SCHEMBL2379102

SCHEMBL2379102

O=[N+]([O-])c1cccc2c(Cl)nccc12

nearest known ligand 0.62

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 5/20 0.62
ALDH1A1 P00352 9/20 0.59
KDM4E B2RXH2 5/20 0.59
MEN1 O00255 5/20 0.59
KMT2A Q03164 5/20 0.59
POLB P06746 1/20 0.56
NCOA1 Q15788 1/20 0.55
NCOA3 Q9Y6Q9 1/20 0.55
MAPT P10636 6/20 0.47
SMN1; SMN2 Q16637 6/20 0.47
HTT P42858 4/20 0.47
LMNA P02545 3/20 0.47
PKM P14618 2/20 0.47
HSP90AA1 P07900 2/20 0.47
OPRK1 P41145 2/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
CYP3A4 P08684 1/20 0.46
APEX1 P27695 1/20 0.46
MAPK1 P28482 1/20 0.46
PMP22 Q01453 1/20 0.46

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
SCHEMBL27415734 0.82 TDP1 (0.67) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL11819002 0.81 TDP1 (0.64) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL29482300 0.80 PDE10A (0.56) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL75026 0.80 PDE10A (0.56) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL27932601 0.79 TDP1 (0.62) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL6595618 0.79 TDP1 (0.62) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL9836130 0.79 TDP1 (0.62) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL10549357 0.79 TDP1 (0.62) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL619830 0.79 TDP1 (0.62) TDP1ALDH1A1KDM4EMEN1KMT2A
SCHEMBL29475175 0.79 TDP1 (1.00) TDP1ALDH1A1POLBNCOA1NCOA3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12281126-B2 Inhibitors of cyclin-dependent kinase 7 and uses thereof DANA-FARBER CANCER INSTITUTE, INC. (US) 2025-04-22 US disclosed
EP-3617213-B1 THIENO[3,2-D]PYRIMIDINE DERIVATIVES HAVING INHIBITORY ACTIVITY FOR PROTEIN KINASES HANMI PHARMACEUTICAL CO LTD (KR) 2025-02-19 EP disclosed
CN-113557017-B Inhibitors of cyclin-dependent kinase 7 and uses thereof 丹娜-法伯癌症研究院 2024-11-29 CN disclosed
CN-118878514-A Heterocyclic compounds for modulating NR2F6 TES制药有限责任公司 2024-11-01 CN disclosed
CN-115427394-A Heterocyclic compounds for modulating NR2F6 TES制药有限责任公司 2022-12-02 CN disclosed
US-20220213061-A9 HETEROCYCLIC COMPOUNDS FOR MODULATING NR2F6 TES PHARMA S.R.L. (IT) 2022-07-07 US disclosed
US-20220213061-A9 HETEROCYCLIC COMPOUNDS FOR MODULATING NR2F6 TES PHARMA S.R.L. (IT) 2022-07-07 US disclosed
US-20220089611-A1 INHIBITORS OF CYCLIN-DEPENDENT KINASE 7 AND USES THEREOF DANA-FARBER CANCER INSTITUTE, INC. (US) 2022-03-24 US disclosed
US-20220064160-A1 BICYCLIC DERIVATIVES ELANCO TIERGESUNDHEIT AG (US) 2022-03-03 US disclosed
EP-3902542-A1 INHIBITORS OF CYCLIN-DEPENDENT KINASE 7 AND USES THEREOF Dana-Farber Cancer Institute, Inc. (US) 2021-11-03 EP disclosed
EP-1228043-B1 ISOQUINOLINE AND QUINAZOLINE DEIVATIVES HAVING A COMBINED 5HT1A, 5HT1B AND 5HT1D RECEPTOR ACTIVITY SMITHKLINE BEECHAM PLC (GB) 2005-01-12 EP disclosed
EP-1373252-A1 CHEMICAL DERIVATIVES AND THEIR USE AS ANTI-TELOMERASE AGENT Aventis Pharma S.A. (FR) 2004-01-02 EP disclosed
WO-2002076975-A1 CHEMICAL DERIVATIVES AND THEIR USE AS ANTI-TELOMERASE AGENT AVENTIS PHARMA S.A. (FR) 2002-10-03 WO disclosed
EP-1233965-A1 ISOQUINOLINE AND QUINAZOLINE DERIVATIVES FOR THE TREATMENT OF CNS DISORDERS SMITHKLINE BEECHAM PLC (GB) 2002-08-28 EP disclosed
EP-1228043-A1 ISOQUINOLINE AND QUINAZOLINE DEIVATIVES HAVING A COMBINED 5HT1A, 5HT1B AND 5HT1D RECEPTOR ACTIVITY SMITHKLINE BEECHAM PLC (GB) 2002-08-07 EP disclosed
WO-2001032659-A1 ISOQUINOLINE AND QUINAZOLINE DERIVATIVES FOR THE TREATMENT OF CNS DISORDERS SMITHKLINE BEECHAM P.L.C. (GB) 2001-05-10 WO disclosed
WO-2001032626-A1 ISOQUINOLINE AND QUINAZOLINE DERIVATIVES HAVING A COMBINED 5HT1A, 5HT1B AND 5HT1D RECEPTOR ACTIVITY SMITHKLINE BEECHAM P.L.C. (GB) 2001-05-10 WO disclosed
EP-0355750-B1 Substituted dihydroisoquinolinones and related compounds as potentiators of the lethal effects of radiation and certain chemotherapeutic agents; selected compounds, analogs and process WARNER LAMBERT CO (US) 1995-01-25 EP disclosed
US-5177075-A Antitumor agents WARNER-LAMBERT COMPANY (US) 1993-01-05 US disclosed
EP-0355750-A1 Substituted dihydroisoquinolinones and related compounds as potentiators of the lethal effects of radiation and certain chemotherapeutic agents; selected compounds, analogs and process WARNER-LAMBERT COMPANY (US) 1990-02-28 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 (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-12281126-B2 Inhibitors of cyclin-dependent kinase 7 and uses thereof CDK9, CDK7, CDK1 TDP1 795/4885ALDH1A1 4202/4885KDM4E 3730/4885
US-20220213061-A9 HETEROCYCLIC COMPOUNDS FOR MODULATING NR2F6 NR2E3, NR2F2, NR2C2 TDP1 2327/4885ALDH1A1 2328/4885KDM4E 2961/4885
US-20220089611-A1 INHIBITORS OF CYCLIN-DEPENDENT KINASE 7 AND USES THEREOF CDK9, CDK7, CDK1 TDP1 795/4885ALDH1A1 4202/4885KDM4E 3730/4885
US-20220064160-A1 BICYCLIC DERIVATIVES FABP3, CYCS, PIGS TDP1 4796/4885ALDH1A1 589/4885KDM4E 2222/4885

“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.