SCHEMBL880134

SCHEMBL880134

CCCC(C)OC(=O)C(C)C

nearest known ligand 0.46

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
FAAH O00519 5/20 0.46
CHRM1 P11229 1/20 0.37
AKR1A1 P14550 1/20 0.37
CHRM3 P20309 1/20 0.37
HTR2A P28223 1/20 0.37
HTR2C P28335 1/20 0.37
ADRA1A P35348 1/20 0.37
HRH1 P35367 1/20 0.37
DRD3 P35462 1/20 0.37
SLC6A3 Q01959 1/20 0.37
HDAC1 Q13547 1/20 0.37
HDAC2 Q92769 1/20 0.37
TDP1 Q9NUW8 1/20 0.37
CNR1 P21554 1/20 0.37
CNR2 P34972 1/20 0.37
TSHR P16473 3/20 0.36
CYP3A4 P08684 2/20 0.36
NFKB1 P19838 2/20 0.36
NPSR1 Q6W5P4 2/20 0.36
CHRNB2 P17787 4/20 0.34

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
SCHEMBL14296417 1.00 FAAH (0.46) FAAHCHRM1AKR1A1CHRM3HTR2A
SCHEMBL14296416 1.00 FAAH (0.46) FAAHCHRM1AKR1A1CHRM3HTR2A
SCHEMBL16665386 0.86 FAAH (0.43) FAAHCHRM1AKR1A1CHRM3HTR2A
SCHEMBL20854298 0.86 FAAH (0.43) FAAHCHRM1AKR1A1CHRM3HTR2A
SCHEMBL2332583 0.86 FAAH (0.56) FAAHTDP1CNR1CNR2TSHR
SCHEMBL16554242 0.86 FAAH (0.43) FAAHCHRM1AKR1A1CHRM3HTR2A
SCHEMBL16554070 0.86 FAAH (0.43) FAAHCHRM1AKR1A1CHRM3HTR2A
SCHEMBL16554241 0.86 FAAH (0.43) FAAHCHRM1AKR1A1CHRM3HTR2A
SCHEMBL16554067 0.86 FAAH (0.43) FAAHCHRM1AKR1A1CHRM3HTR2A
SCHEMBL16554069 0.86 FAAH (0.43) FAAHCHRM1AKR1A1CHRM3HTR2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110981873-B Preparation method for synthesizing pyrroloquinoline quinone by five-step method 江西农业大学 2025-01-24 CN claimed
CN-110981873-B Preparation method for synthesizing pyrroloquinoline quinone by five-step method 江西农业大学 2025-01-24 CN disclosed
CN-109952360-B Quantum dot dispersion, self-luminous photosensitive resin composition, color filter manufactured using the same, and image display device 东友精细化工有限公司 2022-03-22 CN disclosed
US-20170312363-A1 MULTIFUNCTIONALIZED POLYETHYLENE GLYCOL DERIVATIVE AND PREPARATION METHOD THEREFOR XIAMEN SINOPEG BIOTECH CO., LTD. (CN) 2017-11-02 US disclosed
US-20170196848-A1 Prodrugs of NH-Acidic Compounds: Ester, Carbonate, Carbamate and Phosphonate Derivatives ALKERMES PHARMA IRELAND LTD (IE) 2017-07-13 US disclosed
US-9585965-B2 Prodrugs of NH-acidic compounds: ester, carbonate, carbamate and phosphonate derivatives ALKERMES PHARMA IRELAND LIMITED (IE) 2017-03-07 US disclosed
US-20150320875-A1 Prodrugs of NH-Acidic Compounds: Ester, Carbonate, Carbamate and Phosphonate Derivatives ALKERMES PHARMA IRELAND LTD (IE) 2015-11-12 US disclosed
US-9072788-B2 Prodrugs of NH-acidic compounds: ester, carbonate, carbamate and phosphonate derivatives ALKERMES PHARMA IRELAND LIMITED (IE) 2015-07-07 US disclosed
US-8664423-B2 Process for the preparation of acylated secondary alcohol alkoxylates and secondary alcohol alkoxylates SHELL OIL COMPANY (US) 2014-03-04 US disclosed
EP-2181763-B1 Catalyst and process for alkoxylation SHELL INT RESEARCH (NL) 2012-06-20 EP disclosed
US-6313066-B1 Decolorable image forming material and decoloring method of the same KABUSHIKI KAISHA TOSHIBA (JP) 2001-11-06 US disclosed
US-6277208-B1 HEATING IMAGE FORMING MATERIAL, CONTACTING WITH SOLVENT, DESOLVENTIZING, WHERE IMAGE FORMING MATERIAL CONTAINS A COLOR FORMER, A DEVELOPER AND A DECOLORIZER AND WHERE DECOLORIZER COMPRISES AMORPHOUS PHASE SEPARTION INHIBITORS KABUSHIKI KAISHA TOSHIBA (JP) 2001-08-21 US disclosed
US-20010008164-A1 DECOLORIZABLE INK AND PRINTER KABUSHIKI KAISHA TOSHIBA (JP) 2001-07-19 US disclosed
US-6248692-B1 MIXTURE OF COLOR FORMER, DEVELOPER AND DECOLORIZER FORMED BY ACTIVATION KABUSHIKI KAISHA TOSHIBA (JP) 2001-06-19 US disclosed
US-6203603-B1 COLOR FORMER, DEVELOPER, MATRIX AND POLYMER DECOLORIZER KABUSHIKI KAISHA TOSHIBA (JP) 2001-03-20 US disclosed
EP-1041447-A1 Decolorable image forming material and decoloring method of the same Kabushiki Kaisha Toshiba (JP) 2000-10-04 EP disclosed
EP-0987123-A2 Erasable image forming material KABUSHIKI KAISHA TOSHIBA (JP) 2000-03-22 EP disclosed
EP-0980028-A1 Erasable image forming material KABUSHIKI KAISHA TOSHIBA (JP) 2000-02-16 EP disclosed
US-6017386-A A COLOR FORMER, A DEVELOPER AND A DECOLORIZER WHICH COMPRISES A CYCLIC SUGAR ALCOHOL AS HIGHLY AMORPHOUS PHASE SEPARATION INHIBITOR AND A NON AROMATIC SUBSTITUED CYCLIC SUGAR ALCOHOL AS SLIGHTLY AMORPHOUS PHASE SEPARATION INHIBITOR KABUSHIKI KAISHA TOSHIBA (JP) 2000-01-25 US disclosed
EP-0932084-A1 Decoloring method of decolorizable image forming material KABUSHIKI KAISHA TOSHIBA (JP) 1999-07-28 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 (3 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-20150320875-A1 Prodrugs of NH-Acidic Compounds: Ester, Carbonate, Carbamate and Phosphonate Derivatives PHPT1, SI, CA6 FAAH 807/4885CHRM1 2813/4885AKR1A1 1601/4885
US-20170196848-A1 Prodrugs of NH-Acidic Compounds: Ester, Carbonate, Carbamate and Phosphonate Derivatives PHPT1, SI, CA6 FAAH 807/4885CHRM1 2813/4885AKR1A1 1601/4885
US-20170312363-A1 MULTIFUNCTIONALIZED POLYETHYLENE GLYCOL DERIVATIVE AND PREPARATION METHOD THEREFOR HDGF, F11, F12 FAAH 1494/4885CHRM1 1525/4885AKR1A1 875/4885

“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.