SCHEMBL2017132

SCHEMBL2017132

Cc1ccccc1CNC(=O)O

nearest known ligand 0.73

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 5/20 0.73
HPGD P15428 3/20 0.73
KMT2A Q03164 3/20 0.67
GAA P10253 2/20 0.67
HTT P42858 1/20 0.67
KDM4E B2RXH2 3/20 0.60
LMNA P02545 3/20 0.59
NPC1 O15118 2/20 0.57
RAB9A P51151 2/20 0.57
MAPT P10636 1/20 0.56
MEN1 O00255 2/20 0.55
SMN1; SMN2 Q16637 2/20 0.55
POLB P06746 1/20 0.55
L3MBTL1 Q9Y468 1/20 0.55
PKM P14618 1/20 0.55
CA2 P00918 1/20 0.54

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
SCHEMBL24576210 0.88 ALDH1A1 (0.68) ALDH1A1HPGDKMT2AGAAHTT
SCHEMBL29935885 0.87 CYP1A2 (0.55) ALDH1A1HPGDKMT2AGAAHTT
SCHEMBL9156343 0.87 CYP1A2 (0.55) ALDH1A1HPGDKMT2AGAAHTT
SCHEMBL885156 0.86 ALDH1A1 (0.66) ALDH1A1HPGDKMT2AGAAHTT
SCHEMBL11192972 0.85 ALDH1A1 (0.67) ALDH1A1HPGDKMT2AGAAHTT
SCHEMBL4521046 0.85 ALDH1A1 (1.00) ALDH1A1HPGDKMT2AGAAHTT
Hydrochloric Acid SCHEMBL11157053 0.85 CYP1A2 (0.53) ALDH1A1HPGDKMT2AGAAHTT
SCHEMBL935059 0.84 HPGD (0.54) ALDH1A1HPGDKMT2AGAAHTT
SCHEMBL1244426 0.84 ALDH1A1 (0.64) ALDH1A1HPGDKMT2AGAAHTT
SCHEMBL27682450 0.83 ALDH1A1 (0.53) ALDH1A1HPGDKMT2AGAAHTT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-1673347-B1 SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USEFUL AS GAMMA-SECRETASE INHIBITORS HOFFMANN LA ROCHE (CH) 2015-08-19 EP claimed
JP-2007507447-A 2007-03-29 JP claimed
US-7166587-B2 Carbamic acid alkyl ester derivatives HOFFMANN-LA ROCHE INC. (US) 2007-01-23 US claimed
EP-1673347-A1 SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USEFUL AS GAMMA-SECRETASE INHIBITORS F. Hoffman-la Roche AG (CH) 2006-06-28 EP claimed
WO-2005040126-A1 SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USEFUL AS GAMMA-SECRETASE INHIBITORS F. HOFFMAN-LA ROCHE AG (CH) 2005-05-06 WO claimed
US-20050075327-A1 Carbamic acid alkyl ester derivatives HOFFMAN-LA ROCHE INC. 2005-04-07 US claimed
EP-4145995-A1 PESTICIDAL COMPOSITIONS AND RELATED METHODS CJB Applied Technologies, LLC (US) 2023-03-15 EP disclosed
WO-2021226566-A1 PESTICIDAL COMPOSITIONS AND RELATED METHODS CJB APPLIED TECHNOLOGIES, LLC (US) 2021-11-11 WO disclosed
EP-3709804-A1 PESTICIDAL COMPOSITIONS AND RELATED METHODS CJB Applied Technologies, LLC (US) 2020-09-23 EP disclosed
EP-1673347-B1 SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USEFUL AS GAMMA-SECRETASE INHIBITORS HOFFMANN LA ROCHE (CH) 2015-08-19 EP disclosed
US-20110160476-A1 N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester ASAHI KASEI CHEMICALS CORPORATION (JP) 2011-06-30 US disclosed
US-7166587-B2 Carbamic acid alkyl ester derivatives HOFFMANN-LA ROCHE INC. (US) 2007-01-23 US disclosed
EP-1673347-A1 SUBSTITUTED DIBENZO-AZEPINE AND BENZO-DIAZEPINE DERIVATIVES USEFUL AS GAMMA-SECRETASE INHIBITORS F. Hoffman-la Roche AG (CH) 2006-06-28 EP disclosed
US-20050075327-A1 Carbamic acid alkyl ester derivatives HOFFMAN-LA ROCHE INC. 2005-04-07 US disclosed
CN-1087335-A Substituted benzyl carbamates with herbicidal properties CIBA GEIGY AG (CH) 1994-06-01 CN disclosed
CN-1004353-B Process for preparing N-methyl carbamates 埃尼凯姆·辛泰希公司 1989-05-31 CN disclosed
EP-0298419-A2 A protein partial degradation product, process for preparing it and its use Katayama Chemical Works Co., Ltd. (JP) 1989-01-11 EP disclosed
CN-85109417-A The preparation method of N-methyl carbamate class 1986-12-03 CN disclosed
US-4319018-A IN ACID CATALYST MITSUI TOATSU CHEMICALS, INC. (JP) 1982-03-09 US disclosed
EP-0031385-A1 PROCESS FOR PREPARING POLYMETHYLENEPOLYPHENYL POLYCARBAMATE MITSUI TOATSU CHEMICALS, Inc. (JP) 1981-07-08 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-20050075327-A1 Carbamic acid alkyl ester derivatives BCHE, CHRM1, ADCY7 ALDH1A1 1434/4885HPGD 4445/4885KMT2A 2212/4885
US-20110160476-A1 N-Substituted Carbamic Acid Ester Production Method and Isocyanate Production Method Using the N-Substituted Carbamic Acid Ester ALKBH3, CPS1, APEH ALDH1A1 574/4885HPGD 703/4885KMT2A 1122/4885

“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.