SCHEMBL11095014

SCHEMBL11095014

CC(C)C[C@H](NC(=O)[C@@H](O)[C@@H](Cc1ccccc1)NC(=O)OC(C)(C)C)C(=O)O

nearest known ligand 0.61

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
PSEN1 P49768 3/20 0.61
PSEN2 P49810 3/20 0.61
APH1B Q8WW43 3/20 0.61
NCSTN Q92542 3/20 0.61
APH1A Q96BI3 3/20 0.61
PSENEN Q9NZ42 3/20 0.61
APP P05067 1/20 0.61
MME P08473 2/20 0.56
REN P00797 5/20 0.56
KLK5 Q9Y337 1/20 0.53
MAPK1 P28482 1/20 0.53

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
SCHEMBL27041288 1.00 PSEN1 (0.61) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL23302438 1.00 PSEN1 (0.61) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL14725527 1.00 PSEN1 (0.61) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL28525267 0.93 REN (0.59) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL28525268 0.93 REN (0.59) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL28525265 0.93 REN (0.59) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL22393402 0.92 PSEN1 (0.67) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL17899496 0.91 PSEN1 (0.63) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL11089707 0.90 PSEN1 (0.61) PSEN1PSEN2APH1BNCSTNAPH1A
SCHEMBL20506597 0.90 PSEN1 (0.58) PSEN1PSEN2APH1BNCSTNAPH1A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4629981-A2 SMALL MOLECULE DEGRADERS OF C-SRC KINASE The Regents Of The University Of Michigan (US) 2025-10-15 EP claimed
WO-2024145315-A1 TARGETED PROTEIN DEGRADERS OF INDOLEAMINE 2,3-DIOXYGENASE 1 (IDO1) NORTHWESTERN UNIVERSITY (US) 2024-07-04 WO claimed
WO-2024123819-A2 SMALL MOLECULE DEGRADERS OF C-SRC KINASE THE REGENTS OF THE UNIVERSITY OF MICHIGAN (US) 2024-06-13 WO claimed
US-20220023431-A1 PROTEOLYSIS-TARGETING CHIMERIC MOLECULES (PROTACS) THAT INDUCE DEGRADATION OF INDOLEAMINE 2,3-DIOXYGENASE (IDO) PROTEIN NORTHWESTERN UNIVERSITY 2022-01-27 US claimed
US-20260131010-A1 MENIN PROTEOLYSIS TARGETING CHIMERAS (PROTACS) UNIV TEXAS (US) 2026-05-14 US disclosed
US-12492209-B2 Substituted [1,2,4]triazolo[4,3-c]pyrimidines that induce degradation of embryonic ectoderm development (EED) protein NORTHWESTERN UNIVERSITY (US) 2025-12-09 US disclosed
US-12491252-B2 Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 NORTHWESTERN UNIVERSITY (US) 2025-12-09 US disclosed
EP-4629981-A2 SMALL MOLECULE DEGRADERS OF C-SRC KINASE The Regents Of The University Of Michigan (US) 2025-10-15 EP disclosed
US-20250186434-A1 SOS1 PROTEIN DEGRADERS, PHARMACEUTICAL COMPOSITIONS THEREOF, AND THEIR THERAPEUTIC APPLICATIONS BIOTHERYX, INC. 2025-06-12 US disclosed
US-12311029-B2 Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of indoleamine 2,3-dioxygenase (IDO) protein NORTHWESTERN UNIVERSITY (US) 2025-05-27 US disclosed
US-20250049930-A1 PROTAC MOLECULES TARGETING FOXP3 AND USES THEREOF CEDARS-SINAI MEDICAL CENTER (US) 2025-02-13 US disclosed
EP-4460321-A2 PROTAC MOLECULES TARGETING FOXP3 AND USES THEREOF Cedars-Sinai Medical Center (US) 2024-11-13 EP disclosed
CN-112125951-A Impurities in ubenimex bulk drug and preparation method thereof 深圳万乐药业有限公司 2020-12-25 CN disclosed
US-20200276176-A1 COMPOUNDS FOR TARGETING MUTANT HUNTINGTIN PROTEIN AND USES THEREOF CHDI FOUNDATION, INC. 2020-09-03 US disclosed
US-20160193168-A1 Treatment of Pulmonary Arterial Hypertension with Leukotriene Inhibitors THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY 2016-07-07 US disclosed
US-9233089-B2 Treatment of pulmonary hypertension with leukotriene inhibitors THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2016-01-12 US disclosed
US-20130251787-A1 Treatment of Pulmonary Hypertension with Leukotriene Inhibitors THE BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY (US) 2013-09-26 US disclosed
US-4473554-A Bestatin-related compounds as immunopotentiator ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1984-09-25 US disclosed
EP-0083931-A2 New bestatin-related compounds as immunopotentiator ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1983-07-20 EP disclosed
US-4370318-A Bestatin-related compounds as immunopotentiator ZAIDAN HOJIN BISEIBUTSU KAGAKU KENKYU KAI (JP) 1983-01-25 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 (9 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-12311029-B2 Proteolysis-targeting chimeric molecules (PROTACs) that induce degradation of indoleamine 2,3-dioxygenase (IDO) protein IDO1, IDO2, KMO PSEN1 2467/4885PSEN2 2909/4885APH1B 1392/4885
US-20130251787-A1 Treatment of Pulmonary Hypertension with Leukotriene Inhibitors LTA4H, LTB4R2, LTB4R PSEN1 4500/4885PSEN2 4665/4885APH1B 4315/4885
US-20200276176-A1 COMPOUNDS FOR TARGETING MUTANT HUNTINGTIN PROTEIN AND USES THEREOF HTT, HYPK, UBQLN2 PSEN1 212/4885PSEN2 95/4885APH1B 445/4885
US-20260131010-A1 MENIN PROTEOLYSIS TARGETING CHIMERAS (PROTACS) CRBN, UBE3C, PSME3 PSEN1 705/4885PSEN2 755/4885APH1B 684/4885
US-12492209-B2 Substituted [1,2,4]triazolo[4,3-c]pyrimidines that induce degradation of embryonic ectoderm development (EED) protein EED, CUL3, PSME3 PSEN1 2007/4885PSEN2 2587/4885APH1B 1524/4885
US-20160193168-A1 Treatment of Pulmonary Arterial Hypertension with Leukotriene Inhibitors LTA4H, LTB4R2, LTB4R PSEN1 4502/4885PSEN2 4680/4885APH1B 4170/4885
US-20220023431-A1 PROTEOLYSIS-TARGETING CHIMERIC MOLECULES (PROTACS) THAT INDUCE DEGRADATION OF INDOLEAMINE 2,3-DIOXYGENASE (IDO) PROTEIN IDO1, IDO2, KMO PSEN1 2809/4885PSEN2 3170/4885APH1B 1816/4885
US-12491252-B2 Substituted 3-amino-5-phenylbenzamide compounds as covalent inhibitors of enhancer zeste homolog 2 (EZH2) and proteolysis-targeting chimeric derivatives thereof (PROTACs) that induce degradation of EZH2 EZH2, BAZ2A, BAZ2B PSEN1 1145/4885PSEN2 797/4885APH1B 1153/4885
US-20250186434-A1 SOS1 PROTEIN DEGRADERS, PHARMACEUTICAL COMPOSITIONS THEREOF, AND THEIR THERAPEUTIC APPLICATIONS SOS1, CUL1, SOS2 PSEN1 266/4885PSEN2 742/4885APH1B 1369/4885

“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.