SCHEMBL991225

SCHEMBL991225

C=CCCCC=CCOC(C)=O

nearest known ligand 0.53

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
MAPT P10636 4/20 0.53
USP2 O75604 3/20 0.53
LMNA P02545 3/20 0.53
CYP3A4 P08684 2/20 0.53
SMN1; SMN2 Q16637 2/20 0.53
RECQL P46063 1/20 0.53
ALDH1A1 P00352 7/20 0.44
HPGD P15428 1/20 0.44
ALOX15 P16050 1/20 0.38
ABCC4 O15439 1/20 0.35
CNR1 P21554 1/20 0.35
PTPN1 P18031 1/20 0.34
TSHR P16473 1/20 0.33
PRKCA P17252 1/20 0.33
HSD17B10 Q99714 1/20 0.33

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
SCHEMBL991224 1.00 MAPT (0.53) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL9717823 0.85 MAPT (0.53) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL10888549 0.85 MAPT (0.53) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL10886776 0.85 MAPT (0.53) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL10888544 0.85 MAPT (0.53) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL9717827 0.85 MAPT (0.53) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL10886771 0.85 MAPT (0.53) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL9617619 0.84 ALDH1A1 (0.44) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL9617618 0.84 ALDH1A1 (0.44) MAPTUSP2LMNACYP3A4SMN1; SMN2
SCHEMBL16784818 0.84 MAPT (0.46) MAPTUSP2LMNACYP3A4SMN1; 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 107 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2003138-B1 METHOD FOR PRODUCING ALDEHYDE USING BISPHOSPHITE AND GROUP 8-10 METAL COMPOUND, AND SUCH BISPHOSPHITE KURARAY CO (JP) 2013-10-09 EP claimed
US-7745666-B2 Rreacting a nonconjugated diene having a double bond in an end and having from 6-20 carbon atoms with a carbon monoxide and hydrogen in the presence of a bisphosphite and a transition metal compound to provide an unsaturated acyclic aldehyde; KURARAY CO., LTD. (JP) 2010-06-29 US claimed
US-20090259073-A1 Rreacting a nonconjugated diene having a double bond in an end and having from 6-20 carbon atoms with a carbon monoxide and hydrogen in the presence of a bisphosphite and a transition metal compound to provide an unsaturated acyclic aldehyde; KURARAY CO., LTD (JP) 2009-10-15 US claimed
EP-2003138-A1 METHOD FOR PRODUCING ALDEHYDE USING BISPHOSPHITE AND GROUP 8-10 METAL COMPOUND, AND SUCH BISPHOSPHITE Kuraray Co., Ltd. (JP) 2008-12-17 EP claimed
US-5118837-A Reaction of olefinic double bond in presence of other, less reactive olefinic double bonds; modified ruthenium catalyst with trivalent phosphorus or nitrogen or divalent sulfur compound GIVAUDAN CORPORATION (US) 1992-06-02 US claimed
US-4260750-A OF DIENES, TRIARYLPHOSPHINE CATALYST RHONE-POULENC INDUSTRIES (FR) 1981-04-07 US claimed
US-3981907-A Method of producing highly unsaturated compounds by reacting 1,3-conjugated diene compounds with derivatives of dimers of butadienes and products MITSUBISHI CHEMICAL INDUSTRIES LTD. (JA) 1976-09-21 US claimed
WO-2023167201-A1 ACTIVE ENERGY RAY-CURABLE COMPOSITION, AND METHOD FOR PRODUCING CURED PRODUCT 株式会社カネカ 2023-09-07 WO disclosed
EP-4056604-B1 METHOD FOR PRODUCING COPOLYMER OF 1,3,7-OCTATRIENE AND STYRENE KURARAY CO (JP) 2023-08-02 EP disclosed
EP-3564280-B1 COPOLYMER OF 1, 3, 7-OCTATRIENE AND STYRENE AND HYDRIDE THEREOF KURARAY CO (JP) 2023-07-26 EP disclosed
EP-3586961-B1 METHOD FOR MANUFACTURING CATALYST LIQUID KURARAY CO (JP) 2023-06-07 EP disclosed
US-11628430-B2 Method for manufacturing catalyst liquid KURARAY CO., LTD. (JP) 2023-04-18 US disclosed
EP-4163311-A1 COPOLYMER OF 1,3,7-OCTATRIENE AND ISOPRENE, HYDRIDE THEREOF, AND METHOD FOR PRODUCING SAID COPOLYMER Kuraray Co., Ltd. (JP) 2023-04-12 EP disclosed
EP-0296550-A2 Phosphonium salts and processes for production of and uses for the same KURARAY CO., LTD. (JP) 1988-12-28 EP disclosed
US-4399301-A Methylenically-substituted undecadienes RHONE-POULENC INDUSTRIES (FR) 1983-08-16 US disclosed
US-4260750-A OF DIENES, TRIARYLPHOSPHINE CATALYST RHONE-POULENC INDUSTRIES (FR) 1981-04-07 US disclosed
US-4219677-A FOR DIENES IN PRESENCE OF SULFONATED PHOSPHINE CATALYST RHONE-POULENC INDUSTRIES (FR) 1980-08-26 US disclosed
US-4181683-A INTERMEDIATES FOR PERFUMES AND ESTROGEN-DERIVATIVE DRUGS MITSUBISHI PETROCHEMICAL CO., LTD. (JP) 1980-01-01 US disclosed
US-4142060-A DIENES, WATER RHONE-POULENC INDUSTRIES (FR) 1979-02-27 US disclosed
US-3981907-A Method of producing highly unsaturated compounds by reacting 1,3-conjugated diene compounds with derivatives of dimers of butadienes and products MITSUBISHI CHEMICAL INDUSTRIES LTD. (JA) 1976-09-21 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-11628430-B2 Method for manufacturing catalyst liquid OSGEP, PNP, ALK MAPT 1468/4885USP2 2735/4885LMNA 1081/4885
US-20090259073-A1 Rreacting a nonconjugated diene having a double bond in an end and having from 6-20 carbon atoms with a carbon monoxide and hydrogen in the presence of a bisphosphite and a transition metal compound to provide an unsaturated acyclic aldehyde; CBR1, RCN1, CYC1 MAPT 4864/4885USP2 4530/4885LMNA 3380/4885

“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.