Methyl Alcohol

Methyl Alcohol

SCHEMBL2137682

CO.c1ccc(CNC2CCCCC2)cc1

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HRH3 Q9Y5N1 1/20 0.65
GRIN2B Q13224 1/20 0.61
EPHX1 P07099 1/20 0.57
HPGD P15428 1/20 0.57
TAAR1 Q96RJ0 1/20 0.57
FABP6 P51161 1/20 0.56
MEN1 O00255 1/20 0.56
RAB9A P51151 1/20 0.56
KMT2A Q03164 1/20 0.56
POLB P06746 1/20 0.56
BCHE P06276 1/20 0.56
ACHE P22303 1/20 0.56
BACE1 P56817 1/20 0.56
ALDH1A1 P00352 2/20 0.55
HDAC1 Q13547 1/20 0.55
KDM4E B2RXH2 1/20 0.54
PKM P14618 1/20 0.54
OPRM1 P35372 2/20 0.54
OPRL1 P41146 2/20 0.54
EPHX2 P34913 1/20 0.53

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
SCHEMBL1847296 0.94 HRH3 (0.71) HRH3GRIN2BEPHX1HPGDTAAR1
SCHEMBL24574127 0.94 HRH3 (0.71) HRH3GRIN2BEPHX1HPGDTAAR1
SCHEMBL10789534 0.94 HRH3 (0.71) HRH3GRIN2BEPHX1HPGDTAAR1
SCHEMBL294763 0.94 HRH3 (0.71) HRH3GRIN2BEPHX1HPGDTAAR1
Hydrochloric Acid SCHEMBL11781778 0.92 HRH3 (0.69) HRH3GRIN2BEPHX1HPGDTAAR1
Hydrochloric Acid SCHEMBL11782513 0.92 HRH3 (0.69) HRH3GRIN2BEPHX1HPGDTAAR1
SCHEMBL433970 0.92 GRIN2B (0.69) HRH3GRIN2BEPHX1HPGDTAAR1
Acetic Acid SCHEMBL8071956 0.91 EPHX1 (0.60) HRH3GRIN2BEPHX1HPGDTAAR1
Bromide SCHEMBL18131548 0.91 HRH3 (0.67) HRH3GRIN2BEPHX1HPGDTAAR1
Hydrochloric Acid SCHEMBL11785266 0.90 GRIN2B (0.67) HRH3GRIN2BEPHX1HPGDTAAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-6210816-B1 Translucent xerographic recording substrates XEROX CORPORATION 2001-04-03 US claimed
US-11760750-B1 Process for preparing levoketoconazole NURAY CHEMICALS PRIVATE LIMITED (IN) 2023-09-19 US disclosed
CN-108925135-A Synthetic method for preparing (S) - (2R,3R,11bR) -3-isobutyl-9, 10-dimethoxy-2, 3,4,6,7,11 b-hexahydro-1H-pyrido [2,1-a ] isoquinolin-2-yl-2-amino-3-methylbutyrate bis (4-methylbenzenesulfonate) 纽罗克里生物科学有限公司 2018-11-30 CN disclosed
CN-104024241-B Uracil derivatives and their use for medical purposes DAINIPPON SUMITOMO PHARMA CO.,LTD. (JP) 2016-01-20 CN disclosed
US-9040516-B2 Uracil derivative and use thereof for medical purposes SUMITOMO DAINIPPON PHARMA CO., LTD. (JP) 2015-05-26 US disclosed
CN-104024241-A Uracil derivatives and their use for medical purposes DAINIPPON SUMITOMO PHARMA CO 2014-09-03 CN disclosed
US-20140179670-A1 URACIL DERIVATIVE AND USE THEREOF FOR MEDICAL PURPOSES DAINIPPON SUMITOMO PHARMA CO., LTD. (JP) 2014-06-26 US disclosed
EP-2740728-A1 URACIL DERIVATIVE AND USE THEREOF FOR MEDICAL PURPOSES Dainippon Sumitomo Pharma Co., Ltd. (JP) 2014-06-11 EP disclosed
EP-2392400-B1 Homogeneous asymmetric hydrogenation method TAKASAGO PERFUMERY CO LTD (JP) 2014-05-07 EP disclosed
CN-101970572-B Photocurable composition SEKISUI CHEMICAL CO LTD 2014-01-29 CN disclosed
EP-1911516-A1 HOMOGENEOUS ASYMMETRIC HYDROGENATION CATALYST Takasago International Corporation (JP) 2008-04-16 EP disclosed
US-7199260-B2 Process for reductive dehalogenation DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2007-04-03 US disclosed
US-20060052626-A1 Process for reductive dehaloganation DAIICHI PHARMACEUTICAL CO., LTD. (JP) 2006-03-09 US disclosed
US-6825191-B2 ANTICOAGULANT AJINOMOTO CO., INC. (JP) 2004-11-30 US disclosed
US-20030186969-A1 Benzodiazepine derivatives AJINOMOTO CO. INC (JP) 2003-10-02 US disclosed
EP-1329450-A1 BENZODIAZEPINE DERIVATIVE Ajinomoto Co., Inc. (JP) 2003-07-23 EP disclosed
CN-1358170-A Process for preparing (-)-(1S, 4R) N-protected 4-amino-2-cyclopentene-1-carboxylate esters BIOCRYST PHARMACEUTICAL INC (US) 2002-07-10 CN disclosed
US-6407096-B1 1,4-BENZOTHIAZINE AND 1,4-BENZOXAZINE DERIVATIVES; HYPOTENSIVE, ANTIISCHEMIC, ANTIALLERGEN, ANTIASTHMATIC AND ANTICOAGULANT AGENTS; CARDIOVASCULAR DISORDERS TORAY INDUSTRIES, INC. (JP) 2002-06-18 US disclosed
US-6210816-B1 Translucent xerographic recording substrates XEROX CORPORATION 2001-04-03 US disclosed
EP-1028113-A1 FUSED BENZENE HETEROCYCLE DERIVATIVES AND UTILIZATION THEREOF TORAY INDUSTRIES, INC. (JP) 2000-08-16 EP 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 (4 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-20030186969-A1 Benzodiazepine derivatives GABRA1, F11, GABRA4 HRH3 418/4885GRIN2B 221/4885EPHX1 1008/4885
US-20060052626-A1 Process for reductive dehaloganation IDUA, CYP2F1, DEK HRH3 1879/4885GRIN2B 3183/4885EPHX1 710/4885
US-20140179670-A1 URACIL DERIVATIVE AND USE THEREOF FOR MEDICAL PURPOSES URB2, ELANE, NUDT1 HRH3 51/4885GRIN2B 3111/4885EPHX1 1257/4885
US-11760750-B1 Process for preparing levoketoconazole KHK, KYAT3, PLK3 HRH3 4157/4885GRIN2B 4393/4885EPHX1 3838/4885

“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.