PROLIFERATION AND PROTEIN SYNTHESIS IC DISCOVERY GMBH (DE) 2019-03-13 EP disclosed
WO-2017178301-A1 CONTRAST AGENTS BRACCO IMAGING SPA (IT) 2017-10-19 WO disclosed
WO-2017098038-A1 CONTRAST AGENTS BRACCO IMAGING SPA (IT) 2017-06-15 WO disclosed
EP-2905283-B1 Oxazolidinone antibiotics ACTELION PHARMACEUTICALS LTD (CH) 2016-12-14 EP disclosed
US-9505750-B2 5-aminocyclylmethyl-oxazolidin-2-one derivatives ACTELION PHARMACEUTICALS LTD. (CH) 2016-11-29 US disclosed
EP-2144910-B1 OXAZOLIDINONE ANTIBIOTICS ACTELION PHARMACEUTICALS LTD (CH) 2015-10-28 EP disclosed
US-20070155728-A1 Substituted Heterocyclic Compounds PALLE VENKATA 2007-07-05 US disclosed
US-7205303-B2 Substituted heterocyclic compounds CV THERAPEUTICS, INC. (US) 2007-04-17 US disclosed
US-7205303-B2 Substituted heterocyclic compounds CV THERAPEUTICS, INC. (US) 2007-04-17 US disclosed
EP-1339701-B1 HETEROARYL ALKYL PIPERAZINE DERIVATIVES AS FATTY ACID OXIDATION INHIBITORS CV THERAPEUTICS INC (US) 2007-02-14 EP disclosed
US-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2006-05-04 US disclosed
US-20050215801-A1 Process for preparation of optically active 1-substituted amino-2,3-epoxypropanes, intermediates for synthesis thereof and process for preparation of the intermediates KANEKA CORPORATION (JP) 2005-09-29 US disclosed
EP-1555267-A1 2,3-DIHYDRO-6-NITROIMIDAZO 2,1-b OXAZOLES OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2005-07-20 EP disclosed
EP-1553093-A1 PROCESS FOR PREPARATION OF OPTICALLY ACTIVE 1-SUBSTITUTED AMINO-2,3-EPOXYPROPANES, INTERMEDIATES FOR THE SYNTHESIS THEREOF AND PROCESS FOR PREPARATION OF THE INTERMEDIATES KANEKA CORPORATION (JP) 2005-07-13 EP disclosed
EP-1071654-B1 A PROCESS FOR PREPARING CHIRAL (S)-2,3-DISUBSTITUTED-1-PROPYLAMINE DERIVATIVES SAMSUNG FINE CHEMICALS CO LTD (KR) 2003-10-22 EP disclosed
US-6417403-B1 AMINATION OF 3,4-DISUBSTITUTED-1-BUTANECARBONYL DERIVATIVE THROUGH CURTIUS OR HOFMAN REARRANGEMENT; SALT FORMATION, CARBAMYLATION SAMSUNG FINE CHEMICALS CO., LTD. (KR) 2002-07-09 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 (5 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-20060094767-A1 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles NR2C2, NR4A3, NR4A2 LMNA 4152/4885SMN1; SMN2 3985/4885CYP1A2 659/4885
US-11007283-B2 Contrast agents PHOSPHO1, ITPA, PPIP5K2 LMNA 2726/4885SMN1; SMN2 1789/4885CYP1A2 4864/4885
US-20190167819-A1 CONTRAST AGENTS PHOSPHO1, ITPA, PPIP5K2 LMNA 2726/4885SMN1; SMN2 1789/4885CYP1A2 4864/4885
US-20050215801-A1 Process for preparation of optically active 1-substituted amino-2,3-epoxypropanes, intermediates for synthesis thereof and process for preparation of the intermediates OXER1, RCC2, CBR3 LMNA 3686/4885SMN1; SMN2 4620/4885CYP1A2 62/4885
US-20070155728-A1 Substituted Heterocyclic Compounds KCNH1, SDHA, COQ8A LMNA 2300/4885SMN1; SMN2 2336/4885CYP1A2 782/4885

“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.