SCHEMBL83775

SCHEMBL83775

Cn1c(NO)nc2c3cccnc3ccc21

nearest known ligand 0.48

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
PDE10A Q9Y233 12/20 0.48
LMNA P02545 1/20 0.46
KDM4E B2RXH2 1/20 0.43
MAPT P10636 1/20 0.43
CYP3A4 P08684 1/20 0.40
TLR7 Q9NYK1 2/20 0.40
BRD4 O60885 1/20 0.38
HTR2A P28223 1/20 0.36
HTR2C P28335 1/20 0.36
HTR2B P41595 1/20 0.36

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
SCHEMBL29350478 0.80 PDE10A (0.45) PDE10ALMNAKDM4EMAPTHTR2C
SCHEMBL12068237 0.80 PDE10A (0.54) PDE10ALMNAKDM4EMAPTCYP3A4
SCHEMBL605923 0.79 PDE10A (0.50) PDE10ALMNAKDM4EMAPTCYP3A4
SCHEMBL2546975 0.79 CCR1 (0.50) PDE10ALMNAKDM4EMAPTCYP3A4
SCHEMBL4952115 0.78 PDE10A (0.47) PDE10ALMNAKDM4EMAPTCYP3A4
SCHEMBL10309409 0.78 PDE10A (0.59) PDE10ALMNAKDM4EMAPTCYP3A4
SCHEMBL10345238 0.78 PDE10A (0.72) PDE10ALMNAKDM4EMAPTTLR7
Ammonia Solution, Strong SCHEMBL17583545 0.78 PDE10A (0.49) PDE10ALMNAKDM4EMAPTCYP3A4
Bromide SCHEMBL13822734 0.77 PDE10A (0.48) PDE10ALMNAKDM4EMAPTCYP3A4
SCHEMBL15033539 0.77 PDE10A (0.48) PDE10ALMNAKDM4EMAPTCYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20050208515-A1 Method of DNA shuffling with polynucleotides produced by blocking or interrupting a synthesis or amplification process DIVERSA CORPORATION 2005-09-22 US claimed
US-20030113759-A1 Method of DNA shuffling with polynucleotides produced by blocking or interrupting a synthesis or amplification process SHORT JAY M (US) 2003-06-19 US claimed
US-6440668-B1 Method of DNA shuffling with polynucleotides produced by blocking or interrupting a synthesis or amplification process DIVERSA CORPORATION 2002-08-27 US claimed
US-20020028443-A1 METHOD OF DNA SHUFFLING WITH POLYNUCLEOTIDES PRODUCED BY BLOCKING OR INTERRUPTING A SYNTHESIS OR AMPLIFICATION PROCESS DIVERSA CORPORATION 2002-03-07 US claimed
US-5965408-A Method of DNA reassembly by interrupting synthesis DIVERSA CORPORATION (US) 1999-10-12 US claimed
CN-113789316-A Phytases, nucleic acids encoding them and methods of making and using them 巴斯夫酶有限责任公司 2021-12-14 CN disclosed
CN-106222185-B Glucanases, nucleic acids encoding them and methods of making and using them 维莱尼姆公司 2021-12-03 CN disclosed
CN-104450754-B Phytases, nucleic acids encoding them and methods of making and using them 巴斯夫酶有限责任公司 2021-10-01 CN disclosed
CN-110577945-A xylanases, nucleic acids encoding them, and methods for making and using them 维莱尼姆公司 2019-12-17 CN disclosed
US-10428340-B2 Phytases, nucleic acids encoding them and methods for making and using them SYNGENTA PARTICIPATIONS AG (CH) 2019-10-01 US disclosed
US-10329549-B2 Glucanases, nucleic acids encoding them and methods for making and using them BP CORPORATION NORTH AMERICA INC. (US) 2019-06-25 US disclosed
US-20190127712-A1 Phytases, Nucleic Acids Encoding Them and Methods for Making and Using Them SYNGENTA PARTICIPATIONS AG (CH) 2019-05-02 US disclosed
US-20020012974-A1 Genetic engineered nucleic acid promoter VERENIUM CORPORATION 2002-01-31 US disclosed
US-20020006620-A1 Morphatides: novel shape and structure libraries INVITROGEN CORPORATION 2002-01-17 US disclosed
WO-2001048175-A2 METHODS FOR PRODUCING ENANTIOMERICALLY PURE α-SUBSTITUTED CARBOXYLIC ACIDS DIVERSA CORPORATION (US) 2001-07-05 WO disclosed
US-6238884-B1 SUBJECTING POLYNUCLEOTIDES TO SIMULTANEOUS MUTAGENESIS BY AMPLIFYING USING DEGENERATE OLIGONUCLEOTIDES, THEN SUBJECTING PROGENY POLYNUCLEOTIDES TO END SELECTION-BASED SCREENING AND ENRICHMENT PROCESS TO CREATE LIGATION-COMPATIBLE ENDS DIVERSA CORPORATION 2001-05-29 US disclosed
US-6171820-B1 Saturation mutagenesis in directed evolution DIVERSA CORPORATION 2001-01-09 US disclosed
EP-0954600-A2 MORPHATIDES: NOVEL SHAPE AND STRUCTURE LIBRARIES Morphagen (US) 1999-11-10 EP disclosed
US-5965408-A Method of DNA reassembly by interrupting synthesis DIVERSA CORPORATION (US) 1999-10-12 US disclosed
WO-1998016661-A2 MORPHATIDES: NOVEL SHAPE AND STRUCTURE LIBRARIES MORPHAGEN (US) 1998-04-23 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-20020012974-A1 Genetic engineered nucleic acid promoter RNGTT, ASPH, ALKBH3 PDE10A 4357/4885LMNA 1933/4885KDM4E 2443/4885

“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.