SCHEMBL7093747

SCHEMBL7093747

O=C1c2ccccc2C(=O)N1Cc1cc2ccccc2oc1=O

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ MAOA P21397 2/20 0.61
▸ TSHR P16473 3/20 0.49
▸ MAPT P10636 2/20 0.49
▸ MAOB P27338 4/20 0.49
▸ MMP2 P08253 1/20 0.48
▸ MMP9 P14780 1/20 0.48
▸ ADAM17 P78536 1/20 0.48
▸ RAB9A P51151 4/20 0.47
▸ ALDH1A1 P00352 3/20 0.47
▸ KDM4E B2RXH2 1/20 0.47
▸ SMN1; SMN2 Q16637 3/20 0.46
▸ HPGD P15428 2/20 0.46
▸ TYR P14679 1/20 0.46
▸ DAO P14920 1/20 0.46
▸ AKR1B1 P15121 1/20 0.46
▸ POLB P06746 1/20 0.46
▸ KMT2A Q03164 3/20 0.43
▸ PKM P14618 1/20 0.43
▸ NPC1 O15118 3/20 0.43
▸ NCOA1 Q15788 1/20 0.43

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
SCHEMBL6989186 0.85 MIF (0.53) MAOAMAOBRAB9AALDH1A1KDM4E
SCHEMBL10405182 0.83 MAOA (0.44) MAOATSHRMAPTMAOBALDH1A1
SCHEMBL29841388 0.81 MAPT (0.51) TSHRMAPTALDH1A1KDM4ESMN1; SMN2
SCHEMBL1418873 0.81 MAPT (0.51) TSHRMAPTALDH1A1KDM4ESMN1; SMN2
SCHEMBL6995943 0.79 GLA (0.61) MAPTMAOBRAB9AALDH1A1KDM4E
SCHEMBL27625488 0.77 MMP2 (0.67) MAOATSHRMAOBMMP2MMP9
SCHEMBL13612673 0.77 MAOA (0.61) MAOATSHRMAOBMMP2MMP9
SCHEMBL7001341 0.76 RAB9A (0.63) MAPTMAOBRAB9AALDH1A1KDM4E
SCHEMBL1619109 0.75 MAOB (0.67) MAOATSHRMAOBMMP2MMP9
SCHEMBL30594160 0.75 MAOB (0.67) MAOATSHRMAOBMMP2MMP9

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
EP-1032265-B1 NEW PSORALENS FOR PATHOGEN INACTIVATION CERUS CORP (US) 2003-10-29 — — EP disclosed
US-20030082510-A1 Psoralens for pathogen inactivation CERUS CORPORATION (US) 2003-05-01 — — US disclosed
US-6455286-B1 MIXING PSORALEN COMPOUND OF DEFINED STRUCTURE WITH BIOLOGICAL COMPOSITION SUCH AS BLOOD OR PLATELETS, THEN PHOTOACTIVATING COMPOUND TO DEACTIVATE PATHOGEN CERUS CORPORATION 2002-09-24 — — US disclosed
EP-1032265-A4 NEW PSORALENS FOR PATHOGEN INACTIVATION CERUS CORP (US) 2001-05-30 — — EP disclosed
US-6133460-A HAVE PRIMARY AMINO SUBSTITUTIONS ON THE 3-, 4-, 5-, AND 8-POSITIONS OF THE PSORALEN WHICH PERMIT BINDING TO NUCLEIC ACID OF PATHOGENS; CONDITIONS THAT PHOTOACTIVATE THESE PSORALENS RESULT IN INACTIVATION OF PATHOGENS WHICH CONTAIN NUCLEIC ACID CERUS CORPORATION (US) 2000-10-17 — — US disclosed
EP-1032265-A1 NEW PSORALENS FOR PATHOGEN INACTIVATION Cerus Corporation (US) 2000-09-06 — — EP disclosed
WO-1999026476-A1 NEW PSORALENS FOR PATHOGEN INACTIVATION CERUS CORPORATION (US) 1999-06-03 — — 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 (1 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-20030082510-A1 Psoralens for pathogen inactivation BPGM, XPA, RAD50 MAOA 2213/4885TSHR 3453/4885MAPT 2933/4885

“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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