SCHEMBL154453

SCHEMBL154453

CC(C)(C)OC(=O)N1CCOCC1C(=O)O

nearest known ligand 0.50

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.50
USP2 O75604 1/20 0.50
HSD17B10 Q99714 1/20 0.47
RECQL P46063 1/20 0.44
FKBP1A P62942 1/20 0.41
CA12 O43570 1/20 0.38
CA1 P00915 1/20 0.38
CA2 P00918 1/20 0.38
CA9 Q16790 1/20 0.38
KLK7 P49862 1/20 0.36
NPC1 O15118 1/20 0.36
LMNA P02545 1/20 0.35
NPSR1 Q6W5P4 1/20 0.35
ATM Q13315 2/20 0.34

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
SCHEMBL186174 1.00 SMN1; SMN2 (0.50) SMN1; SMN2USP2HSD17B10RECQLFKBP1A
SCHEMBL185522 1.00 SMN1; SMN2 (0.50) SMN1; SMN2USP2HSD17B10RECQLFKBP1A
Ammonia Solution, Strong SCHEMBL28111366 0.98 SMN1; SMN2 (0.49) SMN1; SMN2USP2HSD17B10RECQLFKBP1A
SCHEMBL18555204 0.91 HSD17B10 (0.51) SMN1; SMN2USP2HSD17B10RECQLKLK7
SCHEMBL31148667 0.91 HSD17B10 (0.51) SMN1; SMN2USP2HSD17B10RECQLKLK7
SCHEMBL18555206 0.91 HSD17B10 (0.51) SMN1; SMN2USP2HSD17B10RECQLKLK7
SCHEMBL13804186 0.88 SMN1; SMN2 (0.50) SMN1; SMN2USP2HSD17B10RECQLCA12
SCHEMBL15116754 0.88 SMN1; SMN2 (0.50) SMN1; SMN2USP2HSD17B10RECQLCA12
SCHEMBL3511572 0.86 SMN1; SMN2 (0.49) SMN1; SMN2USP2HSD17B10RECQLCA12
SCHEMBL16359137 0.86 SMN1; SMN2 (0.49) SMN1; SMN2USP2HSD17B10RECQLCA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4059934-A1 COMPOUNDS AND COMPOSITIONS AS INHIBITORS OF ENDOSOMAL TOLL-LIKE RECEPTORS Novartis AG (CH) 2022-09-21 EP claimed
CN-111533708-B Preparation method of chiral N-tert-butoxycarbonylmorpholine-3-carboxylic acid 上海馨远医药科技有限公司 2021-03-16 CN claimed
CN-111533708-A Preparation method of chiral N-tert-butoxycarbonylmorpholine-3-carboxylic acid 上海馨远医药科技有限公司 2020-08-14 CN claimed
EP-1581525-A2 COMPOUNDS HAVING AN ACTIVITY AT METABOTROPIC GLUTAMATE RECEPTORS AstraZeneca AB (SE) 2005-10-05 EP claimed
US-20040106607-A1 New compounds ASTRAZENECA AB AND NPS PHARMACEUTICALS, INC. 2004-06-03 US claimed
WO-2004014902-A2 COMPOUNDS HAVING AN ACTIVITY AT METABOTROPIC GLUTAMATE RECEPTORS ASTRAZENECA AB (SE) 2004-02-19 WO claimed
WO-2026102082-A1 ALKYLPHENYL SUBSTITUTED COMPOUNDS, COMPOSITIONS AND METHODS OF USE DEEP APPLE THERAPEUTICS, INC. (US) 2026-05-15 WO disclosed
US-20260132119-A1 Alkylphenyl Substituted Compounds, Compositions and Methods of Use DEEP APPLE THERAPEUTICS, INC. (US) 2026-05-14 US disclosed
EP-4463455-B1 HETEROALICYCLIC DERIVATIVES AND THEIR USE IN THE TREATMENT OF CNS DISORDERS SUVEN LIFE SCIENCES LTD (IN) 2026-04-29 EP disclosed
EP-4558507-B1 MACROCYCLE COMPOUNDS FOR THE TREATMENT OF CANCER HOFFMANN LA ROCHE (CH) 2026-04-29 EP disclosed
EP-4731626-A1 PI3K INHIBITORS AND USE THEREOF Regor Pharmaceuticals, Inc. (US) 2026-04-29 EP disclosed
US-20260049054-A1 NOVEL POTASSIUM CHANNEL INHIBITORS SANIONA AS (DK) 2026-02-19 US disclosed
US-20260015313-A1 AMINO ACID ACTIVE ESTER AND SALT THEREOF PEPTIDREAM INC (JP) 2026-01-15 US disclosed
US-20030004137-A1 N-heterocyclic derivatives as NOS inhibitors BERLEX LABORATORIES, INC. (US) 2003-01-02 US disclosed
US-20020183323-A1 N-heterocyclic derivatives as NOS inhibitors BERLEX LABORATORIES, INC. 2002-12-05 US disclosed
US-20020165203-A1 N-heterocyclic derivatives as NOS inhibitors BERLEX LABORATORIES, INC. 2002-11-07 US disclosed
US-6432947-B1 NERVOUS SYSTEM DISORDERS; MUSCLE RELAXANTS; ANTIDIABETIC AGENTS BERLEX LABORATORIES, INC. 2002-08-13 US disclosed
CN-1252799-A N-heterocyclic derivatives as NOS inhibitor BERLEX LAB (US) 2000-05-10 CN disclosed
EP-0968206-A1 N-HETEROCYCLIC DERIVATIVES AS NOS INHIBITORS BERLEX LABORATORIES, INC. (US) 2000-01-05 EP disclosed
WO-1998037079-A1 N-HETEROCYCLIC DERIVATIVES AS NOS INHIBITORS BERLEX LABORATORIES, INC. (US) 1998-08-27 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-20030004137-A1 N-heterocyclic derivatives as NOS inhibitors NOS1, NOS2, NOS3 SMN1; SMN2 2568/4885USP2 1630/4885HSD17B10 334/4885
US-20260015313-A1 AMINO ACID ACTIVE ESTER AND SALT THEREOF NSUN3, BCAT1, SLC43A1 SMN1; SMN2 1555/4885USP2 4448/4885HSD17B10 1075/4885
US-20040106607-A1 New compounds MTX1, MLX, TPX2 SMN1; SMN2 2508/4885USP2 4226/4885HSD17B10 3279/4885
US-20020165203-A1 N-heterocyclic derivatives as NOS inhibitors NOS1, NOS2, NOS3 SMN1; SMN2 2568/4885USP2 1630/4885HSD17B10 334/4885
US-20260049054-A1 NOVEL POTASSIUM CHANNEL INHIBITORS SCN10A, KCNK10, KCNJ2 SMN1; SMN2 3226/4885USP2 4447/4885HSD17B10 1259/4885
US-20260132119-A1 Alkylphenyl Substituted Compounds, Compositions and Methods of Use GIPR, MC2R, GRPR SMN1; SMN2 881/4885USP2 3255/4885HSD17B10 1168/4885
US-20020183323-A1 N-heterocyclic derivatives as NOS inhibitors NOS1, NOS2, NOS3 SMN1; SMN2 2568/4885USP2 1630/4885HSD17B10 334/4885

“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.