SCHEMBL29393422

SCHEMBL29393422

COc1ccccc1C=CC=O

nearest known ligand 0.61

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NFE2L2 Q16236 5/20 0.61
▸ TFEB P19484 1/20 0.61
▸ TRPA1 O75762 1/20 0.60
▸ KDM4E B2RXH2 2/20 0.59
▸ CDK4 P11802 3/20 0.56
▸ CCND1 P24385 3/20 0.56
▸ CCNB2 O95067 1/20 0.56
▸ CDK1 P06493 1/20 0.56
▸ CCNB1 P14635 1/20 0.56
▸ CCNB3 Q8WWL7 1/20 0.56
▸ CYP1A1 P04798 2/20 0.55
▸ CYP1A2 P05177 2/20 0.55
▸ CYP1B1 Q16678 2/20 0.55
▸ NPC1 O15118 2/20 0.54
▸ MAPT P10636 2/20 0.54
▸ RAB9A P51151 2/20 0.54
▸ BCHE P06276 2/20 0.54
▸ LMNA P02545 1/20 0.54
▸ CYP19A1 P11511 1/20 0.53
▸ MAPK1 P28482 1/20 0.53

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
SCHEMBL228813 1.00 NFE2L2 (0.61) NFE2L2TFEBTRPA1KDM4ECDK4
SCHEMBL31004887 1.00 NFE2L2 (0.61) NFE2L2TFEBTRPA1KDM4ECDK4
SCHEMBL9900345 1.00 NFE2L2 (0.61) NFE2L2TFEBTRPA1KDM4ECDK4
SCHEMBL43264 1.00 NFE2L2 (0.61) NFE2L2TFEBTRPA1KDM4ECDK4
SCHEMBL18570324 0.86 CDK4 (0.50) NFE2L2TFEBTRPA1KDM4ECDK4
SCHEMBL2119793 0.85 NFE2L2 (0.63) NFE2L2KDM4ECYP1A1CYP1A2CYP1B1
SCHEMBL8494360 0.85 NFE2L2 (0.63) NFE2L2KDM4ECYP1A1CYP1A2CYP1B1
SCHEMBL4019329 0.84 NFE2L2 (0.79) NFE2L2TFEBTRPA1KDM4ECYP1A1
SCHEMBL1603719 0.84 NFE2L2 (0.79) NFE2L2TFEBTRPA1KDM4ECYP1A1
SCHEMBL7915752 0.84 NFE2L2 (0.79) NFE2L2TFEBTRPA1KDM4ECYP1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117402051-A Compound containing alpha, beta-unsaturated aldehyde and having conjugated structure and application thereof 广东远思南药生物科技有限公司 2024-01-16 — — CN claimed
US-20220125696-A1 INFLAMMATION REDUCING COMPOSITION CONTAINING A CANNABIS SATIVA COMPOUND HAUGHT JOHN CHRISTIAN (US) 2022-04-28 — — US claimed
WO-2022087052-A1 INFLAMMATION REDUCING COMPOSITION CONTAINING A CANNABIS SATIVA COMPOUND HAUGHT JOHN CHRISTIAN (US) 2022-04-28 — — WO claimed
EP-4544016-A1 METHODS AND COMPOSITIONS FOR CLEANING COMPRISING A POLYPEPTIDE HAVING THERMOLYSIN ACTIVITY Danisco US Inc. (US) 2025-04-30 — — EP disclosed
WO-2025081158-A1 EMULSIONS INCLUDING ESSENTIAL OIL COMPONENTS APEEL TECHNOLOGY, INC. (US) 2025-04-17 — — WO disclosed
CN-113651682-B Synthesis method of 2-methoxy cinnamaldehyde 八叶草健康产业研究院(厦门)有限公司 2025-01-14 — — CN disclosed
US-20240376409-A1 FRAGRANCE BEAD COMPOSITION AND USE THEREOF NOVOZYMES A/S (DK) 2024-11-14 — — US disclosed
CN-118844491-A Preservative for sauced duck meat products and preparation method and application thereof 江西师范大学 2024-10-29 — — CN disclosed
CN-118666731-A 2-Phenylindole derivative and preparation method and application thereof 东南大学 2024-09-20 — — CN disclosed
CN-118576720-A Application of cinnamon oil as absorption promoter to improvement of puerarin bioavailability 安徽中医药大学 2024-09-03 — — CN disclosed
EP-4229169-B1 LAUNDRY DETERGENT PORTION UNIT HENKEL AG & CO KGAA (DE) 2024-08-07 — — EP disclosed
WO-2022084303-A2 USE OF POLYPEPTIDES HAVING DNASE ACTIVITY NOVOZYMES A/S (DK) 2022-04-28 — — WO disclosed
US-20220125696-A1 INFLAMMATION REDUCING COMPOSITION CONTAINING A CANNABIS SATIVA COMPOUND HAUGHT JOHN CHRISTIAN (US) 2022-04-28 — — US disclosed
WO-2022087052-A1 INFLAMMATION REDUCING COMPOSITION CONTAINING A CANNABIS SATIVA COMPOUND HAUGHT JOHN CHRISTIAN (US) 2022-04-28 — — WO disclosed
EP-3982985-A1 SAKE REPLICAS PRODUCED FROM INDIVIDUAL COMPONENTS AVA FOOD LABS, INC. (US) 2022-04-20 — — EP disclosed
CN-109851570-B Chalcone derivative containing 1,2, 4-triazine, preparation method and application thereof 贵州大学 2022-04-19 — — CN disclosed
US-20220105012-A1 REDUCTION OF TOOTH STAINING DERIVED FROM CATIONIC ANTIBACTERIALS PROCTER & GAMBLE (US) 2022-04-07 — — US disclosed
CN-114085199-A Chalcone derivative containing sulfonyl piperazine and preparation method and application thereof 贵州大学 2022-02-25 — — CN disclosed
US-11253451-B2 Reduction of tooth staining derived from cationic antibacterials THE PROCTER & GAMBLE COMPANY (US) 2022-02-22 — — US disclosed
US-20220047484-A1 Reduction Of Tooth Staining Derived From Cationic Antimicrobials PROCTER & GAMBLE (US) 2022-02-17 — — 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 (3 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-20220047484-A1 Reduction Of Tooth Staining Derived From Cationic Antimicrobials PHOSPHO1, PEF1, DNM1L NFE2L2 4181/4885TFEB 365/4885TRPA1 1436/4885
US-11253451-B2 Reduction of tooth staining derived from cationic antibacterials SOD1, ZRANB2, HDAC10 NFE2L2 291/4885TFEB 78/4885TRPA1 340/4885
US-20220105012-A1 REDUCTION OF TOOTH STAINING DERIVED FROM CATIONIC ANTIBACTERIALS SOD1, ZRANB2, HDAC10 NFE2L2 291/4885TFEB 78/4885TRPA1 340/4885

“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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