SCHEMBL5619699

SCHEMBL5619699

O=C(O)N1C(=O)Cc2ccccc21

nearest known ligand 0.71

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NOTUM Q6P988 1/20 0.71
HPGD P15428 1/20 0.55
MEN1 O00255 3/20 0.50
KMT2A Q03164 3/20 0.50
KDM4E B2RXH2 3/20 0.50
ALDH1A1 P00352 2/20 0.50
CYP3A4 P08684 2/20 0.50
MAPT P10636 2/20 0.50
PABPC1 P11940 1/20 0.50
BLM P54132 1/20 0.50
PDE5A O76074 2/20 0.49
NPC1 O15118 1/20 0.43
MITF O75030 1/20 0.43
RAB9A P51151 1/20 0.43
DDB1 Q16531 1/20 0.43
CRBN Q96SW2 1/20 0.43
RNASEH1 O60930 1/20 0.42
TUBB4A P04350 1/20 0.41
TUBB P07437 1/20 0.41
TUBA3C P0DPH7 1/20 0.41

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
SCHEMBL31220020 1.00 NOTUM (0.71) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL28767800 0.86 NOTUM (0.73) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL27489322 0.86 NOTUM (0.56) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL8489445 0.84 PDE5A (0.68) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL29850056 0.83 NOTUM (1.00) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL30600284 0.83 MEN1 (0.54) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL6251744 0.83 NOTUM (0.69) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL8733182 0.83 MEN1 (0.54) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL1304374 0.83 NOTUM (1.00) NOTUMHPGDMEN1KMT2AKDM4E
SCHEMBL5682752 0.80 NPC1 (0.70) NOTUMHPGDMEN1KMT2AKDM4E

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 20 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110423212-B Hydroxy indole carboxylic acid-based inhibitors of SHP2 美国印第安纳大学研究和技术公司 2023-05-09 CN claimed
CN-105142634-B Oxindole carboxylic acid-based inhibitors of oncogenic protein tyrosine phosphatase-2(SHP2) comprising Src homology-2domain 美国印第安纳大学研究和技术公司 2020-06-12 CN claimed
US-20230234938-A1 NOVEL COMPOUNDS USEFUL AS POLY(ADP-RIBOSE) POLYMERASE (PARP) INHIBITORS RHIZEN PHARMACEUTICALS AG (CH) 2023-07-27 US disclosed
CN-110423212-B Hydroxy indole carboxylic acid-based inhibitors of SHP2 美国印第安纳大学研究和技术公司 2023-05-09 CN disclosed
CN-105142634-B Oxindole carboxylic acid-based inhibitors of oncogenic protein tyrosine phosphatase-2(SHP2) comprising Src homology-2domain 美国印第安纳大学研究和技术公司 2020-06-12 CN disclosed
CN-105142634-B Oxindole carboxylic acid-based inhibitors of oncogenic protein tyrosine phosphatase-2(SHP2) comprising Src homology-2domain 美国印第安纳大学研究和技术公司 2020-06-12 CN disclosed
CN-105142634-B Oxindole carboxylic acid-based inhibitors of oncogenic protein tyrosine phosphatase-2(SHP2) comprising Src homology-2domain 美国印第安纳大学研究和技术公司 2020-06-12 CN disclosed
CN-110709396-A Novel compound inhibitors of the YAP/TAZ-TEAD interaction and their use in the treatment of malignant mesothelioma 伊文蒂瓦公司 2020-01-17 CN disclosed
WO-2016131789-A1 BENZOPYRROLIDONE DERIVATIVES POSSESSING ANTIVIRAL AND ANTICANCER PROPERTIES MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2016-08-25 WO disclosed
EP-3056202-A1 BENZOPYRROLIDONE DERIVATIVES POSSESSING ANTIVIRAL AND ANTICANCER PROPERTIES Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2016-08-17 EP disclosed
CN-103328478-B Piperidinone carboxamide azaindane CGRP receptor antagonists MERCK SHARP & DOHME CORP. (US) 2015-10-07 CN disclosed
EP-2654421-A1 FUSED HETEROCYCLIC INDANE CARBOXAMIDE CGRP RECEPTOR ANTAGONISTS Merck Sharp & Dohme Corp. (US) 2013-10-30 EP disclosed
CN-103328478-A Piperidinone carboxamide azaindane cgrp receptor antagonists MERCK SHARP & DOHME 2013-09-25 CN disclosed
WO-2012087777-A1 FUSED HETEROCYCLIC INDANE CARBOXAMIDE CGRP RECEPTOR ANTAGONISTS MERCK SHARP & DOHME CORP. (US) 2012-06-28 WO disclosed
US-7214700-B2 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors SUGEN INC. (US) 2007-05-08 US disclosed
US-20040039196-A1 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors SUGEN, INC. 2004-02-26 US disclosed
US-20030216462-A1 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors SUGEN, INC. 2003-11-20 US disclosed
EP-1299355-A2 (2-OXINDOL-3-YLIDENYL)ACETIC ACID DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS Sugen, Inc. (US) 2003-04-09 EP disclosed
US-20020028828-A1 (2-oxindol-3-ylidenyl)acetic acid derivatives and their use as protein kinase inhibitors SUGEN, INC. 2002-03-07 US disclosed
WO-2001083450-A2 (2-OXINDOL-3-YLIDENYL)ACETIC ACID DERIVATIVES AND THEIR USE AS PROTEIN KINASE INHIBITORS SUGEN, INC. (US) 2001-11-08 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 (4 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-20020028828-A1 (2-oxindol-3-ylidenyl)acetic acid derivatives and their use as protein kinase inhibitors MAPKAPK2, MAPKAPK3, MAP3K2 NOTUM 3421/4885HPGD 559/4885MEN1 4217/4885
US-20040039196-A1 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors MAPKAPK2, MAPKAPK3, MAP3K2 NOTUM 3421/4885HPGD 559/4885MEN1 4217/4885
US-20030216462-A1 (2-Oxindol-3-ylidenyl) acetic acid derivatives and their use as protein kinase inhibitors MAPKAPK2, MAPKAPK3, MAP3K2 NOTUM 3421/4885HPGD 559/4885MEN1 4217/4885
US-20230234938-A1 NOVEL COMPOUNDS USEFUL AS POLY(ADP-RIBOSE) POLYMERASE (PARP) INHIBITORS PARP1, PARP2, PARP3 NOTUM 2168/4885HPGD 198/4885MEN1 3978/4885

“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.