Thiourea

Thiourea

SCHEMBL933625

CS(=O)(=O)O.N=C(N)S

nearest known ligand 0.00

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of Thiourea. 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
Thiourea SCHEMBL28009945 0.97 KDM4E (0.46)
Sulfuric Acid SCHEMBL28217737 0.86 KDM4E (0.53)
Sulfuric Acid SCHEMBL5315249 0.86 KDM4E (0.53)
Sulfuric Acid SCHEMBL526776 0.86
Guanidine SCHEMBL5503970 0.86 KDM4E (0.53)
Guanidine SCHEMBL2136925 0.86
Guanidine SCHEMBL19458437 0.86 KDM4E (0.53)
Sulfuric Acid SCHEMBL27434030 0.84 KDM4E (0.52)
Thiourea SCHEMBL8576993 0.81 BLM (0.43)
Thiourea SCHEMBL7362564 0.79 KDM4E (0.42)

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 19 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-103788164-A Preparation method of fulvestrant CHIA TAI TIANQING PHARMACEUTICAL GROUP CO LTD 2014-05-14 CN claimed
CN-114685593-B Fulvestrant preparation method and fulvestrant intermediate 鲁南制药集团股份有限公司 2024-01-23 CN disclosed
CN-104447447-B Novel compound and methods for preparing and eliminating same 天津孚音生物科技发展有限公司 2017-02-22 CN disclosed
CN-104447447-A Novel compound and methods for preparing and eliminating same TIANJIN FUYIN BIOTECHNOLOGY DEV CO LTD 2015-03-25 CN disclosed
CN-104387435-A New compound and preparation method and application thereof TIANJIN FUYIN BIOTECHNOLOGY DEV CO LTD 2015-03-04 CN disclosed
CN-103788164-A Preparation method of fulvestrant CHIA TAI TIANQING PHARMACEUTICAL GROUP CO LTD 2014-05-14 CN disclosed
CN-103493799-A Improved organ protection, preservation and recovery HIBERNATION THERAPEUTICS LTD 2014-01-08 CN disclosed
US-20120323001-A1 BACE INHIBITORS ELI LILLY AND COMPANY (US) 2012-12-20 US disclosed
US-8278441-B2 BACE inhibitors ELI LILLY AND COMPANY (US) 2012-10-02 US disclosed
EP-2451793-A1 BACE INHIBITORS Eli Lilly and Company (US) 2012-05-16 EP disclosed
CN-102188705-A Medicament composition containing bis cyclooctane derivatives LIYAN WANG 2011-09-21 CN disclosed
CN-102166215-A Pharmaceutical composition containing piperazine derivatives LIYAN WANG 2011-08-31 CN disclosed
CN-102166357-A Medicinal composition containing bicyclic aza-alkane derivative LIYAN WANG 2011-08-31 CN disclosed
US-20110009395-A1 BACE INHIBITORS ELI LILLY AND COMPANY (US) 2011-01-13 US disclosed
WO-2011005738-A1 BACE INHIBITORS ELI LILLY AND COMPANY (US) 2011-01-13 WO disclosed
EP-1526140-B1 POTASSIUM-DEPENDENT SODIUM-CALCIUM EXCHANGER ASTELLAS PHARMA INC (JP) 2008-11-05 EP disclosed
US-4377693-A 2-Chloro-4,5-disubstituted-thiazoles useful as herbicidal safeners MONSANTO COMPANY (US) 1983-03-22 US disclosed
EP-0027019-B1 2-CHLORO-4,5-DISUBSTITUTED-THIAZOLES, PROCESS FOR THEIR PREPARATION, USE AS ANTIDOTES AGAINST DAMAGE CAUSED BY HERBICIDES AND MIXTURES CONTAINING THEM MONSANTO COMPANY (US) 1983-02-16 EP disclosed
EP-0027019-A1 2-Chloro-4,5-disubstituted-thiazoles, process for their preparation, use as antidotes against damage caused by herbicides and mixtures containing them MONSANTO COMPANY (US) 1981-04-15 EP disclosed