SCHEMBL4110433

SCHEMBL4110433

CC(=O)N[C@@H]1[C@@H](OC(C)=O)[C@H](OC(C)=O)[C@@H](COC(C)=O)O[C@H]1N

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 3/20 0.56
▸ KMT2A Q03164 1/20 0.56
▸ POLB P06746 2/20 0.55
▸ ALDH1A1 P00352 2/20 0.55
▸ CA1 P00915 9/20 0.52
▸ CA2 P00918 9/20 0.52
▸ CA9 Q16790 9/20 0.52
▸ CA12 O43570 8/20 0.52
▸ CYP3A4 P08684 1/20 0.48
▸ MAPT P10636 1/20 0.48
▸ CYP2C9 P11712 1/20 0.48
▸ CYP2C19 P33261 1/20 0.48
▸ CYP2D6 P10635 1/20 0.48
▸ THRB P10828 1/20 0.48
▸ HSD17B10 Q99714 1/20 0.48
▸ TSHR P16473 1/20 0.47
▸ NR3C1 P04150 1/20 0.47
▸ FYN P06241 1/20 0.47
▸ ADRA2A P08913 1/20 0.47
▸ ADORA3 P0DMS8 1/20 0.47

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
SCHEMBL14401482 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL14302583 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL4110436 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL7899944 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL16340705 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL15165006 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL15910017 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL13903997 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL8747631 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1
SCHEMBL7899946 1.00 LMNA (0.56) LMNAKMT2APOLBALDH1A1CA1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6462183-B1 SOLID PHASE OLIGOSACCHARIDE SYNTHESIS ALCHEMIA PTY LTD (AU) 2002-10-08 — — US claimed
US-20240016828-A1 INHIBITION OF NGLY1 FOR THE TREATMENT OF CANCER UNIVERSITY OF NORTH TEXAS HEALTH SCIENCE CENTER (US) 2024-01-18 — — US disclosed
US-20240016828-A1 INHIBITION OF NGLY1 FOR THE TREATMENT OF CANCER UNIVERSITY OF NORTH TEXAS HEALTH SCIENCE CENTER (US) 2024-01-18 — — US disclosed
US-20240016828-A1 INHIBITION OF NGLY1 FOR THE TREATMENT OF CANCER UNIVERSITY OF NORTH TEXAS HEALTH SCIENCE CENTER (US) 2024-01-18 — — US disclosed
US-11779592-B2 Inhibition of NGLY1 for the treatment of cancer UNIVERSITY OF NORTH TEXAS HEALTH SCIENCE CENTER (US) 2023-10-10 — — US disclosed
US-11779592-B2 Inhibition of NGLY1 for the treatment of cancer UNIVERSITY OF NORTH TEXAS HEALTH SCIENCE CENTER (US) 2023-10-10 — — US disclosed
US-11779592-B2 Inhibition of NGLY1 for the treatment of cancer UNIVERSITY OF NORTH TEXAS HEALTH SCIENCE CENTER (US) 2023-10-10 — — US disclosed
US-20230272002-A1 PHOTOREDOX PROTEIN MODIFICATION THE ROSALIND FRANKLIN INSTITUTE (GB) 2023-08-31 — — US disclosed
EP-4182327-A1 PHOTOREDOX PROTEIN MODIFICATION The Rosalind Franklin Institute (GB) 2023-05-24 — — EP disclosed
WO-2023011597-A1 LIGAND CONJUGATES FOR DELIVERY OF THERAPEUTICALLY ACTIVE AGENTS Hepagene Therapeutics (HK) Limited (CN) 2023-02-09 — — WO disclosed
US-5556941-A ANTICOAGULANTS, THROMBIN INHIBITORS BEHRINGWERKE AKTIENGESELLSCHAFT (DE) 1996-09-17 — — US disclosed
US-5543514-A Water-soluble sapphyrins BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1996-08-06 — — US disclosed
US-5530123-A ANTIVIRAL AND CHEMOTHERAPEUTICAL AGENT FOR CANCER BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1996-06-25 — — US disclosed
US-5457195-A Sapphyrin derivatives and conjugates BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1995-10-10 — — US disclosed
EP-0413675-B1 Method for producing synthetic N-linked glycoconjugates MONSANTO CO (US) 1995-05-03 — — EP disclosed
WO-1994009003-A1 SAPPHYRIN DERIVATIVES, CONJUGATES AND POLYMERS THEREOF AND EXPANDED PORPHYRIN CHROMATOGRAPHIC SUPPORTS BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1994-04-28 — — WO disclosed
EP-0558961-A2 Glycopeptide derivatives, process for their manufacture and pharmaceutical compositions comprising them BEHRINGWERKE Aktiengesellschaft (DE) 1993-09-08 — — EP disclosed
US-5091523-A Bactericides, antitumor agent GEORGETOWN UNIVERSITY (US) 1992-02-25 — — US disclosed
US-4280953-A Glycosylated analogs of somatostatin THE SALK INSTITUTE FOR BIOLOGICAL STUDIES (US) 1981-07-28 — — US disclosed
US-4157439-A ANTITUMOR, LOW TOXICITY, NONHYDROLYZING SUAMI T (JP) 1979-06-05 — — 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-20230272002-A1 PHOTOREDOX PROTEIN MODIFICATION PPOX, CACYBP, BRI3BP LMNA 4279/4885KMT2A 3404/4885POLB 3843/4885
US-11779592-B2 Inhibition of NGLY1 for the treatment of cancer NGLY1, GALNT1, GALNT10 LMNA 2369/4885KMT2A 4129/4885POLB 3957/4885
US-20240016828-A1 INHIBITION OF NGLY1 FOR THE TREATMENT OF CANCER NGLY1, GALNT1, GALNT10 LMNA 2401/4885KMT2A 3992/4885POLB 4014/4885

“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.

Send feedback