SCHEMBL7687

SCHEMBL7687

CC(C)(C)OC(=O)N1CCN(CCCN)CC1

nearest known ligand 0.48

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
TLR8 Q9NR97 1/20 0.48
USP2 O75604 1/20 0.47
SMN1; SMN2 Q16637 1/20 0.47
CHRM2 P08172 2/20 0.45
CHRM1 P11229 2/20 0.45
CHRM4 P08173 1/20 0.45
CHRM3 P20309 1/20 0.45
ACKR3 P25106 4/20 0.44
EPHX2 P34913 3/20 0.43
HPGD P15428 1/20 0.41

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
SCHEMBL6221438 1.00 TLR8 (0.48) TLR8USP2SMN1; SMN2CHRM2CHRM1
SCHEMBL943825 0.95 TLR8 (0.47) TLR8USP2SMN1; SMN2CHRM2CHRM1
SCHEMBL7989266 0.94 TLR8 (0.45) TLR8USP2SMN1; SMN2CHRM2CHRM1
SCHEMBL12264373 0.94 TLR8 (0.47) TLR8USP2SMN1; SMN2CHRM2CHRM1
SCHEMBL29263655 0.94 TLR8 (0.47) TLR8USP2SMN1; SMN2CHRM2CHRM1
SCHEMBL18751236 0.94 TLR8 (0.47) TLR8USP2SMN1; SMN2CHRM2CHRM1
Trifluoroacetic Acid SCHEMBL27848401 0.92 TLR8 (0.43) TLR8USP2SMN1; SMN2CHRM2CHRM1
SCHEMBL13496025 0.90 TLR8 (0.43) TLR8USP2SMN1; SMN2CHRM2CHRM1
SCHEMBL12644325 0.90 USP2 (0.50) TLR8USP2SMN1; SMN2CHRM2CHRM1
SCHEMBL46682 0.90 USP2 (0.50) TLR8USP2SMN1; SMN2CHRM2CHRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112142733-A Synthetic route of pan FGFR covalent inhibitor PRN1371 湖南师范大学 2020-12-29 CN claimed
US-20260115297-A1 HETEROBIFUNCTIONAL COMPOUNDS AS DEGRADERS OF HPK1 ICAHN SCHOOL MED MOUNT SINAI (US) 2026-04-30 US disclosed
US-20260115187-A1 TRICYCLIC SKELETON COMPOUND AND USE THEREOF IN PREPARATION OF ANTITUMOR DRUG ZHONGSHAN HOSPITAL, FUDAN UNIVERSITY (CN) 2026-04-30 US disclosed
US-20260092057-A1 BCL-XL/BCL-2 DEGRADERS AND USES THEREOF KYMERA THERAPEUTICS INC (US) 2026-04-02 US disclosed
US-12582645-B2 Chemokine CXCR4 receptor modulators and uses related thereto EMORY UNIVERSITY (US) 2026-03-24 US disclosed
US-12583818-B2 Compound, preparation method thereof, and use thereof DAEGU-GYEONGBUK MEDICAL INNOVATION FOUNDATION (KR) 2026-03-24 US disclosed
US-12465648-B2 Heterobifunctional compounds as degraders of HPK1 ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI (US) 2025-11-11 US disclosed
EP-4620949-A1 ACKR3 MODULATORS FOR CARDIOVASCULAR OR ANTIPLATELET THERAPY Eberhard Karls Universität Tübingen (Medizinische Fakultät) (DE) 2025-09-24 EP disclosed
EP-4608454-A1 SELF-HYDROLYZING MALEIMIDES FOR BIOCONJUGATION Eli Lilly and Company (US) 2025-09-03 EP disclosed
EP-4463452-B1 C-MYC MRNA TRANSLATION MODULATORS AND USES THEREOF IN THE TREATMENT OF CANCER ANIMA BIOTECH INC (US) 2025-07-30 EP disclosed
WO-2007092095-A2 [4-(BENZO [B] THI0PHEN-2-YL) PYRIMIDIN-2YL] -AMINE DERIVATIVES AS IKK-BETA INHIBITORS FOR THE TREATMENT OF CANCER AND INFLAMMATORY DISEASES. ELI LILLY AND COMPANY (US) 2007-08-16 WO disclosed
EP-1778670-A2 MEDICINAL USE OF RECEPTOR LIGANDS 7TM Pharma A/S (DK) 2007-05-02 EP disclosed
EP-1737463-A1 PYRIMIDINES WITH TIE2 (TEK) ACTIVITY AstraZeneca AB (SE) 2007-01-03 EP disclosed
US-7132295-B2 Isotopically coded affinity markers 3 BAYER AKTIENGESELLSCHAFT (DE) 2006-11-07 US disclosed
WO-2006071035-A1 NOVEL ([1,3]THIAZOLO[5,4-B]PYRIDIN-2-YL)-2-CARBOXAMIDE DERIVATIVES LG LIFE SCIENCES, LTD. (KR) 2006-07-06 WO disclosed
WO-2006010446-A2 MEDICINAL USE OF RECEPTOR LIGANDS 7TM PHARMA A/S (DK) 2006-02-02 WO disclosed
WO-2005060970-A1 PYRIMIDINES WITH TIE2 (TEK) ACTIVITY ASTRAZENECA AB (SE) 2005-07-07 WO disclosed
US-20050049406-A1 Isotopically coded affinity markers 3 BAYER AKTIENGESELLSCHAFT (DE) 2005-03-03 US disclosed
EP-1446665-A2 ISOTOPICALLY CODED AFFINITY MARKERS 3 Bayer HealthCare AG (DE) 2004-08-18 EP disclosed
WO-2003040288-A2 ISOTOPICALLY CODED AFFINITY MARKERS 3 BAYER HEALTHCARE AG (DE) 2003-05-15 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 (7 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-12583818-B2 Compound, preparation method thereof, and use thereof TYRO3, TH, SRMS TLR8 264/4885USP2 4057/4885SMN1; SMN2 1810/4885
US-12465648-B2 Heterobifunctional compounds as degraders of HPK1 HIPK1, MCL1, HYPK TLR8 4145/4885USP2 331/4885SMN1; SMN2 3222/4885
US-20260115187-A1 TRICYCLIC SKELETON COMPOUND AND USE THEREOF IN PREPARATION OF ANTITUMOR DRUG HCCS, H4C1; H4C2; H4C3; H4C4; H4C5; H4C6; H4C8; H4C9; H4C11; H4C12; H4C13; H4C14; H4C15; H4C16, MCL1 TLR8 4519/4885USP2 4607/4885SMN1; SMN2 2240/4885
US-20260092057-A1 BCL-XL/BCL-2 DEGRADERS AND USES THEREOF BCL2L2, BCL2A1, BCL2L1 TLR8 4512/4885USP2 1066/4885SMN1; SMN2 744/4885
US-20260115297-A1 HETEROBIFUNCTIONAL COMPOUNDS AS DEGRADERS OF HPK1 TTK, ITK, CLK1 TLR8 3906/4885USP2 337/4885SMN1; SMN2 4005/4885
US-20050049406-A1 Isotopically coded affinity markers 3 IGFBP3, FABP3, LGALS3BP TLR8 4869/4885USP2 1633/4885SMN1; SMN2 2814/4885
US-12582645-B2 Chemokine CXCR4 receptor modulators and uses related thereto CXCR4, CXCR2, CXCR1 TLR8 366/4885USP2 2703/4885SMN1; SMN2 2592/4885

“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.