SCHEMBL2441202

SCHEMBL2441202

CNC1CCCCC1N1CCCC1

nearest known ligand 0.51

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 1/20 0.41
CYP2D6 P10635 3/20 0.40
MEN1 O00255 1/20 0.40
KMT2A Q03164 1/20 0.40
LMNA P02545 1/20 0.40
SIGMAR1 Q99720 4/20 0.40
CHRNA7 P36544 1/20 0.39
MCOLN2 Q8IZK6 1/20 0.38
MCOLN1 Q9GZU1 1/20 0.38
CHRNB4 P30926 1/20 0.37
CHRNA3 P32297 1/20 0.37

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
SCHEMBL2441220 1.00 TDP1 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL7343637 1.00 TDP1 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL8762939 1.00 TDP1 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL8761967 0.98 CHRNA7 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL10366437 0.98 CHRNA7 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL8761961 0.98 CHRNA7 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL11465447 0.98 CHRNA7 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL10366436 0.98 CHRNA7 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL10366438 0.98 CHRNA7 (0.41) TDP1CYP2D6MEN1KMT2ALMNA
SCHEMBL13463493 0.95 CHRNB4 (0.37) TDP1CYP2D6MEN1KMT2ALMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2215085-B1 PYRIDINE AND PYRAZINE DERIVATIVES USEFUL IN THE TREATMENT OF CELL PROLIFERATIVE DISORDERS ASTRAZENECA AB (SE) 2011-09-07 EP disclosed
US-7294647-B2 Kappa agonist compounds and pharmaceutical formulations thereof ADOLOR CORPORATION (US) 2007-11-13 US disclosed
US-6960612-B2 Kappa agonist compounds, pharmaceutical formulations and method of prevention and treatment of pruritus therewith ADOLOR CORPORATION (US) 2005-11-01 US disclosed
US-20050020576-A1 Kappa agonist compounds and pharmaceutical formulations thereof ADOLOR CORPORATION 2005-01-27 US disclosed
US-20040220112-A1 Kappa agonist compounds, pharmaceutical formulations and method of prevention and treatment of pruritus therewith ADOLOR CORPORATION 2004-11-04 US disclosed
EP-1112252-A4 KAPPA AGONIST COMPOUNDS AND PHARMACEUTICAL FORMULATIONS THEREOF ADOLOR CORP (US) 2004-07-14 EP disclosed
US-6750216-B2 HETEROCYCLIC AMINES SUCH AS 2-(2-(N-METHYLSULFAMOYL)-4-METHOXY -PHENYL)-N-METHYL-N-((1S)-1-PHENYL-2-((1-PYRROLIDINYL)ETHYL)) ACETAMIDE, ADMINISTERED AS ANALGESICS ADOLOR CORPORATION 2004-06-15 US disclosed
US-20030236248-A1 Kappa agonist compounds and pharmaceutical formulations thereof KRUSE LAWRENCE I (US) 2003-12-25 US disclosed
US-20030144272-A1 Kappa agonist compounds and pharmaceutical formulations thereof ADOLOR CORPORATION 2003-07-31 US disclosed
US-RE38133-E1 N-Arylalkylenecarbonyl-N-methyl-benzylamine derivatives; analgesics, opioid agonists, antiinflammatory agents ADOLOR CORPORATION 2003-06-03 US disclosed
US-4663343-A ANAGESICS, DIURETICS WARNER-LAMBERT COMPANY (US) 1987-05-05 US disclosed
US-4656182-A ANALGESICS, DIURETICS, PSYCHOTHERAPEUTIC AGENTS WARNER-LAMBERT COMPANY (US) 1987-04-07 US disclosed
EP-0110869-B1 THIENYLACETIC-ACID AMIDE DERIVATIVES, PHARMACEUTICALLY ACCEPTABLE SALTS THEROF AND PROCESS FOR THEIR PREPARATION Laevosan-Gesellschaft m.b.H. (AT) 1987-03-18 EP disclosed
US-4598087-A DIURETICS; ANALGESICS, PSYCHOTHERAPEUTICS WARNER-LAMBERT COMPANY (US) 1986-07-01 US disclosed
US-4579863-A Substituted trans-1,2-diaminocyclohexyl amide compounds WARNER-LAMBERT COMPANY (US) 1986-04-01 US disclosed
EP-0147085-A2 Substituted trans-1.2-diaminocyclohexyl amide compounds WARNER-LAMBERT COMPANY (US) 1985-07-03 EP disclosed
EP-0146297-A1 Substituted trans-1,2-diaminocyclohexyl amide compounds WARNER-LAMBERT COMPANY (US) 1985-06-26 EP disclosed
US-4499286-A Derivatives of thienylacetic acid amides and their pharmaceutically acceptable acid salts and a process for the preparation thereof Leavoson-Gesellschaft m.b.H. & Co. KG (AT) 1985-02-12 US disclosed
EP-0110869-A1 Thienylacetic-acid amide derivatives, pharmaceutically acceptable salts therof and process for their preparation Laevosan-Gesellschaft m.b.H. (AT) 1984-06-13 EP disclosed
US-4145435-A 2-AMINOCYCLOALIPHATIC AMIDE COMPOUNDS THE UPJOHN COMPANY (US) 1979-03-20 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-20030236248-A1 Kappa agonist compounds and pharmaceutical formulations thereof OPRK1, OPRD1, OPRM1 TDP1 4215/4885CYP2D6 946/4885MEN1 4703/4885
US-20030144272-A1 Kappa agonist compounds and pharmaceutical formulations thereof OPRK1, OPRD1, OPRM1 TDP1 4084/4885CYP2D6 659/4885MEN1 4734/4885
US-20040220112-A1 Kappa agonist compounds, pharmaceutical formulations and method of prevention and treatment of pruritus therewith OPRK1, OPRD1, OPRM1 TDP1 4486/4885CYP2D6 886/4885MEN1 4678/4885
US-20050020576-A1 Kappa agonist compounds and pharmaceutical formulations thereof OPRK1, OPRD1, OPRM1 TDP1 4174/4885CYP2D6 541/4885MEN1 4710/4885

“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.