SCHEMBL19982

SCHEMBL19982

O=C1Cc2ccc(Br)cc2N1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
AHR P35869 4/20 1.00
CMA1 P23946 2/20 1.00
TDP2 O95551 3/20 0.62
EIF2AK2 P19525 1/20 0.59
PDK2 Q15119 1/20 0.53
CRBN Q96SW2 3/20 0.46
IDO1 P14902 1/20 0.44
CCNB2 O95067 5/20 0.44
CDK1 P06493 5/20 0.44
CCNB1 P14635 5/20 0.44
GSK3B P49841 5/20 0.44
CDK5 Q00535 5/20 0.44
CDK5R1 Q15078 5/20 0.44
CCNB3 Q8WWL7 5/20 0.44
MAOA P21397 1/20 0.43
MAOB P27338 1/20 0.43
MEN1 O00255 2/20 0.42
KMT2A Q03164 2/20 0.42
KDM4E B2RXH2 1/20 0.42
CDC7 O00311 1/20 0.42

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
SCHEMBL29584808 1.00 AHR (1.00) AHRCMA1TDP2EIF2AK2PDK2
SCHEMBL1233125 0.98 AHR (0.96) AHRCMA1TDP2EIF2AK2PDK2
SCHEMBL8131472 0.98 AHR (0.96) AHRCMA1TDP2EIF2AK2PDK2
Methylamine SCHEMBL27858404 0.94 AHR (0.89) AHRCMA1TDP2EIF2AK2PDK2
SCHEMBL6431 0.84 AHR (0.72) AHRCMA1TDP2EIF2AK2PDK2
SCHEMBL28382093 0.83 CMA1 (0.70) AHRCMA1TDP2EIF2AK2CDK5
SCHEMBL29754270 0.82 CMA1 (0.70) AHRCMA1TDP2CRBNIDO1
SCHEMBL2220942 0.82 CMA1 (0.70) AHRCMA1TDP2CRBNIDO1
SCHEMBL1233674 0.82 AHR (0.68) AHRCMA1TDP2EIF2AK2PDK2
SCHEMBL31734661 0.82 AHR (0.69) AHRCMA1TDP2IDO1CCNB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108530481-A A kind of preparation method of indolone phosphono hydrazine compound and its derivative 广西大学 2018-09-14 CN claimed
CN-103467711-B Connect the semi-conducting polymer of two thiophene oxindole bases and preparation thereof, purposes SHANGHAI JIAO TONG UNIVERSITY (CN) 2015-10-14 CN claimed
CN-103467711-A Bi-thiophene oxindolyl semiconductor polymer, and preparation and application thereof UNIV SHANGHAI JIAOTONG 2013-12-25 CN claimed
US-6469181-B1 PREPARING 2-OXINDOLES AND N-HYROXY-2- OXINDOLES VIA REDUCTION OF 2-NITROARYLMALONATE DIESTERS WITHOUT ISOLATION OF INTERMEDIATES CATALYTICA, INC. 2002-10-22 US claimed
CN-1078590-C Process for preparing 2-oxindoles and N-hydroxy-2-oxindoles CATALYTICA INC (US) 2002-01-30 CN claimed
EP-0809631-A4 PROCESS FOR PREPARING 2-OXINDOLES AND N-HYDROXY-2-OXINDOLES CATALYTICA INC (US) 1998-07-08 EP claimed
EP-0809631-A1 PROCESS FOR PREPARING 2-OXINDOLES AND N-HYDROXY-2-OXINDOLES CATALYTICA, INC. (US) 1997-12-03 EP claimed
WO-1996023770-A1 PROCESS FOR PREPARING 2-OXINDOLES AND N-HYDROXY-2-OXINDOLES CATALYTICA, INC. (US) 1996-08-08 WO claimed
EP-4747242-A1 HETEROCYCLIC INHIBITORS OF IGF-1R FOR TREATMENT OF DISEASE Horizon Therapeutics Ireland Dac (IE) 2026-05-27 EP disclosed
US-12630516-B2 Compounds NRG THERAPEUTICS LTD. (GB) 2026-05-19 US disclosed
EP-4713096-A1 CDK INHIBITOR COMPOUNDS Aleksia Therapeutics, Inc. (US) 2026-03-25 EP disclosed
US-20260070902-A1 SULFONYL DERIVATIVES AS CCR6 INHIBITORS HOFFMANN-LA ROCHE INC. (US) 2026-03-12 US disclosed
US-20260049092-A1 ANTIBACTERIAL COMPOUNDS BLACKSMITH MEDICINES INC (US) 2026-02-19 US disclosed
EP-3950682-B1 PREPARATION METHOD FOR AMIDE COMPOUNDS AND USE THEREOF IN MEDICAL FIELD SHANGHAI SYNERGY PHARMACEUTICAL SCIENCES CO LTD (CN) 2026-02-11 EP disclosed
EP-0175551-A1 Analgesic and antiinflammatory 1,3-diacyl-2-oxindole compounds PFIZER INC. (US) 1986-03-26 EP disclosed
US-4569942-A N,3-Disubstituted 2-oxindole-1-carboxamides as analgesic and antiinflammatory agents PFIZER INC. (US) 1986-02-11 US disclosed
EP-0164860-A1 N,3-disubstituted 2-oxindole-1-carboxamides as analgesic and antiinflammatory agents PFIZER INC. (US) 1985-12-18 EP disclosed
US-4556672-A 3-Substituted 2-oxindole-1-carboxamides as analgesic and anti-inflammatory agents PFIZER INC. (US) 1985-12-03 US disclosed
EP-0156603-A2 3-Substituted 2-oxindole-1-carboxamides as analgesic and anti-inflammatory agents PFIZER INC. (US) 1985-10-02 EP disclosed
EP-0153818-A2 1,3-Disubstituted 2-oxindoles as analgesic and anti-inflammatory agents PFIZER INC. (US) 1985-09-04 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 (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-12630516-B2 Compounds CYP4B1, CYP1B1, NR4A1 AHR 29/4885CMA1 2165/4885TDP2 3367/4885
US-20260049092-A1 ANTIBACTERIAL COMPOUNDS H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, CBR1, FPR1 AHR 1311/4885CMA1 1371/4885TDP2 4807/4885
US-20260070902-A1 SULFONYL DERIVATIVES AS CCR6 INHIBITORS CCR6, CCR1, CCR4 AHR 271/4885CMA1 491/4885TDP2 3949/4885

“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.