SCHEMBL6489247

SCHEMBL6489247

O=C(N[C@@H](Cc1ccc(F)cc1)C(=O)CCl)OCc1ccccc1

nearest known ligand 0.58

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
TACR1 P25103 2/20 0.55
CTSL P07711 2/20 0.54
CTSB P07858 2/20 0.54
CTSS P25774 2/20 0.54
CTSK P43235 2/20 0.54
ALDH1A1 P00352 1/20 0.53
ALOX15 P16050 1/20 0.53
CTRB1 P17538 2/20 0.51
ITGB3 P05106 4/20 0.50
ITGA2B P08514 4/20 0.50
OPRK1 P41145 1/20 0.50
CTSG P08311 1/20 0.50
CMA1 P23946 1/20 0.50
GPR34 Q9UPC5 1/20 0.50

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
SCHEMBL7267663 1.00 TACR1 (0.55) TACR1CTSLCTSBCTSSCTSK
SCHEMBL7490981 0.92 TACR1 (0.62) TACR1CTSLCTSBCTSSCTSK
SCHEMBL4980616 0.92 TACR1 (0.62) TACR1CTSLCTSBCTSSCTSK
SCHEMBL6439753 0.92 TACR1 (0.62) TACR1CTSLCTSBCTSSCTSK
SCHEMBL7291131 0.87 GPR34 (0.63) TACR1CTSLCTSBCTSSCTSK
SCHEMBL8258487 0.87 GPR34 (0.63) TACR1CTSLCTSBCTSSCTSK
SCHEMBL2511842 0.87 GPR34 (0.63) TACR1CTSLCTSBCTSSCTSK
SCHEMBL10722503 0.87 GPR34 (0.63) TACR1CTSLCTSBCTSSCTSK
SCHEMBL7269586 0.86 HDAC8 (0.59) TACR1CTSLCTSBCTSSCTSK
SCHEMBL11145746 0.84 CTSL (0.58) TACR1CTSLCTSBCTSSCTSK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6888012-B2 Reducing an alpha -haloketone compound by asymmetric hydrogen transfer in presence of a group 9 transition metal compound having a substituted or unsubstituted cyclopentadienyl group and an optically active diamine compound AJINOMOTO CO., INC. (JP) 2005-05-03 US disclosed
US-20040082820-A1 Hydrogen transfer reduction; useful as intermediate for production of pharmaceuticals/agricultural chemicals AJINOMOTO CO., INC. (JP) 2004-04-29 US disclosed
EP-1346972-A1 PROCESS FOR PRODUCING OPTICALLY ACTIVE HALOHYDRIN COMPOUND Ajinomoto Co., Inc. (JP) 2003-09-24 EP disclosed
US-5652369-A PROTEASE INHIBITOR HOFFMANN-LA ROCHE INC. (US) 1997-07-29 US disclosed
US-5620987-A Amino acid derivatives HOFFMANN-LA ROCHE INC. (US) 1997-04-15 US disclosed
US-5554756-A PROTEASE INHIBITOR HOFFMANN-LA ROCHE INC. (US) 1996-09-10 US disclosed
US-5446161-A Protease inhibitor, viricides HOFFMANN-LA ROCHE INC. (US) 1995-08-29 US disclosed
EP-0346847-B1 Amino acid derivatives HOFFMANN LA ROCHE (CH) 1994-05-11 EP disclosed
US-5157041-A Viricides HOFFMANN-LA ROCHE INC. (US) 1992-10-20 US disclosed
EP-0346847-A2 Amino acid derivatives F. HOFFMANN-LA ROCHE AG (CH) 1989-12-20 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-20040082820-A1 Hydrogen transfer reduction; useful as intermediate for production of pharmaceuticals/agricultural chemicals DHPS, HDHD5, HYPK TACR1 4567/4885CTSL 3492/4885CTSB 2595/4885

“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.