SCHEMBL5614873

SCHEMBL5614873

Clc1cccc(C(Cl)[Zr])c1Cl

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PNMT P11086 2/20 0.54
CYP1A2 P05177 2/20 0.54
CYP3A4 P08684 2/20 0.54
CYP2D6 P10635 1/20 0.54
NFKB1 P19838 1/20 0.54
LMNA P02545 3/20 0.52
ALDH1A1 P00352 1/20 0.52
GLA P06280 1/20 0.52
IDO1 P14902 2/20 0.43
TDO2 P48775 1/20 0.43
TSHR P16473 5/20 0.41
MEN1 O00255 1/20 0.39
KMT2A Q03164 1/20 0.39
CYP2A6 P11509 1/20 0.36
KCNH2 Q12809 1/20 0.36
HIF1A Q16665 2/20 0.35
CYP2C9 P11712 1/20 0.35
CYP2C19 P33261 1/20 0.35
KDM4E B2RXH2 1/20 0.35
NR1I2 O75469 1/20 0.35

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
SCHEMBL1872442 0.80 CYP1A2 (0.58) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL11501928 0.76 CYP1A2 (0.65) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL5617277 0.76 PNMT (0.54) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL5933878 0.76 PNMT (0.65) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL5614982 0.76 PNMT (0.54) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL14910625 0.76 LMNA (0.57) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL4940577 0.76 CYP1A2 (0.54) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL9409630 0.76 PNMT (0.54) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL28905220 0.74 IDO1 (0.54) PNMTCYP1A2CYP3A4CYP2D6NFKB1
SCHEMBL11499495 0.73 CYP1A2 (0.56) PNMTCYP1A2CYP3A4CYP2D6NFKB1

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 58 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3288953-B1 BIS(AMINOPHENYLPHENOL) LIGANDS AND TRANSITION METAL COMPOUNDS PREPARED THEREFROM UNIVATION TECH LLC (US) 2021-01-06 EP disclosed
US-10696641-B2 Bis(aminophenylphenol) ligands and transition metal catalysts prepared therefrom UNIVATION TECHNOLOGIES, LLC (US) 2020-06-30 US disclosed
US-10689314-B2 Methods for preparing bridged bi-aromatic ligands UNIVATION TECHNOLOGIES, LLC (US) 2020-06-23 US disclosed
US-10654029-B2 Bridged bi-aromatic ligands and olefin polymerization catalysts prepared therefrom UNIVATION TECHNOLOGIES, LLC (US) 2020-05-19 US disclosed
EP-3632920-A1 METHODS FOR PREPARING BRIDGED BI-AROMATIC LIGANDS Univation Technologies, LLC (US) 2020-04-08 EP disclosed
EP-3286162-B1 METHODS FOR PREPARING BRIDGED BI-AROMATIC LIGANDS UNIVATION TECH LLC (US) 2019-10-23 EP disclosed
EP-3285923-B1 BRIDGED BI-AROMATIC LIGANDS AND OLEFIN POLYMERIZATION CATALYSTS PREPARED THEREFROM UNIVATION TECH LLC (US) 2019-07-17 EP disclosed
US-20190111414-A1 BRIDGED BI-AROMATIC LIGANDS AND OLEFIN POLYMERIZATION CATALYSTS PREPARED THEREFROM UNIVATION TECHNOLOGIES, LLC (US) 2019-04-18 US disclosed
US-10252967-B2 Bridged bi-aromatic ligands and transition metal compounds prepared therefrom UNIVATION TECHNOLOGIES, LLC (US) 2019-04-09 US disclosed
US-10239809-B2 Methods for preparing bridged bi-aromatic ligands UNIVATION TECHNOLOGIES, LLC (US) 2019-03-26 US disclosed
EP-0993464-B1 CATALYST FOR THE PRODUCTION OF OLEFIN POLYMERS UNION CARBIDE CHEM PLASTIC (US) 2003-04-16 EP disclosed
US-20020086960-A1 Polymerization catalyst system, polymerization process and polymer therefrom UNIVATION TECHNOLOGIES, LLC 2002-07-04 US disclosed
US-20020065379-A1 Catalyst for the production of olefin polymers MURRAY REX EUGENE (US) 2002-05-30 US disclosed
US-6320005-B1 CYCLIC HETEROATOM-CONTAINING CATALYST PRECURSOR COMPLEXES OF GROUP 3 TO 6 ELEMENTS AND LANTHANIDES; E.G., (N-(2-PYRIDYL)(BENZYL)METHYL(N-2,6-DIISOPROPYLPHENYL)AMINO)ZIR CONIUM TRIBENZYL UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION 2001-11-20 US disclosed
US-6103657-A Catalyst for the production of olefin polymers UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 2000-08-15 US disclosed
US-6096676-A METALLOCENE COORDINATION CATALYSTS BASED ON A GROUP IVB METAL AND AN ACTIVATING COCATALYST; ADDITION POLYMERATION OF OLEFINS, ALPHA-OLEFINS AND DIENES; HOMOGENEITY; KINETICS UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 2000-08-01 US disclosed
EP-0993464-A1 CATALYST FOR THE PRODUCTION OF OLEFIN POLYMERS UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 2000-04-19 EP disclosed
EP-0993471-A2 CATALYST FOR THE PRODUCTION OF OLEFIN POLYMERS UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 2000-04-19 EP disclosed
WO-1999001460-A1 CATALYST FOR THE PRODUCTION OF OLEFIN POLYMERS UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1999-01-14 WO disclosed
WO-1999001481-A2 CATALYST FOR THE PRODUCTION OF OLEFIN POLYMERS UNION CARBIDE CHEMICALS & PLASTICS TECHNOLOGY CORPORATION (US) 1999-01-14 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 (6 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-10696641-B2 Bis(aminophenylphenol) ligands and transition metal catalysts prepared therefrom WASF2, WEE2, THEM6 PNMT 171/4885CYP1A2 1065/4885CYP3A4 390/4885
US-10689314-B2 Methods for preparing bridged bi-aromatic ligands TYR, AOC2, BICRA PNMT 347/4885CYP1A2 146/4885CYP3A4 120/4885
US-10654029-B2 Bridged bi-aromatic ligands and olefin polymerization catalysts prepared therefrom WASF2, WEE2, PICALM PNMT 33/4885CYP1A2 776/4885CYP3A4 554/4885
US-10239809-B2 Methods for preparing bridged bi-aromatic ligands AOC1, TYR, DDT PNMT 826/4885CYP1A2 166/4885CYP3A4 164/4885
US-20190111414-A1 BRIDGED BI-AROMATIC LIGANDS AND OLEFIN POLYMERIZATION CATALYSTS PREPARED THEREFROM WASF2, WEE2, PICALM PNMT 33/4885CYP1A2 776/4885CYP3A4 554/4885
US-10252967-B2 Bridged bi-aromatic ligands and transition metal compounds prepared therefrom WEE2, WEE1, AHR PNMT 249/4885CYP1A2 644/4885CYP3A4 479/4885

“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.