SCHEMBL281203

SCHEMBL281203

O=C1Nc2cccc(Br)c2C1=O

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES1 P23141 5/20 0.60
MAOA P21397 1/20 0.47
MAOB P27338 1/20 0.47
TGM2 P21980 2/20 0.43
RET P07949 1/20 0.43
IDO1 P14902 1/20 0.41
TDO2 P48775 1/20 0.41
PBRM1 Q86U86 2/20 0.41
MEN1 O00255 2/20 0.40
KMT2A Q03164 2/20 0.40
CA1 P00915 1/20 0.40
CA2 P00918 1/20 0.40
CA7 P43166 1/20 0.40
CA9 Q16790 1/20 0.40
POLB P06746 1/20 0.40
MAPT P10636 1/20 0.40
DUSP3 P51452 1/20 0.40
BLM P54132 1/20 0.40
PTPN5 P54829 1/20 0.40
PTPN11 Q06124 1/20 0.40

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
SCHEMBL11921526 0.83 CES1 (0.41) CES1MAOAMAOBTGM2RET
SCHEMBL31107461 0.80 CES1 (0.43) CES1MAOAMAOBTGM2RET
SCHEMBL30835279 0.75 CES1 (0.60) CES1MAOAMAOBTGM2RET
SCHEMBL5975593 0.75 CES1 (0.60) CES1MAOAMAOBTGM2RET
SCHEMBL30716604 0.75 CES1 (1.00) CES1MAOAMAOBTGM2PBRM1
SCHEMBL4242823 0.75 CES1 (0.60) CES1MAOAMAOBTGM2PBRM1
SCHEMBL282066 0.75 CES1 (1.00) CES1MAOAMAOBTGM2PBRM1
SCHEMBL2136384 0.75 CES1 (0.60) CES1MAOAMAOBRETPBRM1
SCHEMBL2838571 0.75 CES1 (0.60) CES1MAOAMAOBTGM2RET
SCHEMBL31728330 0.73 CES1 (0.48) CES1MAOAMAOBTGM2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115215782-B Preparation method of 4-bromoindole 常州琦诺生物科技有限公司 2024-09-03 CN claimed
CN-114950159-B Preparation method of aromatic polymer separation membrane based on super acid catalysis 南京工业大学 2023-06-06 CN claimed
CN-116217460-A Preparation and application of indoline-2-one compound derivative 合肥工业大学 2023-06-06 CN claimed
CN-115215782-A Preparation method of 4-bromoindole 常州琦诺生物科技有限公司 2022-10-21 CN claimed
CN-114950159-A Preparation method of aromatic polymer separation membrane based on super-acid catalysis preparation 南京工业大学 2022-08-30 CN claimed
CN-113912609-A Preparation method of natural alkaloid tryptanthrin and derivative thereof 江苏大学 2022-01-11 CN claimed
CN-111574426-A Diamine monomer containing isoindigo structure and black polyimide synthesized from diamine monomer 湘潭大学 2020-08-25 CN claimed
CN-105693717-A Preparation method of pyrrolo[4,3,2-de]quinoline 中国药科大学 2016-06-22 CN claimed
CN-103554117-B A kind of preparation method of chiral spiro naphthoquinone benzopyran hydroxyindole compound ZHANGJIAGANG INSTITUTE OF INDUSTRIAL TECHNOLOGIES SOOCHOW UNIVERSITY (CN) 2015-09-23 CN claimed
CN-102351777-B Preparation method for chiral 3-hydroxyl-3-methylene nitro indole-2-ketone derivative UNIV SOOCHOW 2014-03-19 CN claimed
CN-103554117-A Preparation method of chiral spiro naphthoquinone benzopyran hydroxyindole compound ZHANGJIAGANG INST IND TECHNOLOGIES SOOCHOW UNIV 2014-02-05 CN claimed
CN-102690226-A Multi-nitrogen substituted isatin derivative and synthetic method of multi-nitrogen substituted isatin derivative UNIV GUANGDONG TECHNOLOGY 2012-09-26 CN claimed
CN-102351777-A Preparation method for chiral 3-hydroxyl-3-methylene nitro indole-2-ketone derivative UNIV SOOCHOW 2012-02-15 CN claimed
US-20070130702-A1 Dyeing process using a specific compound containing active methylene and a compound chosen from a specific aldehyde, a specific ketone, a quinone and a diiminoisoindoline or 3-aminoisoindolone derivative L'OREAL S.A. 2007-06-14 US claimed
US-7204857-B1 Dyeing method using a specific active methylene compound and a compound selected among a specific aldehyde, a specific ketone, a quinone and a di-imino-isoindoline or 3-amino-isoindolone derivative L'OREAL S.A. (FR) 2007-04-17 US claimed
US-6635090-B1 Dyeing method using a specific cationic derivative and a compound selected among a specific aldehyde, a specific ketone, a quinone and a di-imino-isoindoline or 3-amino-isoindolone derivative L'OREAL, S.A. (FR) 2003-10-21 US claimed
US-6458168-B1 Hair dyeing method using an aliphatic cationic amine and compound chosen from an aldehyde, a ketone, a quinone, a di-imino-isoindoline, and a 3-aminoisoindolone derivative L'OREAL S.A. (FR) 2002-10-01 US claimed
US-6451067-B1 HAIR DYE MIXTURE L'OREAL S.A. (FR) 2002-09-17 US claimed
CN-122094937-A Cannabinoid compounds and uses thereof 2026-05-26 CN disclosed
EP-0002624-A1 2-Benzazepine compounds, processes for their preparation and pharmaceutical compositions containing them SMITHKLINE BECKMAN CORPORATION (US) 1979-06-27 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 (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-20070130702-A1 Dyeing process using a specific compound containing active methylene and a compound chosen from a specific aldehyde, a specific ketone, a quinone and a diiminoisoindoline or 3-aminoisoindolone derivative KRT18, NDUFB5, NDUFB7 CES1 3158/4885MAOA 467/4885MAOB 514/4885

“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.