SCHEMBL8267288

SCHEMBL8267288

O=C(O)COCCN1CCOCC1

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GLA P06280 1/20 0.56
HSD17B10 Q99714 1/20 0.50
KDM4E B2RXH2 2/20 0.49
ALDH1A1 P00352 4/20 0.47
POLB P06746 2/20 0.46
L3MBTL1 Q9Y468 2/20 0.46
MEN1 O00255 1/20 0.46
KMT2A Q03164 1/20 0.46
ATM Q13315 1/20 0.45
TDP1 Q9NUW8 1/20 0.44
HRH1 P35367 2/20 0.44
SLC6A2 P23975 1/20 0.44
HRH2 P25021 1/20 0.44
HTR2A P28223 1/20 0.44
SLC6A4 P31645 1/20 0.44
DRD3 P35462 1/20 0.44
HTR2B P41595 1/20 0.44
SLC6A3 Q01959 1/20 0.44
TEK Q02763 1/20 0.44
KCNH2 Q12809 1/20 0.44

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
Hydrochloric Acid SCHEMBL9794692 0.98 GLA (0.59) GLAHSD17B10KDM4EALDH1A1POLB
SCHEMBL4710666 0.84 KDM4E (0.53) GLAKDM4EALDH1A1POLBL3MBTL1
SCHEMBL526447 0.82 GLA (0.62) GLAHSD17B10KDM4EALDH1A1POLB
SCHEMBL6786534 0.81 SMN1; SMN2 (0.57) KDM4EALDH1A1POLBL3MBTL1MEN1
SCHEMBL12120192 0.81 TDP1 (0.51) GLAKDM4EALDH1A1MEN1KMT2A
SCHEMBL111438 0.80 TSHR (0.58) GLAKDM4EALDH1A1HTR2AHTR2B
SCHEMBL7608229 0.79 GLA (0.48) GLAALDH1A1POLBMEN1KMT2A
SCHEMBL6691875 0.79 TDP1 (0.45) KDM4EALDH1A1L3MBTL1TDP1HTR2A
SCHEMBL3830838 0.79 GLA (0.49) GLAHSD17B10KDM4EALDH1A1POLB
SCHEMBL11281615 0.78 KDM4E (0.50) GLAKDM4EALDH1A1POLBL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210179663-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PROTEOLIX, INC. 2021-06-17 US disclosed
US-20200325172-A1 Compounds for proteasome enzyme inhibition PROTEOLIX, INC. 2020-10-15 US disclosed
US-20190211058-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PROTEOLIX, INC. 2019-07-11 US disclosed
US-20180170962-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION ONYX THERAPEUTICS INC (US) 2018-06-21 US disclosed
US-20180170962-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION ONYX THERAPEUTICS INC (US) 2018-06-21 US disclosed
US-20170075218-A1 RESIST COMPOSITION AND PATTERNING PROCESS SHIN-ETSU CHEMICAL CO., LTD. (JP) 2017-03-16 US disclosed
US-20170075218-A1 RESIST COMPOSITION AND PATTERNING PROCESS SHIN-ETSU CHEMICAL CO., LTD. (JP) 2017-03-16 US disclosed
US-20160222057-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION ONYX THERAPEUTICS INC (US) 2016-08-04 US disclosed
US-20160222057-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION ONYX THERAPEUTICS INC (US) 2016-08-04 US disclosed
EP-2270026-B1 Compounds for proteasome enzyme inhibition ONYX THERAPEUTICS INC (US) 2016-05-18 EP disclosed
EP-2270026-A2 Compounds for proteasome enzyme inhibition Onyx Therapeutics, Inc. (US) 2011-01-05 EP disclosed
EP-2266999-A2 Compounds for proteasome enzym inhibition Onyx Therapeutics, Inc. (US) 2010-12-29 EP disclosed
US-20090131421-A1 Compounds for proteasome enzyme inhibition ONYX THERAPEUTICS, INC. 2009-05-21 US disclosed
US-20090131421-A1 Compounds for proteasome enzyme inhibition ONYX THERAPEUTICS, INC. 2009-05-21 US disclosed
US-7417042-B2 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2008-08-26 US disclosed
US-7417042-B2 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2008-08-26 US disclosed
WO-2006017842-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PROTEOLIX, INC. (US) 2006-02-16 WO disclosed
US-20060030533-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2006-02-09 US disclosed
US-20060030533-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents PROTEOLIX, INC. (US) 2006-02-09 US disclosed
CN-1039248-A The preparation method of new bisphosphate derivative BOEHRINGER MANNHEIM GMBH (DE) 1990-01-31 CN 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 (7 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-20160222057-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PSMB1, PSMB9, PSMB3 GLA 2224/4885HSD17B10 3931/4885KDM4E 2768/4885
US-20180170962-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PSMB1, PSMB9, PSMB3 GLA 2224/4885HSD17B10 3931/4885KDM4E 2768/4885
US-20200325172-A1 Compounds for proteasome enzyme inhibition PSMB1, PSMB9, PSMB3 GLA 2224/4885HSD17B10 3931/4885KDM4E 2768/4885
US-20190211058-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PSMB1, PSMB9, PSMB3 GLA 2224/4885HSD17B10 3931/4885KDM4E 2768/4885
US-20090131421-A1 Compounds for proteasome enzyme inhibition PSMB1, PSMB9, PSMB3 GLA 2224/4885HSD17B10 3931/4885KDM4E 2768/4885
US-20210179663-A1 COMPOUNDS FOR PROTEASOME ENZYME INHIBITION PSMB1, PSMB9, PSMB3 GLA 2224/4885HSD17B10 3931/4885KDM4E 2768/4885
US-20060030533-A1 Peptide-based compounds include at least three peptide units, an epoxide or aziridine, and functionalization at the N-terminus inhibit specific activities of N-terminal nucleophile (Ntn) hydrolases, e.g., the chymotrypsin-like activity of the 20S proteasome; antiproliferative and antiinflammatory agents ANPEP, DNPEP, CPN1 GLA 2091/4885HSD17B10 4280/4885KDM4E 3260/4885

“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.