SCHEMBL270793

SCHEMBL270793

CC(C)(C)c1ccc(OCCO)cc1

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 4/20 0.68
CYP3A4 P08684 1/20 0.68
KDM4E B2RXH2 2/20 0.54
ALDH1A1 P00352 1/20 0.54
RECQL P46063 1/20 0.54
NR1I2 O75469 1/20 0.53
HRH3 Q9Y5N1 2/20 0.51
APP P05067 1/20 0.49
KMT2A Q03164 2/20 0.48
XBP1 P17861 1/20 0.48
NPSR1 Q6W5P4 1/20 0.48
POLB P06746 3/20 0.47
RAB9A P51151 3/20 0.47
NPC1 O15118 2/20 0.47
MITF O75030 2/20 0.47
CASP3 P42574 1/20 0.47
SENP7 Q9BQF6 1/20 0.47
LMNA P02545 1/20 0.47
TP53 P04637 1/20 0.47
MEN1 O00255 1/20 0.47

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
Alcohol SCHEMBL15135686 0.96 SMN1; SMN2 (0.64) SMN1; SMN2CYP3A4KDM4EALDH1A1RECQL
SCHEMBL967441 0.90 SMN1; SMN2 (0.56) SMN1; SMN2CYP3A4KDM4EALDH1A1HRH3
SCHEMBL970571 0.89 SMN1; SMN2 (0.56) SMN1; SMN2CYP3A4KDM4EALDH1A1HRH3
SCHEMBL12391998 0.89 SMN1; SMN2 (0.56) SMN1; SMN2CYP3A4KDM4EALDH1A1HRH3
SCHEMBL970017 0.89 SMN1; SMN2 (0.56) SMN1; SMN2CYP3A4KDM4EALDH1A1HRH3
SCHEMBL9592076 0.88 SMN1; SMN2 (0.54) SMN1; SMN2CYP3A4KDM4EALDH1A1HRH3
SCHEMBL4254052 0.88 SMN1; SMN2 (0.68) SMN1; SMN2CYP3A4KDM4EALDH1A1RECQL
SCHEMBL9818198 0.88 SMN1; SMN2 (0.68) SMN1; SMN2CYP3A4KDM4EALDH1A1RECQL
SCHEMBL79031 0.88 SMN1; SMN2 (0.68) SMN1; SMN2CYP3A4KDM4EALDH1A1RECQL
SCHEMBL9590081 0.86 HRH3 (0.56) SMN1; SMN2CYP3A4KDM4EALDH1A1HRH3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2020995-A2 ZERO-ORDER MODIFIED RELEASE SOLID DOSAGE FORMS Mallinckrodt Inc. (US) 2009-02-11 EP claimed
WO-2007133583-A2 ZERO-ORDER MODIFIED RELEASE SOLID DOSAGE FORMS MALLINCKRODT INC. (US) 2007-11-22 WO claimed
US-20050080260-A1 Preparation of prodrugs for selective drug delivery LUMINIDE 2005-04-14 US claimed
CN-118829433-A Respiratory stimulant parenteral formulations 依那拉治疗股份有限公司 2024-10-22 CN disclosed
CN-118488840-A Methods of treating respiratory depression modulated by non-opioid agents 依那拉治疗股份有限公司 2024-08-13 CN disclosed
US-20240238303-A1 LARGE-CONDUCTANCE POTASSIUM CHANNEL MODULATORS, COMPOSITIONS THEREOF, METHODS OF MANUFACTURING THEREOF, AND METHODS OF USE THEREOF ENALARE THERAPEUTICS INC (US) 2024-07-18 US disclosed
US-20240226007-A1 NICOTINAMIDE ADENINE DINUCLEOTIDE (NAD) COMPOSITIONS, METHODS OF MANUFACTURING THEREOF, AND METHODS OF USE THEREOF Sovida Solutions Ltd. (GB) 2024-07-11 US disclosed
EP-4333807-A1 NICOTINAMIDE ADENINE DINUCLEOTIDE (NAD) COMPOSITIONS, METHODS OF MANUFACTURING THEREOF, AND METHODS OF USE THEREOF Sovida Solutions Ltd. (GB) 2024-03-13 EP disclosed
EP-4333852-A1 LARGE-CONDUCTANCE POTASSIUM CHANNEL MODULATORS, COMPOSITIONS THEREOF, METHODS OF MANUFACTURING THEREOF, AND METHODS OF USE THEREOF Enalare Therapeutics Inc. (US) 2024-03-13 EP disclosed
CN-117529306-A Nicotinamide Adenine Dinucleotide (NAD) compositions, methods of making and methods of using the same 索维达解决方案有限公司 2024-02-06 CN disclosed
CN-117479945-A Large conductance potassium channel modulators, compositions thereof, methods of making and methods of using the same 依那拉治疗股份有限公司 2024-01-30 CN disclosed
EP-0162975-B1 P-ALKYL OR CYCLOALKYL PHENOXY ALKANOLS AND ALKANOL ESTERS AND USE FOR THE TREATMENT OF ALLERGIC CONDITIONS PHARMACO DEVELOPMENT PARTNERS (US) 1988-07-27 EP disclosed
EP-0162975-A1 P-alkyl or cycloalkyl phenoxy alkanols and alkanol esters and use for the treatment of allergic conditions PHARMACO DEVELOPMENT PARTNERS (US) 1985-12-04 EP disclosed
US-4543362-A P-Alkyl or cycloalkyl phenoxy alkanols and alkanol esters and process for the treatment of allergic conditions Berger, Frank M. (US) 1985-09-24 US disclosed
US-4504412-A Cyclohexane derivatives in fragrance compositions NATIONAL DISTILLERS AND CHEMICAL CORPORATION (US) 1985-03-12 US disclosed
US-4451474-A T-Butyl-phenoxy-alkylene esters of benzoic and nicotinic acids, compositions containing same and their antihistaminic method of use Berger, Frank M. (US) 1984-05-29 US disclosed
US-4388081-A CONTAINING PHENOXYALCOHOL AS ANTINKNOCK ADDITIVE PHILLIPS PETROLEUM COMPANY (US) 1983-06-14 US disclosed
US-4255152-A USING A DISPERSE DYE, WATER, AND AN ADDUCT OF ETHYLENE, PROPYLENE, OR STYRENE OXIDE AND A CYCLIC-SUBSTITUTED PHENOL; LEVELLING CIBA-GEIGY CORPORATION (US) 1981-03-10 US disclosed
US-4238625-A ACTIVATORS OF LEAD AND/OR BISMUTH AND/OR THEIR COMPOUNDS FOR OXIDATION WITH PLATINUM OR PALLADIUM CATALYST BAYER AKTIENGESELLSCHAFT (DE) 1980-12-09 US disclosed
US-4125732-A HYPOLIPIDEMIC AMERICAN CYANAMID COMPANY (US) 1978-11-14 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-20050080260-A1 Preparation of prodrugs for selective drug delivery APEH, PAH, ALAD SMN1; SMN2 3228/4885CYP3A4 84/4885KDM4E 3072/4885
US-20240238303-A1 LARGE-CONDUCTANCE POTASSIUM CHANNEL MODULATORS, COMPOSITIONS THEREOF, METHODS OF MANUFACTURING THEREOF, AND METHODS OF USE THEREOF KCNN2, KCNN1, KCNN3 SMN1; SMN2 630/4885CYP3A4 2106/4885KDM4E 1119/4885

“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.