SCHEMBL4189286

SCHEMBL4189286

CC(C(=O)O)C1CCCNC1

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CPN1 P15169 3/20 0.57
CPB2 Q96IY4 3/20 0.57
SLC6A1 P30531 3/20 0.47
SLC6A11 P48066 2/20 0.47
SLC6A13 Q9NSD5 2/20 0.47
TSHR P16473 1/20 0.47
LMNA P02545 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47
KDM4E B2RXH2 1/20 0.41
MAPT P10636 1/20 0.41
KMT2A Q03164 1/20 0.41
ATM Q13315 1/20 0.41
CYP2D6 P10635 1/20 0.41
APLNR P35414 2/20 0.33
NOS2 P35228 1/20 0.33
GABRA5 P31644 1/20 0.33
GABRB2 P47870 1/20 0.33
SLC6A12 P48065 1/20 0.33
MAPK1 P28482 1/20 0.33
OPRK1 P41145 1/20 0.33

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
SCHEMBL25662157 1.00 CPN1 (0.57) CPN1CPB2SLC6A1SLC6A11SLC6A13
SCHEMBL25662164 1.00 CPN1 (0.57) CPN1CPB2SLC6A1SLC6A11SLC6A13
SCHEMBL5313699 0.94 CPN1 (0.51) CPN1CPB2SLC6A1SLC6A11SLC6A13
SCHEMBL27607144 0.88 CPN1 (0.44) CPN1CPB2SLC6A1SLC6A11SLC6A13
SCHEMBL31167584 0.88 CPN1 (0.44) CPN1CPB2SLC6A1SLC6A11SLC6A13
SCHEMBL29508636 0.88 CPN1 (0.44) CPN1CPB2SLC6A1SLC6A11SLC6A13
SCHEMBL5499047 0.88 CPN1 (0.44) CPN1CPB2SLC6A1SLC6A11SLC6A13
Hydrochloric Acid SCHEMBL25263972 0.86 CPN1 (0.43) CPN1CPB2SLC6A1SLC6A11SLC6A13
Hydrochloric Acid SCHEMBL31603105 0.86 CPN1 (0.43) CPN1CPB2SLC6A1SLC6A11SLC6A13
Hydrochloric Acid SCHEMBL29508656 0.86 CPN1 (0.43) CPN1CPB2SLC6A1SLC6A11SLC6A13

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0316809-B1 Salts of amino-(poly)percarboxylic acids AUSIMONT SPA (IT) 1993-11-03 EP claimed
CN-113773289-B Naphthalene [1,2-b ] heterocycle-4, 5-diketone compound and preparation method and application thereof 沈阳药科大学 2023-05-12 CN disclosed
CN-113950471-A Charged ion channel blockers and methods of use thereof 诺西恩医疗公司 2022-01-18 CN disclosed
WO-2018021977-A1 GLYCINE METABOLISM MODULATORS AND USES THEREOF AGENCY FOR SCIENCE, TECHNOLOGY AND RESEARCH (SG) 2018-02-01 WO disclosed
US-7569569-B2 Pyrrolo[2,3-d]pyrimidine compounds PFIZER INC. (US) 2009-08-04 US disclosed
US-7402583-B2 Substituted quinolines as antitumor agents ASTRZENCA AB (SE) 2008-07-22 US disclosed
US-20070238721-A1 Highly Selective Novel Amidation Method TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2007-10-11 US disclosed
US-7220771-B2 Methods of using indazole derivatives as JNK inhibitors SIGNAL PHARMACEUTICALS, LLC (US) 2007-05-22 US disclosed
US-7211594-B2 Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith SIGNAL PHARMACEUTICALS, LLC (US) 2007-05-01 US disclosed
US-7208513-B2 Indazole compounds and compositions thereof as JNK inhibitors and for the treatment of diseases associated therewith SIGNAL PHARMACEUTICALS, LLC (US) 2007-04-24 US disclosed
US-5294362-A Bleach AUSIMONT S.R.L. (IT) 1994-03-15 US disclosed
EP-0316809-B1 Salts of amino-(poly)percarboxylic acids AUSIMONT SPA (IT) 1993-11-03 EP disclosed
US-5245075-A Bleaching agents AUSIMONT S.R.L. (IT) 1993-09-14 US disclosed
US-5236678-A Process for absorption of sulfur compounds from fluids using piperidines THE DOW CHEMICAL COMPANY (US) 1993-08-17 US disclosed
EP-0552360-A1 A COMPOSITION AND METHOD FOR SIMULTANEOUS ABSORPTION OF SULFUR DIOXIDE AND NITRIC OXIDE THE DOW CHEMICAL COMPANY (US) 1993-07-28 EP disclosed
WO-1993003825-A1 A COMPOSITION AND METHOD FOR SIMULTANEOUS ABSORPTION OF SULFUR DIOXIDE AND NITRIC OXIDE THE DOW CHEMICAL COMPANY (US) 1993-03-04 WO disclosed
US-5167941-A Sulfur dioxide; cationic polyelectrolyte stabilizers THE DOW CHEMICAL COMPANY (US) 1992-12-01 US disclosed
EP-0471592-A2 Process for absorption of sulfur compounds from fluids using certain piperidines, piperazines, or anhydrides of monocarboxylic amino acids THE DOW CHEMICAL COMPANY (US) 1992-02-19 EP disclosed
EP-0316809-A2 Salts of amino-(poly)percarboxylic acids AUSIMONT S.p.A. (IT) 1989-05-24 EP disclosed
US-4433152-A ANTIINFLAMMATORY AGENT, ANTIALLERGEN OR ANTICOAGULANT NIPPON CHEMIPHAR CO., LTD. (JP) 1984-02-21 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 (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-20070238721-A1 Highly Selective Novel Amidation Method NAAA, CPS1, COASY CPN1 286/4885CPB2 559/4885SLC6A1 3877/4885

“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.