SCHEMBL6139928

SCHEMBL6139928

CCOC(=O)C(F)=Cc1csc(C)n1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
BACE1 P56817 1/20 0.39
MAPT P10636 5/20 0.39
SMN1; SMN2 Q16637 3/20 0.39
KMT2A Q03164 8/20 0.37
MEN1 O00255 7/20 0.37
LMNA P02545 2/20 0.37
NPSR1 Q6W5P4 2/20 0.37
CYP1A2 P05177 2/20 0.37
CYP2C19 P33261 2/20 0.37
CYP2C9 P11712 1/20 0.37
ALDH1A1 P00352 2/20 0.36
NPC1 O15118 2/20 0.36
RAB9A P51151 2/20 0.36
PKM P14618 2/20 0.35
GAA P10253 1/20 0.35
HDAC1 Q13547 1/20 0.34
HDAC2 Q92769 1/20 0.34
S1PR4 O95977 1/20 0.34
S1PR1 P21453 1/20 0.34
MAPK1 P28482 1/20 0.34

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
SCHEMBL5225981 1.00 BACE1 (0.39) BACE1MAPTSMN1; SMN2KMT2AMEN1
SCHEMBL5229354 1.00 BACE1 (0.39) BACE1MAPTSMN1; SMN2KMT2AMEN1
SCHEMBL23180607 0.84 HPGD (0.41) MAPTSMN1; SMN2KMT2AMEN1LMNA
SCHEMBL5229133 0.82 MAPT (0.39) MAPTSMN1; SMN2KMT2AMEN1LMNA
SCHEMBL6139668 0.82 MAPT (0.39) MAPTSMN1; SMN2KMT2AMEN1LMNA
SCHEMBL6139665 0.82 MAPT (0.39) MAPTSMN1; SMN2KMT2AMEN1LMNA
SCHEMBL22346626 0.76 MAPT (0.34) MAPTSMN1; SMN2KMT2AMEN1LMNA
SCHEMBL22346625 0.76 MAPT (0.34) MAPTSMN1; SMN2KMT2AMEN1LMNA
SCHEMBL23179936 0.76 MAPT (0.34) MAPTSMN1; SMN2KMT2AMEN1LMNA
SCHEMBL30704148 0.74 MEN1 (0.38) BACE1MAPTSMN1; SMN2KMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050187270-A1 16-Halogen-epothilone derivatives, method for producing them and their pharmaceutical use BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2005-08-25 US disclosed
US-6930102-B2 16-halogen-epothilone derivatives, process for their production, and their pharmaceutical use SCHERING AG (DE) 2005-08-16 US disclosed
US-20040014978-A1 16-halogen-epothilone derivatives, process for their production, and their pharmaceutical use SCHERING AG (DE) 2004-01-22 US disclosed
US-6610736-B1 Antitumor SCHERING AG (DE) 2003-08-26 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 (2 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-20040014978-A1 16-halogen-epothilone derivatives, process for their production, and their pharmaceutical use EPOR, CYP2F1, REV1 BACE1 4355/4885MAPT 4595/4885SMN1; SMN2 4827/4885
US-20050187270-A1 16-Halogen-epothilone derivatives, method for producing them and their pharmaceutical use ABCB1, UGT2B17, CYP7B1 BACE1 2844/4885MAPT 3989/4885SMN1; SMN2 4832/4885

“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.