SCHEMBL1783890

SCHEMBL1783890

CCCCCCCC(C)=CC=O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.48
CES2 O00748 4/20 0.46
CES1 P23141 4/20 0.46
TRPA1 O75762 1/20 0.45
GPR84 Q9NQS5 7/20 0.44
PPARG P37231 7/20 0.44
PPARD Q03181 7/20 0.44
PPARA Q07869 7/20 0.44
HDAC11 Q96DB2 5/20 0.44
TSHR P16473 5/20 0.44
PTPN1 P18031 3/20 0.44
TLR2 O60603 2/20 0.44
TDP1 Q9NUW8 2/20 0.44
FABP4 P15090 2/20 0.44
SLC22A6 Q4U2R8 1/20 0.44
SLC22A8 Q8TCC7 1/20 0.44
MEN1 O00255 1/20 0.44
ESR1 P03372 1/20 0.44
ALOX15 P16050 1/20 0.44
PDE4A P27815 1/20 0.44

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
SCHEMBL18531572 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL788457 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL1783889 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL20942874 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL20942892 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL20942870 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL20942872 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL20942871 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL20942893 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84
SCHEMBL788458 1.00 ALDH1A1 (0.48) ALDH1A1CES2CES1TRPA1GPR84

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2703407-B1 METHOD FOR MANUFACTURING PHOSPHONOCROTONIC ACID DERIVATIVE KOWA CO (JP) 2017-07-26 EP claimed
US-9540301-B2 Method for manufacturing phosphonocrotonic acid derivative KOWA COMPANY, LTD. (JP) 2017-01-10 US claimed
EP-2703407-A1 METHOD FOR MANUFACTURING PHOSPHONOCROTONIC ACID DERIVATIVE Kowa Company, Ltd. (JP) 2014-03-05 EP claimed
US-20140051876-A1 METHOD FOR MANUFACTURING PHOSPHONOCROTONIC ACID DERIVATIVE MANAC INCORPORATED (JP) 2014-02-20 US claimed
US-20080311175-A1 Compositions and Methods for Promoting Weight Gain and Feed Conversion CHEMAPHOR, INC. (CA) 2008-12-18 US claimed
EP-1806982-A4 COMPOSITIONS AND METHODS FOR PROMOTING WEIGHT GAIN AND FEED CONVERSION CHEMAPHOR INC (CA) 2008-03-19 EP claimed
EP-1806982-A1 COMPOSITIONS AND METHODS FOR PROMOTING WEIGHT GAIN AND FEED CONVERSION Chemaphor Inc. (CA) 2007-07-18 EP claimed
WO-2006034570-A1 COMPOSITIONS AND METHODS FOR PROMOTING WEIGHT GAIN AND FEED CONVERSION CHEMAPHOR INC. (CA) 2006-04-06 WO claimed
EP-0430808-B1 Dihydropyran derivatives, their processes of preparation and their use RHONE POULENC NUTRITION ANIMAL (FR) 1995-03-29 EP claimed
EP-0430807-A1 Process for the preparation of halogeno-acetals from enamines RHONE-POULENC NUTRITION ANIMALE (FR) 1991-06-05 EP claimed
EP-0430808-A1 Dihydropyran derivatives, their processes of preparation and their use RHONE-POULENC NUTRITION ANIMALE (FR) 1991-06-05 EP claimed
CN-111499662-B Isotretinoin C15-triphenylphosphine chloride and preparation method and application thereof 上海新华联制药有限公司 2022-12-20 CN disclosed
US-11291947-B2 Composition for removing sulfur-containing compound KURARAY CO., LTD. (JP) 2022-04-05 US disclosed
US-20190329175-A1 COMPOSITION FOR REMOVING SULFUR-CONTAINING COMPOUND KURARAY CO., LTD. (JP) 2019-10-31 US disclosed
US-10449247-B2 Compositions and methods for enhancing immune response AVIVAGEN INC. (CA) 2019-10-22 US disclosed
EP-0430806-A1 Process for the preparation of haloketals from enamines RHONE-POULENC NUTRITION ANIMALE (FR) 1991-06-05 EP disclosed
EP-0430807-A1 Process for the preparation of halogeno-acetals from enamines RHONE-POULENC NUTRITION ANIMALE (FR) 1991-06-05 EP disclosed
EP-0430808-A1 Dihydropyran derivatives, their processes of preparation and their use RHONE-POULENC NUTRITION ANIMALE (FR) 1991-06-05 EP disclosed
US-3989758-A Monoacetals of unsaturated aliphatic dialdehydes HOFFMANN-LA ROCHE INC. (US) 1976-11-02 US disclosed
US-3974181-A Trimethyl-1,4-dioxaspiro[4,5]dec-7-en-8-methanol HOFFMANN-LA ROCHE INC. (US) 1976-08-10 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 (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-20140051876-A1 METHOD FOR MANUFACTURING PHOSPHONOCROTONIC ACID DERIVATIVE C1S, C3AR1, C9 ALDH1A1 1492/4885CES2 2825/4885CES1 690/4885

“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.