SCHEMBL369647

SCHEMBL369647

C=CCC(OC)c1ccccc1

nearest known ligand 0.47

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2C19 P33261 2/20 0.47
SMN1; SMN2 Q16637 2/20 0.43
ALDH1A1 P00352 3/20 0.40
KDM4E B2RXH2 1/20 0.39
MAPT P10636 1/20 0.39
ALOX15 P16050 1/20 0.39
HSD17B10 Q99714 1/20 0.39
PPARG P37231 1/20 0.37
PPARA Q07869 1/20 0.37
SLC6A4 P31645 3/20 0.36
SLC6A2 P23975 2/20 0.36
KMT2A Q03164 2/20 0.36
MEN1 O00255 1/20 0.36
CYP1A2 P05177 1/20 0.36
CYP3A4 P08684 1/20 0.36
CYP2D6 P10635 1/20 0.36
TSHR P16473 1/20 0.36
AOC3 Q16853 1/20 0.36
SLC6A3 Q01959 1/20 0.36
ATM Q13315 1/20 0.35

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
SCHEMBL939842 0.83 CYP2C19 (0.50) CYP2C19SMN1; SMN2ALDH1A1KDM4EMAPT
SCHEMBL8680427 0.83 CYP2C19 (0.50) CYP2C19SMN1; SMN2ALDH1A1KDM4EMAPT
Methane SCHEMBL28626702 0.82 CYP2C19 (0.48) CYP2C19SMN1; SMN2ALDH1A1KDM4EMAPT
SCHEMBL28089324 0.81 CYP2C19 (0.44) CYP2C19SMN1; SMN2ALDH1A1KDM4EMAPT
SCHEMBL9721626 0.81 AOC3 (0.53) SLC6A4SLC6A2CYP2D6AOC3SLC6A3
SCHEMBL28422465 0.80 CYP2C19 (0.47) CYP2C19SMN1; SMN2ALDH1A1KDM4EMAPT
SCHEMBL27756586 0.80 KMT2A (0.42) CYP2C19ALDH1A1MAPTSLC6A4SLC6A2
SCHEMBL6200840 0.80 SMN1; SMN2 (0.47) CYP2C19SMN1; SMN2ALDH1A1KDM4EMAPT
SCHEMBL18236072 0.80 SMN1; SMN2 (0.47) CYP2C19SMN1; SMN2ALDH1A1KDM4EMAPT
SCHEMBL27547164 0.80 CYP2C19 (0.52) CYP2C19SMN1; SMN2ALDH1A1KDM4EMAPT

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 12 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117486836-A Preparation method of 2-aryl-3-carbonyl substituted tetrahydrofuran and tetrahydropyran compound 遵义医科大学 2024-02-02 CN disclosed
US-8889920-B2 Process for preparing 4-isopropylcyclohexylmethanol BASF SE (DE) 2014-11-18 US disclosed
CN-102365393-B Electrochemical method for producing 3 tert.-butyl benzaldehyde- dimethylacetal BASF SE (DE) 2014-10-29 CN disclosed
US-8629304-B2 Electrochemical method for producing 3-tert-butylbenzaldehyde dimethyl acetal BASF SE (DE) 2014-01-14 US disclosed
CN-102762774-A Process for producing 4-isopropylcyclohexylmethanol BASF SE 2012-10-31 CN disclosed
CN-102365393-A Electrochemical method for producing 3 tert.-butyl benzaldehyde- dimethylacetal BASF SE 2012-02-29 CN disclosed
US-20120016162-A1 ELECTROCHEMICAL METHOD FOR PRODUCING 3-TERT-BUTYLBENZALDEHYDE DIMETHYL ACETAL BASF SE (DE) 2012-01-19 US disclosed
US-20110207968-A1 PROCESS FOR PREPARING 4-ISOPROPYLCYCLOHEXYLMETHANOL BASF SE (DE) 2011-08-25 US disclosed
CN-101231468-A Radiation sensitive resin composition and color filter JSR CORP (JP) 2008-07-30 CN disclosed
CN-101105627-A Radiation-sensitive composition for forming a colored layer, color filter and color liquid crystal display device JSR CORP (JP) 2008-01-16 CN disclosed
EP-1478403-A1 RESPONSIVE MICROGEL AND METHODS RELATED THERETO SUPRATEK PHARMA, INC. (CA) 2004-11-24 EP disclosed
WO-2003063909-A1 RESPONSIVE MICROGEL AND METHODS RELATED THERETO SUPRATEK PHARMA INC. (US) 2003-08-07 WO 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-20110207968-A1 PROCESS FOR PREPARING 4-ISOPROPYLCYCLOHEXYLMETHANOL CYP2E1, CYP3A4, DHPS CYP2C19 63/4885SMN1; SMN2 4447/4885ALDH1A1 147/4885
US-20120016162-A1 ELECTROCHEMICAL METHOD FOR PRODUCING 3-TERT-BUTYLBENZALDEHYDE DIMETHYL ACETAL TET3, TERT, ALKBH2 CYP2C19 998/4885SMN1; SMN2 3493/4885ALDH1A1 56/4885

“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.