SCHEMBL264362

SCHEMBL264362

CC(C)(C)OC(=O)N[C@H](C(=O)O)c1ccccc1

nearest known ligand 0.66

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
CTSK P43235 3/20 0.66
CTSS P25774 2/20 0.66
ATM Q13315 3/20 0.52
GABRB1 P18505 1/20 0.48
GABRB2 P47870 1/20 0.48
MAPT P10636 1/20 0.48
PPARA Q07869 5/20 0.48
PPARG P37231 4/20 0.48
S1PR3 Q99500 1/20 0.47
ACE P12821 1/20 0.47
PPARD Q03181 2/20 0.46

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
SCHEMBL116386 1.00 CTSK (0.66) CTSKCTSSATMGABRB1GABRB2
SCHEMBL525862 1.00 CTSK (0.66) CTSKCTSSATMGABRB1GABRB2
Hydrochloric Acid SCHEMBL28350663 0.98 CTSK (0.64) CTSKCTSSATMGABRB1GABRB2
Bromide SCHEMBL8184293 0.98 CTSK (0.64) CTSKCTSSATMGABRB1GABRB2
SCHEMBL15671568 0.94 CTSK (0.67) CTSKCTSSATMGABRB1GABRB2
SCHEMBL15671569 0.94 CTSK (0.67) CTSKCTSSATMGABRB1GABRB2
SCHEMBL3759870 0.91 CTSK (0.56) CTSKCTSSATMPPARAPPARG
SCHEMBL27158950 0.91 CTSK (0.56) CTSKCTSSATMPPARAPPARG
SCHEMBL16171655 0.90 CTSK (0.66) CTSKCTSSATMGABRB1GABRB2
SCHEMBL16174111 0.90 CTSK (0.66) CTSKCTSSATMGABRB1GABRB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112500361-B Preparation method of (S) -4-phenyl-2-oxazolidinone 甘肃瀚聚药业有限公司 2023-05-12 CN claimed
CN-114085201-A Preparation method of chiral bicyclic gamma-butyrolactone compound 山东第一医科大学(山东省医学科学院) 2022-02-25 CN claimed
US-20090036679-A1 METHOD FOR RESOLVING ENANTIOMERS FROM RACEMIC MIXTURE HAVING CHIRAL CARBON IN ALPHA POSITION OF NITROGEN CHONG KUN DANG PHARMACEUTICAL CORP. (KR) 2009-02-05 US claimed
EP-1984358-A1 METHOD FOR RESOLVING ENANTIOMERS FROM RACEMIC MIXTURE HAVING CHIRAL CARBON IN ALPHA POSITION OF NITROGEN Chong Kun Dang Pharmaceutical Corp. (KR) 2008-10-29 EP claimed
WO-2007091753-A1 METHOD FOR RESOLVING ENANTIOMERS FROM RACEMIC MIXTURE HAVING CHIRAL CARBON IN ALPHA POSITION OF NITROGEN CHONG KUN DANG PHARMACEUTICAL CORP. (KR) 2007-08-16 WO claimed
EP-4702033-A1 DESMURAMYLPEPTIDE DIACIDS AS NOD2 AGONISTS AND USE THEREOF Imhotex Limited (GB) 2026-03-04 EP disclosed
US-20260000781-A1 FC CONJUGATES INCLUDING AN INHIBITOR OF CD73 AND USES THEREOF CIDARA THERAPEUTICS INC (US) 2026-01-01 US disclosed
US-20250388544-A1 HETEROAROMATIC INHIBITORS OF ASTACIN PROTEINASES VIVORYON THERAPEUTICS N.V. (DE) 2025-12-25 US disclosed
EP-4662204-A2 TELOMERASE INHIBITOR COMPOUNDS Geron Corporation (US) 2025-12-17 EP disclosed
WO-2025243042-A1 COMPOUNDS FOR THE INHIBITION OF CYCLOPHILIN D THE UNIVERSITY OF LIVERPOOL (GB) 2025-11-27 WO disclosed
EP-4651872-A1 COMPOUNDS, COMPOSITIONS AND METHODS OF USE TO TREAT HYPOPARATHYROIDISM AND OSTEOPOROSIS Septerna, Inc. (US) 2025-11-26 EP disclosed
US-12435181-B2 Formulations capable of reacting with or removal of molecular oxygen LI SHENSHEN (US) 2025-10-07 US disclosed
US-4172832-A Mercaptoalcohols and process for their manufacture CIBA-GEIGY CORPORATION (US) 1979-10-30 US disclosed
EP-0004134-A1 Beta-lactam antibacterial agents, their pharmaceutical compositions and process for their preparation BEECHAM GROUP PLC (GB) 1979-09-19 EP disclosed
US-4112086-A BACTERICIDE SMITHKLINE CORPORATION (US) 1978-09-05 US disclosed
US-4108992-A BACTERICIDES BEECHAM GROUP LIMITED (GB) 1978-08-22 US disclosed
US-4101656-A 7β-Acylamino-3-(alkanesulfonamidoalkyl substituted tetrazolylthiomethyl) cephalosporins, antibacterial compositions containing them and methods of treating bacterial infections with them SMITHKLINE CORPORATION (US) 1978-07-18 US disclosed
US-4013650-A PROCESS FOR THE MANUFACTURE OF 3-METHYLENE-CEPHAM COMPOUNDS CIBA-GEIGY CORPORATION (US) 1977-03-22 US disclosed
US-3989695-A 7β-Amino-cepham-3-ol-4-carboxylic acid compounds CIBA-GEIGY CORPORATION (US) 1976-11-02 US disclosed
US-3968226-A 3-Heterocyclic thiomethylcephalosporins as antibacterial agents SMITHKLINE CORPORATION (US) 1976-07-06 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 (3 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-20250388544-A1 HETEROAROMATIC INHIBITORS OF ASTACIN PROTEINASES BMP1, BMPR1A, BMPR1B CTSK 319/4885CTSS 254/4885ATM 4630/4885
US-20090036679-A1 METHOD FOR RESOLVING ENANTIOMERS FROM RACEMIC MIXTURE HAVING CHIRAL CARBON IN ALPHA POSITION OF NITROGEN SRR, NPEPPS, DNPEP CTSK 2431/4885CTSS 898/4885ATM 4636/4885
US-20260000781-A1 FC CONJUGATES INCLUDING AN INHIBITOR OF CD73 AND USES THEREOF FCGR2A, FCGR1A, FCGR3B CTSK 2406/4885CTSS 1555/4885ATM 4379/4885

“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.