Sulfanilamide

Sulfanilamide

SCHEMBL28036092

F.Nc1ccc(S(N)(=O)=O)cc1.c1ccccc1

nearest known ligand 0.85

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

folP

The experimentally established mechanism targets of Sulfanilamide. 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
CA2 P00918 18/20 0.85
CA9 Q16790 17/20 0.85
CA12 O43570 15/20 0.85
CA1 P00915 15/20 0.85
CA14 Q9ULX7 6/20 0.85
CA7 P43166 6/20 0.85
CA6 P23280 5/20 0.85
CA5A P35218 5/20 0.85
CA5B Q9Y2D0 5/20 0.85
CA4 P22748 4/20 0.85
CA13 Q8N1Q1 3/20 0.85
TSHR P16473 2/20 0.85
USP2 O75604 1/20 0.85
TDP1 Q9NUW8 1/20 0.85
AGO2 Q9UKV8 1/20 0.85
CA3 P07451 3/20 0.64
PLA2G7 Q13093 1/20 0.64
HTT P42858 1/20 0.59
LMNA P02545 1/20 0.56
MPO P05164 1/20 0.56

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
Sulfanilamide SCHEMBL8449748 0.97 CA2 (0.90) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL27545160 0.95 CA2 (0.85) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL27440502 0.95 CA2 (0.85) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL27352502 0.95 CA2 (0.94) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL8380125 0.93 CA2 (0.81) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL27911829 0.93 CA2 (0.81) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL2798899 0.92 CA2 (1.00) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL740 0.92 CA2 (1.00) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL30659052 0.92 CA2 (1.00) CA2CA9CA12CA1CA14
Sulfanilamide SCHEMBL31544839 0.92 CA2 (1.00) CA2CA9CA12CA1CA14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106535637-A Molecules having certain pesticidal utilities, and intermediates, compositions, and processes related thereto 美国陶氏益农公司 2017-03-22 CN claimed
CN-110505874-A Molecule and relative intermediate, composition and method with desinsection effectiveness DOW AGROSCIENCES LLC 2019-11-26 CN disclosed
CN-110087469-A Molecule and relative intermediate, composition and method with certain desinsection effectiveness 美国陶氏益农公司 2019-08-02 CN disclosed
CN-109475126-A Control the composition and method of spider type guiding principle species fecundity FMC有限公司 2019-03-15 CN disclosed
CN-109152360-A IN SITU TREATMENT OF SEED IN FURROW FMC有限公司 2019-01-04 CN disclosed
CN-109068644-A Insect repellant FMC有限公司 2018-12-21 CN disclosed
CN-108368125-A Acc inhibitors and uses thereof 吉利德阿波罗公司 2018-08-03 CN disclosed
CN-108349995-A Pyrazoles ACC inhibitor and application thereof 吉利德阿波罗公司 2018-07-31 CN disclosed
CN-108349994-A Triazole ACC inhibitor and application thereof 吉利德阿波罗公司 2018-07-31 CN disclosed
CN-108290902-A Esters ACC inhibitor and application thereof 吉利德阿波罗公司 2018-07-17 CN disclosed
CN-107616168-A Aqueous suspension shape composition pesticide 日产化学工业株式会社 2018-01-23 CN disclosed
CN-107372525-A A kind of Herbicidal combinations of humulone of sulphur containing triazole and its application 青岛清原化合物有限公司 2017-11-24 CN disclosed
CN-107108383-A Nitrification inhibitor composition and process for preparing same 美国陶氏益农公司 2017-08-29 CN disclosed
CN-103635089-B Comprise the reactive compound compound of (sulfur generation) carboxamide derivative and Fungicidal compounds 拜耳知识产权有限责任公司 2016-12-14 CN disclosed
CN-105007737-A 3-alkyl-5-fluoro-4-substituted-imino-3, 4-dihydropyrimidin-2 (1H) -one derivatives as fungicides DOW AGROSCIENCES LLC 2015-10-28 CN disclosed