SCHEMBL1748567

SCHEMBL1748567

CC1(C)C=Cc2ccccc2O1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HTR2C P28335 1/20 0.49
HTR2B P41595 1/20 0.49
HIF1A Q16665 8/20 0.44
EPAS1 Q99814 8/20 0.44
ALDH1A1 P00352 2/20 0.42
HPGD P15428 2/20 0.42
KDM4E B2RXH2 1/20 0.42
NPC1 O15118 1/20 0.42
CA12 O43570 1/20 0.42
CA1 P00915 1/20 0.42
TP53 P04637 1/20 0.42
POLB P06746 1/20 0.42
MAPT P10636 1/20 0.42
CA7 P43166 1/20 0.42
RAB9A P51151 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
CA9 Q16790 1/20 0.42
CA13 Q8N1Q1 1/20 0.42
HSD17B10 Q99714 1/20 0.42
CYP3A4 P08684 1/20 0.41

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
SCHEMBL29644871 1.00 HTR2C (0.49) HTR2CHTR2BHIF1AEPAS1ALDH1A1
Ethane SCHEMBL10720474 0.98 HTR2C (0.47) HTR2CHTR2BHIF1AEPAS1ALDH1A1
SCHEMBL29038389 0.92 HTR2C (0.44) HTR2CHTR2BHIF1AEPAS1ALDH1A1
Formamide SCHEMBL29013842 0.89 HTR2C (0.41) HTR2CHTR2BHIF1AEPAS1ALDH1A1
Acrylamide SCHEMBL29013882 0.82 ALDH1A1 (0.40) HTR2CHTR2BHIF1AEPAS1ALDH1A1
SCHEMBL12640789 0.79 HTR2C (0.46) HTR2CHTR2BHIF1AEPAS1ALDH1A1
SCHEMBL381889 0.77 HTR2C (0.52) HTR2CHTR2BALDH1A1KDM4ETP53
SCHEMBL15989633 0.76 ALDH1A1 (0.56) HIF1AEPAS1ALDH1A1HPGDKDM4E
SCHEMBL11098662 0.76 HTR2C (0.44) HTR2CHTR2BHIF1AEPAS1ALDH1A1
SCHEMBL2558890 0.76 PTGS1 (0.46) HTR2CHTR2BHIF1AEPAS1TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116041300-B 2, 2-Dimethyl benzopyran derivative and preparation method and application thereof 沈阳药科大学 2024-04-26 CN claimed
CN-117186049-A 2, 2-dimethyl-2H chromene derivative containing sulfonamide unit, and preparation method and application thereof 贵州大学 2023-12-08 CN claimed
CN-116283936-A Substituted amino ether-containing 2, 2-dimethyl benzopyran derivative and salt or solvate thereof, preparation and application thereof, and composition 沈阳药科大学 2023-06-23 CN claimed
CN-116041300-A 2, 2-dimethyl benzopyran derivative and preparation method and application thereof 沈阳药科大学 2023-05-02 CN claimed
CN-109096235-B 2, 2-dimethyl benzopyran derivative and preparation method and application thereof 沈阳药科大学 2022-06-21 CN claimed
US-20220105054-A1 ABSORPTION ENHANCER OF CINNAMIC ACID DERIVATIVE YAMADA BEE COMPANY, INC. (JP) 2022-04-07 US claimed
EP-1535918-B1 PROCESS FOR PRODUCING AMINOBENZOPYRAN COMPOUND NISSAN CHEMICAL IND LTD (JP) 2010-11-03 EP claimed
US-7683189-B2 Process for producing aminobenzopyran compound NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2010-03-23 US claimed
CN-100363358-C Process for producing aminobenzopyran compound NISSAN CHEMICAL IND LTD (JP) 2008-01-23 CN claimed
EP-1716141-A1 BENZOPYRAN DERIVATIVES, METHOD OF PRODUCTION AND USE THEREOF Université de Liège (BE) 2006-11-02 EP claimed
US-5605703-A REDUCE TOXICITY OF DRUG WHEN ADMINISTERED BY INJECTION LIPOTEC, S.A. (ES) 1997-02-25 US claimed
US-5602267-A Organometallic catalysts for epoxidizing prochiral olefins and a new class of amid-salicylidene ligands HOECHST CELANESE (US) 1997-02-11 US claimed
EP-0643626-A4 CHIRAL CATALYSTS, CATALYTIC OXIDATION AND DISPROPORTIONATION REACTIONS, AND METHODS OF PRODUCING EPOXYCHROMANS AND TAXOL. RES CORP TECHNOLOGIES INC (US) 1995-12-06 EP claimed
EP-0643626-A1 CHIRAL CATALYSTS, CATALYTIC OXIDATION AND DISPROPORTIONATION REACTIONS, AND METHODS OF PRODUCING EPOXYCHROMANS AND TAXOL RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1995-03-22 EP claimed
US-5391751-A Hypotensive, antiarrhythmia, antiasthmatic agents RED BALLOON INVESTMENT LIMITED (JE) 1995-02-21 US claimed
EP-0312432-B1 2,2-Dimethyl chromene derivatives, preparation process and pharmaceutical compositions containing them SANOFI ELF (FR) 1994-01-12 EP claimed
EP-0521099-A4 CHIRAL CATALYSTS AND EPOXIDATION REACTIONS CATALYZED THEREBY 1993-10-20 EP claimed
WO-1993003838-A1 CHIRAL CATALYSTS, CATALYTIC OXIDATION AND DISPROPORTIONATION REACTIONS, AND METHODS OF PRODUCING EPOXYCHROMANS AND TAXOL RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1993-03-04 WO claimed
EP-0521099-A1 CHIRAL CATALYSTS AND EPOXIDATION REACTIONS CATALYZED THEREBY RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1993-01-07 EP claimed
WO-1991014694-A1 CHIRAL CATALYSTS AND EPOXIDATION REACTIONS CATALYZED THEREBY RESEARCH CORPORATION TECHNOLOGIES, INC. (US) 1991-10-03 WO claimed

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-20220105054-A1 ABSORPTION ENHANCER OF CINNAMIC ACID DERIVATIVE FABP2, SLC16A3, SLC16A7 HTR2C 937/4885HTR2B 515/4885HIF1A 314/4885

“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.