SCHEMBL2180249

SCHEMBL2180249

CC(C)(C)OC(=O)N[C@H]1CCNC[C@@H]1O

nearest known ligand 0.43

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
BTK Q06187 1/20 0.43
GAA P10253 2/20 0.39
EPHX1 P07099 1/20 0.38
EPHX2 P34913 1/20 0.38
NFKB1 P19838 1/20 0.38
NFKB2 Q00653 1/20 0.38
RELA Q04206 1/20 0.38
CTSK P43235 2/20 0.38
KDM1A O60341 1/20 0.37
CA1 P00915 1/20 0.37
CA2 P00918 1/20 0.37
SSTR4 P31391 2/20 0.37
SSTR1 P30872 1/20 0.37

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
SCHEMBL2490021 1.00 BTK (0.43) BTKGAAEPHX1EPHX2NFKB1
SCHEMBL13767380 1.00 BTK (0.43) BTKGAAEPHX1EPHX2NFKB1
SCHEMBL30111928 1.00 BTK (0.43) BTKGAAEPHX1EPHX2NFKB1
SCHEMBL2490017 1.00 BTK (0.43) BTKGAAEPHX1EPHX2NFKB1
SCHEMBL2180252 1.00 BTK (0.43) BTKGAAEPHX1EPHX2NFKB1
SCHEMBL2180246 1.00 BTK (0.43) BTKGAAEPHX1EPHX2NFKB1
Carbamic Acid SCHEMBL4770752 0.94 BTK (0.43) BTKGAAEPHX1EPHX2NFKB1
SCHEMBL4765504 0.92 BTK (0.42) BTKGAAEPHX1EPHX2NFKB1
SCHEMBL14040699 0.92 BTK (0.42) BTKGAAEPHX1EPHX2NFKB1
SCHEMBL14131624 0.92 BTK (0.42) BTKGAAEPHX1EPHX2NFKB1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12617782-B2 Pyridazinones as PARP7 inhibitors RIBON THERAPEUTICS, INC. (US) 2026-05-05 US disclosed
EP-4511368-A2 CCR4 ANTAGONISTS ChemoCentryx, Inc. (US) 2025-02-26 EP disclosed
US-20240174674-A1 NITROGEN-CONTAINING POLYCYCLIC FUSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND USE THEREOF APPLIED PHARMACEUTICAL SCIENCE, INC. (CN) 2024-05-30 US disclosed
CN-114907338-B Nitrogen-containing polycyclic condensed ring compound, pharmaceutical composition, preparation method and application thereof 北京志健金瑞生物医药科技有限公司 2024-02-06 CN disclosed
US-20240034728-A1 PYRIDAZINONES AS PARP7 INHIBITORS RIBON THERAPEUTICS, INC. 2024-02-01 US disclosed
EP-4289428-A1 NITROGEN-CONTAINING POLYCYCLIC FUSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND USE THEREOF Applied Pharmaceutical Science, Inc. (CN) 2023-12-13 EP disclosed
US-20230382894-A1 CCR4 ANTAGONISTS CHEMOCENTRYX, INC. 2023-11-30 US disclosed
WO-2023205618-A2 CCR4 ANTAGONISTS CHEMOCENTRYX, INC. (US) 2023-10-26 WO disclosed
US-11691969-B2 Pyridazinones as PARP7 inhibtors RIBON THERAPEUTICS, INC. (US) 2023-07-04 US disclosed
US-11648243-B2 Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors ARRAY BIOPHARMA INC. (US) 2023-05-16 US disclosed
US-20110172431-A1 PROCESS FOR PRODUCING 1-SUBSTITUTED TRANS-4-(SUBSTITUTED AMINO) PIPERIDIN-3-OL SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2011-07-14 US disclosed
US-20110166357-A1 METHOD FOR PRODUCING N-SUBSTITUTED-TRANS-4-AZIDOPIPERIDINE-3-OL SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2011-07-07 US disclosed
US-7803816-B2 MCH receptor antagonists HOFFMANN-LA ROCHE INC. (US) 2010-09-28 US disclosed
EP-1934199-B1 INDANE DERIVATIVES AS MCH RECEPTOR ANTAGONISTS HOFFMANN LA ROCHE (CH) 2009-04-22 EP disclosed
US-20070078165-A1 MCH receptor antagonists BERTHEL STEVEN J 2007-04-05 US disclosed
WO-2007016610-A2 ANTIBACTERIAL AGENTS GLAXO GROUP LIMITED (GB) 2007-02-08 WO disclosed
EP-1578743-A4 ANTIBACTERIAL AGENTS GLAXO GROUP LTD (GB) 2006-11-29 EP disclosed
US-20060041123-A1 Antibacterial agents GLAXO GROUP LIMITED (GB) 2006-02-23 US disclosed
EP-1578743-A2 ANTIBACTERIAL AGENTS GLAXO GROUP LIMITED (GB) 2005-09-28 EP disclosed
WO-2004058144-A2 ANTIBACTERIAL AGENTS GLAXO GROUP LIMITED (GB) 2004-07-15 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 (10 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-20230382894-A1 CCR4 ANTAGONISTS CCR4, CCR1, CCR3 BTK 3520/4885GAA 3231/4885EPHX1 1228/4885
US-20070078165-A1 MCH receptor antagonists MCHR1, MCHR2, MC5R BTK 4536/4885GAA 1229/4885EPHX1 2389/4885
US-11648243-B2 Substituted pyrazolo[1,5-A]pyridine compounds as RET kinase inhibitors RET, BRAF, RAF1 BTK 444/4885GAA 3183/4885EPHX1 1481/4885
US-12617782-B2 Pyridazinones as PARP7 inhibitors PARP3, PARP2, PARP1 BTK 2174/4885GAA 4352/4885EPHX1 2674/4885
US-20060041123-A1 Antibacterial agents NQO2, NRDC, IFNG BTK 3378/4885GAA 314/4885EPHX1 3422/4885
US-11691969-B2 Pyridazinones as PARP7 inhibtors PARP2, PARP1, PARP4 BTK 2100/4885GAA 3105/4885EPHX1 4220/4885
US-20110166357-A1 METHOD FOR PRODUCING N-SUBSTITUTED-TRANS-4-AZIDOPIPERIDINE-3-OL RPS27L, OSGEP, RPLP1 BTK 2044/4885GAA 1683/4885EPHX1 824/4885
US-20110172431-A1 PROCESS FOR PRODUCING 1-SUBSTITUTED TRANS-4-(SUBSTITUTED AMINO) PIPERIDIN-3-OL TEAD4, TEAD3, TEAD2 BTK 3125/4885GAA 2624/4885EPHX1 697/4885
US-20240174674-A1 NITROGEN-CONTAINING POLYCYCLIC FUSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND USE THEREOF RET, WEE1, JAK2 BTK 92/4885GAA 3924/4885EPHX1 2626/4885
US-20240034728-A1 PYRIDAZINONES AS PARP7 INHIBITORS PARP2, PARP1, PARP4 BTK 2308/4885GAA 3492/4885EPHX1 3302/4885

“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.