Sulfacytine

Sulfacytine

SCHEMBL49377

CCn1ccc(NS(=O)(=O)c2ccc(N)cc2)nc1=O

nearest known ligand 0.50

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PPPK-DHPS

The experimentally established mechanism targets of Sulfacytine. 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
HTR6 P50406 5/20 0.50
MAPT P10636 4/20 0.50
ALDH1A1 P00352 4/20 0.50
CYP3A4 P08684 3/20 0.50
CYP2C9 P11712 3/20 0.50
CYP2C19 P33261 3/20 0.50
L3MBTL1 Q9Y468 2/20 0.50
RAB9A P51151 1/20 0.50
KDM4E B2RXH2 2/20 0.49
NPSR1 Q6W5P4 2/20 0.49
APEX1 P27695 1/20 0.49
BLM P54132 1/20 0.49
PDE4A P27815 1/20 0.48
AGO2 Q9UKV8 1/20 0.48
SMN1; SMN2 Q16637 3/20 0.48
TDP1 Q9NUW8 1/20 0.48
ADRA1A P35348 1/20 0.46
LMNA P02545 5/20 0.45
AURKA O14965 1/20 0.44
DHFR P00374 1/20 0.44

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
Sulfacytine SCHEMBL28251252 0.95 CA1 (0.48) HTR6MAPTALDH1A1CYP3A4CYP2C9
Sulfacytine SCHEMBL28122249 0.92 LMNA (0.60) HTR6MAPTALDH1A1CYP3A4CYP2C9
SCHEMBL10697070 0.86 KDM4E (0.51) MAPTALDH1A1KDM4ENPSR1SMN1; SMN2
SCHEMBL9806949 0.77 MAPT (0.43) MAPTSMN1; SMN2
Sulfachrysoidine SCHEMBL5886196 0.77 MAPT (0.38) HTR6MAPTALDH1A1CYP3A4CYP2C9
SCHEMBL14639242 0.70 MAPT (0.47) MAPTALDH1A1L3MBTL1KDM4ELMNA
SCHEMBL11882075 0.69 L3MBTL1 (0.77) HTR6MAPTALDH1A1CYP3A4CYP2C9
SCHEMBL11884662 0.69 HTR6 (0.52) HTR6MAPTALDH1A1CYP3A4CYP2C9
SCHEMBL10031608 0.69 ALDH1A1 (0.74) HTR6MAPTALDH1A1CYP3A4CYP2C9
SCHEMBL1892698 0.68 FGFR1 (0.44) MAPTLMNA

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

Appears in 4022 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025111482-A1 COMPLEXING AGENT SALT FORMULATIONS OF PHARMACEUTICAL COMPOUNDS AT LOW STOICHIOMETRIC RATIOS BEXSON BIOMEDICAL, INC. (US) 2025-05-30 WO claimed
US-20220169680-A1 CELL-PENETRATING PEPTIDE BASED ON INFLUENZA VIRUS M2 PROTEIN INSTITUTE OF BASIC MEDICAL SCIENCES CHINESE ACADEMY OF MEDICAL SCIENCES (CN) 2022-06-02 US claimed
EP-3912989-A1 CELL-PENETRATING PEPTIDE BASED ON INFLUENZA VIRUS M2 PROTEIN Institute of Basic Medical Sciences Chinese Academy of Medical Sciences (CN) 2021-11-24 EP claimed
EP-3841119-A1 COMPOSITIONS AND METHODS FOR REDUCING BACTERIAL AGGREGATION La Trobe University (AU) 2021-06-30 EP claimed
EP-2459227-B1 Prodrugs containing an aromatic amine connected by an amide bond to a carrier ASCENDIS PHARMA AS (DK) 2021-03-17 EP claimed
WO-2020037376-A1 COMPOSITIONS AND METHODS FOR REDUCING BACTERIAL AGGREGATION LA TROBE UNIVERSITY (AU) 2020-02-27 WO claimed
US-10449247-B2 Compositions and methods for enhancing immune response AVIVAGEN INC. (CA) 2019-10-22 US claimed
EP-2953624-B1 METHODS OF TREATING MICROBIAL INFECTIONS, INCLUDING MASTITIS LUODA PHARMA LTD (IE) 2019-08-21 EP claimed
CN-103857440-B Antimycotic and antibacterium prodrug based on conjugate 维奥姆生物科学有限公司 2018-09-25 CN claimed
CN-101094658-B For improving the medicinal preparation for oral administration of the many microencapsulated form discharging at least one active component 弗拉梅爱尔兰有限公司 2016-10-05 CN claimed
EP-0792371-A1 COMBINATION METHOD FOR ACNE TREATMENT Merck & Co., Inc. (US) 1997-09-03 EP claimed
EP-0786999-A1 COMBINATION METHOD FOR ACNE TREATMENT Merck & Co., Inc. (US) 1997-08-06 EP claimed
EP-0741570-A1 METHOD FOR PREVENTING OR REDUCING PHOTOSENSITIVITY AND/OR PHOTOTOXICITY REACTIONS TO MEDICATIONS G.D. SEARLE & CO. (US) 1996-11-13 EP claimed
US-5543417-A 5 Alpha-reductase inhibitor and at least one of an antibacterial agent, a keratolytic agent or an anti-inflammatory agent MERCK & CO., INC. (US) 1996-08-06 US claimed
WO-1996012487-A1 COMBINATION METHOD FOR ACNE TREATMENT MERCK & CO., INC. (US) 1996-05-02 WO claimed
WO-1996012817-A1 COMBINATION METHOD FOR ACNE TREATMENT MERCK & CO., INC. (US) 1996-05-02 WO claimed
WO-1995020387-A1 METHOD FOR PREVENTING OR REDUCING PHOTOSENSITIVITY AND/OR PHOTOTOXICITY REACTIONS TO MEDICATIONS G.D. SEARLE & CO. (US) 1995-08-03 WO claimed
WO-1992014456-A1 USE OF PHARMACEUTICAL COMPOUNDS IN THE TREATMENT OF SYMPTOMS OF DISORDERS RELATED TO NEUROLOGICAL DISEASES AND ETIOLOGICALLY RELATED SYMPTOMOLOGY SHAPIRO HOWARD K (US) 1992-09-03 WO claimed
EP-0255100-A2 Use of trimetrexate and its salts for the preparation of pharmaceutical compositions for treating infections of the mycobacterium-avium-intracellulare complex WARNER-LAMBERT COMPANY (US) 1988-02-03 EP claimed
US-4039667-A N-SULFANILYL-1-ETHYL-CYTOSINE HOFFMANN-LA ROCHE INC. (US) 1977-08-02 US claimed