SCHEMBL86228

SCHEMBL86228

CC(C)(C)OC(=O)N1CCC[C@H]1CCN

nearest known ligand 0.48

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
HSD17B10 Q99714 1/20 0.46
ATM Q13315 2/20 0.46
SMN1; SMN2 Q16637 1/20 0.43
PDE8B O95263 1/20 0.43
ALDH1A1 P00352 1/20 0.43
CHEK2 O96017 1/20 0.42
NPC1 O15118 1/20 0.41
OPRD1 P41143 1/20 0.41
ALOX5AP P20292 1/20 0.40
FEN1 P39748 1/20 0.40
TSHR P16473 1/20 0.40

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
SCHEMBL1427736 1.00 HSD17B10 (0.46) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL1061613 1.00 HSD17B10 (0.46) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL23015233 0.95 PDE8B (0.47) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL1009587 0.95 PDE8B (0.47) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL31037649 0.95 PDE8B (0.47) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL3815408 0.91 ATM (0.44) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL6345733 0.91 ATM (0.44) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL7923096 0.91 ATM (0.42) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL31420888 0.91 ATM (0.42) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1
SCHEMBL4574708 0.91 ATM (0.42) HSD17B10ATMSMN1; SMN2PDE8BALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250129021-A1 SMALL MOLECULE PROTEIN SYNTHESIS MODULATORS Interdict Bio, Inc. (US) 2025-04-24 US disclosed
WO-2025064718-A1 SMALL MOLECULE PROTEIN SYNTHESIS MODULATORS Interdict Bio, Inc. (US) 2025-03-27 WO disclosed
US-20250034200-A1 Prodrugs of Neurosteroid Analogs and Uses Thereof UNIV EMORY (US) 2025-01-30 US disclosed
CN-115894447-B METTL3 inhibitors and uses thereof 成都先导药物开发股份有限公司 2024-10-01 CN disclosed
WO-2023086438-A1 PRODRUGS OF NEUROSTEROID ANALOGS AND USES THEREOF EMORY UNIVERSITY (US) 2023-05-19 WO disclosed
CN-115894447-A METTL3 inhibitors and uses thereof 成都先导药物开发股份有限公司 2023-04-04 CN disclosed
EP-3045206-B2 POLYCYCLIC CARBAMOYLPYRIDONE DERIVATIVE HAVING HIV INTEGRASE INHIBITORY ACTIVITY VIIV HEALTHCARE CO (US) 2023-02-15 EP disclosed
US-20220213121-A1 SUBSTITUTED 1,2,3,3a,4,5,7,9,13,13a-DECAHYDROPYRIDO[1',2':4,5]PYRAZINO[1,2-a]PYRROLO[1,2-c]PYRIMIDINES HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO., LTD. (JP) 2022-07-07 US disclosed
CN-114340616-A Pyrazole and imidazole derivatives as orexin antagonists, compositions and methods 海格生物科学有限责任公司 2022-04-12 CN disclosed
CN-110204537-B 1,2, 5-oxadiazole derivatives as inhibitors of indoleamine 2, 3-dioxygenase 盛世泰科生物医药技术(苏州)有限公司 2021-10-08 CN disclosed
US-20070225270-A1 Pyrazolopyrimidines as cyclin dependent kinase inhibitors SCHERING CORPORATION 2007-09-27 US disclosed
US-7196078-B2 Trisubstituted and tetrasubstituted pyrazolopyrimidines as cyclin dependent kinase inhibitors SCHERING CORPOARTION (US) 2007-03-27 US disclosed
US-6878736-B1 Histamine H3 receptor ligands JAMES BLACK FOUNDATION LIMITED (GB) 2005-04-12 US disclosed
US-6806279-B2 FOR THERAPY OF AUTOIMMUNE DISEASES SUCH AS RHEUMATOID ARTHRITIS, MULTIPLE SCLEROSIS, UVEITIS, AND PSORIASIS, ALLOGRAFT REJECTION, AND GRAFT-VERSUS-HOST DISEASE SUNESIS PHARMACEUTICALS, INC. 2004-10-19 US disclosed
US-20040167128-A1 Sulfonamides having antiangiogenic and anticancer activity ABBVIE INC. 2004-08-26 US disclosed
US-20040157836-A1 Sulfonamides having antiangiogenic and anticancer activity ABBOTT LABORATORIES 2004-08-12 US disclosed
US-20030149049-A1 Small-molecule inhibitors of interleukin-2 SUNESIS PHARMACEUTICALS, INC. 2003-08-07 US disclosed
WO-2003051797-A2 SMALL-MOLECULE INHIBITORS OF INTERLEUKIN-2 SUNESIS PHARMACEUTICALS, INC. (US) 2003-06-26 WO disclosed
EP-1056733-A1 HISTAMINE H3 RECEPTOR LIGANDS JAMES BLACK FOUNDATION LIMITED (GB) 2000-12-06 EP disclosed
WO-1999042458-A1 HISTAMINE H3 RECEPTOR LIGANDS JAMES BLACK FOUNDATION LIMITED (GB) 1999-08-26 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 (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-20070225270-A1 Pyrazolopyrimidines as cyclin dependent kinase inhibitors CDK2, CDKN1A, CDK1 HSD17B10 4224/4885ATM 457/4885SMN1; SMN2 2284/4885
US-20220213121-A1 SUBSTITUTED 1,2,3,3a,4,5,7,9,13,13a-DECAHYDROPYRIDO[1',2':4,5]PYRAZINO[1,2-a]PYRROLO[1,2-c]PYRIMIDINES HAVING HIV INTEGRASE INHIBITORY ACTIVITY TYMP, TYMS, POLA1 HSD17B10 2403/4885ATM 4740/4885SMN1; SMN2 3758/4885
US-20040167128-A1 Sulfonamides having antiangiogenic and anticancer activity METAP2, METAP1, DNPEP HSD17B10 3758/4885ATM 2591/4885SMN1; SMN2 1949/4885
US-20250034200-A1 Prodrugs of Neurosteroid Analogs and Uses Thereof CYP11B2, CYP11B1, CYP21A2 HSD17B10 60/4885ATM 2713/4885SMN1; SMN2 708/4885
US-20030149049-A1 Small-molecule inhibitors of interleukin-2 IL2, IL2RA, HLA-DRB1 HSD17B10 2354/4885ATM 4790/4885SMN1; SMN2 3620/4885
US-20250129021-A1 SMALL MOLECULE PROTEIN SYNTHESIS MODULATORS MYC, KRAS, NRAS HSD17B10 3549/4885ATM 835/4885SMN1; SMN2 1576/4885
US-20040157836-A1 Sulfonamides having antiangiogenic and anticancer activity METAP2, METAP1, DNPEP HSD17B10 3758/4885ATM 2591/4885SMN1; SMN2 1949/4885

“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.