SCHEMBL2748081

SCHEMBL2748081

CCN1c2ccccc2SC1Br

nearest known ligand 0.38

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 4/20 0.37
▸ SMN1; SMN2 Q16637 1/20 0.37
▸ MAOA P21397 1/20 0.35
▸ KDM1A O60341 2/20 0.35
▸ PPARG P37231 1/20 0.34
▸ GSK3B P49841 1/20 0.34
▸ BCHE P06276 3/20 0.33
▸ POLB P06746 2/20 0.33
▸ PKM P14618 1/20 0.33
▸ TSHR P16473 1/20 0.33
▸ MAPT P10636 2/20 0.33
▸ HPGD P15428 1/20 0.33
▸ HTT P42858 1/20 0.33
▸ GAA P10253 1/20 0.33
▸ ATM Q13315 1/20 0.33

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
SCHEMBL27757015 0.86 ALDH1A1 (0.39) ALDH1A1SMN1; SMN2MAOAKDM1APPARG
SCHEMBL30702419 0.79 SMN1; SMN2 (0.38) ALDH1A1SMN1; SMN2MAOAKDM1APPARG
SCHEMBL1046284 0.79 SMN1; SMN2 (0.38) ALDH1A1SMN1; SMN2MAOAKDM1APPARG
SCHEMBL27757096 0.79 GSK3B (0.48) ALDH1A1SMN1; SMN2KDM1APPARGGSK3B
Iodide SCHEMBL8924984 0.78 SMN1; SMN2 (0.37) ALDH1A1SMN1; SMN2MAOAKDM1APPARG
SCHEMBL31571120 0.78 ALDH1A1 (0.37) ALDH1A1SMN1; SMN2MAOAKDM1APPARG
SCHEMBL1573679 0.78 PPARG (0.37) ALDH1A1SMN1; SMN2MAOAKDM1APPARG
SCHEMBL29973993 0.78 ALDH1A1 (0.37) ALDH1A1SMN1; SMN2MAOAKDM1APPARG
SCHEMBL9305366 0.78 ALDH1A1 (0.37) ALDH1A1SMN1; SMN2MAOAKDM1APPARG
SCHEMBL1412788 0.78 PPARG (0.37) ALDH1A1SMN1; SMN2MAOAKDM1APPARG

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106478366-A A kind of preparation method of 1,2- pentanediol 衡阳春天医药化工设备有限公司 2017-03-08 — — CN claimed
CN-120025293-A Difunctional aza-carbene catalyst and preparation method and application thereof 中国科学院大连化学物理研究所 2025-05-23 — — CN disclosed
CN-112442038-B Industrial preparation method of pemetrexed disodium 德州德药制药有限公司 2022-09-02 — — CN disclosed
CN-112174970-B Method for preparing pemetrexed disodium with high yield 德州德药制药有限公司 2022-06-07 — — CN disclosed
CN-109704921-B Economic and green preparation method of vicinal dihydric alcohol 淄博诺奥化工有限公司 2022-01-04 — — CN disclosed
CN-112442038-A Industrial preparation method of pemetrexed disodium 德州德药制药有限公司 2021-03-05 — — CN disclosed
CN-112174970-A Method for preparing pemetrexed disodium in high yield 德州德药制药有限公司 2021-01-05 — — CN disclosed
CN-109704921-A The economical and eco-friendly preparation method of adjacent dihydric alcohol 淄博诺奥化工股份有限公司 2019-05-03 — — CN disclosed
CN-106478366-A A kind of preparation method of 1,2- pentanediol 衡阳春天医药化工设备有限公司 2017-03-08 — — CN disclosed
CN-106478366-A A kind of preparation method of 1,2- pentanediol 衡阳春天医药化工设备有限公司 2017-03-08 — — CN disclosed
CN-101489998-B Process for producing 2-hydroxy-4- (methylthio) butanoic acid or butyrate compound and intermediate thereof SUMITOMO CO LTD 2013-01-02 — — CN disclosed
US-8178325-B2 Process for producing sulfur-containing hydroxycarboxylic acid SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2012-05-15 — — US disclosed
CN-101517087-B Process for the preparation of 2-hydr0xy-4- (alkylthio or arylthio) butanoic acid by microbial conversion of 2-0x0-4- (alkylthio or arylthio) 1-butanol employing bacteria of the genus pseud0m0nas, rh0 SUMITOMO CHEMICAL CO 2011-11-23 — — CN disclosed
EP-2066798-B1 PROCESS FOR THE PREPARATION OF 2-HYDROXY CARBOXYLIC ACIDS EMPLOYING BACTERIA OF THE GENUS PSEUDOMONAS, RHODOCOCCUS OR BACILLUS SUMITOMO CHEMICAL CO (JP) 2010-12-29 — — EP disclosed
US-20090275094-A1 PROCESS FOR PRODUCING SULFUR-CONTAINING HYDROXYCARBOXYLIC ACID SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2009-11-05 — — US disclosed
CN-101517087-A Process for the preparation of 2-hydr0xy-4- (alkylthio or arylthio) butanoic acid by microbial conversion of 2-0x0-4- (alkylthio or arylthio) 1-butanol employing bacteria of the genus pseud0m0nas, rh0 SUMITOMO CHEMICAL CO (JP) 2009-08-26 — — CN disclosed
CN-101489998-A Process for producing 2-hydroxy-4- (methylthio) butanoic acid or butyrate compound and intermediate thereof SUMITOMO CHEMICAL CO (JP) 2009-07-22 — — CN disclosed
EP-2066798-A1 PROCESS FOR THE PREPARATION OF 2-HYDR0XY-4- (ALKYLTHIO OR ARYLTHIO) BUTANOIC ACID BY MICROBIAL CONVERSION OF 2-0X0-4- (ALKYLTHIO OR ARYLTHIO) 1-BUTANOL EMPLOYING BACTERIA OF THE GENUS PSEUD0M0NAS, RH0D0C0CCUS, OR BACILLUS Sumitomo Chemical Company, Limited (JP) 2009-06-10 — — EP disclosed
WO-2008104875-A1 OXAZOLIDINONES AS CHOLESTEROL ABSORPTION INHIBITORS PFIZER PRODUCTS INC. (US) 2008-09-04 — — WO disclosed
WO-2008038810-A1 PROCESS FOR THE PREPARATION OF 2-HYDR0XY-4- (ALKYLTHIO OR ARYLTHIO) BUTANOIC ACID BY MICROBIAL CONVERSION OF 2-0X0-4- (ALKYLTHIO OR ARYLTHIO) 1-BUTANOL EMPLOYING BACTERIA OF THE GENUS PSEUD0M0NAS, RH0D0C0CCUS, OR BACILLUS SUMITOMO CHEMICAL COMPANY, LIMITED (JP) 2008-04-03 — — WO disclosed
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