SCHEMBL1772196

SCHEMBL1772196

Cc1c(Cl)cccc1B(O)O

nearest known ligand 0.48

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.48
MAPT P10636 2/20 0.40
LMNA P02545 2/20 0.39
POLB P06746 1/20 0.39
CYP1A2 P05177 2/20 0.37
MEN1 O00255 1/20 0.37
USP2 O75604 1/20 0.37
MT-CO2 P00403 1/20 0.37
TTR P02766 1/20 0.37
PLA2G1B P04054 1/20 0.37
PGR P06401 1/20 0.37
CYP3A4 P08684 1/20 0.37
HTR1A P08908 1/20 0.37
ADRA2A P08913 1/20 0.37
ADORA3 P0DMS8 1/20 0.37
AR P10275 1/20 0.37
CYP2C9 P11712 1/20 0.37
HPGD P15428 1/20 0.37
HTR2A P28223 1/20 0.37
CYP2C19 P33261 1/20 0.37

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
SCHEMBL2406662 0.88 ALDH1A1 (0.46) ALDH1A1MAPTLMNAPOLBCYP1A2
SCHEMBL4991 0.78 TSHR (0.48) ALDH1A1LMNACYP1A2MEN1CYP3A4
SCHEMBL29352520 0.78 TSHR (0.48) ALDH1A1LMNACYP1A2MEN1CYP3A4
SCHEMBL4129 0.77 TSHR (0.47) ALDH1A1MAPTLMNAENPP2TSHR
SCHEMBL29404220 0.77 TSHR (0.47) ALDH1A1MAPTLMNAENPP2TSHR
SCHEMBL215780 0.76 TSHR (0.41) ALDH1A1LMNACYP1A2ENPP2CYP2A6
SCHEMBL112040 0.76
SCHEMBL29479067 0.75 TRPA1 (0.50) ALDH1A1MAPTCYP1A2ENPP2CYP2A6
Benzene SCHEMBL28042388 0.75 LMNA (0.45) ALDH1A1LMNAENPP2CYP2A6TSHR
SCHEMBL309076 0.75 TRPA1 (0.50) ALDH1A1MAPTCYP1A2ENPP2CYP2A6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12630566-B2 KRas G12D inhibitors Mirati Therapeutics, Inc. (US) 2026-05-19 US disclosed
EP-4663626-A1 IMINE COMPOUNDS AS WELL AS PREPARATION METHOD THEREFOR AND USE THEREOF Bio Genuine (Shanghai) Biotech Co., Ltd (CN) 2025-12-17 EP disclosed
US-20250368641-A1 QUINOLINE COMPOUNDS AS INHIBITORS OF KRAS INCYTE CORP (US) 2025-12-04 US disclosed
WO-2025235874-A1 HETEROCYCLICS AS EGFR INHIBITORS SCHRÖDINGER, INC. (US) 2025-11-13 WO disclosed
US-12466822-B2 Heterocyclic compounds as immunomodulators INCYTE CORPORATION (US) 2025-11-11 US disclosed
US-20250325660-A1 IMMUNOMODULATOR COMPOUNDS AND METHODS OF USE INCYTE CORP (US) 2025-10-23 US disclosed
US-12410183-B2 Sars-cov2 main protease inhibitors GILEAD SCIENCES, INC. (US) 2025-09-09 US disclosed
US-20250255848-A1 SUBSTITUTED 6,7-DIHYDRO-5H-BENZO[7]ANNULENE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND THERAPEUTIC USES THEREOF SANOFI (FR) 2025-08-14 US disclosed
US-12378243-B2 Quinoline compounds as inhibitors of KRAS INCYTE CORPORATION (US) 2025-08-05 US disclosed
US-20250188073-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS INCYTE CORP (US) 2025-06-12 US disclosed
CN-1370176-A Subsstituted heterocycle fused gamma-carbolines BRISTOL MYERS SQUIBB CO (US) 2002-09-18 CN disclosed
EP-1212303-A2 BICYCLIC ANDROGEN AND PROGESTERONE RECEPTOR MODULATOR COMPOUNDS AND METHODS LIGAND PHARMACEUTICALS INCORPORATED (US) 2002-06-12 EP disclosed
EP-1192165-A2 SUBSTITUTED HETEROCYCLE FUSED GAMMA-CARBOLINES Bristol-Myers Squibb Pharma Company (US) 2002-04-03 EP disclosed
EP-1189905-A1 SUBSTITUTED HETEROCYCLE FUSED GAMMA-CARBOLINES Bristol-Myers Squibb Pharma Company (US) 2002-03-27 EP disclosed
US-20020019393-A1 Inhibitors of p38 VERTEX PHARMACEUTICALS INCORPORATED 2002-02-14 US disclosed
WO-2001016108-A2 BICYCLIC ANDROGEN AND PROGESTERONE RECEPTOR MODULATOR COMPOUNDS AND METHODS LIGAND PHARMACEUTICALS INCORPORATED (US) 2001-03-08 WO disclosed
EP-1077943-A1 HETEROCYCLIC INHIBITORS OF P38 Vertex Pharmaceuticals Incorporated (US) 2001-02-28 EP disclosed
WO-2000077010-A2 SUBSTITUTED HETEROCYCLE FUSED GAMMA-CARBOLINES DU PONT PHARMACEUTICALS COMPANY (US) 2000-12-21 WO disclosed
WO-2000077001-A1 SUBSTITUTED HETEROCYCLE FUSED GAMMA-CARBOLINES DU PONT PHARMACEUTICALS COMPANY (US) 2000-12-21 WO disclosed
WO-1999058502-A1 HETEROCYCLIC INHIBITORS OF P38 VERTEX PHARMACEUTICALS INCORPORATED (US) 1999-11-18 WO 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 (9 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-20250325660-A1 IMMUNOMODULATOR COMPOUNDS AND METHODS OF USE CD274, PDCD1LG2, PDCD1 ALDH1A1 1759/4885MAPT 4007/4885LMNA 4333/4885
US-12466822-B2 Heterocyclic compounds as immunomodulators CD74, IL2, ICOS ALDH1A1 223/4885MAPT 4685/4885LMNA 4857/4885
US-12378243-B2 Quinoline compounds as inhibitors of KRAS KRAS, NRAS, HRAS ALDH1A1 1858/4885MAPT 4504/4885LMNA 2409/4885
US-12630566-B2 KRas G12D inhibitors KRAS, NRAS, HRAS ALDH1A1 1816/4885MAPT 4652/4885LMNA 4684/4885
US-12410183-B2 Sars-cov2 main protease inhibitors ACE2, TMPRSS2, ACE ALDH1A1 3259/4885MAPT 2197/4885LMNA 3885/4885
US-20020019393-A1 Inhibitors of p38 MAPK1, MAPK3, MAP3K1 ALDH1A1 3189/4885MAPT 1883/4885LMNA 2007/4885
US-20250255848-A1 SUBSTITUTED 6,7-DIHYDRO-5H-BENZO[7]ANNULENE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND THERAPEUTIC USES THEREOF CYP19A1, FSHR, GPER1 ALDH1A1 637/4885MAPT 4606/4885LMNA 2311/4885
US-20250188073-A1 TRICYCLIC COMPOUNDS AS INHIBITORS OF KRAS KRAS, NRAS, HRAS ALDH1A1 2204/4885MAPT 4509/4885LMNA 2478/4885
US-20250368641-A1 QUINOLINE COMPOUNDS AS INHIBITORS OF KRAS KRAS, NRAS, HRAS ALDH1A1 1858/4885MAPT 4504/4885LMNA 2409/4885

“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.