SCHEMBL6859660

SCHEMBL6859660

COc1cc(C)c(C(=O)c2c(C)cccc2OC(C)=O)c(OC)c1OC

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PTPN1 P18031 1/20 0.49
POLB P06746 1/20 0.44
HTT P42858 2/20 0.43
TUBB4A P04350 2/20 0.42
TUBB P07437 2/20 0.42
TUBA3C P0DPH7 2/20 0.42
TUBA1B P68363 2/20 0.42
TUBA4A P68366 2/20 0.42
TUBB4B P68371 2/20 0.42
TUBB3 Q13509 2/20 0.42
TUBB2A Q13885 2/20 0.42
TUBB8 Q3ZCM7 2/20 0.42
TUBA3E Q6PEY2 2/20 0.42
TUBA1A Q71U36 2/20 0.42
TUBA1C Q9BQE3 2/20 0.42
TUBB6 Q9BUF5 2/20 0.42
TUBB2B Q9BVA1 2/20 0.42
TUBB1 Q9H4B7 2/20 0.42
KDM4E B2RXH2 1/20 0.41
ALDH1A1 P00352 1/20 0.41

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
SCHEMBL6740389 0.90 KCNB1 (0.47) PTPN1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL7519964 0.87 KRAS (0.47) PTPN1POLBHTTTUBB4ATUBB
SCHEMBL7110651 0.86 ELANE (0.43) PTPN1TUBB4ATUBBTUBA3CTUBA1B
SCHEMBL8464629 0.85 CA12 (0.53) POLBTUBB4ATUBBTUBA3CTUBA1B
SCHEMBL6852540 0.82 CYP19A1 (0.51) TUBB4ATUBBTUBA3CTUBA1BTUBA4A
SCHEMBL27813524 0.81 ACHE (0.45) PTPN1POLBHTTTUBB4ATUBB
SCHEMBL6857968 0.81 POLB (0.44) POLBHTTTUBB4ATUBBTUBA3C
SCHEMBL6860817 0.81 POLB (0.44) PTPN1POLBHTTTUBB4ATUBB
SCHEMBL7943881 0.79 ATM (0.54) POLBTUBB4ATUBBTUBA3CTUBA1B
SCHEMBL6742658 0.78 KCNB1 (0.44) TUBB4ATUBBTUBA3CTUBA1BTUBA4A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0967196-B1 Substituted 2-hydroxybenzophenones, preparation thereof, their use as fungicide and their fungicidal compositions BASF AG (DE) 2003-10-22 EP claimed
EP-0967196-A2 Substituted 2-hydroxybenzophenones, preparation thereof, their use as fungicide and their fungicidal compositions American Cyanamid Company (US) 1999-12-29 EP claimed
US-6790851-B2 Fungicidal compositions SYNGENTA CROP PROTECTION, INC. 2004-09-14 US disclosed
EP-1278414-B1 FUNGICIDAL COMPOSITIONS SYNGENTA PARTICIPATIONS AG (CH) 2003-12-17 EP disclosed
EP-0967196-B1 Substituted 2-hydroxybenzophenones, preparation thereof, their use as fungicide and their fungicidal compositions BASF AG (DE) 2003-10-22 EP disclosed
US-20030166669-A1 Fungicidal compositions SYNGENTA CROP PROTECTION, INC. 2003-09-04 US disclosed
EP-1278414-A1 FUNGICIDAL COMPOSITIONS Syngenta Participations AG (CH) 2003-01-29 EP disclosed
WO-2001080643-A1 FUNGICIDAL COMPOSITIONS SYNGENTA PARTICIPATIONS AG (CH) 2001-11-01 WO disclosed
US-6127570-A USEFUL AS FUNGICIDES HAVING HIGH SYSTEMICITIES AMERICAN CYANAMID COMPANY (US) 2000-10-03 US disclosed
EP-0967196-A2 Substituted 2-hydroxybenzophenones, preparation thereof, their use as fungicide and their fungicidal compositions American Cyanamid Company (US) 1999-12-29 EP 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-20030166669-A1 Fungicidal compositions CBR1, CBR3, CYP1B1 PTPN1 172/4885POLB 2317/4885HTT 3344/4885

“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.