SCHEMBL918337

SCHEMBL918337

O=C(C=Cc1c2ccccc2cc2ccccc12)c1c2ccccc2cc2ccccc12

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2D6 P10635 1/20 0.63
CYP1A2 P05177 3/20 0.53
KMT2A Q03164 3/20 0.53
CYP2C19 P33261 2/20 0.53
KDM4E B2RXH2 2/20 0.53
MEN1 O00255 2/20 0.53
ALDH1A1 P00352 2/20 0.53
HPGD P15428 2/20 0.53
GLA P06280 1/20 0.53
HSD17B10 Q99714 1/20 0.53
ABCG2 Q9UNQ0 7/20 0.50
CYP3A4 P08684 1/20 0.46
CYP2C9 P11712 1/20 0.46
MAOB P27338 1/20 0.44
LMNA P02545 3/20 0.42
POLB P06746 2/20 0.42
MAPT P10636 2/20 0.41
SMN1; SMN2 Q16637 2/20 0.41
PAX8 Q06710 1/20 0.41
CYP1B1 Q16678 2/20 0.40

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
SCHEMBL918336 1.00 CYP2D6 (0.63) CYP2D6CYP1A2KMT2ACYP2C19KDM4E
SCHEMBL973107 0.84 CYP3A4 (0.62) CYP2D6CYP1A2KMT2ACYP2C19KDM4E
SCHEMBL12948677 0.84 CYP3A4 (0.62) CYP2D6CYP1A2KMT2ACYP2C19KDM4E
SCHEMBL973106 0.84 ABCG2 (0.69) CYP2D6CYP1A2KMT2ACYP2C19KDM4E
SCHEMBL11405387 0.84 ABCG2 (0.69) CYP2D6CYP1A2KMT2ACYP2C19KDM4E
SCHEMBL8854345 0.81 CYP2D6 (0.58) CYP2D6CYP1A2KMT2ACYP2C19KDM4E
SCHEMBL970864 0.81 MAPT (0.60) CYP2D6CYP1A2KMT2ACYP2C19KDM4E
SCHEMBL979447 0.80 CYP3A4 (0.58) CYP2D6CYP1A2KMT2ACYP2C19MEN1
SCHEMBL979445 0.80 CYP1B1 (0.65) CYP2D6CYP1A2KMT2ACYP2C19KDM4E
SCHEMBL12948651 0.80 CYP3A4 (0.58) CYP2D6CYP1A2KMT2ACYP2C19MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7875408-B2 comprising photobleachable organic materials can be bleached by 193 nm light, and brought back to their original state by stimuli after exposure; to improve the aerial image effectively seen by the photoresist and thereby improve the contrast INTERNATIONAL BUSINESS MACHINES CORPORATION (US) 2011-01-25 US disclosed
US-7872029-B2 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states BOWEN J PHILLIP 2011-01-18 US disclosed
US-20090018167-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states Robinson, Thomas Philip (US) 2009-01-15 US disclosed
US-7432303-B2 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states Bowen, J. Phillip (US) 2008-10-07 US disclosed
US-20080182178-A1 Bleachable materials for lithography GLOBALFOUNDRIES U.S. INC. 2008-07-31 US disclosed
US-20050148599-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. 2005-07-07 US disclosed
US-6906105-B2 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states BOWEN J PHILLIP (US) 2005-06-14 US disclosed
US-20030027830-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. 2003-02-06 US disclosed
US-6462075-B1 USE OF CHALCONE AND ITS DERIVATIVES AS ANTITUMOR/ANTICANCER AGENTS AND TO TREAT A NUMBER OF CONDITIONS OR DISEASE STATES IN WHICH ANGIOGENESIS IS A FACTOR INCLUDING PSORIASIS, ACNE, ROSACEA, WARTS, ECZEMA, HEMANGIOMAS AND LYMPHANGIOGENESIS THE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. 2002-10-08 US disclosed
EP-1242352-A2 CHALCONE AND ITS ANALOGS AS AGENTS FOR THE INHIBITION OF ANGIOGENESIS AND RELATED DISEASE STATES UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2002-09-25 EP disclosed
US-20020040029-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states BOWEN, J. PHILLIP 2002-04-04 US disclosed
WO-2001046110-A2 CHALCONE AND ITS ANALOGS AS AGENTS FOR THE INHIBITION OF ANGIOGENESIS AND RELATED DISEASE STATES THE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2001-06-28 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 (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-20020040029-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states FLT1, FLT4, VEGFA CYP2D6 1885/4885CYP1A2 795/4885KMT2A 2333/4885
US-20090018167-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states FLT1, FLT4, VEGFA CYP2D6 1826/4885CYP1A2 792/4885KMT2A 2276/4885
US-20030027830-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states FLT1, VEGFA, FLT4 CYP2D6 1861/4885CYP1A2 655/4885KMT2A 2196/4885
US-20050148599-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states FLT1, VEGFA, FLT4 CYP2D6 1861/4885CYP1A2 655/4885KMT2A 2196/4885

“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.