SCHEMBL6995943

SCHEMBL6995943

CC(=O)Oc1ccc2cc(CN3C(=O)c4ccccc4C3=O)c(=O)oc2c1

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ GLA P06280 5/20 0.61
▸ KDM4E B2RXH2 5/20 0.61
▸ RAB9A P51151 4/20 0.61
▸ NPC1 O15118 3/20 0.61
▸ MEN1 O00255 3/20 0.61
▸ KMT2A Q03164 3/20 0.61
▸ SMN1; SMN2 Q16637 5/20 0.53
▸ GAA P10253 4/20 0.53
▸ HPGD P15428 4/20 0.53
▸ CASP1 P29466 2/20 0.53
▸ CASP7 P55210 2/20 0.53
▸ HSD17B10 Q99714 2/20 0.53
▸ ALDH1A1 P00352 4/20 0.53
▸ CA12 O43570 2/20 0.51
▸ CA9 Q16790 2/20 0.51
▸ POLB P06746 1/20 0.51
▸ TDP1 Q9NUW8 1/20 0.51
▸ MAPT P10636 1/20 0.49
▸ GPR55 Q9Y2T6 1/20 0.47
▸ CA2 P00918 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
SCHEMBL7001341 0.88 RAB9A (0.63) GLAKDM4ERAB9ANPC1MEN1
SCHEMBL6989186 0.81 MIF (0.53) GLAKDM4ERAB9ANPC1MEN1
SCHEMBL6996195 0.80 ALDH1A1 (0.60) GLAKDM4EMEN1KMT2ASMN1; SMN2
SCHEMBL7093747 0.79 MAOA (0.61) KDM4ERAB9ANPC1MEN1KMT2A
SCHEMBL6996805 0.78 GLA (0.62) GLAKDM4ERAB9ANPC1MEN1
SCHEMBL27766198 0.77 KMT2A (0.49) NPC1MEN1KMT2ASMN1; SMN2HPGD
SCHEMBL14880118 0.76 NPC1 (1.00) GLAKDM4ERAB9ANPC1MEN1
SCHEMBL23316741 0.75 GLA (0.72) GLAKDM4ERAB9ANPC1MEN1
SCHEMBL10405182 0.74 MAOA (0.44) KDM4EKMT2ASMN1; SMN2CASP1CASP7
SCHEMBL31566290 0.74 NPC1 (0.81) GLAKDM4ERAB9ANPC1MEN1

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 GLA 1490/4885KDM4E 3035/4885RAB9A 4514/4885

“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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