SCHEMBL5038547

SCHEMBL5038547

C(=Cc1ccon1)c1ccccc1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 3/20 0.54
KMT2A Q03164 3/20 0.54
KDM4E B2RXH2 6/20 0.48
ALDH1A1 P00352 5/20 0.48
HPGD P15428 4/20 0.48
GRM4 Q14833 5/20 0.46
HDAC6 Q9UBN7 2/20 0.46
RAB9A P51151 4/20 0.44
NPC1 O15118 3/20 0.44
SMN1; SMN2 Q16637 3/20 0.44
PKM P14618 2/20 0.44
LMNA P02545 2/20 0.44
GRM5 P41594 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
CYP3A4 P08684 1/20 0.44
CYP2D6 P10635 1/20 0.44
CYP2C9 P11712 1/20 0.44
TSHR P16473 1/20 0.44
NFKB1 P19838 1/20 0.44
CYP2C19 P33261 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
SCHEMBL6982031 1.00 MEN1 (0.54) MEN1KMT2AKDM4EALDH1A1HPGD
SCHEMBL1176652 0.81 MEN1 (0.35) MEN1KMT2AKDM4EALDH1A1HPGD
SCHEMBL29089469 0.80 NFE2L2 (0.45) KDM4EHPGDGRM4RAB9ANPC1
SCHEMBL31280552 0.80 RAB9A (0.44) MEN1KMT2AKDM4EALDH1A1HPGD
SCHEMBL29089460 0.76 MAPT (0.59) KDM4EALDH1A1HPGDRAB9ANPC1
SCHEMBL11387702 0.73 ECE2 (0.50) MEN1KMT2ARAB9ANPC1SMN1; SMN2
SCHEMBL2465326 0.73
SCHEMBL710247 0.71 MEN1 (0.54) MEN1KMT2AALDH1A1GRM4RAB9A
(Z)-1,2-Diphenylethene SCHEMBL443 0.71 MAOB (0.73) MEN1KMT2AALDH1A1HDAC6LMNA
(Z)-1,2-Diphenylethene SCHEMBL9134305 0.71 MAOB (0.73) MEN1KMT2AALDH1A1HDAC6LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115536649-B Polysubstituted pyrazoline compound and synthesis method thereof 成都中医药大学 2024-12-20 CN disclosed
CN-115536649-A Polysubstituted pyrazoline compound and synthesis method thereof 四川普康药业有限公司 2022-12-30 CN disclosed
US-9593071-B2 Process for the preparation of gamma amino acids and intermediates used in said process ROYAL COLLEGE OF SURGEONS IN IRELAND (IE) 2017-03-14 US disclosed
CN-104220433-A Process for preparing gamma amino acids and intermediates useful in said process ROYAL COLLEGE OF SURGEONS IE 2014-12-17 CN disclosed
US-20140336412-A1 PROCESS FOR THE PREPARATION OF GAMMA AMINO ACIDS AND INTERMEDIATES USED IN SAID PROCESS ROYAL COLLEGE OF SURGEONS IN IRELAND (IE) 2014-11-13 US disclosed
EP-2782911-A1 PROCESS FOR THE PREPARATION OF GAMMA AMINO ACIDS AND INTERMEDIATES USED IN SAID PROCESS Royal College of Surgeons in Ireland (IE) 2014-10-01 EP disclosed
WO-2013076225-A1 PROCESS FOR THE PREPARATION OF GAMMA AMINO ACIDS AND INTERMEDIATES USED IN SAID PROCESS ROYAL COLLEGE OF SURGEONS IN IRELAND (IE) 2013-05-30 WO disclosed
US-7319150-B2 Method for preparing styryl pyrazole, isoxazole and isothiazole derivatives LABORATOIRES MAYOLY SPINDLER (FR) 2008-01-15 US disclosed
US-7319150-B2 Method for preparing styryl pyrazole, isoxazole and isothiazole derivatives LABORATOIRES MAYOLY SPINDLER (FR) 2008-01-15 US disclosed
US-20060135580-A1 Novel method for preparing styryl pyrazole, isoxazole and isothiazole derivatives UNIVERSITE MONTPELLIER 2 (FR) 2006-06-22 US disclosed
EP-0749429-B1 3,5-DISUBSTITUTED AND 3,5,6-TRISUBSTITUTED 2-ISOXAZOLINES AND ISOXAZOLES, PROCESS FOR PREPARING THE SAME AND THEIR USE AS MEDICAMENTS HOECHST AG (DE) 1999-06-30 EP disclosed
EP-0904272-A1 DIHYDROBENZOFURAN AND RELATED COMPOUNDS USEFUL AS ANTI-INFLAMMATORY AGENTS THE PROCTER & GAMBLE COMPANY (US) 1999-03-31 EP disclosed
CN-1210534-A Dihydrobenzofuran and related compounds useful as anti-inflammatory agents PROCTER & GAMBLE (US) 1999-03-10 CN disclosed
US-5686471-A Dihydrobenzofuran and related compounds useful as anti-inflammatory agents THE PROCTER & GAMBLE COMPANY (US) 1997-11-11 US disclosed
WO-1997028155-A1 DIHYDROBENZOFURAN AND RELATED COMPOUNDS USEFUL AS ANTI-INFLAMMATORY AGENTS THE PROCTER & GAMBLE COMPANY (US) 1997-08-07 WO disclosed
US-5208251-A Compounds for antiinflammatory agents, antiallergens, antiarthritic, antiulcer agents WARNER-LAMBERT COMPANY (US) 1993-05-04 US disclosed
EP-0245825-B1 STYRYL PYRAZOLES, ISOXAZOLES AND ANALOGS THEREOF HAVING ACTIVITY AS 5-LIPOXY-GENASE INHIBITORS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM WARNER-LAMBERT COMPANY (US) 1991-03-13 EP disclosed
US-4924002-A REACTION WITH MOLYBDENUM CARBONYL AND HYDRAZINE WARNER-LAMBERT COMPANY (US) 1990-05-08 US disclosed
US-4877881-A SUNSCREEN WARNER-LAMBERT COMPANY (US) 1989-10-31 US disclosed
EP-0245825-A1 Styryl pyrazoles, isoxazoles and analogs thereof having activity as 5-lipoxy-genase inhibitors and pharmaceutical compositions containing them WARNER-LAMBERT COMPANY (US) 1987-11-19 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 (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-20060135580-A1 Novel method for preparing styryl pyrazole, isoxazole and isothiazole derivatives ADH5, ADH1A, STK35 MEN1 4475/4885KMT2A 3612/4885KDM4E 4089/4885
US-20140336412-A1 PROCESS FOR THE PREPARATION OF GAMMA AMINO ACIDS AND INTERMEDIATES USED IN SAID PROCESS GLRB, GABRP, GABRG1 MEN1 3346/4885KMT2A 3770/4885KDM4E 2847/4885

“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.