SCHEMBL473047

SCHEMBL473047

CC1(C)OC(=O)[C@@H](CC(=O)O)O1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
GLS O94925 1/20 0.47
APEX1 P27695 1/20 0.37
KDM4E B2RXH2 2/20 0.32
TSHR P16473 1/20 0.32
HTT P42858 1/20 0.32
ATM Q13315 1/20 0.32
CYP1A2 P05177 1/20 0.32
CYP2D6 P10635 1/20 0.32
CYP2C9 P11712 1/20 0.32
CYP2C19 P33261 1/20 0.32
HPGD P15428 1/20 0.31
SMN1; SMN2 Q16637 1/20 0.31
BACE1 P56817 1/20 0.31
KMT2A Q03164 1/20 0.31
ITGB3 P05106 1/20 0.31
ITGB2 P05107 1/20 0.31
ITGB1 P05556 1/20 0.31
ITGAV P06756 1/20 0.31
ITGA2B P08514 1/20 0.31
ITGA5 P08648 1/20 0.31

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
SCHEMBL1005092 1.00 GLS (0.47) GLSAPEX1KDM4ETSHRHTT
SCHEMBL200462 1.00 GLS (0.47) GLSAPEX1KDM4ETSHRHTT
Biphenyl SCHEMBL7177377 0.89 GLS (0.41) GLSAPEX1KDM4ETSHRHTT
SCHEMBL9460988 0.86 GLS (0.46) GLS
SCHEMBL18218788 0.85 GLS (0.47) GLSHTTSMN1; SMN2BACE1
SCHEMBL18914987 0.85 GLS (0.47) GLSKDM4EBACE1
SCHEMBL18219056 0.85 GLS (0.47) GLSHTTSMN1; SMN2BACE1
SCHEMBL23296774 0.83 GLS (0.46) GLSBACE1
SCHEMBL183678 0.83 GLS (0.46) GLSBACE1
SCHEMBL2280018 0.83 GLS (0.46) GLSBACE1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108864148-B Rapamycin-40-malic acid sodium salt and preparation method and application thereof 福建省微生物研究所 2021-09-03 CN claimed
US-20260116913-A1 NEUROSTEROID COMPOUNDS AND METHODS FOR THEIR PREPARATION AND USE IN TREATING CENTRAL NERVOUS SYSTEM DISORDERS TEXAS A & M UNIV SYS (US) 2026-04-30 US disclosed
US-12509487-B2 Neurosteroid compounds and methods for their preparation and use in treating central nervous system disorders THE TEXAS A&M UNIVERSITY SYSTEM (US) 2025-12-30 US disclosed
WO-2025037940-A1 PYRAZOLE-1-CARBOXAMIDES AS RIP1 KINASE INHIBITORS BISICHEM CO., LTD. (KR) 2025-02-20 WO disclosed
WO-2023134629-A1 NUCLEAR TRANSPORT REGULATOR AND USE THEREOF 上海海雁医药科技有限公司 2023-07-20 WO disclosed
WO-2023134629-A1 NUCLEAR TRANSPORT REGULATOR AND USE THEREOF 上海海雁医药科技有限公司 2023-07-20 WO disclosed
US-20230151052-A1 NEUROSTEROID COMPOUNDS AND METHODS FOR THEIR PREPARATION AND USE IN TREATING CENTRAL NERVOUS SYSTEM DISORDERS THE TEXAS A&M UNIVERSITY SYSTEM 2023-05-18 US disclosed
US-11542296-B2 Neurosteroid compounds and methods for their preparation and use in treating central nervous system disorders THE TEXAS A&M UNIVERSITY SYSTEM (US) 2023-01-03 US disclosed
CN-108785305-B Heterocyclic inhibitors of glutaminase 卡利泰拉生物科技公司 2021-10-29 CN disclosed
CN-108864148-B Rapamycin-40-malic acid sodium salt and preparation method and application thereof 福建省微生物研究所 2021-09-03 CN disclosed
US-20020143186-A1 Glucagon antagonists/inverse agonists PFIZER INC 2002-10-03 US disclosed
US-6359061-B1 COMBINATORIAL LIBRARIES ARE USEFUL FOR SCREENING IN BIOLOGCAL ASSAYS IN ORDER TO IDENTIFY PHARMACEUTICALLY USEFUL COMPOUNDS ISIS PHARMACEUTICALS, INC. 2002-03-19 US disclosed
EP-1183091-A1 OPTIMIZATION OF LIGAND AFFINITY FOR RNA TARGETS USING MASS SPECTROMETRY ISIS PHARMACEUTICALS, INC. (US) 2002-03-06 EP disclosed
WO-2002000612-A1 GLUCAGON ANTAGONISTS/INVERSE AGONISTS NOVO NORDISK A/S (DK) 2002-01-03 WO disclosed
US-6316623-B1 USEFUL FOR SCREENING IN BIOLOGICAL ASSAYS IN ORDER TO IDENTIFY PHARMACEUTICALLY USEFUL COMPOUNDS ISIS PHARMACEUTICALS, INC. 2001-11-13 US disclosed
WO-2001058573-A1 OPTIMIZATION OF LIGAND AFFINITY FOR RNA TARGETS USING MASS SPECTROMETRY ISIS PHARMACEUTICALS, INC. (US) 2001-08-16 WO disclosed
EP-1091958-A1 SALTS OF PAROXETINE SMITHKLINE BEECHAM PLC (GB) 2001-04-18 EP disclosed
EP-1082323-A2 OXAZOLIDINONE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM AstraZeneca UK Limited (GB) 2001-03-14 EP disclosed
WO-2000001692-A1 SALTS OF PAROXETINE SMITHKLINE BEECHAM PLC (GB) 2000-01-13 WO disclosed
WO-1999064417-A2 OXAZOLIDINONE DERIVATIVES, PROCESS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM ASTRAZENECA AB (SE) 1999-12-16 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 (5 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-20230151052-A1 NEUROSTEROID COMPOUNDS AND METHODS FOR THEIR PREPARATION AND USE IN TREATING CENTRAL NERVOUS SYSTEM DISORDERS CYP11B2, CYP21A2, CYP11B1 GLS 624/4885APEX1 3945/4885KDM4E 4509/4885
US-12509487-B2 Neurosteroid compounds and methods for their preparation and use in treating central nervous system disorders SLC6A11, GABRE, SLC6A13 GLS 1422/4885APEX1 4847/4885KDM4E 2859/4885
US-20260116913-A1 NEUROSTEROID COMPOUNDS AND METHODS FOR THEIR PREPARATION AND USE IN TREATING CENTRAL NERVOUS SYSTEM DISORDERS CHRNA9, HSD3B2, HSD3B1 GLS 2814/4885APEX1 3944/4885KDM4E 2002/4885
US-11542296-B2 Neurosteroid compounds and methods for their preparation and use in treating central nervous system disorders CYP11B2, CYP21A2, CYP11B1 GLS 624/4885APEX1 3945/4885KDM4E 4509/4885
US-20020143186-A1 Glucagon antagonists/inverse agonists GLP1R, GPR119, GCGR GLS 236/4885APEX1 3309/4885KDM4E 3671/4885

“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.