SCHEMBL2843086

SCHEMBL2843086

Nc1c(C(=O)O)cccc1C(=O)C=Cc1ccccc1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 7/20 0.73
CYP1B1 Q16678 4/20 0.61
CYP1A1 P04798 1/20 0.61
BCHE P06276 2/20 0.60
CYP2C19 P33261 1/20 0.60
MAOB P27338 3/20 0.53
LMNA P02545 3/20 0.53
PLIN1 O60240 2/20 0.53
RECQL P46063 2/20 0.53
PLIN5 Q00G26 2/20 0.53
ABHD5 Q8WTS1 2/20 0.53
TNFRSF1A P19438 1/20 0.53
ACHE P22303 1/20 0.53
ALDH1A1 P00352 3/20 0.50
SMN1; SMN2 Q16637 3/20 0.50
KDM4E B2RXH2 2/20 0.50
MEN1 O00255 2/20 0.50
CYP3A4 P08684 2/20 0.50
HPGD P15428 2/20 0.50
ALOX15 P16050 2/20 0.50

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
SCHEMBL2843080 1.00 MAPT (0.73) MAPTCYP1B1CYP1A1BCHECYP2C19
SCHEMBL14801668 0.89 MAPT (0.60) MAPTCYP1B1CYP1A1BCHECYP2C19
SCHEMBL14801670 0.89 MAPT (0.60) MAPTCYP1B1CYP1A1BCHECYP2C19
SCHEMBL27753446 0.87 MAPT (0.78) MAPTCYP1B1CYP1A1BCHECYP2C19
SCHEMBL1501351 0.84 MAPT (1.00) MAPTCYP1B1CYP1A1BCHECYP2C19
SCHEMBL1501349 0.84 MAPT (1.00) MAPTCYP1B1CYP1A1BCHECYP2C19
SCHEMBL25202121 0.84 MAPT (0.73) MAPTCYP1B1BCHECYP2C19MAOB
SCHEMBL17047852 0.84 MAPT (0.73) MAPTCYP1B1BCHECYP2C19MAOB
SCHEMBL31233508 0.84 MAPT (0.73) MAPTCYP1B1BCHECYP2C19MAOB
SCHEMBL30383301 0.84 MAPT (0.73) MAPTCYP1B1BCHECYP2C19MAOB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140072584-A1 NOVEL PHARMACEUTICAL USE OF BENZOIC ACID DERIVATIVES LI, YINGJI (CN) 2014-03-13 US claimed
US-4623724-A Method for the production of nuclear substituted cinnamoylanthranilic acid salts KISSEI PHARMACEUTICAL CO., LTD. (JP) 1986-11-18 US claimed
US-4587356-A Process for the production of nuclear substituted cinnamoylanthranilic acid derivatives KISSEI PHARMACEUTICAL CO., LTD. (JP) 1986-05-06 US claimed
EP-0074725-B1 A METHOD FOR THE PRODUCTION OF NUCLEAR SUBSTITUTED CINNAMOYLANTHRANILIC ACID DERIVATIVES AND INTERMEDIATES THEREOF Kissei Pharmaceutical Co. Ltd. (JP) 1985-12-27 EP claimed
US-4486597-A Method for the production of nuclear substituted cinnamoylanthranilic acid derivatives KISSEI PHARMACEUTICAL CO., LTD. (JP) 1984-12-04 US claimed
EP-0074725-A1 A method for the production of nuclear substituted cinnamoylanthranilic acid derivatives and intermediates thereof Kissei Pharmaceutical Co. Ltd. (JP) 1983-03-23 EP claimed
JP-1246249-A None JP disclosed
US-20230270703-A1 COMPOUNDS AND METHODS FOR THE TREATMENT OF EYE DISORDERS OCCURX PTY LTD (AU) 2023-08-31 US disclosed
CN-116033901-A Compounds and methods for treating ocular disorders 奥克尔克斯有限公司 2023-04-28 CN disclosed
EP-4161527-A1 COMPOUNDS AND METHODS FOR THE TREATMENT OF EYE DISORDERS OccuRx Pty Ltd (AU) 2023-04-12 EP disclosed
EP-2799427-B1 Therapeutic compounds FIBROTECH THERAPEUTICS PTY LTD (AU) 2018-07-04 EP disclosed
CN-107643344-A Utilize high performance liquid chromatography fluoroscopic examination(HPLC‑FLD)Method analysis measure oat alkaloid 北京工商大学 2018-01-30 CN disclosed
US-9561201-B2 Therapeutic compounds FIBROTECH THERAPEUTICS PTY LTD (AU) 2017-02-07 US disclosed
EP-0074725-B1 A METHOD FOR THE PRODUCTION OF NUCLEAR SUBSTITUTED CINNAMOYLANTHRANILIC ACID DERIVATIVES AND INTERMEDIATES THEREOF Kissei Pharmaceutical Co. Ltd. (JP) 1985-12-27 EP disclosed
US-4486597-A Method for the production of nuclear substituted cinnamoylanthranilic acid derivatives KISSEI PHARMACEUTICAL CO., LTD. (JP) 1984-12-04 US disclosed
US-4486597-A Method for the production of nuclear substituted cinnamoylanthranilic acid derivatives KISSEI PHARMACEUTICAL CO., LTD. (JP) 1984-12-04 US disclosed
US-4486597-A Method for the production of nuclear substituted cinnamoylanthranilic acid derivatives KISSEI PHARMACEUTICAL CO., LTD. (JP) 1984-12-04 US disclosed
EP-0074725-A1 A method for the production of nuclear substituted cinnamoylanthranilic acid derivatives and intermediates thereof Kissei Pharmaceutical Co. Ltd. (JP) 1983-03-23 EP disclosed
EP-0074725-A1 A method for the production of nuclear substituted cinnamoylanthranilic acid derivatives and intermediates thereof Kissei Pharmaceutical Co. Ltd. (JP) 1983-03-23 EP disclosed
EP-0074725-A1 A method for the production of nuclear substituted cinnamoylanthranilic acid derivatives and intermediates thereof Kissei Pharmaceutical Co. Ltd. (JP) 1983-03-23 EP 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-20140072584-A1 NOVEL PHARMACEUTICAL USE OF BENZOIC ACID DERIVATIVES NFATC1, GABRA5, GABRA6 MAPT 4128/4885CYP1B1 515/4885CYP1A1 743/4885
US-20230270703-A1 COMPOUNDS AND METHODS FOR THE TREATMENT OF EYE DISORDERS ALDH1A2, RBP4, RARB MAPT 3298/4885CYP1B1 1885/4885CYP1A1 3460/4885

“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.