SCHEMBL2196928

SCHEMBL2196928

CC(O)C(N)c1ccccc1

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DPP4 P27487 2/20 0.62
ADRA2C P18825 2/20 0.60
KDM4E B2RXH2 2/20 0.60
LMNA P02545 2/20 0.60
ADRA2A P08913 1/20 0.60
HIF1A Q16665 1/20 0.60
ALDH1A1 P00352 2/20 0.58
F2 P00734 1/20 0.48
AOC3 Q16853 2/20 0.47
CHRM2 P08172 1/20 0.45
ADRA1A P35348 1/20 0.45
RGS12 O14924 1/20 0.45
GLA P06280 1/20 0.45
CYP3A4 P08684 1/20 0.45
CYP2D6 P10635 1/20 0.45
CYP2C9 P11712 1/20 0.45
PKM P14618 1/20 0.45
ALOX15 P16050 1/20 0.45
TSHR P16473 1/20 0.45
ALOX12 P18054 1/20 0.45

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
SCHEMBL1335056 1.00 DPP4 (0.62) DPP4ADRA2CKDM4ELMNAADRA2A
SCHEMBL516556 1.00 DPP4 (0.62) DPP4ADRA2CKDM4ELMNAADRA2A
SCHEMBL8651376 1.00 DPP4 (0.62) DPP4ADRA2CKDM4ELMNAADRA2A
SCHEMBL12069803 1.00 DPP4 (0.62) DPP4ADRA2CKDM4ELMNAADRA2A
SCHEMBL14440005 1.00 DPP4 (0.62) DPP4ADRA2CKDM4ELMNAADRA2A
SCHEMBL16847208 1.00 DPP4 (0.62) DPP4ADRA2CKDM4ELMNAADRA2A
Hydrochloric Acid SCHEMBL520233 0.98 ALDH1A1 (0.61) DPP4ADRA2CKDM4ELMNAADRA2A
Hydrochloric Acid SCHEMBL520234 0.98 ALDH1A1 (0.61) DPP4ADRA2CKDM4ELMNAADRA2A
Hydrochloric Acid SCHEMBL3589482 0.98 ALDH1A1 (0.61) DPP4ADRA2CKDM4ELMNAADRA2A
Hydrochloric Acid SCHEMBL18765989 0.98 ALDH1A1 (0.61) DPP4ADRA2CKDM4ELMNAADRA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1659154-B Process for the preparation of amine stereoisomers APSINTERM LLC 2012-05-30 CN claimed
CN-101193869-A Glucocortioid mimetics, methods of making them, pharmaceutical compositions, and uses thereof BOEHRINGER INGELHEIM PHARMA (DE) 2008-06-04 CN claimed
EP-1497272-A4 METHOD OF PREPARING AMINE STEREOISOMERS APSINTERM LLC (US) 2007-02-07 EP claimed
CN-1659154-A Process for the preparation of amine stereoisomers APSINTERM LLC (US) 2005-08-24 CN claimed
US-20050165240-A1 Method of preparing amine stereoisomers APSINTERM, LLC 2005-07-28 US claimed
EP-1497272-A2 METHOD OF PREPARING AMINE STEREOISOMERS Apsinterm, LLC. (US) 2005-01-19 EP claimed
WO-2003091207-A2 METHOD OF PREPARING AMINE STEREOISOMERS APSINTERM, LLC. (US) 2003-11-06 WO claimed
WO-2026104834-A1 USE OF A NITROGEN CONTAINING COMPOUND WITH INCREASED WATER REPELLENCY, REDUCED FRICTION, OR IMPROVED VISUAL APPEARANCE, METHOD OF TREATING A SURFACE, COMPOSITION AND TREATED SUBSTRATE INNOSPEC LIMITED (GB) 2026-05-21 WO disclosed
WO-2026104847-A1 USES AND COMPOSITIONS COMPRISING POLYAMIDES INNOSPEC LIMITED (GB) 2026-05-21 WO disclosed
WO-2026104838-A1 POLYAMIDES AND CONCENTRATE COMPOSITIONS COMPRISING THE POLYAMIDES INNOSPEC LIMITED (GB) 2026-05-21 WO disclosed
US-20260078098-A1 PROCESS OF MAKING DERIVATIVES OF SUBSTITUTED MORPHOLINES SUPERNUS PHARMACEUTICALS, INC. (US) 2026-03-19 US disclosed
CN-114948963-B Benzolactam compounds as protein kinase inhibitors 大冢制药株式会社 2025-05-27 CN disclosed
US-20250109343-A1 CORROSION INHIBITOR INNOSPEC LIMITED (GB) 2025-04-03 US disclosed
EP-0222694-A2 Microbicides CIBA-GEIGY AG (CH) 1987-05-20 EP disclosed
US-4639478-A Bismorpholines, a process for their preparation and their use for protection against hydrolysis BAYER AKTIENGESELLSCHAFT (DE) 1987-01-27 US disclosed
US-4617387-A REACTING GLYOXAL WITH AN N-SUBSTITUTED AMINO ALCOHOL BAYER AKTIENGESELLSCHAFT (DE) 1986-10-14 US disclosed
EP-0137251-A2 Bismorpholines, process for their preparation and their use as anti-hydrolysis agents BAYER AG (DE) 1985-04-17 EP disclosed
US-4311840-A ANTIINFLAMMATORY AGENTS E. R. SQUIBB & SONS, INC. (US) 1982-01-19 US disclosed
US-4251660-A Method for preparing tetrahydroisoquinolines SMITHKLINE CORPORATION (US) 1981-02-17 US disclosed
US-4146560-A HYDROGENATION; COPPER-COBALT-CHROMIUM CATALYST TEXACO DEVELOPMENT CORP. (US) 1979-03-27 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 (2 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-20050165240-A1 Method of preparing amine stereoisomers SRM, TST, SMOX DPP4 4826/4885ADRA2C 817/4885KDM4E 2935/4885
US-20260078098-A1 PROCESS OF MAKING DERIVATIVES OF SUBSTITUTED MORPHOLINES HTR2C, SLC6A2, HTR1D DPP4 3132/4885ADRA2C 37/4885KDM4E 970/4885

“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.