SCHEMBL2129167

SCHEMBL2129167

NC(=O)c1ccccc1C(=O)NCO

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 2/20 0.47
HTT P42858 1/20 0.47
BCAT2 O15382 1/20 0.47
HPGD P15428 2/20 0.47
KDM4E B2RXH2 1/20 0.47
ALDH1A1 P00352 1/20 0.47
MAPT P10636 1/20 0.47
HSD17B10 Q99714 1/20 0.47
KMT2A Q03164 1/20 0.46
APEX1 P27695 1/20 0.46
METAP2 P50579 1/20 0.44
LMNA P02545 1/20 0.43
GAA P10253 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43
SIRT2 Q8IXJ6 2/20 0.42
CHRNB2 P17787 1/20 0.42
CHRNB4 P30926 1/20 0.42
CHRNA3 P32297 1/20 0.42
CHRNA4 P43681 1/20 0.42
SIRT1 Q96EB6 1/20 0.42

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
SCHEMBL6903284 0.86 TSHR (0.58) TSHRHTTHPGDKDM4EALDH1A1
SCHEMBL9570919 0.85 ALDH1A1 (0.54) TSHRHTTBCAT2HPGDKDM4E
SCHEMBL9844764 0.83 KDM4E (0.49) TSHRHTTBCAT2HPGDKDM4E
SCHEMBL6566957 0.82 TSHR (0.55) TSHRHTTHPGDKDM4EALDH1A1
SCHEMBL9329299 0.82 TSHR (0.46) TSHRHTTBCAT2HPGDKDM4E
SCHEMBL6075765 0.82 TSHR (0.46) TSHRHTTBCAT2HPGDKDM4E
SCHEMBL7255678 0.82 HTT (0.62) TSHRHTTHPGDKDM4EALDH1A1
SCHEMBL3973663 0.82 KMT2A (0.45) TSHRHTTBCAT2HPGDKDM4E
SCHEMBL15796793 0.82 KMT2A (0.67) HTTKDM4EALDH1A1MAPTKMT2A
SCHEMBL4138337 0.81 CTSD (0.55) TSHRHTTBCAT2HPGDKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-7186538-A None JP disclosed
US-20250340507-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARM INNC (US) 2025-11-06 US disclosed
CN-111527075-A Xanthene compound, photosensitive resin composition containing the same, photosensitive material, color filter, and display device 株式会社LG化学 2020-08-11 CN disclosed
US-20170283368-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS PARATEK PHARMACEUTICALS, INC. 2017-10-05 US disclosed
US-9522872-B2 Methods for synthesizing substituted tetracycline compounds PARATEK PHARMACEUTICALS, INC. (US) 2016-12-20 US disclosed
WO-2014005125-A2 FLUORESCENT COMPOUNDS AND USES THEREOF BIOTIUM, INC. (US) 2014-01-03 WO disclosed
CN-103460086-A Colored composition for color filters, and color filters TOYO INK SC HOLDINGS CO LTD 2013-12-18 CN disclosed
EP-2176216-B1 METHODS FOR SYNTHESIZING 9-SUBSTITUTED MINOCYCLINE PARATEK PHARM INNC (US) 2012-04-25 EP disclosed
EP-2192111-A2 Methods for synthesizing substituted tetracycline compounds Paratek Pharmaceuticals, Inc. (US) 2010-06-02 EP disclosed
EP-2176216-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS Paratek Pharmaceuticals, Inc. (US) 2010-04-21 EP disclosed
US-4791204-A FOR COLORING POLYMERS CIBA-GEIGY CORPORATION (US) 1988-12-13 US disclosed
US-4678611-A Novel dyestuff intermediates and use thereof for the manufacture of novel azo dyes CIBA-GEIGY CORPORATION (US) 1987-07-07 US disclosed
EP-0073826-A1 RAPID SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDES USING PHOSPHORUS OXYCHLORIDE ACTIVATION BIORESEARCH INC. (US) 1983-03-16 EP disclosed
US-4360460-A Novel azo dyes having a 4-sulfo-5-aminomethyl naphthalene coupling moiety CIBA-GEIGY AG (CH) 1982-11-23 US disclosed
WO-1982003079-A1 RAPID SOLID PHASE SYNTHESIS OF OLIGONUCLEOTIDES USING PHOSPHORUS OXYCHLORIDE ACTIVATION BIORESEARCH INC (US) 1982-09-16 WO disclosed
US-4288363-A Novel azo dyes having 2-amino-5-aminomethyl-7-sulfo naphthalene coupling moiety CIBA-GEIGY CORPORATION (US) 1981-09-08 US disclosed
US-4222777-A RADIOGRAPHY, PROCESSING FREE OF SILVER BLEACHING STEP FUJI PHOTO FILM CO., LTD. (JP) 1980-09-16 US disclosed
US-4154615-A GRAFT POLYMERS KONISHIROKU PHOTO INDUSTRY CO., LTD. (JP) 1979-05-15 US disclosed
US-4092414-A 3,4-Dihydrospiro-2H-1,3-benzoxazines and their use in treating edema, abnormal electrolyte retention, and inflammation MERCK & CO., INC. (US) 1978-05-30 US disclosed
US-4070464-A DISPIROBENZOXAZINES MERCK & CO., INC. (US) 1978-01-24 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 (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-20250340507-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS TET3, TET1, DHFR TSHR 2369/4885HTT 571/4885BCAT2 305/4885
US-20170283368-A1 METHODS FOR SYNTHESIZING SUBSTITUTED TETRACYCLINE COMPOUNDS TET3, TET1, DHFR TSHR 2369/4885HTT 571/4885BCAT2 305/4885

“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.