Methyl Alcohol

Methyl Alcohol

SCHEMBL2996522

CO.O=S(=O)(O)c1ccccc1

nearest known ligand 0.89

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

BTKCACNA1CCACNA1DCACNA1FCACNA1SCACNA2D1CACNA2D2DRD2GABRA1GABRA2GABRA3GABRA4GABRA5GABRA6GABRB1GABRB2GABRB3GABRDGABREGABRG1GABRG2GABRG3GABRPGABRQHRH1HTR2AP2RY12

The experimentally established mechanism targets of Methyl Alcohol. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.89
SMN1; SMN2 Q16637 1/20 0.89
POLB P06746 2/20 0.58
CYP2D6 P10635 1/20 0.58
HTR6 P50406 1/20 0.52
LMNA P02545 2/20 0.52
ALDH1A1 P00352 5/20 0.50
NT5E P21589 1/20 0.50
PSIP1 O75475 1/20 0.50
TDP1 Q9NUW8 3/20 0.48
HSD17B10 Q99714 2/20 0.48
NAPRT Q6XQN6 1/20 0.48
CA1 P00915 2/20 0.48
CA2 P00918 2/20 0.48
MMP1 P03956 1/20 0.48
MMP2 P08253 1/20 0.48
MMP9 P14780 1/20 0.48
MMP8 P22894 1/20 0.48
MMP13 P45452 1/20 0.48
CA12 O43570 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
SCHEMBL28293509 0.97 TSHR (0.94) TSHRSMN1; SMN2POLBCYP2D6HTR6
Ethane SCHEMBL4196548 0.94 TSHR (0.89) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL30812783 0.94 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL30671620 0.94 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL1079321 0.94 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
Benzene SCHEMBL9751882 0.94 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL3409457 0.94 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL597672 0.94 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL2509 0.94 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6
SCHEMBL30307036 0.94 TSHR (1.00) TSHRSMN1; SMN2POLBCYP2D6HTR6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106045974-B A kind of bepotastine besilate at salt method 杭州和泽医药科技有限公司 2019-09-13 CN claimed
CN-103572503-A Hydrophobic type glass wool blanket and adhesive proportion thereof CHEN ZHAOFENG 2014-02-12 CN claimed
CN-102618197-A High-glue content adhesive for flexible glass fiber felt JIEMING ZHOU 2012-08-01 CN claimed
CN-100540588-C The preparation method of high-purity nano-sheet polyaniline UNIV TIANJIN (CN) 2009-09-16 CN claimed
CN-101139440-A Method for preparing high-purity nano-sheet polyaniline UNIV TIANJIN (CN) 2008-03-12 CN claimed
WO-2024083204-A1 SALT AND CRYSTAL FORM OF HETEROCYCLIC DERIVATIVE INHIBITOR, AND PREPARATION METHOD THEREFOR AND USE THEREOF 上海翰森生物医药科技有限公司 2024-04-25 WO disclosed
CN-115340529-A Acid addition salt of ROCK inhibitor, crystal form of salt, composition and pharmaceutical application 武汉朗来科技发展有限公司 2022-11-15 CN disclosed
CN-114478586-A Salt or crystal form of inhibitor containing bicyclic derivatives, and preparation method and application thereof 上海翰森生物医药科技有限公司 2022-05-13 CN disclosed
CN-113717194-A Salts of heteroaromatic derivatives and process for preparing the same 上海翰森生物医药科技有限公司 2021-11-30 CN disclosed
CN-113248645-B Low-melting point polyvinyl alcohol and preparation method thereof 天津辛德玛悬浮剂有限公司 2021-10-26 CN disclosed
CN-113493440-A Salt of nitrogen-containing heteroaromatic derivative and crystal form thereof 上海翰森生物医药科技有限公司 2021-10-12 CN disclosed
CN-113248645-A Low-melting point polyvinyl alcohol and preparation method thereof 天津辛德玛悬浮剂有限公司 2021-08-13 CN disclosed
WO-2008155752-A1 (1R,1'R)-ATRACURIUM SALTS SEPARATION PROCESS CHEMAGIS LTD. (IL) 2008-12-24 WO disclosed
CN-101287719-A Cholinergic enhancers with improved blood-brain barrier permeability for the treatment of diseases accompanied by cognitive impairment GALANTOS PHARMA GMBH (DE) 2008-10-15 CN disclosed
CN-101139440-A Method for preparing high-purity nano-sheet polyaniline UNIV TIANJIN (CN) 2008-03-12 CN disclosed
US-20070244058-A1 Galactose Derivative, Drug Carrier and Medicinal Composition NIPPON SHINYAKU CO., LTD. (JP) 2007-10-18 US disclosed
EP-1783137-A1 GALACTOSE DERIVATIVE, DRUG CARRIER AND MEDICINAL COMPOSITION Nippon Shinyaku Co., Ltd. (JP) 2007-05-09 EP disclosed
CN-1269823-C 3, 7-diazabicyclo [3.3.1] formulations as antiarrhythmic compounds ASTRAZENECA AB (SE) 2006-08-16 CN disclosed
CN-1514837-A 3,7-diazabicyclo [3.3.1] for mulations as anti arhythmiccompounds 2004-07-21 CN disclosed
US-5635707-A Photoelectric conversion device for use in sensing light reflected from medium surface NEC CORPORATION (JP) 1997-06-03 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 (1 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-20070244058-A1 Galactose Derivative, Drug Carrier and Medicinal Composition GALK1, GALE, UGGT1 TSHR 2018/4885SMN1; SMN2 2915/4885POLB 472/4885

“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.