SCHEMBL2136384

SCHEMBL2136384

Cc1cccc2c1C(=O)C(=O)N2

nearest known ligand 0.60

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CES1 P23141 3/20 0.60
KDR P35968 2/20 0.51
PDPK1 O15530 1/20 0.51
RET P07949 4/20 0.50
DAO P14920 1/20 0.50
MAOA P21397 1/20 0.47
MAOB P27338 1/20 0.47
ERBB2 P04626 2/20 0.46
POLB P06746 1/20 0.45
FLT3 P36888 1/20 0.43
PDGFRB P09619 3/20 0.43
ROS1 P08922 1/20 0.42
CDK5 Q00535 1/20 0.42
ACVR1 Q04771 1/20 0.42
LRRK2 Q5S007 1/20 0.42
PBRM1 Q86U86 1/20 0.41
IGF1R P08069 1/20 0.41
CA1 P00915 1/20 0.40
CA2 P00918 1/20 0.40
CA7 P43166 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
SCHEMBL14812709 0.83 MAOA (0.53) CES1KDRPDPK1RETDAO
SCHEMBL11700610 0.80 PDPK1 (0.42) CES1KDRPDPK1RETDAO
SCHEMBL8185520 0.80 CES1 (0.58) CES1RETDAOMAOAMAOB
SCHEMBL5975593 0.79 CES1 (0.60) CES1KDRPDPK1RETMAOA
SCHEMBL22525286 0.78 DAO (0.58) CES1DAOPOLBCA1CA2
SCHEMBL5741222 0.77 POLB (0.51) CES1KDRPDPK1RETERBB2
SCHEMBL1871243 0.76 CES1 (0.56) CES1KDRPDPK1RETDAO
SCHEMBL7587270 0.76 POLB (0.50) CES1KDRPDPK1RETERBB2
SCHEMBL10863778 0.76 CES1 (0.51) CES1KDRPDPK1RETDAO
SCHEMBL4861892 0.76 KDR (0.60) KDRPDPK1RETERBB2FLT3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-105732460-A Method for synthesizing indole compound 常州工程职业技术学院 2016-07-06 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
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
JP-4139167-A None JP disclosed
US-12421191-B2 3-hydroxyoxindole derivatives as CRHR2 antagonist RAQUALIA PHARMA INC. (JP) 2025-09-23 US disclosed
CN-119591596-A 4, 5-Dihydro-3H-pyrrolo [2,3-c ] quinolin-4-one derivatives and uses thereof 沈阳药科大学 2025-03-11 CN disclosed
CN-118420517-A Preparation method of indoline-2, 3-diketone compound 河北医科大学 2024-08-02 CN disclosed
CN-117486784-A Ligand precursor compound containing spiro-indolone skeleton and preparation method and application thereof 中国海洋石油集团有限公司 2024-02-02 CN disclosed
US-20240018103-A1 3-HYDROXYOXINDOLE DERIVATIVES AS CRHR2 ANTAGONIST RAQUALIA PHARMA INC. (JP) 2024-01-18 US disclosed
WO-2008121817-A2 QUINOLINE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS COMPRISING THEM FOR SELECTIN INHIBITION WYETH (US) 2008-10-09 WO disclosed
WO-2007132280-A1 ISATIN AND ITS DERIVATIVES FOR USE AS A MEDICAMENT Szegedi Tudományegyetem (HU) 2007-11-22 WO disclosed
US-20070088044-A1 Quinazoline derivatives as antitumor agents ASTRAZENECA AB 2007-04-19 US disclosed
US-20070082921-A1 Quinazoline derivatives as antitumor agents ASTRAZENECA AB 2007-04-12 US disclosed
US-6117885-A Biphenyl-substituted quinoline derivatives E. R. SQUIBB & SONS, INC. (US) 2000-09-12 US disclosed
EP-0556060-A1 Biphenyl-substituted quinoline and naphthyridines derivatives as angiotensine II antagonists E.R. SQUIBB & SONS, INC. (US) 1993-08-18 EP disclosed
JP-H04139167-A NEW METHYLINOLEQUINONE COMPOUND MITSUBISHI GAS CHEM CO INC 1992-05-13 JP 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 (5 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-20240018103-A1 3-HYDROXYOXINDOLE DERIVATIVES AS CRHR2 ANTAGONIST CRHR2, CRHR1, CRH CES1 1763/4885KDR 3868/4885PDPK1 2420/4885
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 3158/4885KDR 4002/4885PDPK1 1258/4885
US-20070088044-A1 Quinazoline derivatives as antitumor agents ERBB2, EGFR, ERBB4 CES1 4214/4885KDR 33/4885PDPK1 372/4885
US-12421191-B2 3-hydroxyoxindole derivatives as CRHR2 antagonist CRHR2, CRHR1, CRH CES1 1763/4885KDR 3868/4885PDPK1 2420/4885
US-20070082921-A1 Quinazoline derivatives as antitumor agents ERBB2, EGFR, ERBB4 CES1 4214/4885KDR 33/4885PDPK1 372/4885

“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.