SCHEMBL253323

SCHEMBL253323

CC1(C)C2CCC1(C)C(O)C2N

nearest known ligand 0.35

Predicted protein targets (top 4)

geneUniProtsupporting neighboursconfidence
CNR2 P34972 2/20 0.35
DPP4 P27487 1/20 0.33
EBP Q15125 1/20 0.32
SHBG P04278 1/20 0.30

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
SCHEMBL50911 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL14889462 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL11645490 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL6507028 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL9360142 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL7673902 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL11882526 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL11771376 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL11882927 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG
SCHEMBL8131815 1.00 CNR2 (0.35) CNR2DPP4EBPSHBG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7563910-B2 Heterocyclic cannabinoid receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2009-07-21 US claimed
EP-1749002-B1 PYRROLE OR IMIDAZOLE AMIDES FOR TREATING OBESITY HOFFMANN LA ROCHE (CH) 2009-05-27 EP claimed
EP-1749002-A1 PYRROLE OR IMIDAZOLE AMIDES FOR TREATING OBESITY F.HOFFMANN-LA ROCHE AG (CH) 2007-02-07 EP claimed
WO-2005108393-A1 PYRROLE OR IMIDAZOLE AMIDES FOR TREATING OBESITY F. HOFFMANN-LA ROCHE AG (CH) 2005-11-17 WO claimed
US-20050250769-A1 Heterocyclic cannabinoid receptor antagonists F. HOFFMANN-LA ROCHE AG (CH) 2005-11-10 US claimed
EP-0431955-B1 3-Amino-2-hydroxybornane derivatives, asymmetric Michael reaction using the same, and process for preparing optically active muscone utilizing Michael reaction NIPPON MINING CO (JP) 1994-03-30 EP claimed
EP-0431955-A2 3-Amino-2-hydroxybornane derivatives, asymmetric Michael reaction using the same, and process for preparing optically active muscone utilizing Michael reaction NIKKO KYODO CO., LTD. (JP) 1991-06-12 EP claimed
JP-3236357-A None JP disclosed
EP-2401280-B1 Cyclopropyl fused indolobenzazepine hcv ns5b inhibitors BRISTOL MYERS SQUIBB CO (US) 2013-05-01 EP disclosed
EP-2401280-A1 Cyclopropyl fused indolobenzazepine hcv ns5b inhibitors Bristol-Myers Squibb Company (US) 2012-01-04 EP disclosed
WO-2010099159-A1 CYCLOPROPYL FUSED INDOLOBENZAZEPINE HCV NS5B INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2010-09-02 WO disclosed
US-7563910-B2 Heterocyclic cannabinoid receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2009-07-21 US disclosed
EP-1749002-B1 PYRROLE OR IMIDAZOLE AMIDES FOR TREATING OBESITY HOFFMANN LA ROCHE (CH) 2009-05-27 EP disclosed
EP-0431955-A2 3-Amino-2-hydroxybornane derivatives, asymmetric Michael reaction using the same, and process for preparing optically active muscone utilizing Michael reaction NIKKO KYODO CO., LTD. (JP) 1991-06-12 EP disclosed
EP-0431955-A2 3-Amino-2-hydroxybornane derivatives, asymmetric Michael reaction using the same, and process for preparing optically active muscone utilizing Michael reaction NIKKO KYODO CO., LTD. (JP) 1991-06-12 EP disclosed
EP-0431955-A2 3-Amino-2-hydroxybornane derivatives, asymmetric Michael reaction using the same, and process for preparing optically active muscone utilizing Michael reaction NIKKO KYODO CO., LTD. (JP) 1991-06-12 EP disclosed
US-4130563-A POLYMER INTERMEDIATES BAYER AKTIENGESELLSCHAFT (DE) 1978-12-19 US disclosed
US-3988362-A ANTIDEPRESSANTS HOFFMANN-LA ROCHE INC. (US) 1976-10-26 US disclosed
US-3860724-A SUBSTITUTED SULFONYL UREA AND ITS STEREOISOMERS AS HYPOGLYCEMIC AGENTS HOFFMANN LA ROCHE 1975-01-14 US disclosed
US-3832397-A PROCESS FOR SUBSTITUTED SULFONYLUREAS HOFFMANN LA ROCHE 1974-08-27 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-20050250769-A1 Heterocyclic cannabinoid receptor antagonists CNR1, CNR2, GPR18 CNR2 2/4885DPP4 3962/4885EBP 1098/4885

“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.