SCHEMBL983965

SCHEMBL983965

CCOC(=O)c1cccc(N)c1.CS(=O)(=O)O.CS(=O)(=O)O

nearest known ligand 0.54

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. 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
ADRB2 known ✓ P07550 2/20 0.53
LMNA P02545 2/20 0.54
CYP1A2 P05177 1/20 0.54
CYP3A4 P08684 1/20 0.54
MAOA P21397 1/20 0.54
ELANE P08246 1/20 0.54
ADRB1 P08588 2/20 0.53
ADRB3 P13945 2/20 0.53
CA2 P00918 3/20 0.51
CDC25B P30305 2/20 0.51
CA1 P00915 2/20 0.51
CA12 O43570 1/20 0.51
CA9 Q16790 1/20 0.51
HPGD P15428 1/20 0.50
RECQL P46063 1/20 0.50
CYP4F2 P78329 1/20 0.50
CYP4A11 Q02928 1/20 0.50
ALDH1A1 P00352 1/20 0.50
TSHR P16473 1/20 0.50
KMT2A Q03164 1/20 0.50

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
SCHEMBL29370485 1.00 LMNA (0.54) LMNACYP1A2CYP3A4MAOAELANE
SCHEMBL285618 1.00 LMNA (0.54) LMNACYP1A2CYP3A4MAOAELANE
Methane SCHEMBL2132580 0.98 ELANE (0.53) LMNACYP1A2CYP3A4MAOAELANE
Hydrochloric Acid SCHEMBL7319745 0.98 ELANE (0.53) LMNACYP1A2CYP3A4MAOAELANE
SCHEMBL29465556 0.92 LMNA (0.62) LMNACYP1A2CYP3A4MAOAELANE
SCHEMBL133366 0.92 LMNA (0.62) LMNACYP1A2CYP3A4MAOAELANE
Methane SCHEMBL15286491 0.91 LMNA (0.61) LMNACYP1A2CYP3A4MAOAELANE
Hydrochloric Acid SCHEMBL642777 0.91 LMNA (0.61) LMNACYP1A2CYP3A4MAOAELANE
Ethylamine SCHEMBL27494386 0.88 LMNA (0.57) LMNACYP1A2CYP3A4MAOAELANE
3-Aminobenzoic Acid SCHEMBL8220213 0.86 LMNA (0.56) LMNACYP1A2CYP3A4MAOAELANE

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-122074420-A Evaluation method of bile acid in relieving intestinal inflammation of east star spots 2026-05-26 CN claimed
CN-121674260-B Microorganism composite flora for treating aquaculture tail water and application thereof 南京万瑞环境科技有限公司 2026-05-19 CN claimed
EP-4460178-A1 METHOD TO DETACH ECTOPARASITES FROM FISH Intervet International B.V. (NL) 2024-11-13 EP claimed
CN-118901628-A Construction method of zebra fish bacterial inflammation model 江苏国生质检科技有限公司 2024-11-08 CN claimed
US-20240207454-A1 NEURO-BEHAVIORAL ASSAY FOR PHYSIOLOGICAL EVALUATION OF WATER-SOLUBLE ANESTHETICS NORTHEASTERN UNIVERSITY 2024-06-27 US claimed
WO-2023131615-A1 METHOD TO DETACH ECTOPARASITES FROM FISH INTERVET INTERNATIONAL B.V. (NL) 2023-07-13 WO claimed
US-20160287528-A1 METHODS AND COMPOSITIONS FOR USE IN AQUACULTURE CHEMAPHOR INC. (CA) 2016-10-06 US claimed
US-20130156816-A1 METHODS AND COMPOSITIONS FOR USE IN AQUACULTURE CHEMAPHOR INC. (CA) 2013-06-20 US claimed
EP-2536293-A1 METHODS AND COMPOSITIONS FOR USE IN AQUACULTURE Chemaphor Inc. (CA) 2012-12-26 EP claimed
WO-2011103464-A1 METHODS AND COMPOSITIONS FOR USE IN AQUACULTURE CHEMAPHOR INC. (CA) 2011-08-25 WO claimed
CN-122074420-A Evaluation method of bile acid in relieving intestinal inflammation of east star spots 2026-05-26 CN disclosed
CN-121674260-B Microorganism composite flora for treating aquaculture tail water and application thereof 南京万瑞环境科技有限公司 2026-05-19 CN disclosed
CN-121674260-B Microorganism composite flora for treating aquaculture tail water and application thereof 南京万瑞环境科技有限公司 2026-05-19 CN disclosed
WO-2026102322-A1 METHODS AND SYSTEMS FOR MODIFYING MOTILITY OF ENGINEERED MULTICELLULAR ORGANISMS TRUSTEES OF TUFTS COLLEGE (US) 2026-05-15 WO disclosed
CN-122006607-A Natural plant compound microcapsule for aquatic product transportation and keep-alive and application thereof 泰山学院 2026-05-12 CN disclosed
US-5434295-A Central nervous system YISSUM RESEARCH DEVELOPMENT COMPANY (IL) 1995-07-18 US disclosed
EP-0642504-A1 (3S,4S)-DELTA-6-TETRAHYDROCANNABINOL-7-OIC ACIDS AND DERIVATIVES THEREOF, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM YISSUM RESEARCH AND DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM (IL) 1995-03-15 EP disclosed
EP-0642504-A4 (3S,4S)-DELTA-6-TETRAHYDROCANNABINOL-7-OIC ACIDS AND DERIVATIVES THEREOF, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. YISSUM RES DEV CO (IL) 1994-08-22 EP disclosed
WO-1993005031-A1 (3S,4S)-DELTA-6-TETRAHYDROCANNABINOL-7-OIC ACIDS AND DERIVATIVES THEREOF, PROCESSES FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM YISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY IN JERUSALEM (IL) 1993-03-18 WO disclosed
EP-0501445-A1 Pharmaceutical composition comprising interleukin-2 YEDA RESEARCH AND DEVELOPMENT CO. LTD. (IL) 1992-09-02 EP disclosed