SCHEMBL293045

SCHEMBL293045

CC1C=Cc2ccccc2O1

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDM4E B2RXH2 5/20 0.37
ALDH1A1 P00352 4/20 0.37
HPGD P15428 3/20 0.37
MAPT P10636 3/20 0.34
MEN1 O00255 2/20 0.34
KMT2A Q03164 2/20 0.34
PARP1 P09874 1/20 0.33
P2RY6 Q15077 1/20 0.32
NPC1 O15118 2/20 0.31
RAB9A P51151 2/20 0.31
SMN1; SMN2 Q16637 2/20 0.31
BRD4 O60885 1/20 0.31
CREBBP Q92793 1/20 0.31
HTR2C P28335 1/20 0.31
HTR2B P41595 1/20 0.31
POLB P06746 2/20 0.30
GAA P10253 1/20 0.30
NPSR1 Q6W5P4 1/20 0.30
LMNA P02545 1/20 0.30
TP53 P04637 1/20 0.30

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
SCHEMBL30485934 1.00 KDM4E (0.37) KDM4EALDH1A1HPGDMAPTMEN1
SCHEMBL15761031 1.00 KDM4E (0.37) KDM4EALDH1A1HPGDMAPTMEN1
SCHEMBL28363725 0.86 KDM4E (0.31) KDM4EALDH1A1HPGD
SCHEMBL12491545 0.79 KDM4E (0.31) KDM4EALDH1A1HPGDMAPTMEN1
SCHEMBL30407118 0.79 KDM4E (0.35) KDM4EALDH1A1HPGDMAPTMEN1
SCHEMBL30096256 0.77 KDM4E (0.38) KDM4EALDH1A1HPGDMAPTMEN1
SCHEMBL3069884 0.76 KDM4E (0.37) KDM4EALDH1A1MAPTMEN1KMT2A
SCHEMBL3209487 0.76 KDM4E (0.33) KDM4EALDH1A1MAPTMEN1KMT2A
SCHEMBL1077043 0.76 P2RY6 (0.34) KDM4EALDH1A1MAPTMEN1KMT2A
SCHEMBL20526421 0.76 KDM4E (0.33) KDM4EALDH1A1MAPTMEN1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-113330004-A Differential solubility driven asymmetric transformation process for substituted 2H-chromene-3-carboxylic acids 株式会社AskAt 2021-08-31 CN claimed
EP-0184257-B1 BENZOXAZOL- AND BENZOTHIAZOLAMINE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 1990-07-25 EP claimed
US-4861785-A Benzoxazol-and benzothiazolamine derivatives, useful as anti-anoxic agents JANSSEN PHARMACEUTICA N.V. (BE) 1989-08-29 US claimed
EP-0184257-A1 Benzoxazol- and benzothiazolamine derivatives JANSSEN PHARMACEUTICA N.V. (BE) 1986-06-11 EP claimed
EP-0027835-A1 Process for producing cis-(+,-)-3,4-dihydro-N,N,2-trimethyl-2H-1-benzopyran-3-amine, intermediates produced thereby and their preparation WARNER-LAMBERT COMPANY (US) 1981-05-06 EP claimed
US-4203895-A Process for the preparation of cis-(±)-3,4-dihydro-N,N,2-trimethyl-2H-1-benzopyran-3-amine and intermediates produced thereby WARNER-LAMBERT COMPANY (US) 1980-05-20 US claimed
US-12577526-B2 Massively parallel on-chip construction of synthetic microbial communities THE BROAD INSTITUTE, INC. (US) 2026-03-17 US disclosed
US-20250376656-A1 MASSIVELY PARALLEL ON-CHIP CONSTRUCTION OF SYNTHETIC MICROBIAL COMMUNITIES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2025-12-11 US disclosed
US-20250154122-A1 PROCESS FOR THE PREPARATION OF COMPOUNDS COMPRISING A 2,5-DIHYDROBENZOXEPINE STRUCTURE BY PHOTOCHEMICAL REARRANGEMENT ECOLE POLYTECHNIQUE (FR) 2025-05-15 US disclosed
CN-118984826-A Method for preparing compounds comprising 2, 5-dihydrobenzoxazepine structures by photochemical rearrangement 巴黎综合理工学院 2024-11-19 CN disclosed
WO-2023156461-A1 PROCESS FOR THE PREPARATION OF COMPOUNDS COMPRISING A 2,5-DIHYDROBENZOXEPINE STRUCTURE BY PHOTOCHEMICAL REARRANGEMENT ECOLE POLYTECHNIQUE (FR) 2023-08-24 WO disclosed
US-20220228190-A1 MASSIVELY PARALLEL ON-CHIP CONSTRUCTION OF SYNTHETIC MICROBIAL COMMUNITIES MASSACHUSETTS INSTITUTE OF TECHNOLOGY (US) 2022-07-21 US disclosed
WO-2022040600-A1 COMPOUNDS AS GLP-1R AGONISTS TERNS PHARMACEUTICALS, INC. (US) 2022-02-24 WO disclosed
US-5941704-A Crown cage for ball bearing and dental hand piece including the same KOYO SEIKO CO., LTD. (JP) 1999-08-24 US disclosed
US-5010198-A Intermediates for the synthesis of benzoxazol- and benzothiazolamine derivatives, useful as anti-anoxic agents JANSSEN PHARMACEUTICA N.V. (BE) 1991-04-23 US disclosed
EP-0184257-B1 BENZOXAZOL- AND BENZOTHIAZOLAMINE DERIVATIVES JANSSEN PHARMACEUTICA N.V. (BE) 1990-07-25 EP disclosed
US-4861785-A Benzoxazol-and benzothiazolamine derivatives, useful as anti-anoxic agents JANSSEN PHARMACEUTICA N.V. (BE) 1989-08-29 US disclosed
EP-0184257-A1 Benzoxazol- and benzothiazolamine derivatives JANSSEN PHARMACEUTICA N.V. (BE) 1986-06-11 EP disclosed
EP-0027835-A1 Process for producing cis-(+,-)-3,4-dihydro-N,N,2-trimethyl-2H-1-benzopyran-3-amine, intermediates produced thereby and their preparation WARNER-LAMBERT COMPANY (US) 1981-05-06 EP disclosed
US-4203895-A Process for the preparation of cis-(±)-3,4-dihydro-N,N,2-trimethyl-2H-1-benzopyran-3-amine and intermediates produced thereby WARNER-LAMBERT COMPANY (US) 1980-05-20 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-20250154122-A1 PROCESS FOR THE PREPARATION OF COMPOUNDS COMPRISING A 2,5-DIHYDROBENZOXEPINE STRUCTURE BY PHOTOCHEMICAL REARRANGEMENT DHPS, DDT, DHX15 KDM4E 259/4885ALDH1A1 1913/4885HPGD 396/4885
US-12577526-B2 Massively parallel on-chip construction of synthetic microbial communities STUB1, SAMM50, CD14 KDM4E 2737/4885ALDH1A1 1629/4885HPGD 4563/4885

“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.