SCHEMBL11246667

SCHEMBL11246667

CCCCc1ccc2cc(OC)ccc2c1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 2/20 0.58
LMNA P02545 2/20 0.58
MAPT P10636 2/20 0.58
SMN1; SMN2 Q16637 2/20 0.58
PTGS2 P35354 2/20 0.58
KDM4E B2RXH2 1/20 0.58
NPC1 O15118 1/20 0.58
TP53 P04637 1/20 0.58
CYP3A4 P08684 1/20 0.58
MAOA P21397 1/20 0.58
SLC6A2 P23975 1/20 0.58
RAB9A P51151 1/20 0.58
SLC6A3 Q01959 1/20 0.58
PTGS1 P23219 1/20 0.53
AKR1C3 P42330 1/20 0.53
AKR1C2 P52895 1/20 0.53
IGF1R P08069 1/20 0.49
ALOX15 P16050 1/20 0.49
CYP2A6 P11509 1/20 0.48
HTR2A P28223 1/20 0.48

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
SCHEMBL28131897 0.96 CYP1A2 (0.55) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL7061128 0.95 PTGS2 (0.57) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL16024600 0.93 HTR2A (0.56) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL19506648 0.93 HTR2A (0.56) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL14783441 0.93 HTR2A (0.56) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL16024605 0.90 HTR2A (0.53) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL28841007 0.90 HTR2A (0.53) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL16024669 0.90 HTR2A (0.53) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL3162663 0.89 CYP1A2 (0.62) CYP1A2LMNAMAPTSMN1; SMN2PTGS2
SCHEMBL3153171 0.86 CASP3 (0.51) CYP1A2LMNAMAPTSMN1; SMN2PTGS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-0003643-B1 PROCESS FOR THE PREPARATION OF 4-(6-METHOXY-2-NAPHTHYL)-BUTAN-2-ONE; 4-(6-METHOXY-2-NAPHTHYL)-4-HYDROXYBUT-3-EN-2-ONE AND A PROCESS FOR ITS PREPARATION BEECHAM GROUP PLC (GB) 1982-09-29 EP claimed
US-20230271988-A1 METHOD FOR PRODUCING ORGANOMETALLIC NUCLEOPHILE AND REACTION METHOD USING ORGANOMETALLIC NUCLEOPHILE NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY (JP) 2023-08-31 US disclosed
US-20230271988-A1 METHOD FOR PRODUCING ORGANOMETALLIC NUCLEOPHILE AND REACTION METHOD USING ORGANOMETALLIC NUCLEOPHILE NATIONAL UNIVERSITY CORPORATION HOKKAIDO UNIVERSITY (JP) 2023-08-31 US disclosed
EP-2316469-A1 Delivery system and methods for protecting and administering dextroamphetamine Shire LLC (US) 2011-05-04 EP disclosed
EP-2316468-A1 Delivery system and methods for protecting and administering dextroamphetamine Shire LLC (US) 2011-05-04 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-20230271988-A1 METHOD FOR PRODUCING ORGANOMETALLIC NUCLEOPHILE AND REACTION METHOD USING ORGANOMETALLIC NUCLEOPHILE HPD, TALDO1, OGG1 CYP1A2 537/4885LMNA 4769/4885MAPT 4173/4885

“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.