SCHEMBL6702285

SCHEMBL6702285

O=C(O)c1cccc(Sc2ccc([N+](=O)[O-])cc2)c1

nearest known ligand 0.66

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ TP53 P04637 1/20 0.61
▸ KDM4E B2RXH2 1/20 0.57
▸ MAPT P10636 4/20 0.55
▸ NPC1 O15118 1/20 0.55
▸ PKM P14618 1/20 0.55
▸ RAB9A P51151 1/20 0.55
▸ PAX8 Q06710 1/20 0.55
▸ TDP1 Q9NUW8 1/20 0.54
▸ HPGD P15428 2/20 0.53
▸ CYP1A2 P05177 1/20 0.53
▸ CYP2C9 P11712 1/20 0.53
▸ HSD17B10 Q99714 1/20 0.53
▸ GSTP1 P09211 1/20 0.52
▸ GSTM2 P28161 1/20 0.52
▸ MEN1 O00255 3/20 0.50
▸ KMT2A Q03164 3/20 0.50
▸ CES2 O00748 2/20 0.50
▸ CES1 P23141 2/20 0.50
▸ SRD5A2 P31213 1/20 0.50
▸ MAPK1 P28482 1/20 0.47

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
SCHEMBL2200367 0.87 ALDH1A1 (0.62) TP53MAPTNPC1HPGDMEN1
SCHEMBL13265968 0.87 TSHR (0.62) TP53KDM4EMAPTHPGDMEN1
SCHEMBL14537799 0.87 ALDH1A1 (0.62) TP53KDM4EMAPTPKMHPGD
SCHEMBL10650255 0.85 TP53 (0.61) TP53KDM4EMAPTNPC1RAB9A
SCHEMBL3197561 0.83 MEN1 (0.53) MAPTRAB9AHPGDCYP1A2MEN1
SCHEMBL1447749 0.82 HPGD (0.66) TP53KDM4EHPGDCYP1A2CYP2C9
SCHEMBL6778027 0.82 HPGD (0.70) HPGDCYP1A2CYP2C9HSD17B10GSTP1
SCHEMBL31383422 0.82 CYP1A2 (0.76) TP53HPGDCYP1A2CYP2C9HSD17B10
SCHEMBL2406839 0.82 CYP1A2 (0.76) TP53HPGDCYP1A2CYP2C9HSD17B10
Hydrochloric Acid SCHEMBL7134403 0.80 HPGD (0.63) TP53KDM4EHPGDCYP1A2CYP2C9

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20070099919-A1 Composition and synthesis of new reagents for inhibition of HIV replication NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2007-05-03 — — US disclosed
EP-1119548-B1 3-(3-CHLORO-4-HYDROXYPHENYLAMINO)-4-(2-NITROPHENYL)-1H-PYRROLE-2,5-DIONE AS GLYCOGEN SYNTHASE KINASE-3 INHIBITOR (GSK-3) SMITHKLINE BEECHAM PLC (GB) 2004-12-08 — — EP disclosed
US-6719520-B2 FOR INHIBITION OF GLYCOGEN SYNTHASE KINASE-3 (GSK-3); TREATMENT AND PROPHYLAXIS FOR DIABETES, CHRONIC NEURODEGENERATIVE CONDITIONS, MOOD DISORDERS SUCH AS SCHIZOPHRENIA AND MANIC DEPRESSION AND HAIR LOSS AND CANCER SMITHKLINE BEECHAM CORPORATION 2004-04-13 — — US disclosed
US-20040010031-A1 Novel method and compounds SMITHKLINE BEECHAM P.L.C. 2004-01-15 — — US disclosed
WO-2001074771-A1 PYRROLE-2,5-DIONE DERIVATIVES FOR THE TREATMENT OF DIABETES SMITHKLINE BEECHAM P.L.C. (GB) 2001-10-11 — — WO disclosed
EP-1119548-A1 PYRROLE-2,5-DIONES AS GSK-3 INHIBITORS SMITHKLINE BEECHAM PLC (GB) 2001-08-01 — — EP disclosed
WO-2000021927-A2 PYRROLE-2,5-DIONES AS GSK-3 INHIBITORS SMITHKLINE BEECHAM PLC (GB) 2000-04-20 — — 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 (2 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-20040010031-A1 Novel method and compounds GSK3A, GSK3B, GSKIP TP53 3964/4885KDM4E 2477/4885MAPT 72/4885
US-20070099919-A1 Composition and synthesis of new reagents for inhibition of HIV replication REV1, MAVS, ISG15 TP53 1596/4885KDM4E 980/4885MAPT 2825/4885

“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.

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