Threonine

Threonine

SCHEMBL442280

C[C@@H](O)[C@H](N)C(=O)O.NCC(=O)O

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ADORA1ADORA2AADORA2BADORA3PDE3APDE3BPDE4APDE4BPDE4CPDE4D

The experimentally established mechanism targets of Threonine. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC7A5 Q01650 2/20 0.50
GLRA1 P23415 1/20 0.48
SLC6A9 P48067 1/20 0.48
OR51E2 Q9H255 1/20 0.48
USP2 O75604 1/20 0.40
SLCO1B1 Q9Y6L6 1/20 0.40
GABRR1 P24046 4/20 0.39
GABRP O00591 2/20 0.39
GABRD O14764 2/20 0.39
GABRA1 P14867 2/20 0.39
GABRB1 P18505 2/20 0.39
GABRG2 P18507 2/20 0.39
GABRB3 P28472 2/20 0.39
GABRA5 P31644 2/20 0.39
GABRA3 P34903 2/20 0.39
GABRA2 P47869 2/20 0.39
GABRB2 P47870 2/20 0.39
GABRA4 P48169 2/20 0.39
GABRE P78334 2/20 0.39
GABRA6 Q16445 2/20 0.39

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
Threonine SCHEMBL1537459 1.00 SLC7A5 (0.50) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL1675354 1.00 SLC7A5 (0.50) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL18729492 1.00 SLC7A5 (0.50) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL442279 1.00 SLC7A5 (0.50) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL2765875 1.00 SLC7A5 (0.50) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL8005616 1.00 SLC7A5 (0.50) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL1514090 1.00 SLC7A5 (0.50) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL8429463 0.96 SLC7A5 (0.46) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL5073181 0.96 SLC7A5 (0.46) SLC7A5GLRA1SLC6A9OR51E2USP2
Threonine SCHEMBL5073185 0.96 SLC7A5 (0.46) SLC7A5GLRA1SLC6A9OR51E2USP2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2024141786-A2 MULTITARGET VACCINES AND THERAPEUTICS POPVAX PRIVATE LIMITED (IN) 2024-07-04 WO claimed
EP-2477962-A1 PRODRUGS OF GUANFACINE Shire LLC (US) 2012-07-25 EP claimed
US-20120178666-A1 PRODRUGS OF GUANFACINE SHIRE LLC (US) 2012-07-12 US claimed
CN-102498094-A Prodrugs of guanfacine SHIRE LLC 2012-06-13 CN claimed
WO-2011033296-A1 PRODRUGS OF GUANFACINE SHIRE LLC (US) 2011-03-24 WO claimed
US-20110065796-A1 PRODRUGS OF GUANFACINE SHIRE LLC (US) 2011-03-17 US claimed
WO-2009043114-A1 ARSENOXIDE COMPOUND AND METHOD OF USE NEWSOUTH INNOVATIONS PTY LIMITED (AU) 2009-04-09 WO claimed
CN-1774259-A Parenteral formulations of peptides for the treatment of systemic lupus erythematosus TEVA PHARMA (IL) 2006-05-17 CN claimed
WO-2005051976-A2 PROTEIN AND PEPTIDE LIGATION PROCESSES AND ONE-STEP PURIFICATION PROCESSES ANSATA THERAPEUTICS, INC. (US) 2005-06-09 WO claimed
US-5252725-A α-1-antichymotrypsin, analogues and methods of production THE TRUSTEES OF THE UNIVERSITY OF PENNSYLVANIA (US) 1993-10-12 US claimed
JP-60027371-A None JP disclosed
EP-3500671-B1 METHOD OF SELECTING TARGET SEQUENCES FOR THE DESIGN OF GUIDE RNAS BROAD INST INC (US) 2024-07-10 EP disclosed
EP-3500670-B1 METHOD FOR SELECTING TARGET SEQUENCES FOR GUIDE RNA OF CRISPR SYSTEMS BROAD INST INC (US) 2024-07-10 EP disclosed
WO-2024141784-A2 BROADLY PROTECTIVE BETACORONAVIRUS VACCINES AND COMPOSITIONS POPVAX PRIVATE LIMITED (IN) 2024-07-04 WO disclosed
WO-2024141786-A2 MULTITARGET VACCINES AND THERAPEUTICS POPVAX PRIVATE LIMITED (IN) 2024-07-04 WO disclosed
EP-0332225-A2 Antibody to polypeptides complementary to peptides or proteins having an amino acid sequence or nucleotide coding sequence at least partially known and methods of design therefor BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1989-09-13 EP disclosed
US-4863857-A Polypeptide complementary to peptides or proteins having an amino acid sequence or nucleotide coding sequence at least partially known BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1989-09-05 US disclosed
EP-0214232-A1 POLYPEPTIDES COMPLEMENTARY TO PEPTIDES OR PROTEINS HAVING AN AMINO ACID SEQUENCE OR NUCLEOTIDE CODING SEQUENCE AT LEAST PARTIALLY KNOWN AND METHODS OF DESIGN THEREFOR. UNIV TEXAS (US) 1987-03-18 EP disclosed
WO-1986005208-A1 POLYPEPTIDES COMPLEMENTARY TO PEPTIDES OR PROTEINS HAVING AN AMINO ACID SEQUENCE OR NUCLEOTIDE CODING SEQUENCE AT LEAST PARTIALLY KNOWN AND METHODS OF DESIGN THEREFOR BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (US) 1986-09-12 WO disclosed
JP-S6027371-A FOOD PRESERVATIVE SANRAKU INC 1985-02-12 JP 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-20120178666-A1 PRODRUGS OF GUANFACINE DNPEP, VIP, GDA SLC7A5 121/4885GLRA1 653/4885SLC6A9 237/4885
US-20110065796-A1 PRODRUGS OF GUANFACINE DNPEP, VIP, GDA SLC7A5 121/4885GLRA1 653/4885SLC6A9 237/4885

“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.