SCHEMBL3899031

SCHEMBL3899031

O=CON1CCc2ccccc21

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 7/20 0.46
MEN1 O00255 4/20 0.46
KMT2A Q03164 4/20 0.46
USP2 O75604 1/20 0.46
CDK4 P11802 1/20 0.46
ALOX15 P16050 1/20 0.46
CCND1 P24385 1/20 0.46
NOTUM Q6P988 1/20 0.44
TSHR P16473 3/20 0.43
SIGMAR1 Q99720 1/20 0.43
HPGD P15428 1/20 0.42
MAPT P10636 5/20 0.41
SMN1; SMN2 Q16637 4/20 0.41
NPC1 O15118 3/20 0.41
RAB9A P51151 3/20 0.41
NPSR1 Q6W5P4 1/20 0.41
TP53 P04637 1/20 0.41
GAA P10253 1/20 0.41
L3MBTL1 Q9Y468 2/20 0.40
KDM4E B2RXH2 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
SCHEMBL8861369 0.89 SMN1; SMN2 (0.50) ALDH1A1MEN1KMT2ANOTUMTSHR
SCHEMBL4685687 0.80 ALDH1A1 (0.48) ALDH1A1MEN1KMT2AUSP2CDK4
SCHEMBL9132803 0.79 ALDH1A1 (0.52) ALDH1A1MEN1KMT2AUSP2CDK4
SCHEMBL28246338 0.78 NOTUM (0.46) ALDH1A1MEN1KMT2ANOTUMTSHR
SCHEMBL1408706 0.76 ALDH1A1 (0.48) ALDH1A1MEN1KMT2AUSP2CDK4
SCHEMBL27754978 0.76 MEN1 (0.47) ALDH1A1MEN1KMT2AUSP2CDK4
SCHEMBL21798510 0.74 NOTUM (0.50) ALDH1A1MEN1KMT2ANOTUMTSHR
SCHEMBL28213553 0.74 ALDH1A1 (0.43) ALDH1A1MEN1KMT2AUSP2CDK4
SCHEMBL14156263 0.73 SMN1; SMN2 (0.46) ALDH1A1MEN1KMT2AUSP2CDK4
SCHEMBL6769554 0.73 MEN1 (0.46) ALDH1A1MEN1KMT2AUSP2CDK4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110256326-B Indoline carboxylic acid alkaloid in purslane and extraction and separation method and application thereof 辽宁中医药大学 2022-05-13 CN claimed
CN-111646999-A Indoline carboxylic acid compound and preparation method thereof 内江师范学院 2020-09-11 CN claimed
US-20090253932-A1 Resolution of Racemic Organic Acids with (1S, 4S)-4[3,4-Dichlorophenyl]-1,2,3,4-Tetrahydro-N-Methyl-1-Naphthaloneamine MATRIX LABORATORIES LTD (IN) 2009-10-08 US claimed
EP-1831132-A2 RESOLUTION OF RACEMIC ORGANIC ACIDS WITH (1S, 4S)-4[3,4-DICHLOROPHENYL]-1,2,3,4- TETRAHYDRO-N-METHYL-1-NAPHTHALONEAMINE Matrix Laboratories Ltd (IN) 2007-09-12 EP claimed
WO-2006013581-A2 RESOLUTION OF RACEMIC ORGANIC ACIDS WITH (1S, 4S)-4[3,4-DICHLOROPHENYL]-1,2,3,4- TETRAHYDRO-N-METHYL-1-NAPHTHALONEAMINE MATRIX LABORATORIES LTD (IN) 2006-02-09 WO claimed
US-6232305-B1 ANTICANCER AGENTS; BONE DISORDERS; ANTIARTHRITIC AGENTS; RESPIRATORY SYSTEM DISORDERS NAEJA PHARMACEUTICAL INC. (CA) 2001-05-15 US claimed
JP-3204666-A None JP disclosed
US-11964037-B2 Hair-dyeing method KAO CORPORATION (JP) 2024-04-23 US disclosed
US-20230110875-A1 ANTI-CD276 POLYPEPTIDES, PROTEINS, AND CHIMERIC ANTIGEN RECEPTORS BIOMED VALLEY DISCOVERIES, INC. 2023-04-13 US disclosed
US-20230048023-A1 HAIR-DYEING METHOD KAO CORPORATION (JP) 2023-02-16 US disclosed
EP-4082620-A1 HAIR-DYEING METHOD Kao Corporation (JP) 2022-11-02 EP disclosed
CN-114828817-A Method for dyeing hair 花王株式会社 2022-07-29 CN disclosed
CN-110256326-B Indoline carboxylic acid alkaloid in purslane and extraction and separation method and application thereof 辽宁中医药大学 2022-05-13 CN disclosed
US-4697016-A Intermediates for the preparation of a carboxylic acid CIBA-GEIGY CORPORATION (US) 1987-09-29 US disclosed
EP-0105919-B1 1-CARBOXYALKANOYLPERHYDROINDOLE-2-CARBOXYLIC ACIDS AND DERIVATIVES CIBA-GEIGY AG (CH) 1987-07-08 EP disclosed
US-4595766-A Process for the preparation of an indoline carboxylic acid CIBA-GEIGY CORPORATION (US) 1986-06-17 US disclosed
US-4595766-A Process for the preparation of an indoline carboxylic acid CIBA-GEIGY CORPORATION (US) 1986-06-17 US disclosed
US-4493843-A Indole and indoline carboxylic acid compounds and method of use MAY & BAKER LIMITED (GB) 1985-01-15 US disclosed
EP-0105919-A1 1-CARBOXYALKANOYLPERHYDROINDOLE-2-CARBOXYLIC ACIDS AND DERIVATIVES. CIBA GEIGY AG (CH) 1984-04-25 EP disclosed
WO-1983003828-A1 1-CARBOXYALKANOYLPERHYDROINDOLE-2-CARBOXYLIC ACIDS AND DERIVATIVES CIBA-GEIGY AG (CH) 1983-11-10 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 (3 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-20090253932-A1 Resolution of Racemic Organic Acids with (1S, 4S)-4[3,4-Dichlorophenyl]-1,2,3,4-Tetrahydro-N-Methyl-1-Naphthaloneamine HTR4, OXER1, CYP2S1 ALDH1A1 464/4885MEN1 1897/4885KMT2A 2489/4885
US-11964037-B2 Hair-dyeing method KAT7, KAT2B, SRD5A1 ALDH1A1 25/4885MEN1 2278/4885KMT2A 824/4885
US-20230048023-A1 HAIR-DYEING METHOD KAT7, KAT2B, SRD5A1 ALDH1A1 25/4885MEN1 2278/4885KMT2A 824/4885

“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.