SCHEMBL1634878

SCHEMBL1634878

CCOC(=O)/C(=C\c1ccccc1)C(=O)C(C)C

nearest known ligand 0.79

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 7/20 0.79
KMT2A Q03164 7/20 0.79
NR1H4 Q96RI1 1/20 0.59
MAPT P10636 9/20 0.59
LMNA P02545 4/20 0.59
NPSR1 Q6W5P4 3/20 0.59
CYP1A2 P05177 1/20 0.59
CYP2C9 P11712 1/20 0.59
CYP2C19 P33261 1/20 0.59
S1PR4 O95977 1/20 0.59
S1PR1 P21453 1/20 0.59
MAPK1 P28482 1/20 0.59
ALDH1A1 P00352 3/20 0.52
KDM4E B2RXH2 2/20 0.52
HSP90AA1 P07900 2/20 0.52
HPGD P15428 1/20 0.52
POLB P06746 2/20 0.51
PLIN1 O60240 1/20 0.51
PLIN5 Q00G26 1/20 0.51
ABHD5 Q8WTS1 1/20 0.51

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
SCHEMBL1633388 1.00 MEN1 (0.79) MEN1KMT2ANR1H4MAPTLMNA
SCHEMBL935186 0.89 MEN1 (1.00) MEN1KMT2ANR1H4MAPTLMNA
Benzene SCHEMBL27988126 0.89 MEN1 (1.00) MEN1KMT2ANR1H4MAPTLMNA
SCHEMBL1682175 0.87 MEN1 (0.59) MEN1KMT2ANR1H4MAPTLMNA
SCHEMBL1682173 0.87 MEN1 (0.59) MEN1KMT2ANR1H4MAPTLMNA
Butane SCHEMBL6828046 0.85 MEN1 (0.93) MEN1KMT2ANR1H4MAPTLMNA
SCHEMBL4142686 0.85 NR1H4 (0.56) MEN1KMT2ANR1H4MAPTLMNA
SCHEMBL4142682 0.85 NR1H4 (0.56) MEN1KMT2ANR1H4MAPTLMNA
SCHEMBL3181515 0.85 MAPT (0.78) MEN1KMT2ANR1H4MAPTLMNA
SCHEMBL3181512 0.85 MAPT (0.78) MEN1KMT2ANR1H4MAPTLMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7932403-B2 Process for preparing pyrrole derivatives and intermediates RATIOPHARM GMBH (DE) 2011-04-26 US disclosed
US-20090012312-A1 Process for Preparing Pyrrole Derivatives and Intermediates RATIOPHARM GMBH (DE) 2009-01-08 US disclosed
WO-2007131528-A1 PROCESS FOR PREPARING C5 INTERMEDIATES AND THEIR USE IN THE PREPARATION OF N-SUBSTITUTED PYRROLE DERIVATIVES RATIOPHARM GMBH (DE) 2007-11-22 WO disclosed
EP-1705175-A1 Process for preparing C5 products and their use for Atorvastatin synthesis ratiopharm GmbH (DE) 2006-09-27 EP disclosed
WO-2006066823-A1 PROCESS FOR PREPARING PYRROLE DERIVATIVES AND INTERMEDIATES RATIOPHARM GMBH (DE) 2006-06-29 WO disclosed
EP-1671947-A1 Process for preparing pyrrole derivatives and intermediates Ratiopharm GmbH (DE) 2006-06-21 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 (1 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-20090012312-A1 Process for Preparing Pyrrole Derivatives and Intermediates DHCR7, DHPS, CYP46A1 MEN1 1533/4885KMT2A 3515/4885NR1H4 235/4885

“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.