SCHEMBL5953069

SCHEMBL5953069

CCCC[Sn](CCCC)(CCCC)c1cccc(O)c1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
DRD3 P35462 6/20 0.40
DRD2 P14416 5/20 0.40
OPRM1 P35372 4/20 0.40
OPRD1 P41143 3/20 0.40
OPRK1 P41145 3/20 0.40
ALDH1A1 P00352 2/20 0.39
CYP3A4 P08684 2/20 0.39
CA12 O43570 1/20 0.39
CA2 P00918 1/20 0.39
LMNA P02545 1/20 0.39
CA5A P35218 1/20 0.39
CA9 Q16790 1/20 0.39
HSD17B10 Q99714 1/20 0.39
CA14 Q9ULX7 1/20 0.39
CA5B Q9Y2D0 1/20 0.39
ACHE P22303 4/20 0.38
TYR P14679 1/20 0.38
TSHR P16473 1/20 0.38
DRD1 P21728 3/20 0.38
DRD4 P21917 3/20 0.38

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
SCHEMBL5953196 0.79 KMT2A (0.41) ALDH1A1
SCHEMBL1453524 0.79 ACHE (0.41) ALDH1A1CYP3A4ACHESMN1; SMN2
SCHEMBL2700589 0.79 ENPP2 (0.38) DRD3DRD2TSHR
SCHEMBL2864353 0.78 ACHE (0.38) ACHE
SCHEMBL3221521 0.78 TSHR (0.45) ALDH1A1CYP3A4CA12CA2CA9
SCHEMBL2482070 0.76 ESR1 (0.45) ALDH1A1CYP3A4LMNAHSD17B10ACHE
SCHEMBL30185957 0.76 KMT2A (0.46) CA12CA2CA9SMN1; SMN2
SCHEMBL2392823 0.76 HPGD (0.47) ALDH1A1LMNATSHRSMN1; SMN2
SCHEMBL1884032 0.76 KMT2A (0.46) CA12CA2CA9SMN1; SMN2
SCHEMBL276811 0.76 LTA4H (0.38) TSHRSMN1; SMN2

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
CN-101679432-B Heteroaryl compounds, compositions thereof, and their use as protein kinase inhibitors SIGNAL PHARM LLC 2015-04-22 CN disclosed
US-7038070-B2 Preparation of preparing substituted indanones BASELL POLYOLEFINE GMBH (DE) 2006-05-02 US disclosed
US-6963017-B2 Preparation of preparing substituted indanones BASELL POLYOLEFINE GMBH (DE) 2005-11-08 US disclosed
EP-0968158-B1 METHOD OF PREPARING SUBSTITUTED INDANONES, THE SUBSTITUTED INDANONES AND METALLOCENES PREPARED THEREFROM BASELL POLYOLEFINE GMBH (DE) 2005-08-10 EP disclosed
US-20050033076-A1 Preparation of preparing substituted indanones EQUISTAR CHEMICALS, LP 2005-02-10 US disclosed
US-20030009046-A1 Preparation of preparing substituted indanones EQUISTAR CHEMICALS, LP 2003-01-09 US disclosed
US-6147169-A LOW TEMPERATURE CURING MIXTURE OF REACTIVE BASE RESIN AND A CLATHRATE COMPRISING A TETRAKISPHENOL HOSTING A CURING AGENT OR CURING CATALYST; STORAGE STABILITY, CORROSION RESISTANCE, ADHESION KANSAI PAINT CO., LTD. (JP) 2000-11-14 US 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 (2 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-20050033076-A1 Preparation of preparing substituted indanones CYP1A2, CYP2J2, IDH3A DRD3 1868/4885DRD2 1803/4885OPRM1 2829/4885
US-20030009046-A1 Preparation of preparing substituted indanones CYP1A2, CYP1B1, CYP1A1 DRD3 1784/4885DRD2 1860/4885OPRM1 2604/4885

“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.