SCHEMBL740140

SCHEMBL740140

CCC1(C(=O)O)CCCNC1

nearest known ligand 0.39

Predicted protein targets (top 8)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 1/20 0.39
SLC6A2 P23975 9/20 0.35
SLC6A4 P31645 9/20 0.35
SLC6A3 Q01959 9/20 0.35
MMP2 P08253 1/20 0.32
MMP14 P50281 1/20 0.32
ADAM17 P78536 1/20 0.32
CYP2D6 P10635 7/20 0.32

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
SCHEMBL4117702 1.00 CYP2C19 (0.39) CYP2C19SLC6A2SLC6A4SLC6A3MMP2
SCHEMBL2423874 1.00 CYP2C19 (0.39) CYP2C19SLC6A2SLC6A4SLC6A3MMP2
Cadaverine Tartrate SCHEMBL18879377 0.90 CYP2C19 (0.37) CYP2C19SLC6A2SLC6A4SLC6A3
SCHEMBL29951019 0.88 SLC6A2 (0.39) CYP2C19SLC6A2SLC6A4SLC6A3CYP2D6
SCHEMBL25962718 0.85 SLC6A2 (0.40) CYP2C19SLC6A2SLC6A4SLC6A3MMP2
Hydrochloric Acid SCHEMBL28328339 0.84 SLC6A2 (0.40) CYP2C19SLC6A2SLC6A4SLC6A3MMP2
SCHEMBL28230632 0.81 CYP2C19 (0.39) CYP2C19SLC6A2SLC6A4SLC6A3MMP2
SCHEMBL21937953 0.80 SLC6A2 (0.33) SLC6A2SLC6A4SLC6A3MMP2MMP14
SCHEMBL10088963 0.79
SCHEMBL2890720 0.79 POLB (0.41) SLC6A2SLC6A4SLC6A3MMP2MMP14

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 32 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110431142-A Alicyclic substituted pyrazolo [1,5-a] pyrimidine derivatives of pharmacological activity RICHTER GEDEON NYRT 2019-11-08 CN disclosed
CN-110402245-A Process for the separation of optical isomers of racemic 3-alkylpiperidine-carboxylic acid ethyl ester RICHTER GEDEON NYRT 2019-11-01 CN disclosed
EP-2430195-A2 COMPOSITIONS AND METHODS FOR BIOLOGICAL SAMPLE STORAGE Biomatrica, INC. (US) 2012-03-21 EP disclosed
WO-2010132508-A2 COMPOSITIONS AND METHODS FOR BIOLOGICAL SAMPLE STORAGE BIOMATRICA, INC. (US) 2010-11-18 WO disclosed
US-20080306054-A1 Pharmaceutical Compounds ASTEX THERAPEUTICS LIMITED (GB) 2008-12-11 US disclosed
CN-101263115-A Substituted indoles and use thereof WYETH CORP (US) 2008-09-10 CN disclosed
EP-0931078-B1 NOVEL TRICYCLIC PIPERIDINYL COMPOUNDS USEFUL AS INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE SCHERING CORP (US) 2006-11-15 EP disclosed
US-20060161004-A1 Novel compounds GLAXOSMITHKLINE SPA 2006-07-20 US disclosed
US-20050070574-A1 Novel compounds GLAXOSMITHKLINE SPA AND LABORATOIRE 2005-03-31 US disclosed
US-20040102633-A1 Novel compounds GLAXOSMITHKLINE S.P.A. (IT) 2004-05-27 US disclosed
WO-2001004119-A1 AMIDO SPIROPIPERIDINES PROMOTE THE RELEASE OF GROWTH HORMONE MERCK & CO., INC. (US) 2001-01-18 WO disclosed
US-5965570-A PHARMACEUTICAL COMPOSITIONS FOR INHIBITING THE ABNORMAL GROWTH OF CELLS; ADMINISTERING TO INHIBIT TUMOR CELLS WHEREIN THE RAS PROTEIN IS ACTIVATED AS A RESULT OF ONCOGENIC MUTATION IN GENES OTHER THAN THE RAS GENE SCHERING CORPORATION (US) 1999-10-12 US disclosed
EP-0931078-A1 NOVEL TRICYCLIC PIPERIDINYL COMPOUNDS USEFUL AS INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE SCHERING CORPORATION (US) 1999-07-28 EP disclosed
WO-1998011098-A1 NOVEL TRICYCLIC PIPERIDINYL COMPOUNDS USEFUL AS INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE SCHERING CORPORATION (US) 1998-03-19 WO disclosed
EP-0522082-B1 MULTI-FUNCTIONAL PHARMACEUTICAL COMPOUNDS AND METHODS OF USE GLASKY ALVIN J (US) 1997-07-02 EP disclosed
EP-0522082-A4 MULTI-FUNCTIONAL PHARMACEUTICAL COMPOUNDS AND METHODS OF USE 1993-06-09 EP disclosed
EP-0522082-A1 MULTI-FUNCTIONAL PHARMACEUTICAL COMPOUNDS AND METHODS OF USE. GLASKY ALVIN J (US) 1993-01-13 EP disclosed
US-5091432-A Synergistic SPECTRUM PHARMACEUTICALS, INC. 1992-02-25 US disclosed
WO-1991014434-A1 MULTI-FUNCTIONAL PHARMACEUTICAL COMPOUNDS AND METHODS OF USE GLASKY ALVIN J (US) 1991-10-03 WO disclosed
US-4950674-A Arylalkylheterocyclic amines,N-substituted by aryloxyalkyl group in a method for allergy treatment A. H. ROBINS COMPANY, INCORPORATED (US) 1990-08-21 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 (4 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-20050070574-A1 Novel compounds NR1H3, NR1H2, CNR1 CYP2C19 433/4885SLC6A2 1238/4885SLC6A4 804/4885
US-20060161004-A1 Novel compounds SLC10A1, ABCB11, AQP1 CYP2C19 88/4885SLC6A2 1414/4885SLC6A4 1587/4885
US-20080306054-A1 Pharmaceutical Compounds HSP90AB1, HSP90AA1, HSP90AB2P CYP2C19 173/4885SLC6A2 492/4885SLC6A4 806/4885
US-20040102633-A1 Novel compounds H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CBR1, NR1H3 CYP2C19 782/4885SLC6A2 1048/4885SLC6A4 702/4885

“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.