SCHEMBL5764697

SCHEMBL5764697

CCc1nc(Cc2ccc(Cl)cc2)sc1C1CCNCC1

nearest known ligand 0.39

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR6 P50406 1/20 0.39
NPC1 O15118 1/20 0.38
RAB9A P51151 1/20 0.38
CCR5 P51681 4/20 0.38
CETP P11597 1/20 0.37
ALDH1A1 P00352 1/20 0.36
HTR3A P46098 2/20 0.35
ABCB1 P08183 1/20 0.35
HTR2C P28335 2/20 0.35
HTR2B P41595 2/20 0.35
GABRA1 P14867 2/20 0.35
GABRG2 P18507 2/20 0.35
GABRB3 P28472 2/20 0.35
PTGDR2 Q9Y5Y4 1/20 0.34
KCNH2 Q12809 2/20 0.34
OPRM1 P35372 1/20 0.34
GPR4 P46093 1/20 0.34
TMEM97 Q5BJF2 1/20 0.34
SIGMAR1 Q99720 1/20 0.34
MEN1 O00255 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
SCHEMBL5762055 0.91 CCR5 (0.39) HTR6CCR5HTR3AGABRA1GABRG2
SCHEMBL5765303 0.89 CCR5 (0.38) CCR5HTR3AHTR2CHTR2BGABRA1
SCHEMBL5763728 0.88 CCR5 (0.40) CCR5HTR3AGABRA1GABRG2GABRB3
SCHEMBL5764678 0.88 CCR5 (0.40) CCR5HTR3AHTR2CHTR2BGABRA1
SCHEMBL5763905 0.88 CCR5 (0.36) HTR6NPC1RAB9ACCR5HTR3A
SCHEMBL5762735 0.88 GABRA1 (0.47) CCR5GABRA1GABRG2GABRB3SIGMAR1
SCHEMBL5765334 0.87 HTR6 (0.40) HTR6NPC1RAB9ACCR5ALDH1A1
Hydrochloric Acid SCHEMBL5764059 0.86 GABRA1 (0.46) CCR5GABRA1GABRG2GABRB3SIGMAR1
SCHEMBL5764323 0.86 HTR6 (0.43) HTR6NPC1RAB9ACCR5HTR2C
SCHEMBL5766275 0.86 HTR6 (0.46) HTR6NPC1RAB9ACETPALDH1A1

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
EP-1192133-B1 N-CYCLOPENTYL MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY MERCK & CO INC (US) 2006-11-02 EP disclosed
US-6593346-B2 Substituted 3-(piperidin-1-ylmethyl)cyclopentylamines, useful as modulators of the chemokine receptors CCR-5 and/or CC R-3. MERCK & CO. INC. 2003-07-15 US disclosed
US-6538002-B1 In particular, these compounds are useful as modulators of the chemokine receptors CCR-5 and/or CCR-3. as antiinflammatory agents MERCK & CO., INC. 2003-03-25 US disclosed
US-20020120146-A1 N-cyclopentyl modulators of chemokine receptor activity MERCK SHARP & DOHME CORP. 2002-08-29 US disclosed
US-6432981-B1 BLOCKS HUMAN IMMUNODEFICIENCY VIRUS (HIV) FROM ENTERING CELLS; AUTOIMMUNE DISEASES; ANTIALLERGENS, ANTIINFLAMMATORY AND ANTIASTHMATIC AGENTS MERCK & CO., INC. 2002-08-13 US disclosed
US-6358979-B1 FOR THERAPY AND PROPHYLAXIS OF ASTHMA, ALLERGIC RHINITIS, DERMATITIS, CONJUNCTIVITIS, ATHEROSCLEROSIS OR RHEUMATOID ARTHRITIS, INFECTION BY HIV, TREATING INFECTION BY HIV, DELAYING OF THE ONSET OF AIDS MERCK & CO., INC. 2002-03-19 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 (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-20020120146-A1 N-cyclopentyl modulators of chemokine receptor activity CCR1, CCR3, CCR5 HTR6 1057/4885NPC1 864/4885RAB9A 1266/4885

“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.