Methyl Alcohol

Methyl Alcohol

SCHEMBL3396777

CO.O=C(Cc1ccccn1)OC(=O)Cc1ccccn1

nearest known ligand 0.53

Full drug profile on Sugi Atlas →

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.53
CYP1A2 P05177 1/20 0.53
TSHR P16473 1/20 0.53
RAB9A P51151 3/20 0.51
NPC1 O15118 2/20 0.51
SMN1; SMN2 Q16637 2/20 0.50
PTPRA P18433 1/20 0.47
KDM4E B2RXH2 1/20 0.47
MAPT P10636 1/20 0.47
POLB P06746 1/20 0.46
IDO1 P14902 1/20 0.45
LMNA P02545 1/20 0.45
PARP10 Q53GL7 1/20 0.45
MEN1 O00255 1/20 0.44
KMT2A Q03164 1/20 0.44

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
SCHEMBL375765 0.98 RAB9A (0.53) ALDH1A1CYP1A2TSHRRAB9ANPC1
Acetic Acid SCHEMBL6285526 0.95 ALDH1A1 (0.53) ALDH1A1CYP1A2TSHRRAB9ANPC1
Acetonitrile SCHEMBL10666479 0.92 ALDH1A1 (0.46) ALDH1A1CYP1A2TSHRRAB9ANPC1
Toluene SCHEMBL10939845 0.92 MAPT (0.48) ALDH1A1CYP1A2TSHRRAB9ANPC1
SCHEMBL1714515 0.91 ALDH1A1 (0.53) ALDH1A1CYP1A2TSHRRAB9ANPC1
SCHEMBL2520545 0.91 RAB9A (0.47) ALDH1A1CYP1A2TSHRRAB9ANPC1
Pyrrole SCHEMBL28308888 0.90 RAB9A (0.46) ALDH1A1CYP1A2TSHRRAB9ANPC1
SCHEMBL9680519 0.87 CYP1A2 (0.43) ALDH1A1CYP1A2TSHRRAB9ANPC1
SCHEMBL78000 0.87 SMN1; SMN2 (0.53) ALDH1A1CYP1A2TSHRRAB9ANPC1
SCHEMBL29390571 0.87 SMN1; SMN2 (0.53) ALDH1A1CYP1A2TSHRRAB9ANPC1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-7705135-B2 Pharmaceutical compositions comprising aloe pectins, and methods for their production and use NANOTHERAPEUTICS, INC. (US) 2010-04-27 US disclosed
US-7691986-B2 High molecular weight, low methoxyl pectins, and their production and uses NANOTHERAPEUTICS, INC. (US) 2010-04-06 US disclosed
US-20060211653-A1 Pharmaceutical compositions comprising Aloe pectins, and methods for their production and use NANOTHERAPEUTICS, INC. 2006-09-21 US disclosed
US-7022683-B1 Pharmacological compositions comprising pectins having high molecular weights and low degrees of methoxylation CARRINGTON LABORATORIES, INC. (US) 2006-04-04 US disclosed
EP-1607407-A2 Aloe pectins Carrington Laboratories, Inc. (US) 2005-12-21 EP disclosed
EP-1086141-B1 ALOE PECTINS CARRINGTON LAB INC (US) 2005-09-28 EP disclosed
US-20030220485-A1 High molecular weight, low methoxyl pectins, and their production and uses CARRINGTON LABORATORIES, INC. 2003-11-27 US disclosed
US-5929051-A ALOE PECTIN CONTAINS 3-O-METHYL RHAMNOSE, BEING CAPABLE OF FORMING GEL IN PRESENCE OF CALCIUM SALT; TEMPERATURE REVERSIBLE FORMS SOLUTION AT ROOM TEMPERATURE; USED AS CONTROLLED RELEASE AGENT CARRINGTON LABORATORIES, INC. (US) 1999-07-27 US disclosed