SCHEMBL721707

SCHEMBL721707

Cn1ccc2cc(N)ccc21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PRKCI P41743 1/20 1.00
BRPF1 P55201 2/20 0.53
CYP2A6 P11509 2/20 0.53
PIK3CB P42338 2/20 0.53
EGFR P00533 2/20 0.51
HSD11B1 P28845 1/20 0.44
LRRK2 Q5S007 1/20 0.41
ABL1 P00519 3/20 0.40
SRC P12931 3/20 0.40
TUBB4A P04350 1/20 0.40
TUBB P07437 1/20 0.40
TUBA3C P0DPH7 1/20 0.40
TUBA1B P68363 1/20 0.40
TUBA4A P68366 1/20 0.40
TUBB4B P68371 1/20 0.40
TUBB3 Q13509 1/20 0.40
TUBB2A Q13885 1/20 0.40
TUBB8 Q3ZCM7 1/20 0.40
TUBA3E Q6PEY2 1/20 0.40
TUBA1A Q71U36 1/20 0.40

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
SCHEMBL30006940 1.00 PRKCI (1.00) PRKCIBRPF1CYP2A6PIK3CBEGFR
Hydrochloric Acid SCHEMBL7350283 0.98 PRKCI (0.96) PRKCIBRPF1CYP2A6PIK3CBEGFR
SCHEMBL5718697 0.83 PRKCI (0.70) PRKCIBRPF1CYP2A6PIK3CBEGFR
SCHEMBL29507010 0.83 PRKCI (0.70) PRKCIBRPF1CYP2A6PIK3CBEGFR
SCHEMBL398452 0.83 PRKCI (0.70) PRKCIBRPF1CYP2A6PIK3CBEGFR
Tert-Butyl Formate SCHEMBL28273704 0.82 PRKCI (0.68) PRKCIBRPF1CYP2A6PIK3CBEGFR
Hydrochloric Acid SCHEMBL397061 0.81 PRKCI (0.68) PRKCIBRPF1CYP2A6PIK3CBEGFR
SCHEMBL981889 0.80 PRKCI (0.66) PRKCICYP2A6PIK3CBEGFRHSD11B1
SCHEMBL18683804 0.76 PRKCI (0.60) PRKCIBRPF1CYP2A6PIK3CBHSD11B1
SCHEMBL29624271 0.76 PRKCI (0.61) PRKCICYP2A6PIK3CBHSD11B1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115746017-B Thienopyrimidine compound and preparation method and application thereof 英维沃化工科技(广州)有限公司 2024-06-07 CN claimed
CN-116332950-A Indazole substituted podophyllotoxin derivative and preparation method and application thereof 汤亚杰 2023-06-27 CN claimed
CN-115746017-A Thienopyrimidine compound and preparation method and application thereof 英维沃化工科技(广州)有限公司 2023-03-07 CN claimed
EP-2116547-A1 Substituted N-imidazo(2, 1-b) thiazole-5-sulfonamide derivatives as 5-TH6 ligands Laboratorios Del. Dr. Esteve, S.A. (ES) 2009-11-11 EP claimed
US-5752982-A DYEING HAIR IN LIGHTFAST, WASHFAST COLORS L'OREAL (FR) 1998-05-19 US claimed
EP-0578735-B1 NOVEL KERATIN FIBRE DYEING METHOD USING AMINOINDOLES, WITH ACID pH, COMPOSITIONS THEREFOR AND NOVEL AMINOINDOLE COMPOUNDS OREAL (FR) 1996-01-03 EP claimed
EP-0460996-B1 Keratinic fibres dyeing process with an aminoindol associated with a quinone derivative OREAL (FR) 1994-09-14 EP claimed
US-5180400-A METHOD FOR DYEING KERATINOUS FIBRES USING AN AMINOINDOLE IN COMBINATION WITH A QUINONE DERIVATIVE L'OREAL (FR) 1993-01-19 US claimed
CN-122036587-A Zalutst compound and application thereof in inhibiting MLL1-WDR5 interaction 暨南大学 2026-05-15 CN disclosed
EP-4724443-A1 PYRAZOLO-PYRIMIDINONE COMPOUNDS FOR USE IN METHODS OF INHIBITING WEE1 A KINASE Acrivon Therapeutics, Inc. (US) 2026-04-15 EP disclosed
US-12590071-B2 Hydrazone derivative in which terminal amine group is substituted with aryl group or heteroaryl group, and use thereof KOREA INSTITUTE OF SCIENCE AND TECHNOLOGY (KR) 2026-03-31 US disclosed
WO-2025245484-A1 FOXN1 ACTIVATORS THYMOFOX INC. (US) 2025-11-27 WO disclosed
US-12479845-B2 Imidazopyridine derivative compounds and use of same HANMI PHARM. CO., LTD. (KR) 2025-11-25 US disclosed
US-20250263760-A1 MODIFIED BACTERIA FOR PRODUCTION OF NITROAROMATICS UNIVERSITY OF FLORIDA RESEARCH FOUNDATION, INCORPORATED (US) 2025-08-21 US disclosed
WO-1992005170-A1 INDOLE UREAS AS 5 HT RECEPTOR ANTAGONIST BEECHAM GROUP PLC (GB) 1992-04-02 WO disclosed
EP-0460996-A1 Keratinic fibres dyeing process with an aminoindol associated with a quinone derivative L'OREAL (FR) 1991-12-11 EP disclosed
US-5034403-A Topical antiinflammatory agents for skin disorders HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1991-07-23 US disclosed
US-4983615-A ANTIINFLAMMATORY AGENTS HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1991-01-08 US disclosed
EP-0405425-A2 Heteroarylamino- and heteroaryloxypyridinamines and related compounds, a process for their preparation and their use as medicaments HOECHST-ROUSSEL PHARMACEUTICALS INCORPORATED (US) 1991-01-02 EP disclosed
US-4970219-A TOPICAL ANTIINFLAMMATORY AGENTS HOECHST-ROUSSEL PHARMACEUTICALS INC. (US) 1990-11-13 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 (2 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-12590071-B2 Hydrazone derivative in which terminal amine group is substituted with aryl group or heteroaryl group, and use thereof ABL1, TH, CYP3A43 PRKCI 4447/4885BRPF1 1796/4885CYP2A6 545/4885
US-12479845-B2 Imidazopyridine derivative compounds and use of same KDM1A, KDM1B, KDM2A PRKCI 1408/4885BRPF1 3393/4885CYP2A6 1199/4885

“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.