SCHEMBL4076360

SCHEMBL4076360

Nc1cccc2cccc(Cl)c12

nearest known ligand 0.52

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 6/20 0.52
ALDH1A1 P00352 5/20 0.50
NR4A2 P43354 2/20 0.50
JAK2 O60674 1/20 0.45
RPS6KA3 P51812 1/20 0.45
MELK Q14680 1/20 0.45
STK24 Q9Y6E0 1/20 0.45
CYP3A4 P08684 4/20 0.42
HSD17B10 Q99714 4/20 0.42
HPGD P15428 3/20 0.42
CYP1A2 P05177 3/20 0.42
CYP2A6 P11509 2/20 0.42
KEAP1 Q14145 1/20 0.42
PIK3CA P42336 1/20 0.42
MEN1 O00255 3/20 0.41
KMT2A Q03164 3/20 0.41
KDM4E B2RXH2 1/20 0.41
RXFP1 Q9HBX9 1/20 0.41
CYP1A1 P04798 1/20 0.41
CYP1B1 Q16678 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
SCHEMBL30064915 1.00 TSHR (0.52) TSHRALDH1A1NR4A2JAK2RPS6KA3
SCHEMBL29620230 0.81 TSHR (0.53) TSHRALDH1A1CYP3A4HSD17B10HPGD
SCHEMBL4103602 0.81 TSHR (0.53) TSHRALDH1A1CYP3A4HSD17B10HPGD
SCHEMBL29349435 0.81 JAK2 (0.54) TSHRALDH1A1JAK2RPS6KA3MELK
SCHEMBL29620231 0.81 TSHR (0.53) TSHRALDH1A1CYP3A4HSD17B10HPGD
SCHEMBL65699 0.81 JAK2 (0.54) TSHRALDH1A1JAK2RPS6KA3MELK
SCHEMBL6629381 0.79 TSHR (0.42) TSHRALDH1A1NR4A2JAK2RPS6KA3
Hydrochloric Acid SCHEMBL11277860 0.78 JAK2 (0.52) TSHRALDH1A1JAK2RPS6KA3MELK
SCHEMBL14742902 0.78 ALDH1A1 (0.59) TSHRALDH1A1JAK2RPS6KA3MELK
SCHEMBL9627127 0.78 JAK2 (0.52) TSHRALDH1A1JAK2RPS6KA3MELK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117839592-A Preparation device and extraction method of 8-chloro-1-aminonaphthalene 南京康德祥医药科技有限公司 2024-04-09 CN claimed
US-12630566-B2 KRas G12D inhibitors Mirati Therapeutics, Inc. (US) 2026-05-19 US disclosed
US-20260062412-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY CHUGAI PHARMACEUTICAL CO LTD (JP) 2026-03-05 US disclosed
EP-4647424-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY CHUGAI SEIYAKU KABUSHIKI KAISHA (JP) 2025-11-12 EP disclosed
EP-4501932-A2 KRAS G12C INHIBITORS Mirati Therapeutics, Inc. (US) 2025-02-05 EP disclosed
EP-3880208-B1 KRAS G12C INHIBITORS MIRATI THERAPEUTICS INC (US) 2024-11-20 EP disclosed
US-20240309020-A1 KRAS G12D INHIBITORS ARRAY BIOPHARMA INC. 2024-09-19 US disclosed
WO-2024181437-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY 中外製薬株式会社 2024-09-06 WO disclosed
CN-111989321-B KRAS G12C inhibitors 米拉蒂治疗股份有限公司 2024-05-14 CN disclosed
CN-113135924-B Pyrimidine derivatives and their use in medicine 广东东阳光药业股份有限公司 2024-04-26 CN disclosed
US-20060281738-A1 2-Naphthylimino-1,3-thiazine derivative SHIONOGI AND CO., LTD. (JP) 2006-12-14 US disclosed
CN-1863784-A 2-naphthylimino-1,3-thiazine derivative SHIONOGI & CO (JP) 2006-11-15 CN disclosed
EP-1659117-A1 2-NAPHTHYLIMINO-1,3-THIAZINE DERIVATIVE SHIONOGI & CO., LTD. (JP) 2006-05-24 EP disclosed
EP-0894799-B1 INDOLOMORPHINANE DERIVATIVES AND REMEDIES/PREVENTIVES FOR CEREBRAL DISORDERS TORAY INDUSTRIES (JP) 2004-04-07 EP disclosed
US-6156762-A Indolomorphinan derivative and agent for curing and preventing cerebral disorder TORAY INDUSTRIES, INC. (JP) 2000-12-05 US disclosed
EP-0894799-A1 INDOLOMORPHINANE DERIVATIVES AND REMEDIES/PREVENTIVES FOR CEREBRAL DISORDERS TORAY INDUSTRIES, INC. (JP) 1999-02-03 EP disclosed
US-4247456-A Water-insoluble monoazo pyridone dye CASSELLA AKTIENGESELLSCHAFT (DE) 1981-01-27 US disclosed
US-4237019-A PROTECTING AQUEOUS MEDIUM SUCH AS WATER BASED PAINTS OR METAL WORKING FLUIDS IMPERIAL CHEMICAL INDUSTRIES LIMITED (GB) 1980-12-02 US disclosed
EP-0002041-A1 Processes for synthesizing bisazomethine-bisazo pigments CIBA-GEIGY AG (CH) 1979-05-30 EP disclosed
US-3957749-A WATER-INSOLUBLE MONOAZO PYRIDINE DYES CASSELLA FARBWERKE MAINKUR AKTIENGESELLSCHAFT (DT) 1976-05-18 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 (4 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-12630566-B2 KRas G12D inhibitors KRAS, NRAS, HRAS TSHR 4213/4885ALDH1A1 1816/4885NR4A2 4644/4885
US-20260062412-A1 NITROGEN-CONTAINING HETEROCYCLIC COMPOUND HAVING MYT1 INHIBITORY ACTIVITY MYT1, NTMT1, MYL6 TSHR 439/4885ALDH1A1 2880/4885NR4A2 2643/4885
US-20060281738-A1 2-Naphthylimino-1,3-thiazine derivative NPM1, OXTR, CYP2S1 TSHR 440/4885ALDH1A1 1571/4885NR4A2 337/4885
US-20240309020-A1 KRAS G12D INHIBITORS KRAS, NRAS, HRAS TSHR 4393/4885ALDH1A1 2681/4885NR4A2 4022/4885

“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.