Isopropyl Alcohol

Isopropyl Alcohol

SCHEMBL476732

CC(C)O.[Cl-].[H+]

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEBDKRB2CHRM1CHRM2CHRM3CHRNA1CHRNB1CHRNDCHRNECHRNGGUCY1A1GUCY1A2GUCY1B1GUCY1B2NAMPTPTAFRSLC10A2SLC6A2SLC6A3TACR1dacAdacBdacCftsImrcAmrcBmrdA

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

⚠ Novel chemotype — no close known analogue (best Tanimoto < 0.3). Unexplored chemical space relative to ChEMBL.

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.

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240343738-A1 Method for preparing pranoprofen and composition comprising pranoprofen and impurity SHENYANG XINGQI PHARMACEUTICAL CO., LTD. (CN) 2024-10-17 US claimed
US-20240239791-A1 PROCESSES FOR THE SYNTHESIS OF VALBENAZINE NEUROCRINE BIOSCIENCES, INC. 2024-07-18 US claimed
WO-2024119985-A1 METHOD FOR PREPARING SITAGLIPTIN INTERMEDIATE PYRAZINE HYDROCHLORIDE 台州达辰药业有限公司 2024-06-13 WO claimed
CN-118108612-A Preparation method of high-purity L-phenylephrine hydrochloride 南京海融制药有限公司 2024-05-31 CN claimed
EP-4361155-A1 METHOD FOR PREPARING PRANOPROFEN AND COMPOSITION CONTAINING PRANOPROFEN AND IMPURITY Shenyang Xingqi Pharmaceutical Co., Ltd. (CN) 2024-05-01 EP claimed
CN-117209387-B Salifying and purifying process of esmolol hydrochloride 中国海洋大学 2024-04-26 CN claimed
EP-4330255-A1 PROCESSES FOR THE SYNTHESIS OF VALBENAZINE Neurocrine Biosciences, Inc. (US) 2024-03-06 EP claimed
CN-114507184-B Synthesis method and application of 1-methyl hexahydroazepin-4-one hydrochloride 好医生药业集团有限公司 2024-02-13 CN claimed
CN-113620826-B Preparation method of D-p-hydroxyphenylglycine methyl ester hydrochloride suitable for industrial production 湖北省宏源药业科技股份有限公司 2024-02-02 CN claimed
CN-117480170-A Method for synthesizing valphenazine 纽罗克里生物科学有限公司 2024-01-30 CN claimed
CN-110734405-A Synthesis method of N- (6-aminohexyl) -N '-methyl-2, 2' -biimidazole 华东数字医学工程研究院 2020-01-31 CN claimed
CN-110668951-A Synthesis process of selegiline hydrochloride 安徽贝克生物制药有限公司 2020-01-10 CN claimed
CN-110642721-A Preparation method of selegiline hydrochloride 安徽贝克生物制药有限公司 2020-01-03 CN claimed
CN-109705112-A The preparation method of the novel crystal forms of Lurasidone HCl 江苏恩华药业股份有限公司 2019-05-03 CN claimed
CN-109251175-A The preparation method of pyrimidinones 广东东阳光药业有限公司 2019-01-22 CN claimed
CN-105524057-A Lurasidone hydrochloride new crystal form and preparation method thereof JIANGSU NHWA PHARMACEUTICAL CO LTD 2016-04-27 CN claimed
US-7880015-B2 treating N-[[2'-(1-triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyl]-L-valine methyl ester with oxalic acid to produce N-[[2'-(1-triphenylmethyltetrazol-5-yl)biphenyl-4-yl]methyl]-L-valine methyl ester oxalate, treating intermediate with a base and vlaeryl chloride , deprotecting; Valsartan product AUROBINDO PHARMA LTD. (IN) 2011-02-01 US claimed
US-20090281326-A1 Process For the Preparation of Angiotensin II Antagonist AUROBINDO PHARMA LTD (IN) 2009-11-12 US claimed
EP-2057132-A2 PROCESS FOR THE PREPARATION OF THE ANGIOTENSIN II ANTAGONIST VALSARTAN Aurobindo Pharma Limited (IN) 2009-05-13 EP claimed
WO-2008004110-A2 PROCESS FOR THE PREPARATION OF THE ANGIOTENSIN II ANTAGONIST VALSARTAN AUROBINDO PHARMA LIMITED (IN) 2008-01-10 WO claimed