Aniline

Aniline

SCHEMBL167326

Nc1ccccc1.Nc1ccccc1.O=S(=O)(O)O

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

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

The experimentally established mechanism targets of Aniline. 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
TSHR P16473 7/20 0.65
ALDH1A1 P00352 4/20 0.52
NT5E P21589 1/20 0.52
HSD17B10 Q99714 3/20 0.50
TDP1 Q9NUW8 3/20 0.50
SMN1; SMN2 Q16637 1/20 0.50
KDM4E B2RXH2 2/20 0.46
MAPT P10636 2/20 0.46
HPGD P15428 2/20 0.46
CYP3A4 P08684 4/20 0.46
TAAR1 Q96RJ0 1/20 0.46
LMNA P02545 4/20 0.45
KMT2A Q03164 2/20 0.45
KEAP1 Q14145 1/20 0.45
GAA P10253 1/20 0.45
BLM P54132 1/20 0.45
GFER P55789 1/20 0.45
PMP22 Q01453 1/20 0.45
MEN1 O00255 1/20 0.44
CA12 O43570 2/20 0.43

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
Aniline SCHEMBL167327 1.00 TSHR (0.65) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL676147 1.00 TSHR (0.65) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL5693986 0.97 TSHR (0.61) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL28037884 0.97 TSHR (0.61) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL28305697 0.95 TSHR (0.58) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL3156113 0.92 TSHR (0.61) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL7863425 0.90 TSHR (0.52) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL8022436 0.90 TSHR (0.52) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL3783271 0.89 TSHR (0.58) TSHRALDH1A1NT5EHSD17B10TDP1
Aniline SCHEMBL6026655 0.89 TSHR (0.58) TSHRALDH1A1NT5EHSD17B10TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119584440-A Processing method of large back cavity circuit board 东莞市科佳电路有限公司 2025-03-07 CN disclosed
CN-112074736-B UV filter composition, method for the production thereof and use thereof 巴斯夫欧洲公司 2024-10-01 CN disclosed
US-11793742-B2 Mixtures of cosmetic UV absorbers BASF SE (DE) 2023-10-24 US disclosed
US-11666050-B2 Enhancing the antimicrobial activity of biocides with polymers BASF SE (DE) 2023-06-06 US disclosed
US-11647746-B2 Enhancing the antimicrobial activity of biocides with polymers BASF SE (DE) 2023-05-16 US disclosed
US-11458083-B2 Cosmetic and/or dermatological composition containing a merocyanine derivative comprising specific polar groups consisting of hydroxyl- and ether-functionalities L'OREAL (FR) 2022-10-04 US disclosed
US-20220047483-A1 MICRO-PARTICULATE ORGANIC UV ABSORBER COMPOSITION BASF SE (DE) 2022-02-17 US disclosed
EP-2315502-B1 Electroluminescent device UDC IRELAND LTD (IE) 2020-10-14 EP disclosed
EP-2265092-B1 Electroluminescent device UDC IRELAND LTD (IE) 2018-03-14 EP disclosed
EP-1520450-B1 ELECTROLUMINESCENT DEVICE UDC IRELAND LTD (IE) 2017-08-02 EP disclosed
CN-1654337-A Method for preparing iron oxide black by reducing nitrobenzene using ferrous powder with side product of aniline sulfate salts HUBEI KAIYUAN CHEMICALS & TECH (CN) 2005-08-17 CN disclosed
US-20050175856-A1 Blue emitting, durable, organoelectrouminescent layers containing 2H-benzotriazole compounds; full color display panels; light emission efficiency and brightness UDC IRELAND LIMITED (IE) 2005-08-11 US disclosed
EP-1520450-A1 ELECTROLUMINESCENT DEVICE Ciba Specialty Chemicals Holding Inc. (CH) 2005-04-06 EP disclosed
WO-2003105538-A1 ELECTROLUMINESCENT DEVICE SIBA SPELCIALTY CHEMICALS HOLDING INC. (CH) 2003-12-18 WO disclosed
US-5874547-A REACTING A PRIMARY AROMATIC AMINE WITH DIAZOTIZING AGENT IN SOLUTION; AZO DYES CROMPTON & KNOWLES CORPORATION (US) 1999-02-23 US disclosed
US-5344980-A Process for the preparation of 1,3,5-tris(4'-hydroxyaryl)benzene HOECHST CELANESE CORP. (US) 1994-09-06 US disclosed
US-5300698-A Process for the prepartion of 1,3,5-tris(4'-hydroxyaryl)benzene HOECHST CELANESE CORPORATION (US) 1994-04-05 US disclosed
US-4447368-A Process for the preparation of aminoarylsulphonic acids in sulfolene solvent SIEMENS-ALLIS, INC. (US) 1984-05-08 US disclosed
US-4435336-A FROM ARYLAMINE AND SULFONIC ACID, OR CORRESPONDING ARYLAMMONIUM HY BAYER AKTIENGESELLSCHAFT (DE) 1984-03-06 US disclosed
EP-0000247-B1 WATER-ABSORBENT STARCH COPOLYMERISATES AND METHOD FOR THEIR PREPARATION. A.E. STALEY MANUFACTURING COMPANY (US) 1982-08-04 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (5 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-11458083-B2 Cosmetic and/or dermatological composition containing a merocyanine derivative comprising specific polar groups consisting of hydroxyl- and ether-functionalities KRT18, LAGE3, TYR TSHR 3849/4885ALDH1A1 1018/4885NT5E 4261/4885
US-11647746-B2 Enhancing the antimicrobial activity of biocides with polymers CAT, AOC1, DDT TSHR 3558/4885ALDH1A1 787/4885NT5E 950/4885
US-20220047483-A1 MICRO-PARTICULATE ORGANIC UV ABSORBER COMPOSITION MCM4, UGT1A4, CCNB1 TSHR 4166/4885ALDH1A1 454/4885NT5E 4667/4885
US-11666050-B2 Enhancing the antimicrobial activity of biocides with polymers CAT, AOC1, DDT TSHR 3558/4885ALDH1A1 787/4885NT5E 950/4885
US-11793742-B2 Mixtures of cosmetic UV absorbers BTD, TMSB10, TH TSHR 1026/4885ALDH1A1 734/4885NT5E 1931/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.