SCHEMBL1806308

SCHEMBL1806308

CCN(CC)C(=O)c1ccc(O)cc1

nearest known ligand 0.63

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
HPGD P15428 5/20 0.63
ALDH1A1 P00352 4/20 0.63
MAPT P10636 2/20 0.63
MLYCD O95822 1/20 0.61
HSP90AA1 P07900 5/20 0.59
HSP90AB1 P08238 5/20 0.59
OPRM1 P35372 2/20 0.59
OPRD1 P41143 2/20 0.59
LMNA P02545 2/20 0.56
MEN1 O00255 1/20 0.56
KMT2A Q03164 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.56
L3MBTL1 Q9Y468 1/20 0.56
RAB9A P51151 2/20 0.56
NPC1 O15118 1/20 0.56
CYP1A2 P05177 1/20 0.54
BLM P54132 1/20 0.54
TDP1 Q9NUW8 1/20 0.52

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
SCHEMBL5703500 0.91 HPGD (0.73) HPGDALDH1A1MAPTMLYCDHSP90AA1
SCHEMBL13236606 0.85 HPGD (0.49) HPGDALDH1A1MAPTMLYCDHSP90AA1
SCHEMBL4489409 0.83 MLYCD (0.64) HPGDALDH1A1MLYCDTDP1
SCHEMBL6802252 0.83 HPGD (0.69) HPGDALDH1A1MAPTMLYCDHSP90AA1
SCHEMBL121475 0.83 HPGD (0.66) HPGDALDH1A1MAPTMLYCDHSP90AA1
SCHEMBL26015713 0.82 HPGD (0.61) HPGDALDH1A1LMNA
SCHEMBL24629175 0.81 HPGD (0.57) HPGDALDH1A1MAPTMLYCDHSP90AA1
SCHEMBL1018549 0.81 HPGD (0.61) HPGDALDH1A1MAPTMLYCDHSP90AA1
SCHEMBL471629 0.81 HPGD (0.61) HPGDALDH1A1MAPTMLYCDHSP90AA1
SCHEMBL3081053 0.81 HPGD (0.61) HPGDALDH1A1MAPTMLYCDHSP90AA1

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
CN-115473001-B Battery separator, preparation method thereof and battery 江苏中兴派能电池有限公司 2023-08-29 CN claimed
CN-115473001-A Battery diaphragm, preparation method thereof and battery 江苏中兴派能电池有限公司 2022-12-13 CN claimed
CN-1294519-A Pharmaceutical composition containing a compound having an activity of promoting the absorption of an active ingredient INPHARMA SA (CH) 2001-05-09 CN claimed
EP-4630813-A2 IMPROVED METHOD FOR SCALABLE UNTARGETED METABOLOMIC WORKFLOW Washington University (US) 2025-10-15 EP disclosed
WO-2024123681-A2 IMPROVED METHOD FOR SCALABLE UNTARGETED METABOLOMIC WORKFLOW WASHINGTON UNIVERSITY (US) 2024-06-13 WO disclosed
CN-115473001-B Battery separator, preparation method thereof and battery 江苏中兴派能电池有限公司 2023-08-29 CN disclosed
US-11735772-B2 Electrolytes for electrochemical energy storage UCHICAGO ARGONNE, LLC (US) 2023-08-22 US disclosed
CN-115473001-A Battery diaphragm, preparation method thereof and battery 江苏中兴派能电池有限公司 2022-12-13 CN disclosed
EP-2493863-B1 PHENOXY-SUBSTITUTED PYRIMIDINES AS OPIOID RECEPTOR MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2015-02-25 EP disclosed
EP-2493863-B1 PHENOXY-SUBSTITUTED PYRIMIDINES AS OPIOID RECEPTOR MODULATORS JANSSEN PHARMACEUTICA NV (BE) 2015-02-25 EP disclosed
CN-102686569-B Phenoxy substituted pyrimidines as opioid receptor modulators JANSSEN PHARMACEUTICA NV 2014-11-26 CN disclosed
WO-2005089747-A1 NOVEL AZABICYCLIC DERIVATIVES, PREPARATION METHOD THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME LES LABORATOIRES SERVIER (FR) 2005-09-29 WO disclosed
CN-1178699-C Pharmaceutical Compsns. contg. compounds with activity for enhancement of absorption of active ingredients 2004-12-08 CN disclosed
CN-1294519-A Pharmaceutical composition containing a compound having an activity of promoting the absorption of an active ingredient INPHARMA SA (CH) 2001-05-09 CN disclosed
US-5866611-A PHENOXYPROPYLAMINE INHIBITORS OF SQUALENE SYNTHESE, USEFUL IN TREATING DISEASES IN WHICH A LOWERING OF CHOLESTEROL IS DESIRABLE. ZENECA LIMITED (GB) 1999-02-02 US disclosed
EP-0589018-A1 AMINES AS INHIBITORS OF SQUALENE SYNTHASE ZENECA LIMITED (GB) 1994-03-30 EP disclosed
EP-0393513-B1 Preparation of a difluorohalomethoxybenzene MITSUI TOATSU CHEMICALS (JP) 1994-03-09 EP disclosed
WO-1993020807-A1 AMINES AS INHIBITORS OF SQUALENE SYNTHASE ZENECA LIMITED (GB) 1993-10-28 WO disclosed
US-5105021-A Reacting metal phenolate with (di)bromo(chloro)difluoromethane in presence of promoter MITSUI TOATSU CHEMICALS, INCORPORATED (JP) 1992-04-14 US disclosed
EP-0393513-A1 Preparation of a difluorohalomethoxybenzene MITSUI TOATSU CHEMICALS, Inc. (JP) 1990-10-24 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-11735772-B2 Electrolytes for electrochemical energy storage HCN2, SLC9A2, HCN3 HPGD 26/4885ALDH1A1 433/4885MAPT 2581/4885

“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.