SCHEMBL9490660

SCHEMBL9490660

Cc1ccc([PH](=O)Cl)cc1

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ACHE P22303 5/20 0.44
▸ TDP1 Q9NUW8 2/20 0.44
▸ ALDH1A1 P00352 3/20 0.36
▸ CES2 O00748 2/20 0.36
▸ CES1 P23141 2/20 0.36
▸ LMNA P02545 2/20 0.36
▸ CYP2A6 P11509 1/20 0.36
▸ GAA P10253 1/20 0.36
▸ CA1 P00915 2/20 0.35
▸ CA2 P00918 2/20 0.35
▸ CA7 P43166 2/20 0.35
▸ CA9 Q16790 2/20 0.35
▸ HPGD P15428 2/20 0.35
▸ SMN1; SMN2 Q16637 1/20 0.35
▸ HSD17B10 Q99714 2/20 0.34
▸ CYP2D6 P10635 1/20 0.34
▸ CYP2C9 P11712 1/20 0.34
▸ ALOX15 P16050 1/20 0.34
▸ CYP2C19 P33261 1/20 0.34
▸ KDM4E B2RXH2 1/20 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
SCHEMBL183975 0.77 ACHE (0.50) ACHETDP1ALDH1A1CES2CES1
SCHEMBL2680100 0.74 LMNA (0.47) ALDH1A1CES2CES1LMNACYP2A6
SCHEMBL13412455 0.74 ACHE (0.47) ACHETDP1ALDH1A1CES2CES1
SCHEMBL28664090 0.72 ACHE (0.44) ACHETDP1ALDH1A1CES2CES1
SCHEMBL14246454 0.72 ALDH1A1 (0.36) ACHETDP1ALDH1A1TSHR
SCHEMBL230854 0.72 TDP1 (0.44) ACHETDP1ALDH1A1CES2CES1
SCHEMBL14246416 0.72 CA1 (0.52) ACHETDP1ALDH1A1CES2CES1
SCHEMBL14246524 0.72 TSHR (0.44) ALDH1A1LMNACA1CA2CA9
P-Xylene SCHEMBL28865890 0.71 ACHE (0.73) ACHETDP1ALDH1A1CES2CES1
SCHEMBL4838271 0.71 — —

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103396464-A Preparation method of ivermectin HEBEI VEYON ANIMAL PHARMACEUTICAL CO LTD 2013-11-20 — — CN claimed
EP-2537839-B1 B-DIHYDROFURAN DERIVING COMPOUND, METHOD FOR PRODUCING B-DIHYDROFURAN DERIVING COMPOUND OR B-TETRAHYDROFURAN DERIVING COMPOUND, B -GLYCOSIDE COMPOUND, METHOD FOR PRODUCING B-GLYCOSIDE COMPOUND, AND METHOD FOR PRODUCING 4'-ETHYNYL D4T AND ANALOGUE COMPOUNDS THEREOF NISSAN CHEMICAL IND LTD (JP) 2016-12-14 — — EP disclosed
US-9212174-B2 Certain β-dihydrofuran derivatives NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2015-12-15 — — US disclosed
CN-102741237-B Method for producing beta-dihydrofuran deriving compound NISSAN CHEMICAL IND LTD 2015-04-29 — — CN disclosed
CN-104395329-A Method for producing phosphoric acid ester amides DAIKYO CHEMICAL CO LTD 2015-03-04 — — CN disclosed
EP-2537839-A1 B-DIHYDROFURAN DERIVING COMPOUND, METHOD FOR PRODUCING B-DIHYDROFURAN DERIVING COMPOUND OR B-TETRAHYDROFURAN DERIVING COMPOUND, B -GLYCOSIDE COMPOUND, METHOD FOR PRODUCING B-GLYCOSIDE COMPOUND, AND METHOD FOR PRODUCING 4'-ETHYNYL D4T AND ANALOGUE COMPOUNDS THEREOF Nissan Chemical Industries, Ltd. (JP) 2012-12-26 — — EP disclosed
US-20120322995-A1 beta-DIHYDROFURAN DERIVING COMPOUND, METHOD FOR PRODUCING beta-DIHYDROFURAN DERIVING COMPOUND OR beta-TETRAHYDROFURAN DERIVING COMPOUND, beta-GLYCOSIDE COMPOUND, METHOD FOR PRODUCING beta GLYCOSIDE COMPOUND, AND METHOD FOR PRODUCING 4'-ETHYNYL D4T AND ANALOGUE COMPOUNDS THEREOF NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2012-12-20 — — US disclosed
CN-102741237-A Beta-dihydrofuran deriving compound, method for producing beta-dihydrofuran deriving compound or beta-tetrahydrofuran deriving compound, beta-glycoside compound, method for producing beta-glycoside compound, and method for producing 4'-ethynyl d4t and analogue comp NISSAN CHEMICAL IND LTD 2012-10-17 — — CN disclosed
EP-0269395-B1 RUTHENIUM-PHOSPHINE COMPLEX CATALYSTS Takasago International Corporation (JP) 1993-02-17 — — EP disclosed
EP-0271310-A2 Ruthenium-phosphine complexes Takasago International Corporation (JP) 1988-06-15 — — EP disclosed
EP-0271311-A2 Ruthenium-phosphine complexes Takasago International Corporation (JP) 1988-06-15 — — EP disclosed
EP-0269395-A2 Ruthenium-phosphine complex catalysts Takasago International Corporation (JP) 1988-06-01 — — 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-20120322995-A1 beta-DIHYDROFURAN DERIVING COMPOUND, METHOD FOR PRODUCING beta-DIHYDROFURAN DERIVING COMPOUND OR beta-TETRAHYDROFURAN DERIVING COMPOUND, beta-GLYCOSIDE COMPOUND, METHOD FOR PRODUCING beta GLYCOSIDE COMPOUND, AND METHOD FOR PRODUCING 4'-ETHYNYL D4T AND ANALOGUE COMPOUNDS THEREOF DHPS, B4GALT1, STT3A ACHE 2462/4885TDP1 1496/4885ALDH1A1 495/4885

“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.

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