SCHEMBL1496544

SCHEMBL1496544

CC(O)COc1ccc(Oc2ccccc2)cc1

nearest known ligand 0.85

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
LMNA P02545 1/20 0.85
LTA4H P09960 5/20 0.57
CYP2D6 P10635 2/20 0.53
ADRB2 P07550 1/20 0.53
ADRB1 P08588 1/20 0.53
ADRB3 P13945 1/20 0.53
MAOA P21397 1/20 0.50
PTGS1 P23219 1/20 0.50
MTNR1A P48039 3/20 0.49
MTNR1B P49286 3/20 0.49
SMN1; SMN2 Q16637 1/20 0.49
PLA2G2A P14555 1/20 0.48
HTR1D P28221 1/20 0.48
HTR1B P28222 1/20 0.48

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
SCHEMBL9713476 1.00 LMNA (0.85) LMNALTA4HCYP2D6ADRB2ADRB1
SCHEMBL4046461 1.00 LMNA (0.85) LMNALTA4HCYP2D6ADRB2ADRB1
Toluene SCHEMBL28503513 0.93 LMNA (0.73) LMNALTA4HCYP2D6ADRB2ADRB1
SCHEMBL1618880 0.92 LMNA (1.00) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL50453 0.92 LMNA (1.00) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL3254859 0.92 LMNA (1.00) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL2943775 0.92 LMNA (1.00) LMNACYP2D6ADRB2ADRB1ADRB3
Methoxymethane SCHEMBL9729148 0.88 LMNA (0.92) LMNACYP2D6ADRB2ADRB1ADRB3
Alcohol SCHEMBL5067801 0.86 LMNA (0.88) LMNACYP2D6ADRB2ADRB1ADRB3
SCHEMBL5949941 0.85 LMNA (0.78) LMNACYP2D6ADRB2ADRB1ADRB3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119613237-A Synthesis method of 1- (4-phenoxy) -2-propanol 山东省分析测试中心 2025-03-14 CN claimed
CN-118878399-A Preparation method and application of crude drug intermediate ether alcohol 山东润青前线生物科技股份有限公司 2024-11-01 CN claimed
CN-112174784-A Crystal form A of 1- (4-phenoxyphenoxy) -2-propanol and preparation method and application thereof 江苏龙灯化学有限公司 2021-01-05 CN claimed
JP-61104797-A None JP disclosed
JP-61104797-A None JP disclosed
JP-60176592-A None JP disclosed
JP-60176592-A None JP disclosed
CN-120904022-A Synthesis method of pyriproxyfen key intermediate 1- (4-phenoxy) -2-propanol 南京逸嘉云数据信息有限公司 2025-11-07 CN disclosed
CN-119613237-A Synthesis method of 1- (4-phenoxy) -2-propanol 山东省分析测试中心 2025-03-14 CN disclosed
CN-119613237-A Synthesis method of 1- (4-phenoxy) -2-propanol 山东省分析测试中心 2025-03-14 CN disclosed
CN-118878399-A Preparation method and application of crude drug intermediate ether alcohol 山东润青前线生物科技股份有限公司 2024-11-01 CN disclosed
EP-0246713-A2 Intermediates for the production of nitrogen-containing substituted heterocyclic compounds SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1987-11-25 EP disclosed
JP-S61104797-A BIOCHEMICAL PREPARATION OF OPTICALLY ACTIVE 1-(4-PHENOXYPHENOXY)PROPAN-2-OL SUMITOMO CHEM CO LTD 1986-05-23 JP disclosed
JP-S61104797-A BIOCHEMICAL PREPARATION OF OPTICALLY ACTIVE 1-(4-PHENOXYPHENOXY)PROPAN-2-OL SUMITOMO CHEM CO LTD 1986-05-23 JP disclosed
JP-S60176592-A BIOCHEMICAL PREPARATION OF OPTICALLY ACTIVE 1-(4-PHENOXYPHENOXY)PROPAN-2-OL SUMITOMO CHEM CO LTD 1985-09-10 JP disclosed
JP-S60176592-A BIOCHEMICAL PREPARATION OF OPTICALLY ACTIVE 1-(4-PHENOXYPHENOXY)PROPAN-2-OL SUMITOMO CHEM CO LTD 1985-09-10 JP disclosed
EP-0128648-A1 Nitrogen-containing heterocyclic compounds, and their production and use SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 1984-12-19 EP disclosed
US-4058627-A INSECTICIDE, MITICIDE CIBA-GEIGY CORPORATION (US) 1977-11-15 US disclosed
US-3998891-A INSECTICIDES, MITICIDES CIBA-GEIGY CORPORATION (US) 1976-12-21 US disclosed
US-3963786-A Phenoxyphenylalkoxy-, alkenyloxy-, alkinyloxy- and benzyloxy-alkoxy ethers CIBA-GEIGY CORPORATION (US) 1976-06-15 US disclosed