SCHEMBL1853597

SCHEMBL1853597

COc1nnc(Cl)cc1N

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TDP1 Q9NUW8 2/20 0.52
MAPT P10636 2/20 0.38
CASP1 P29466 1/20 0.38
GAA P10253 3/20 0.38
NPC1 O15118 1/20 0.38
AURKA O14965 1/20 0.37
TTK P33981 1/20 0.37
AURKB Q96GD4 1/20 0.37
INCENP Q9NQS7 1/20 0.37
ALDH1A1 P00352 4/20 0.37
CYP1A2 P05177 1/20 0.37
CYP2C19 P33261 1/20 0.37
PKM P14618 1/20 0.33
HSP90AA1 P07900 5/20 0.32
HSP90AB1 P08238 5/20 0.32
PIK3CA P42336 1/20 0.31
G6PD P11413 1/20 0.31
LMNA P02545 1/20 0.30
POLB P06746 2/20 0.30
CYP3A4 P08684 1/20 0.30

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
SCHEMBL25131711 0.78 TDP1 (0.47) TDP1MAPTGAANPC1ALDH1A1
SCHEMBL29284057 0.77 TDP1 (0.42) TDP1ALDH1A1POLBTSHRL3MBTL1
SCHEMBL29206809 0.77 ALDH1A1 (0.39) TDP1MAPTGAANPC1ALDH1A1
SCHEMBL29770615 0.76 ALDH1A1 (0.38) TDP1ALDH1A1CYP1A2CYP2C19LMNA
SCHEMBL15577470 0.76 ALDH1A1 (0.38) TDP1MAPTGAANPC1ALDH1A1
SCHEMBL16387120 0.76 ALDH1A1 (0.38) TDP1ALDH1A1CYP1A2CYP2C19LMNA
SCHEMBL15941543 0.76 MAPT (0.43) TDP1MAPTCASP1GAANPC1
SCHEMBL13351317 0.76 MAPT (0.39) TDP1MAPTCASP1GAANPC1
SCHEMBL1750877 0.74 ALDH1A1 (0.37) TDP1ALDH1A1CYP1A2CYP2C19LMNA
SCHEMBL27238766 0.74 ALDH1A1 (0.37) TDP1MAPTALDH1A1CYP1A2CYP2C19

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250276977-A1 TYK2 INHIBITORS AND USES THEREOF ALUMIS INC (US) 2025-09-04 US disclosed
US-12312339-B2 Polo like kinase 4 inhibitors ORIC PHARMACEUTICALS, INC. (US) 2025-05-27 US disclosed
WO-2025090809-A1 MACROCYCLIC HETEROCYCLES AND USES THEREOF KUMQUAT BIOSCIENCES INC. (US) 2025-05-01 WO disclosed
CN-119161346-A Pyrrolo-ring compound and application thereof in medicine 康百达(四川)生物医药科技有限公司 2024-12-20 CN disclosed
CN-113811534-B TYK2 inhibitors and uses thereof 阿鲁米斯公司 2024-10-29 CN disclosed
US-20240270722-A1 POLO LIKE KINASE 4 INHIBITORS ORIC PHARMACEUTICALS, INC. 2024-08-15 US disclosed
CN-118005615-A Pyridazine compound and preparation method, pharmaceutical composition and application thereof 中国药科大学 2024-05-10 CN disclosed
US-20240124426-A1 POLO LIKE KINASE 4 INHIBITORS ORIC PHARMACEUTICALS, INC. 2024-04-18 US disclosed
CN-117794529-A POLO-like kinase 4 inhibitors 欧瑞克制药公司 2024-03-29 CN disclosed
EP-4337198-A1 POLO LIKE KINASE 4 INHIBITORS Oric Pharmaceuticals, Inc. (US) 2024-03-20 EP disclosed
WO-2008001076-A1 FUSED THIAZOLE DERIVATIVES AS KINASE INHIBITORS UCB PHARMA S.A. (BE) 2008-01-03 WO disclosed
WO-2004108707-A1 PYRIDAZINIL QUINAZOLINE DERIVATIVES FOR USE IN THE TREATMENT OF TUMOURS ASTRAZENECA AB (SE) 2004-12-16 WO disclosed
EP-0948495-B1 ARYL AND HETEROARYL SUBSTITUTED FUSED PYRROLE ANTIINFLAMMATORY AGENTS AMGEN INC (US) 2004-04-14 EP disclosed
US-6605634-B2 Tumor necrosis factor alpha and interleukin-1 (IL-1) mediated diseases; pain, diabetes; cyclooxygenase inhibition AMGEN, INC. 2003-08-12 US disclosed
US-20030096819-A1 Aryl and heteroaryl substituted fused pyrrole anti-inflammatory agents AMGEN INC. 2003-05-22 US disclosed
US-6440973-B1 Aryl and heteroaryl substituted fused pyrrole antiinflammatory agents AMGEN INC. 2002-08-27 US disclosed
US-6180643-B1 ANTAGONIST OF INTERLEUKINS, TUMOR NECROSIS FACTOR AMGEN INC. 2001-01-30 US disclosed
EP-0948495-A1 ARYL AND HETEROARYL SUBSTITUTED FUSED PYRROLE ANTIINFLAMMATORY AGENTS Amgen Inc., (US) 1999-10-13 EP disclosed
WO-1998022457-A9 ARYL AND HETEROARYL SUBSTITUTED FUSED PYRROLE ANTIINFLAMMATORY AGENTS 1998-08-20 WO disclosed
WO-1998022457-A1 ARYL AND HETEROARYL SUBSTITUTED FUSED PYRROLE ANTIINFLAMMATORY AGENTS AMGEN INC. (US) 1998-05-28 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 (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-20250276977-A1 TYK2 INHIBITORS AND USES THEREOF TYK2, JAK1, JAK2 TDP1 252/4885MAPT 669/4885CASP1 1831/4885
US-20240124426-A1 POLO LIKE KINASE 4 INHIBITORS PLK4, PLK2, PLK3 TDP1 659/4885MAPT 1102/4885CASP1 3608/4885
US-20030096819-A1 Aryl and heteroaryl substituted fused pyrrole anti-inflammatory agents TNF, IL1A, IL6 TDP1 1813/4885MAPT 4243/4885CASP1 120/4885
US-12312339-B2 Polo like kinase 4 inhibitors PLK4, PLK2, PLK3 TDP1 659/4885MAPT 1102/4885CASP1 3608/4885
US-20240270722-A1 POLO LIKE KINASE 4 INHIBITORS PLK4, PLK2, PLK3 TDP1 649/4885MAPT 1151/4885CASP1 3548/4885

“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.