SCHEMBL973106

SCHEMBL973106

O=C(C=Cc1ccccc1)c1c2ccccc2cc2ccccc12

nearest known ligand 0.69

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ABCG2 Q9UNQ0 5/20 0.69
▸ SLC5A1 P13866 1/20 0.58
▸ SLC5A2 P31639 1/20 0.58
▸ CYP1B1 Q16678 6/20 0.57
▸ CYP1A2 P05177 4/20 0.56
▸ KMT2A Q03164 3/20 0.56
▸ CYP2C19 P33261 3/20 0.56
▸ MEN1 O00255 2/20 0.56
▸ ALDH1A1 P00352 2/20 0.56
▸ KDM4E B2RXH2 1/20 0.56
▸ GLA P06280 1/20 0.56
▸ HPGD P15428 1/20 0.56
▸ HSD17B10 Q99714 1/20 0.56
▸ CYP1A1 P04798 3/20 0.55
▸ MAPT P10636 4/20 0.55
▸ LMNA P02545 3/20 0.55
▸ MAOB P27338 2/20 0.55
▸ PLIN1 O60240 2/20 0.55
▸ RECQL P46063 2/20 0.55
▸ PLIN5 Q00G26 2/20 0.55

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
SCHEMBL11405387 1.00 ABCG2 (0.69) ABCG2SLC5A1SLC5A2CYP1B1CYP1A2
SCHEMBL12948651 0.85 CYP3A4 (0.58) ABCG2CYP1B1CYP1A2KMT2ACYP2C19
SCHEMBL979447 0.85 CYP3A4 (0.58) ABCG2CYP1B1CYP1A2KMT2ACYP2C19
SCHEMBL918336 0.84 CYP2D6 (0.63) ABCG2SLC5A1SLC5A2CYP1B1CYP1A2
SCHEMBL918337 0.84 CYP2D6 (0.63) ABCG2SLC5A1SLC5A2CYP1B1CYP1A2
SCHEMBL11139519 0.84 MAPT (0.58) ABCG2CYP1B1CYP1A2KMT2AMEN1
SCHEMBL11139521 0.84 MAPT (0.58) ABCG2CYP1B1CYP1A2KMT2AMEN1
SCHEMBL7840056 0.83 CYP1B1 (0.57) ABCG2SLC5A1SLC5A2CYP1B1CYP1A2
SCHEMBL970864 0.80 MAPT (0.60) ABCG2CYP1B1CYP1A2KMT2ACYP2C19
Chalcone SCHEMBL28873552 0.79 CYP1B1 (0.63) ABCG2CYP1B1CYP1A2KMT2ACYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
JP-55120535-A — — None — — JP 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-7867629-B2 Nitrogenous heterocyclic derivative and organic electroluminescent element employing the same IDEMITSU KOSAN CO., LTD. (JP) 2011-01-11 — — 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-20060154105-A1 Nitrogenous heterocyclic derivative and organic elecrtroluminescent element employing the same IDEMITSU KOSAN CO., LTD. (JP) 2006-07-13 — — US disclosed
EP-1582516-A1 NITROGENOUS HETEROCYCLIC DERIVATIVE AND ORGANIC ELECTROLUMINESCENT ELEMENT EMPLOYING THE SAME IDEMITSU KOSAN CO., LTD. (JP) 2005-10-05 — — EP 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
JP-S55120535-A ANTHRACENE DERIVATIVE AND LUMINESCENT COMPOSITION TEIJIN LTD 1980-09-17 — — JP 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 (5 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 ABCG2 635/4885SLC5A1 3358/4885SLC5A2 4074/4885
US-20090018167-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states FLT1, FLT4, VEGFA ABCG2 659/4885SLC5A1 3563/4885SLC5A2 4224/4885
US-20030027830-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states FLT1, VEGFA, FLT4 ABCG2 535/4885SLC5A1 3282/4885SLC5A2 3799/4885
US-20050148599-A1 Chalcone and its analogs as agents for the inhibition of angiogenesis and related disease states FLT1, VEGFA, FLT4 ABCG2 535/4885SLC5A1 3282/4885SLC5A2 3799/4885
US-20060154105-A1 Nitrogenous heterocyclic derivative and organic elecrtroluminescent element employing the same L1CAM, NOTCH1, NUDC ABCG2 2886/4885SLC5A1 4240/4885SLC5A2 3817/4885

“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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