SCHEMBL4385122

SCHEMBL4385122

OC[C@@H]1CCCN1C1CCC1

nearest known ligand 0.47

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
POLB P06746 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
LMNA P02545 2/20 0.37
MEN1 O00255 2/20 0.33
KMT2A Q03164 2/20 0.33
ALDH1A1 P00352 1/20 0.33
TDP1 Q9NUW8 1/20 0.32
SIGMAR1 Q99720 2/20 0.32
SPHK2 Q9NRA0 5/20 0.31
SPHK1 Q9NYA1 5/20 0.31
HRH3 Q9Y5N1 1/20 0.31

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
SCHEMBL20144886 1.00 POLB (0.47) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL20144697 0.95 L3MBTL1 (0.47) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL20144698 0.95 L3MBTL1 (0.47) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL20095597 0.93 POLB (0.45) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL22220339 0.93 POLB (0.48) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL19172490 0.93 POLB (0.48) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL31282369 0.91 POLB (0.42) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL30706645 0.91 POLB (0.42) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL2266863 0.91 POLB (0.42) POLBL3MBTL1LMNAMEN1KMT2A
SCHEMBL20144884 0.91 L3MBTL1 (0.42) POLBL3MBTL1LMNAMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11548888-B2 KRas G12C inhibitors Mirati Therapeutics, Inc. (US) 2023-01-10 US disclosed
US-11548888-B2 KRas G12C inhibitors Mirati Therapeutics, Inc. (US) 2023-01-10 US disclosed
US-20200331911-A1 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. 2020-10-22 US disclosed
US-20200331911-A1 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. 2020-10-22 US disclosed
WO-2020146613-A1 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. (US) 2020-07-16 WO disclosed
US-20120108748-A1 SOLID PHASE PEPTIDE SYNTHESIS OF PEPTIDE ALCOHOLS CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (FR) 2012-05-03 US disclosed
WO-2011000848-A1 SOLID PHASE PEPTIDE SYNTHESIS OF PEPTIDE ALCOHOLS CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS) (FR) 2011-01-06 WO disclosed
EP-2270025-A1 Solid phase peptide synthesis of peptide alcohols Centre National pour la Recherche Scientifique (CNRS) (FR) 2011-01-05 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 (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-20120108748-A1 SOLID PHASE PEPTIDE SYNTHESIS OF PEPTIDE ALCOHOLS VIP, ERG28, PSAP POLB 866/4885L3MBTL1 970/4885LMNA 3745/4885
US-11548888-B2 KRas G12C inhibitors KRAS, NRAS, HRAS POLB 1699/4885L3MBTL1 2112/4885LMNA 2991/4885
US-20200331911-A1 KRAS G12C INHIBITORS KRAS, NRAS, HRAS POLB 1699/4885L3MBTL1 2112/4885LMNA 2991/4885

“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.