SCHEMBL7000396

SCHEMBL7000396

Cc1oc2c(COCCO)c3oc(=O)cc(C)c3cc2c1C

nearest known ligand 0.41

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MCL1 Q07820 2/20 0.41
KDM4E B2RXH2 9/20 0.41
GLA P06280 6/20 0.41
GAA P10253 6/20 0.41
ALDH1A1 P00352 6/20 0.41
ERAP1 Q9NZ08 4/20 0.41
L3MBTL1 Q9Y468 4/20 0.41
POLB P06746 3/20 0.41
KMT2A Q03164 3/20 0.41
MEN1 O00255 2/20 0.41
RXFP1 Q9HBX9 2/20 0.41
TDP1 Q9NUW8 2/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
PABPC1 P11940 1/20 0.41
APEX1 P27695 1/20 0.41
RECQL P46063 1/20 0.41
ATM Q13315 1/20 0.41
HPGD P15428 5/20 0.39
STAT6 P42226 1/20 0.39
HIF1A Q16665 1/20 0.39

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
SCHEMBL1115728 0.88 L3MBTL1 (0.44) MCL1KDM4EGLAGAAALDH1A1
SCHEMBL6993313 0.88 MCL1 (0.41) MCL1KDM4EGLAGAAALDH1A1
Hydrochloric Acid SCHEMBL7001517 0.86 MCL1 (0.41) MCL1KDM4EGLAGAAALDH1A1
SCHEMBL4373485 0.85 L3MBTL1 (0.43) MCL1KDM4EGLAGAAALDH1A1
SCHEMBL6996930 0.83 HSD17B10 (0.39) MCL1KDM4EGLAGAAALDH1A1
SCHEMBL6990104 0.83 KDM4E (0.44) MCL1KDM4EGLAGAAALDH1A1
SCHEMBL6994361 0.81 ALDH1A1 (0.41) KDM4EGLAGAAALDH1A1POLB
SCHEMBL7519245 0.80 L3MBTL1 (0.42) MCL1KDM4EGLAGAAALDH1A1
SCHEMBL1115532 0.79 L3MBTL1 (0.41) MCL1KDM4EGLAGAAALDH1A1
SCHEMBL6996035 0.77 MCL1 (0.45) MCL1KDM4EGLAGAAALDH1A1

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 MCL1 1419/4885KDM4E 3035/4885GLA 1490/4885

“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.