SCHEMBL506640

SCHEMBL506640

CC(O)c1ncccc1F

nearest known ligand 0.41

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
TRPM8 Q7Z2W7 2/20 0.41
CYP2D6 P10635 1/20 0.38
CHRM1 P11229 1/20 0.38
HRH1 P35367 1/20 0.38
KCNH2 Q12809 1/20 0.38
L3MBTL1 Q9Y468 3/20 0.37
KDM4E B2RXH2 3/20 0.36
MPI P34949 1/20 0.36
PDK2 Q15119 1/20 0.35
NAPRT Q6XQN6 1/20 0.34
ALDH1A1 P00352 2/20 0.34
CTH P32929 1/20 0.33
NPC1 O15118 2/20 0.33
PKM P14618 1/20 0.33
AGTR1 P30556 1/20 0.33
RAB9A P51151 1/20 0.33
MAPK1 P28482 1/20 0.32
CNR1 P21554 1/20 0.32
ALOX12 P18054 1/20 0.32

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
SCHEMBL25211250 1.00 TRPM8 (0.41) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL29858175 1.00 TRPM8 (0.41) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL1858360 1.00 TRPM8 (0.41) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL9963324 0.85 CYP2D6 (0.40) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL12468617 0.83 CYP2D6 (0.38) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL20738494 0.79 CYP2D6 (0.38) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL21547452 0.79 CYP2D6 (0.41) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL20738495 0.79 CYP2D6 (0.38) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL30824594 0.79 CYP2D6 (0.38) TRPM8CYP2D6CHRM1HRH1KCNH2
SCHEMBL6961060 0.79 CYP2D6 (0.38) TRPM8CYP2D6CHRM1HRH1KCNH2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12545684-B2 CDK2 inhibitors BLUEPRINT MEDICINES CORPORATION (US) 2026-02-10 US disclosed
CN-116134035-B 3- (1H-imidazol-2-yl) -2,3,8 a-tetrahydroindol-5 (1H) -one derivatives useful as factor XIA inhibitors 詹森药业有限公司 2025-03-11 CN disclosed
CN-119431313-A Antifungal compound, preparation method and application thereof 上海交通大学 2025-02-14 CN disclosed
US-20240383902-A1 CDK2 INHIBITORS BLUEPRINT MEDICINES CORPORATION 2024-11-21 US disclosed
US-20240174683-A1 MAP4K1 INHIBITORS BAYER AKTIENGESELLSCHAFT (DE) 2024-05-30 US disclosed
US-11970498-B2 CDK2 inhibitors BLUEPRINT MEDICINES CORPORATION (US) 2024-04-30 US disclosed
US-11932648-B2 CDK2 inhibitors BLUEPRINT MEDICINES CORPORATION (US) 2024-03-19 US disclosed
EP-4288437-A1 MAP4K1 INHIBITORS Bayer Aktiengesellschaft (DE) 2023-12-13 EP disclosed
US-20230322791-A1 CDK2 INHIBITORS BLUEPRINT MEDICINES CORPORATION 2023-10-12 US disclosed
US-20230295157-A1 3-(1H-IMIDAZOL-2-YL)-2,3,8,8A-TETRAHYDROINDOLIZIN-5(1H)-ONE DERIVATIVES USEFUL AS FACTOR XIA INHIBITORS JANSSEN RESEARCH & DEVELOPMENT, LLC 2023-09-21 US disclosed
CN-102311387-A 6-substituted 2,3,4, 5-tetrahydro-1H-benzo [d] aza as 5-HT2Creceptor agonists LILLY CO ELI 2012-01-11 CN disclosed
CN-101522693-B Novel 5,7-disubstituted [1, 3] thiazolo [4, 5] pyrimidin-2 (3h)-amine deirvatives and their use in therapy ASTRAZENECA AB 2012-01-04 CN disclosed
CN-101516893-B 5, 7-disubstituted [1,3] thiazolo [4,5-D ] pyrimidin-2 (3H) -one derivatives and their use in therapy ASTRAZENECA AB (SE) 2011-11-30 CN disclosed
US-8022062-B2 6-substituted 2,3,4,5-tetrahydro-1H-benzo[d]azepines as 5-HT2C receptor agonists ELI LILLY AND COMPANY (US) 2011-09-20 US disclosed
CN-101522693-A Novel 5,7-disubstituted [1, 3] thiazolo [4, 5] pyrimidin-2 (3h)-amine deirvatives and their use in therapy ASTRAZENECA AB (SE) 2009-09-02 CN disclosed
CN-101516893-A Novel 5, 7-disubstituted [1,3] thiazolo [4, 5-D ] pyrimidin-2 (3H) -one derivatives and their use in therapy ASTRAZENECA AB (SE) 2009-08-26 CN disclosed
US-20090099155-A1 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS ARRAY BIOPHARMA, INC. 2009-04-16 US disclosed
CN-1934088-A As 5-HT2c6-substituted 2,3,4, 5-tetrahydro-1H-benzo [ d ] receptor agonists]Aza * LILLY CO ELI (US) 2007-03-21 CN disclosed
EP-1720836-A1 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO [D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS ELI LILLY AND COMPANY (US) 2006-11-15 EP disclosed
WO-2005082859-A1 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS ELI LILLY AND COMPANY (US) 2005-09-09 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 (8 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-20090099155-A1 6-SUBSTITUTED 2,3,4,5-TETRAHYDRO-1H-BENZO[D]AZEPINES AS 5-HT2C RECEPTOR AGONISTS HTR2C, HTR5A, HTR4 TRPM8 1364/4885CYP2D6 567/4885CHRM1 458/4885
US-11932648-B2 CDK2 inhibitors CDK2, CDK20, CDK2AP1 TRPM8 4428/4885CYP2D6 2839/4885CHRM1 4883/4885
US-20230322791-A1 CDK2 INHIBITORS CDK2, CDK20, CDK2AP1 TRPM8 4428/4885CYP2D6 2839/4885CHRM1 4883/4885
US-20230295157-A1 3-(1H-IMIDAZOL-2-YL)-2,3,8,8A-TETRAHYDROINDOLIZIN-5(1H)-ONE DERIVATIVES USEFUL AS FACTOR XIA INHIBITORS SERPINC1, F11, TFPI2 TRPM8 3319/4885CYP2D6 2325/4885CHRM1 4412/4885
US-20240174683-A1 MAP4K1 INHIBITORS MAP3K4, MAP4K4, MAP4K1 TRPM8 2069/4885CYP2D6 4249/4885CHRM1 1091/4885
US-11970498-B2 CDK2 inhibitors CDK2, CDK20, CDK2AP1 TRPM8 4428/4885CYP2D6 2839/4885CHRM1 4883/4885
US-20240383902-A1 CDK2 INHIBITORS CDK2, CDK20, CDK2AP1 TRPM8 4428/4885CYP2D6 2839/4885CHRM1 4883/4885
US-12545684-B2 CDK2 inhibitors CDK2, CDK4, CDK1 TRPM8 4463/4885CYP2D6 1707/4885CHRM1 4067/4885

“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.