SCHEMBL405225

SCHEMBL405225

CC(=O)c1ccc(C)c2ccccc12

nearest known ligand 0.56

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 3/20 0.56
KDM4E B2RXH2 2/20 0.47
ALDH1A1 P00352 2/20 0.47
HPGD P15428 2/20 0.47
BRD4 O60885 1/20 0.47
L3MBTL1 Q9Y468 1/20 0.47
GAA P10253 1/20 0.46
TSHR P16473 1/20 0.46
BRPF1 P55201 1/20 0.46
MAPT P10636 2/20 0.46
PBRM1 Q86U86 1/20 0.46
MEN1 O00255 1/20 0.46
NSD2 O96028 1/20 0.46
POLB P06746 1/20 0.46
KMT2A Q03164 1/20 0.46
MCL1 Q07820 1/20 0.46
CNR2 P34972 4/20 0.45
CNR1 P21554 1/20 0.45
CYP2A6 P11509 1/20 0.44
AKR1C4 P17516 1/20 0.43

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
SCHEMBL31347531 1.00 CYP1A2 (0.56) CYP1A2KDM4EALDH1A1HPGDBRD4
SCHEMBL38471077 0.89 KDM4E (0.55) KDM4EALDH1A1HPGDBRD4L3MBTL1
SCHEMBL10391045 0.89 KDM4E (0.55) KDM4EALDH1A1HPGDBRD4L3MBTL1
SCHEMBL8471483 0.87 CYP1A2 (0.56) CYP1A2KDM4EALDH1A1HPGDBRD4
SCHEMBL7717844 0.84 CYP1A2 (0.59) CYP1A2MAPTPOLBCNR2CNR1
SCHEMBL7829452 0.83 CYP1A2 (0.56) CYP1A2ALDH1A1TSHRKMT2AMCL1
SCHEMBL669648 0.83 CYP1A2 (0.56) CYP1A2KDM4EALDH1A1HPGDTSHR
SCHEMBL10884829 0.81 UGT2B7 (0.42) CYP1A2TSHRMEN1KMT2AMCL1
SCHEMBL6914442 0.81 CYP1A2 (0.54) CYP1A2KDM4EALDH1A1HPGDTSHR
SCHEMBL3914643 0.81 ATM (0.60) CYP1A2KDM4EALDH1A1HPGDGAA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117384028-B Synthesis method of 4-acetyl-1-naphthoic acid 济南久隆医药科技有限公司 2025-02-14 CN claimed
CN-117384028-A Synthesis method of 4-acetyl-1-naphthoic acid 济南久隆医药科技有限公司 2024-01-12 CN claimed
CN-114113388-B Method for detecting related substances in 4-oxime methyl-1-naphthoic acid 丽珠集团新北江制药股份有限公司 2023-05-23 CN claimed
CN-114113388-A Method for detecting related substances in 4-oximinomethyl-1-naphthoic acid 丽珠集团新北江制药股份有限公司 2022-03-01 CN claimed
CN-109761775-B Method for purifying 4-acetyl-1-methylnaphthalene from acetyl methylnaphthalene mixture 湖北海力环保科技股份有限公司 2022-02-01 CN claimed
EP-0087269-B1 PLANT GROWTH REGULATORS COALITE GROUP PLC (GB) 1986-11-20 EP claimed
CN-119638567-A Refining method of 1, 4-naphthalene dicarboxylic acid 江苏八巨药业有限公司 2025-03-18 CN disclosed
CN-117384028-B Synthesis method of 4-acetyl-1-naphthoic acid 济南久隆医药科技有限公司 2025-02-14 CN disclosed
CN-117384028-B Synthesis method of 4-acetyl-1-naphthoic acid 济南久隆医药科技有限公司 2025-02-14 CN disclosed
US-20240390333-A1 NEUROPROTECTIVE COMPOSITIONS AND METHODS OF USING THE SAME THE BOARD OF SUPERVISORS OF LOUISIANA STATE UNIV AND AGRICULTURAL AND MECHANICAL COLLEGE (US) 2024-11-28 US disclosed
US-11974988-B2 Neuroprotective compositions and methods of using the same BOARD OF SUPERVISORS OF LOUISIANA STATE UNIVERSITY AND AGRICULTURAL AND MECHANICAL COLLEGE (US) 2024-05-07 US disclosed
CN-117384028-A Synthesis method of 4-acetyl-1-naphthoic acid 济南久隆医药科技有限公司 2024-01-12 CN disclosed
CN-117384028-A Synthesis method of 4-acetyl-1-naphthoic acid 济南久隆医药科技有限公司 2024-01-12 CN disclosed
WO-2009148290-A2 3-SUBSTITUTED PROPANAMINE COMPOUNDS SK HOLDINGS CO., LTD. (KR) 2009-12-10 WO disclosed
EP-0087269-B1 PLANT GROWTH REGULATORS COALITE GROUP PLC (GB) 1986-11-20 EP disclosed
EP-0087269-A1 Plant growth regulators COALITE GROUP PLC (GB) 1983-08-31 EP disclosed
US-4249022-A Process for the manufacture of 1,4-disubstituted bicyclic or tricyclic compounds and new 1,4-disubstituted bicyclic compounds CIBA-GEIGY CORPORATION (US) 1981-02-03 US disclosed
US-4154754-A 1,4-Dicyanonaphthalenes CIBA-GEIGY CORPORATION (US) 1979-05-15 US disclosed
US-4048212-A Process for the manufacture of 1,4-dicyanonaphthalenes CIBA-GEIGY CORPORATION (US) 1977-09-13 US disclosed
US-4011261-A PROCESS FOR THE MANUFACTURE OF 1,4-DISUBSTITUTED BICYCLIC OR TRICYCLIC COMPOUNDS AND NEW 1,4-DISUBSTITUTED BICYCLIC COMPOUNDS CIBA-GEIGY CORPORATION (US) 1977-03-08 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-11974988-B2 Neuroprotective compositions and methods of using the same GAP43, NLN, SMN1; SMN2 CYP1A2 4648/4885KDM4E 3736/4885ALDH1A1 1731/4885
US-20240390333-A1 NEUROPROTECTIVE COMPOSITIONS AND METHODS OF USING THE SAME GAP43, NLN, SMN1; SMN2 CYP1A2 4648/4885KDM4E 3736/4885ALDH1A1 1731/4885

“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.