SCHEMBL6182684

SCHEMBL6182684

CCOC(=O)C1(C2CCOCC2)CCNCC1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
OPRM1 P35372 1/20 0.43
CYP3A4 P08684 2/20 0.38
TSHR P16473 2/20 0.38
ABCB11 O95342 1/20 0.38
LMNA P02545 1/20 0.38
CYP1A2 P05177 1/20 0.38
CHRM2 P08172 1/20 0.38
CHRM4 P08173 1/20 0.38
CHRM5 P08912 1/20 0.38
CYP2D6 P10635 1/20 0.38
CHRM1 P11229 1/20 0.38
CYP2C9 P11712 1/20 0.38
CHRM3 P20309 1/20 0.38
DRD1 P21728 1/20 0.38
HRH2 P25021 1/20 0.38
HTR2A P28223 1/20 0.38
HTR2C P28335 1/20 0.38
HRH1 P35367 1/20 0.38
DRD3 P35462 1/20 0.38
SCN1A P35498 1/20 0.38

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
Hydrochloric Acid SCHEMBL7560277 0.99 OPRM1 (0.42) OPRM1CYP3A4TSHRABCB11LMNA
SCHEMBL3465278 0.89 TSHR (0.42) CYP3A4TSHRABCB11LMNACYP1A2
SCHEMBL1684100 0.89 OPRM1 (0.48) OPRM1CYP3A4TSHRABCB11LMNA
Hydrochloric Acid SCHEMBL1282252 0.88 OPRM1 (0.47) OPRM1CYP3A4TSHRABCB11LMNA
SCHEMBL1311224 0.85 CYP3A4 (0.52) OPRM1CYP3A4TSHRABCB11LMNA
SCHEMBL2007741 0.84 OPRM1 (0.45) OPRM1CYP3A4TSHRABCB11LMNA
Hydrochloric Acid SCHEMBL5729678 0.84 CYP3A4 (0.53) OPRM1CYP3A4TSHRABCB11LMNA
Hydrochloric Acid SCHEMBL19410760 0.83 CYP3A4 (0.44) OPRM1CYP3A4TSHRABCB11LMNA
SCHEMBL1976918 0.81 CYP3A4 (0.48) OPRM1CYP3A4TSHRABCB11LMNA
SCHEMBL2925260 0.81 CYP3A4 (0.51) OPRM1CYP3A4TSHRABCB11LMNA

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 8 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4724435-A1 BIFUNCTIONAL AZINES CONJOGATES AS SELECTIVE DEGRADERS OF SMARCA2 AND THERAPEUTIC USES THEREOF Nurix Therapeutics, Inc. (US) 2026-04-15 EP disclosed
US-20250051344-A1 BIFUNCTIONAL SELECTIVE DEGRADERS OF SMARCA2 AND THERAPEUTIC USES THEREOF NURIX THERAPEUTICS, INC. 2025-02-13 US disclosed
WO-2024254532-A1 BIFUNCTIONAL AZINES CONJOGATES AS SELECTIVE DEGRADERS OF SMARCA2 AND THERAPEUTIC USES THEREOF NURIX THERAPEUTICS, INC. (US) 2024-12-12 WO disclosed
EP-1187614-A4 SUBSTITUTED PIPERIDINES AS MELANOCORTIN-4 RECEPTOR AGONISTS MERCK & CO INC (US) 2005-06-22 EP disclosed
US-20020137664-A1 Substituted piperidines as melanocortin-4 receptor agonists MERCK & CO., INC. 2002-09-26 US disclosed
EP-1187614-A1 SUBSTITUTED PIPERIDINES AS MELANOCORTIN-4 RECEPTOR AGONISTS Merck & Co., Inc. (US) 2002-03-20 EP disclosed
US-6350760-B1 OBESITY, DIABETES, SEXUAL DYSFUNCTION; MERCK & CO., INC. 2002-02-26 US disclosed
WO-2000074679-A1 SUBSTITUTED PIPERIDINES AS MELANOCORTIN-4 RECEPTOR AGONISTS MERCK & CO., INC. (US) 2000-12-14 WO 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 (2 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-20020137664-A1 Substituted piperidines as melanocortin-4 receptor agonists MC4R, MC5R, MC3R OPRM1 86/4885CYP3A4 1106/4885TSHR 342/4885
US-20250051344-A1 BIFUNCTIONAL SELECTIVE DEGRADERS OF SMARCA2 AND THERAPEUTIC USES THEREOF SMARCA2, SMARCE1, SMARCB1 OPRM1 4448/4885CYP3A4 4516/4885TSHR 3787/4885

“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.