SCHEMBL3591425

SCHEMBL3591425

CN1CCC(O)(c2ccc(Cl)cc2)CC1

nearest known ligand 0.57

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
▸ CCR3 P51677 2/20 0.57
▸ DRD2 P14416 4/20 0.56
▸ OPRM1 P35372 4/20 0.56
▸ OPRL1 P41146 3/20 0.55
▸ OPRD1 P41143 1/20 0.55
▸ OPRK1 P41145 1/20 0.55
▸ SLC18A3 Q16572 1/20 0.54
▸ ADRA1A P35348 1/20 0.52
▸ MEN1 O00255 1/20 0.51
▸ KMT2A Q03164 1/20 0.51

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
SCHEMBL9910962 0.93 OPRM1 (0.52) CCR3DRD2OPRM1OPRL1OPRD1
SCHEMBL10028305 0.90 OPRL1 (0.46) CCR3OPRM1OPRL1OPRD1OPRK1
SCHEMBL9910960 0.89 CCR3 (0.50) CCR3DRD2OPRM1OPRL1OPRD1
SCHEMBL5471021 0.84 KMT2A (0.56) CCR3DRD2OPRM1ADRA1AMEN1
SCHEMBL14307260 0.83 CCR3 (0.69) CCR3DRD2OPRM1OPRL1ADRA1A
SCHEMBL10424458 0.82 OPRM1 (0.57) DRD2OPRM1OPRL1OPRD1OPRK1
SCHEMBL17888226 0.82 CYP2D6 (0.48) DRD2OPRM1OPRL1OPRD1OPRK1
SCHEMBL10287607 0.82 OPRM1 (0.63) CCR3DRD2OPRM1OPRL1ADRA1A
SCHEMBL12925944 0.81 OPRM1 (0.49) OPRM1OPRL1OPRD1OPRK1
SCHEMBL15543779 0.81 MAPT (0.55) CCR3DRD2OPRM1OPRL1OPRD1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20130210769-A1 COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF CANNABINOID RECEPTOR 1 ACTIVITY IRM LLC (BM) 2013-08-15 — — US claimed
US-20100234365-A1 COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF CANNABINOID RECEPTOR 1 ACTIVITY IRM LLC (BM) 2010-09-16 — — US claimed
EP-2121598-A2 COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF CANNABINOID RECEPTOR 1 ACTIVITY IRM LLC (BM) 2009-11-25 — — EP claimed
WO-2008076754-A2 COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF CANNABINOID RECEPTOR 1 ACTIVITY IRM LLC (BM) 2008-06-26 — — WO claimed
US-20240016775-A1 ANTI-CORONAVIRUS APPLICATION OF POLY ADP RIBOSE POLYMERASE INHIBITOR FUKANG (SHANGHAI) HEALTH TECHNOLOGY CO., LTD (CN) 2024-01-18 — — US disclosed
US-20210317134-A1 UBIQUITIN-SPECIFIC-PROCESSING PROTEASE 7 (USP7) MODULATORS AND USES THEREOF RAPT THERAPEUTICS INC (US) 2021-10-14 — — US disclosed
CN-113214102-A Amine-containing transfection reagents and methods of making and using same 生命技术公司 2021-08-06 — — CN disclosed
CN-108358812-B Amine-containing transfection reagents and methods of making and using same 生命技术公司 2021-05-11 — — CN disclosed
US-10414771-B2 Compounds useful for inhibiting metastasis from cancer and methods using same DREXEL UNIVERSITY (US) 2019-09-17 — — US disclosed
US-20190233441-A1 TRIAZOLOPYRIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF GENENTECH, INC. (US) 2019-08-01 — — US disclosed
CN-104910025-B Alkamine lipid and its purposes 麻省理工学院 2019-07-16 — — CN disclosed
EP-3041841-B1 TRIAZOLOPYRIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF HOFFMANN LA ROCHE (CH) 2019-06-05 — — EP disclosed
CN-1680418-A Ketolactones, their use and process for their preparation and pharmaceutical compositions containing them ABBOTT LAB (US) 2005-10-12 — — CN disclosed
US-6844333-B1 Method of treating atherosclerosis THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 2005-01-18 — — US disclosed
US-20040072849-A1 Dioxanes and uses thereof NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2004-04-15 — — US disclosed
WO-2003020721-A1 PYRROLO PYRIMIDINES AS AGENTS FOR THE INHIBITION OF CYSTEIN PROTEASES NOVARTIS AG (CH) 2003-03-13 — — WO disclosed
CN-1271363-A 3' -N-modified 6-O-substituted erythromycin ketolide derivatives having antibacterial activity ABBOTT LAB (US) 2000-10-25 — — CN disclosed
CN-1237183-A 6-0-substituted ketolides with antibacterial activity ABBOTT CO (US) 1999-12-01 — — CN disclosed
CN-1224427-A 6-O-substituted erythromycin compounds and preparation method thereof ABBOTT LAB (US) 1999-07-28 — — CN disclosed
US-4325953-A 4-Aryl-4-aryloxypiperidines JOHN WYETH AND BROTHER LIMITED (GB) 1982-04-20 — — 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 (7 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-10414771-B2 Compounds useful for inhibiting metastasis from cancer and methods using same CX3CR1, CCL2, CCR5 CCR3 17/4885DRD2 2074/4885OPRM1 703/4885
US-20240016775-A1 ANTI-CORONAVIRUS APPLICATION OF POLY ADP RIBOSE POLYMERASE INHIBITOR PARP3, PARP1, PARP4 CCR3 1998/4885DRD2 4607/4885OPRM1 3967/4885
US-20040072849-A1 Dioxanes and uses thereof UTS2R, HDAC5, AMDHD2 CCR3 3530/4885DRD2 3983/4885OPRM1 4575/4885
US-20210317134-A1 UBIQUITIN-SPECIFIC-PROCESSING PROTEASE 7 (USP7) MODULATORS AND USES THEREOF USP7, SENP7, USP8 CCR3 4635/4885DRD2 4829/4885OPRM1 4147/4885
US-20190233441-A1 TRIAZOLOPYRIDINE COMPOUNDS, COMPOSITIONS AND METHODS OF USE THEREOF ABL1, JAK2, JAK1 CCR3 2380/4885DRD2 4124/4885OPRM1 1787/4885
US-20130210769-A1 COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF CANNABINOID RECEPTOR 1 ACTIVITY CNR1, CNR2, FAAH CCR3 974/4885DRD2 889/4885OPRM1 18/4885
US-20100234365-A1 COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF CANNABINOID RECEPTOR 1 ACTIVITY CNR1, CNR2, FAAH CCR3 974/4885DRD2 889/4885OPRM1 18/4885

“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.

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