SCHEMBL19897940

SCHEMBL19897940

N#Cc1cccc2[nH]cc(CC(N)C(=O)O)c12

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 4/20 0.58
KDM4E B2RXH2 4/20 0.58
MAPT P10636 4/20 0.58
MEN1 O00255 3/20 0.58
LMNA P02545 2/20 0.58
TSHR P16473 2/20 0.58
BLM P54132 2/20 0.58
PMP22 Q01453 2/20 0.58
MPO P05164 1/20 0.58
HIF1A Q16665 1/20 0.58
ALDH1A1 P00352 2/20 0.48
NPSR1 Q6W5P4 2/20 0.48
CYP3A4 P08684 1/20 0.48
HTR1A P08908 1/20 0.48
ADORA3 P0DMS8 1/20 0.48
ALOX15 P16050 1/20 0.48
NFKB1 P19838 1/20 0.48
HTR2A P28223 1/20 0.48
HTR2C P28335 1/20 0.48
SLC6A4 P31645 1/20 0.48

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
SCHEMBL30688366 1.00 KMT2A (0.58) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL19897942 1.00 KMT2A (0.58) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL18029006 0.87 KMT2A (0.58) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL18029332 0.87 KMT2A (0.58) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL24328916 0.86 SMN1; SMN2 (0.57) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL2286478 0.84 SCN9A (0.48) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL2286482 0.84 SCN9A (0.48) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL24328254 0.82 NR3C2 (0.47) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL18029267 0.81 KMT2A (0.68) KMT2AKDM4EMAPTMEN1LMNA
SCHEMBL1460641 0.81 KMT2A (0.68) KMT2AKDM4EMAPTMEN1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3759227-A1 IMPROVED METHOD FOR THE SYNTHESIS OF TRYPTOPHAN ANALOGS IN AQUEOUS SOLVENTS AT REDUCED TEMPERATURES California Institute of Technology (US) 2021-01-06 EP claimed
US-10752927-B2 Method for the synthesis of tryptophan analogs in aqueous solvents at reduced temperatures CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2020-08-25 US claimed
US-20190271016-A1 METHOD FOR THE SYNTHESIS OF TRYPTOPHAN ANALOGS IN AQUEOUS SOLVENTS AT REDUCED TEMPERATURES CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2019-09-05 US claimed
US-20260048134-A1 PEPTIDE-BASED DELIVERY AGENT AND METHOD OF MAKING AND USING THE SAME ENDOREL BIOSCIENCES LLC (US) 2026-02-19 US disclosed
US-20250382646-A1 ENGINEERED ENZYMES AND METHODS FOR THE SYNTHESIS OF DIVERSE TYROSINE ANALOGS CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2025-12-18 US disclosed
US-12421534-B2 Engineered enzymes and method for the synthesis of diverse tyrosine analogs CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2025-09-23 US disclosed
US-20250250569-A1 PEPTIDE-BASED DELIVERY AGENT WITH ASPARAGINE-CONTAINING MASK PEPTIDE GROUP AND METHOD OF MAKING AND USING THE SAME ENDOREL BIOSCIENCES LLC (US) 2025-08-07 US disclosed
WO-2025128626-A1 HYBRID PEPTIDE COMPOUNDS HAVING A MODIFIED LYSINE RESIDUE CARMOT THERAPEUTICS, INC. (US) 2025-06-19 WO disclosed
WO-2025128624-A2 HYBRID PEPTIDE COMPOUNDS HAVING A SUBSTITUTED TRYPTOPHAN RESIDUE OR A TERMINAL SUBSTITUENT CARMOT THERAPEUTICS, INC. (US) 2025-06-19 WO disclosed
EP-4568707-A1 PEPTIDE-BASED DELIVERY AGENT AND METHOD OF MAKING AND USING THE SAME EndoRel Biosciences LLC (US) 2025-06-18 EP disclosed
CN-120076830-A Peptide-based delivery agents and methods of making and using the same 恩多雷尔生物科学有限责任公司 2025-05-30 CN disclosed
US-20210315826-A1 NATURAL FLUORESCENT POLYDEDRAL AMINO ACID CRYSTALS FOR EFFICIENT ENTRAPMENT AND SYSTEMIC DELIVERY OF HYDROPHOBIC SMALL MOLECULES CORNELL UNIVERSITY 2021-10-14 US disclosed
EP-3759227-A1 IMPROVED METHOD FOR THE SYNTHESIS OF TRYPTOPHAN ANALOGS IN AQUEOUS SOLVENTS AT REDUCED TEMPERATURES California Institute of Technology (US) 2021-01-06 EP disclosed
WO-2020208191-A1 NOVEL DHAP SYNTHASE TECHNISCHE UNIVERSITÄT HAMBURG (DE) 2020-10-15 WO disclosed
US-10752927-B2 Method for the synthesis of tryptophan analogs in aqueous solvents at reduced temperatures CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2020-08-25 US disclosed
WO-2020023507-A1 NATURAL FLUORESCENT POLYHEDRAL AMINO ACID CRYSTALS FOR EFFICIENT ENTRAPMENT AND SYSTEMIC DELIVERY OF HYDROPHOBIC SMALL MOLECULES CORNELL UNIVERSITY (US) 2020-01-30 WO disclosed
US-20190271016-A1 METHOD FOR THE SYNTHESIS OF TRYPTOPHAN ANALOGS IN AQUEOUS SOLVENTS AT REDUCED TEMPERATURES CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2019-09-05 US disclosed
EP-3504332-A1 ENGINEERED SYNTHASE FOR PRODUCTION OF TRYPTOPHAN DERIVATIVES AND INTRANSIGENT SUBSTRATES California Institute of Technology (US) 2019-07-03 EP disclosed
WO-2018039495-A1 ENGINEERED SYNTHASE FOR PRODUCTION OF TRYPTOPHAN DERIVATIVES AND INTRANSIGENT SUBSTRATES CALIFORNIA INSTITUTE OF TECHNOLOGY (US) 2018-03-01 WO disclosed
US-20180057806-A1 ENGINEERED SYNTHASE FOR PRODUCTION OF TRYPTOPHAN DERIVATIVES AND INTRANSIGENT SUBSTRATES CALIFORNIA INSTITUTE OF TECHNOLOGY 2018-03-01 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-20260048134-A1 PEPTIDE-BASED DELIVERY AGENT AND METHOD OF MAKING AND USING THE SAME FABP1, LAMP1, SLC7A1 KMT2A 2388/4885KDM4E 3700/4885MAPT 3343/4885
US-20250250569-A1 PEPTIDE-BASED DELIVERY AGENT WITH ASPARAGINE-CONTAINING MASK PEPTIDE GROUP AND METHOD OF MAKING AND USING THE SAME LNPEP, ASNS, DNPEP KMT2A 4087/4885KDM4E 4641/4885MAPT 849/4885
US-20180057806-A1 ENGINEERED SYNTHASE FOR PRODUCTION OF TRYPTOPHAN DERIVATIVES AND INTRANSIGENT SUBSTRATES WARS1, TPH1, TPH2 KMT2A 1560/4885KDM4E 2269/4885MAPT 2121/4885

“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.