SCHEMBL347342

SCHEMBL347342

Nc1ncnc2c1ncn2[C@@H]1O[C@H](COP(=O)(O)OC(=O)[C@@H](N)Cc2ccc(O)cc2)[C@@H](O)[C@H]1O

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
P2RY1 P47900 7/20 0.68
P2RY2 P41231 3/20 0.68
SRC P12931 2/20 0.68
SMN1; SMN2 Q16637 2/20 0.68
P2RX1 P51575 2/20 0.68
P2RX3 P56373 2/20 0.68
ALDH1A1 P00352 2/20 0.68
P2RX4 Q99571 1/20 0.68
P2RX2 Q9UBL9 1/20 0.68
TRPM2 O94759 2/20 0.65
TAS1R3 Q7RTX0 2/20 0.65
TAS1R1 Q7RTX1 2/20 0.65
DNPH1 O43598 1/20 0.65
PRKAB2 O43741 1/20 0.65
LDHA P00338 1/20 0.65
ADRB2 P07550 1/20 0.65
FBP1 P09467 1/20 0.65
ADORA1 P30542 1/20 0.65
PRKAG1 P54619 1/20 0.65
PRKAA2 P54646 1/20 0.65

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
SCHEMBL30903856 1.00 P2RY1 (0.68) P2RY1P2RY2SRCSMN1; SMN2P2RX1
SCHEMBL4945718 0.93 P2RY1 (0.69) P2RY1P2RY2SRCSMN1; SMN2P2RX1
SCHEMBL27695784 0.93 P2RY1 (0.63) P2RY1P2RY2SRCSMN1; SMN2P2RX1
SCHEMBL30051599 0.93 P2RY1 (0.69) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Phosphate SCHEMBL11576227 0.90 P2RY1 (0.69) P2RY1P2RY2SRCSMN1; SMN2P2RX1
Adenosine Phosphate SCHEMBL15670947 0.90 P2RY1 (0.73) P2RY1P2RY2SRCSMN1; SMN2P2RX1
SCHEMBL18423487 0.86 P2RY1 (0.73) P2RY1P2RY2SRCSMN1; SMN2P2RX1
SCHEMBL17148064 0.85 P2RY1 (0.67) P2RY1P2RY2SRCSMN1; SMN2P2RX1
SCHEMBL5063172 0.85 P2RY1 (0.71) P2RY1P2RY2SRCSMN1; SMN2P2RX1
SCHEMBL1332848 0.84 P2RY1 (0.81) P2RY1P2RY2SRCSMN1; SMN2P2RX1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8293512-B2 Polypeptide having activity of aminoacyl-tRNA synthetase and use thereof RIKEN (JP) 2012-10-23 US claimed
US-20120028330-A1 POLYPEPTIDE HAVING ACTIVITY OF AMINOACYL-tRNA SYNTHETASE AND USE THEREOF RIKEN (JP) 2012-02-02 US claimed
US-20090226966-A1 Polypeptide having activity of aminoacyl-tRNA synthetase and use thereof RIKEN (JP) 2009-09-10 US claimed
CN-119970725-A Use of substituted isoxazol-5-one derivative 河南省人民医院 2025-05-13 CN disclosed
US-20230279378-A1 CHIMERIC THERMOSTABLE AMINOACYL-TRNA SYNTHETASE FOR ENHANCED UNNATURAL AMINO ACID INCORPORATION NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2023-09-07 US disclosed
EP-4045639-A1 CHIMERIC THERMOSTABLE AMINOACYL-TRNA SYNTHETASE FOR ENHANCED UNNATURAL AMINO ACID INCORPORATION Trustees of Boston College (US) 2022-08-24 EP disclosed
CN-114555645-A Chimeric thermostable aminoacyl tRNA synthetases for enhanced incorporation of unnatural amino acids 波士顿学院董事会 2022-05-27 CN disclosed
CN-108658916-B Substituent 6, 8-dimercapto-2-phenyl-4H-chromen-4-one derivative and preparation method and application thereof 四川大学 2021-09-24 CN disclosed
WO-2021076795-A1 CHIMERIC THERMOSTABLE AMINOACYL-TRNA SYNTHETASE FOR ENHANCED UNNATURAL AMINO ACID INCORPORATION TRUSTEES OF BOSTON COLLEGE (US) 2021-04-22 WO disclosed
CN-108658916-A 6,8- dimercapto -2- phenyl -4H- chromen-4-one derivatives of substituent group and its preparation method and application 四川大学 2018-10-16 CN disclosed
EP-2796546-B1 Incorporation of unnatural amino acids SCRIPPS RESEARCH INST (US) 2017-08-09 EP disclosed
EP-1456360-A2 METHODS AND COMPOSITION FOR THE PRODUCTION OF ORTHOGANAL TRNA-AMINOACYLTRNA SYNTHETASE PAIRS The Scripps Research Institute (US) 2004-09-15 EP disclosed
WO-2003091418-A2 NOVEL ESSENTIAL FUNGAL POLYNUCLEOTIDES, POLYPEPTIDES, AND METHODS OF USE BRISTOL-MYERS SQUIBB COMPANY (US) 2003-11-06 WO disclosed
US-6631329-B1 Complexed with mupirocin and tRNAile; streak-seedingm vapor equilibrating; replacing with cryoprotectant; flash-freezing YALE UNIVERSITY 2003-10-07 US disclosed
US-20030108885-A1 Comprises ribonuclease barnase marker gene; recombination/genetic engineering; libraries; drug resistance THE SCRIPPS RESEARCH INSTITUTE (US) 2003-06-12 US disclosed
US-20030082575-A1 Translation system for use in the generation of protein containing adjusted amino acid sequences THE SCRIPPS RESEARCH INSTITUTE (US) 2003-05-01 US disclosed
WO-2002086075-A2 METHODS AND COMPOSITION FOR THE PRODUCTION OF ORTHOGANAL TRNA-AMINOACYLTRNA SYNTHETASE PAIRS THE SCRIPPS RESEARCH INSTITUTE (US) 2002-10-31 WO disclosed
WO-2002085923-A2 IN VIVO INCORPORATION OF UNNATURAL AMINO ACIDS THE SCRIPPS RESEARCH INSTITUTE (US) 2002-10-31 WO disclosed
EP-1200564-A2 USE OF THE CRYSTAL STRUCTURE OF STAPHYLOCOCCUS AUREUS ISOLEUCYL-tRNA SYNTHETASE IN ANTIBIOTIC DESIGN YALE UNIVERSITY (US) 2002-05-02 EP disclosed
WO-2001009154-A2 USE OF THE CRYSTAL STRUCTURE OF STAPHYLOCOCCUS AUREUS ISOLEUCYL-tRNA SYNTHETASE IN ANTIBIOTIC DESIGN YALE UNIVERSITY (US) 2001-02-08 WO 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 (1 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-20030108885-A1 Comprises ribonuclease barnase marker gene; recombination/genetic engineering; libraries; drug resistance RNASEL, RNASEH1, RNASE1 P2RY1 4740/4885P2RY2 4690/4885SRC 4566/4885

“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.