SCHEMBL601569

SCHEMBL601569

Fc1cccc(Cl)c1CCl

nearest known ligand 0.63

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 2/20 0.63
GAA P10253 1/20 0.59
HTT P42858 2/20 0.50
BACE1 P56817 1/20 0.50
KDM4E B2RXH2 2/20 0.49
CYP2A13 Q16696 1/20 0.49
ATM Q13315 2/20 0.47
NPSR1 Q6W5P4 1/20 0.47
TDP1 Q9NUW8 1/20 0.47
KMT2A Q03164 4/20 0.46
MEN1 O00255 3/20 0.46
SMN1; SMN2 Q16637 1/20 0.46
MAPT P10636 1/20 0.46
DAO P14920 1/20 0.45
LMNA P02545 1/20 0.45
TP53 P04637 1/20 0.44
CYP1A2 P05177 1/20 0.44
CYP3A4 P08684 1/20 0.44
CYP2C19 P33261 1/20 0.44
HSD17B10 Q99714 1/20 0.44

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
SCHEMBL30776827 1.00 TAAR1 (0.63) TAAR1GAAHTTBACE1KDM4E
SCHEMBL5045977 0.98 TAAR1 (0.61) TAAR1GAAHTTBACE1KDM4E
SCHEMBL723742 0.85 TAAR1 (0.48) TAAR1GAAHTTBACE1KDM4E
SCHEMBL3115865 0.82 TAAR1 (0.70) TAAR1GAAHTTBACE1KDM4E
SCHEMBL1007397 0.82 TAAR1 (0.52) TAAR1GAAHTTCYP2A13NPSR1
SCHEMBL28596017 0.81 TAAR1 (0.63) TAAR1GAAHTTBACE1KDM4E
Ammonia Solution, Strong SCHEMBL28327987 0.79 TAAR1 (0.50) TAAR1GAAHTTCYP2A13NPSR1
SCHEMBL11029627 0.79 TAAR1 (0.50) TAAR1GAAHTTCYP2A13NPSR1
SCHEMBL5042264 0.79 TAAR1 (0.50) TAAR1GAAHTTCYP2A13NPSR1
SCHEMBL24686248 0.79 TAAR1 (0.61) TAAR1GAAHTTBACE1KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-214932216-U 2-chlorine-6-fluorobenzyl chloride storage barrel with good sealing performance 江苏万隆化学有限公司 2021-11-30 CN claimed
CN-102617312-A Method for preparing 2-chloro-6-fluorobenzaldehyde DANYANG WANLONG CHEMICAL CO LTD 2012-08-01 CN claimed
US-6137009-A ADMIXING MONOALKYLAMINE, ALKALI, AND 2-HALO-6-HALO-BENZYL HALIDE; HEATING TO FORM N-ALKYL-2-HALO-6-HALO-BENZYLAMINE AND SALT SRM CHEMICAL, LTD. CO. (US) 2000-10-24 US claimed
US-4100159-A REACTING 2,6-DIHALOBENZYL HALIDES WITH A SALT OF ADENINE IN PRESENCE OF ONIUM SALT PHASE TRANSFER CATALYST MERCK & CO., INC. (US) 1978-07-11 US claimed
JP-57085388-A None JP disclosed
EP-4587438-A1 BICYCLIC COMPOUNDS AS CDK INHIBITORS BeiGene Switzerland GmbH (CH) 2025-07-23 EP disclosed
CN-119894890-A Bicyclic compounds as CDK inhibitors 百济神州(苏州)生物科技有限公司 2025-04-25 CN disclosed
WO-2025062334-A1 4-((5-(3-(4-(PYRIDIN-2-YL)CYCLOPENTYL)-1 H-PYRAZOL-3-YL)AMINO)-BENZENESULFONAMIDE DERIVATIVES AND SIMILAR COMPOUNDS AS CDK INHIBITORS FOR THE TREATMENT OF CANCER BEIGENE SWITZERLAND GMBH (CH) 2025-03-27 WO disclosed
CN-116178100-B Dechlorination reduction method for 2-chloro-6-fluorotrichlorobenzyl 浙江大洋生物科技集团股份有限公司 2025-01-28 CN disclosed
CN-114516844-B Quinoxaline derivative, preparation method and application 贵州大学 2024-07-19 CN disclosed
US-20240174674-A1 NITROGEN-CONTAINING POLYCYCLIC FUSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND USE THEREOF APPLIED PHARMACEUTICAL SCIENCE, INC. (CN) 2024-05-30 US disclosed
CN-110770214-B Heterocyclic P2X7 antagonists 布雷耶疗法有限公司 2024-03-29 CN disclosed
US-4189485-A ANTICOCCIDIAL ACTIVITY TAKEDA CHEMICAL INDUSTRIES, LTD. (JP) 1980-02-19 US disclosed
US-4171440-A Process for purification of 9-(2,6-dihalobenzyl)adenines MERCK & CO., INC. (US) 1979-10-16 US disclosed
EP-0002214-A1 Benzyl ethers of cyclic 1,2-diols, methods for their preparation and their use as herbicides BAYER AG (DE) 1979-06-13 EP disclosed
US-4146384-A Tetrahydrofuran-ether compounds and herbicidal compositions BAYER AKTIENGESELLSCHAFT (DE) 1979-03-27 US disclosed
EP-0000002-A1 Tetrahydrofurane derivatives, processes for their preparation and their use as herbicides BAYER AG (DE) 1978-12-20 EP disclosed
US-4127721-A Derivatives of thiadiazolo[3,4-d]pyrimidine MERCK & CO., INC. (US) 1978-11-28 US disclosed
US-4100159-A REACTING 2,6-DIHALOBENZYL HALIDES WITH A SALT OF ADENINE IN PRESENCE OF ONIUM SALT PHASE TRANSFER CATALYST MERCK & CO., INC. (US) 1978-07-11 US disclosed
US-4098787-A Process for preparation of 9-(dihalobenzyl) adenines MERCK & CO., INC. (US) 1978-07-04 US 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 (1 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-20240174674-A1 NITROGEN-CONTAINING POLYCYCLIC FUSED RING COMPOUND, PHARMACEUTICAL COMPOSITION THEREOF, PREPARATION METHOD THEREFOR, AND USE THEREOF RET, WEE1, JAK2 TAAR1 1120/4885GAA 3924/4885HTT 4004/4885

“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.