Dimethyl Sulfoxide

Dimethyl Sulfoxide

SCHEMBL177271

C[S+](C)[O-].O=C(OC(=O)C(F)(F)F)C(F)(F)F

nearest known ligand 0.00

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Known targets — ChEMBL curated mechanism

MAP2K1MAP2K2

The experimentally established mechanism targets of Dimethyl Sulfoxide. 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.

Compoundsimilaritytop predictedshared targets
Dimethyl Sulfoxide SCHEMBL8483068 1.00
Dimethyl Sulfoxide SCHEMBL6082696 0.88 ALDH1A1 (0.39)
Dimethyl Sulfoxide SCHEMBL9877938 0.85 PPIP5K2 (0.31)
SCHEMBL28021775 0.84
Ethane SCHEMBL23013321 0.83 CES2 (0.33)
Methyl Alcohol SCHEMBL7718124 0.83 CA2 (0.32)
Chloromethane SCHEMBL28080031 0.83 CA2 (0.32)
SCHEMBL27623481 0.83 CA2 (0.35)
SCHEMBL52 0.83 CA2 (0.35)
Hydrochloric Acid SCHEMBL8958370 0.80 CA2 (0.33)

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-116462724-A Preparation method of tulathromycin intermediate epoxide 新发药业有限公司 2023-07-21 CN claimed
CN-113666978-A Preparation method of macrolide compound and intermediate used by same 洛阳惠中兽药有限公司 2021-11-19 CN claimed
CN-109678811-B Asymmetric preparation method of florfenicol intermediate cyclic compound 湖北中牧安达药业有限公司 2020-12-29 CN claimed
CN-109678811-A A kind of asymmetric preparation method of florfenicol intermediate cyclic product 湖北中牧安达药业有限公司 2019-04-26 CN claimed
CN-102786569-B The preparation method of Tulathromycin intermediate and preparation method thereof and Tulathromycin 安徽中升药业有限公司 2016-12-07 CN claimed
CN-102260306-B Novel method for preparing tulathromycin SHANDONG LUKANG SHELILE PHARMACEUTICAL CO LTD 2012-07-18 CN claimed
CN-102260306-A Novel method for preparing tulathromycin 2011-11-30 CN claimed
EP-1327637-B1 Process for the preparation of L-Ribose UNIV GEORGIA RES FOUND (US) 2005-09-14 EP claimed
US-6894159-B2 Process for the preparation of 2′-fluoro-5-methyl-beta-L-arabino-furanosyluridine THE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION (US) 2005-05-17 US claimed
US-20030139593-A1 Process for the preparation of 2'-fluoro-5-methyl-beta-L-arabino-furanosyluridine UNIVERSITY OF GEORGIA RESEARCH FOUNDATION INC. 2003-07-24 US claimed
EP-1327637-A1 Process for the preparation of L-Ribose UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2003-07-16 EP claimed
EP-0998482-B1 PROCESS FOR THE PREPARATION OF 2'-FLUORO-5-METHYL-BETA-L-ARABINOFURANOSYLURIDINE UNIV GEORGIA RES FOUND (US) 2003-04-02 EP claimed
US-6512107-B2 Generating preferential uridine derivative THE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION 2003-01-28 US claimed
US-20020062018-A1 PROCESS FOR THE PREPARATION OF 2'- FLUORO-5-METHYL-BETA-L-ARABINO- FURANOSYLURIDINE GEORGIA, UNIVERSITY OF, RESEARCH FOUNDATION INC., THE 2002-05-23 US claimed
EP-0998482-A1 PROCESS FOR THE PREPARATION OF 2'-FLUORO-5-METHYL-$g(b) -L-ARABINOFURANOSYLURIDINE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 2000-05-10 EP claimed
WO-1999005158-A1 PROCESS FOR THE PREPARATION OF 2'-FLUORO-5-METHYL-β -L-ARABINOFURANOSYLURIDINE THE UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC. (US) 1999-02-04 WO claimed
WO-2023229032-A1 THERAPEUTIC FOR CANCER REFRACTORY TO IMMUNE CHECKPOINT INHIBITOR 住友ファーマ株式会社 2023-11-30 WO disclosed
EP-4253377-A1 5-HETEROARYL-1H-PYRAZOL-3-AMINE DERIVATIVE Sumitomo Pharma Co., Ltd. (JP) 2023-10-04 EP disclosed
US-4180654-A 4\"-Deoxy-4\"-acylamido derivatives of oleandomycin, erythromycin and erythromycin carbonate PFIZER INC. (US) 1979-12-25 US disclosed
US-4150220-A Semi-synthetic 4\"-erythromycin A derivatives PFIZER INC. (US) 1979-04-17 US disclosed