SCHEMBL4451546

SCHEMBL4451546

COc1cc2c(Oc3ccc4[nH]c(C)cc4c3F)ccnc2cc1OCC1CC1

nearest known ligand 0.73

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 7/20 0.73
PDGFRB P09619 3/20 0.73
MET P08581 5/20 0.53
RET P07949 2/20 0.53
FLT3 P36888 2/20 0.53
PDGFRA P16234 2/20 0.53
PLK4 O00444 1/20 0.53
GAK O14976 1/20 0.53
EPHB6 O15197 1/20 0.53
RIPK2 O43353 1/20 0.53
ERN1 O75460 1/20 0.53
STK10 O94804 1/20 0.53
MAP4K4 O95819 1/20 0.53
CHEK2 O96017 1/20 0.53
ABL1 P00519 1/20 0.53
EGFR P00533 1/20 0.53
ERBB2 P04626 1/20 0.53
LCK P06239 1/20 0.53
FYN P06241 1/20 0.53
CSF1R P07333 1/20 0.53

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
SCHEMBL29902450 0.92 KDR (0.70) KDRPDGFRBMETRETFLT3
SCHEMBL28516088 0.92 KDR (0.68) KDRPDGFRBMETRETFLT3
SCHEMBL28571054 0.92 KDR (0.70) KDRPDGFRBMETRETFLT3
SCHEMBL28519841 0.92 KDR (0.70) KDRPDGFRBMETRETFLT3
SCHEMBL28572514 0.92 KDR (0.70) KDRPDGFRBMETRETFLT3
Hydrochloric Acid SCHEMBL29902483 0.91 KDR (0.69) KDRPDGFRBMETRETFLT3
Hydrochloric Acid SCHEMBL28573091 0.91 KDR (0.69) KDRPDGFRBMETRETFLT3
Hydrochloric Acid SCHEMBL28569161 0.91 KDR (0.69) KDRPDGFRBMETRETFLT3
Hydrochloric Acid SCHEMBL28569162 0.91 KDR (0.69) KDRPDGFRBMETRETFLT3
SCHEMBL28528916 0.90 KDR (0.66) KDRPDGFRBMETRETFLT3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2125776-A1 SPIRO SUBSTITUTED COMPOUNDS AS ANGIOGENESIS INHIBITORS Advenchen Laboratories, LLC (US) 2009-12-02 EP claimed
WO-2008112407-A1 SPIRO SUBSTITUTED COMPOUNDS AS ANGIOGENESIS INHIBITORS ADVENCHEN LABORATORIES, LLC (US) 2008-09-18 WO claimed
US-20080227811-A1 Spiro Substituted Compounds As Angiogenesis Inhibitors ADVENCHEN LABORATORIES, LLC 2008-09-18 US claimed
EP-3513809-B9 MEDICINAL COMPOSITION COMPRISING TIVOZANIB KYOWA KIRIN CO LTD (JP) 2022-07-13 EP disclosed
EP-3400942-B1 USE OF QUINOLINE DERIVATIVES FOR TREATING OESOPHAGEAL CANCER AND TREATMENT METHOD, PHARMACEUTICAL COMPOSITION AND KIT THEREOF CHIA TAI TIANQING PHARMACEUTICAL GROUP CO LTD (CN) 2022-04-13 EP disclosed
EP-3973964-A1 QUINOLINE DERIVATIVE USED FOR COMBINATION TREATMENT OF SMALL CELL LUNG CANCER Chia Tai Tianqing Pharmaceutical Group Co., Ltd. (CN) 2022-03-30 EP disclosed
EP-3967310-A1 QUINOLINE DERIVATIVE USED FOR SOFT TISSUE SARCOMA COMBINATION THERAPY CHIA TAI TIANQING PHARMACEUTICAL GROUP CO., LTD. (CN) 2022-03-16 EP disclosed
EP-3513809-B1 MEDICINAL COMPOSITION COMPRISING TIVOZANIB KYOWA KIRIN CO LTD (JP) 2022-03-02 EP disclosed
EP-3854396-A1 QUINOLINE DERIVATIVE USED FOR TREATING SMALL CELL LUNG CANCER Chia Tai Tianqing Pharmaceutical Group Co., Ltd. (CN) 2021-07-28 EP disclosed
EP-3766496-A1 QUINOLINE DERIVATIVE FOR TREATMENT OF NASOPHARYNGEAL CARCINOMA Chia Tai Tianqing Pharmaceutical Group Co., Ltd. (CN) 2021-01-20 EP disclosed
WO-2020233723-A1 QUINOLINE DERIVATIVES FOR TREATMENT OF HEAD AND NECK CANCER 正大天晴药业集团股份有限公司 (CN) 2020-11-26 WO disclosed
WO-2020057536-A1 QUINOLINE DERIVATIVE FOR TREATING BRAIN TUMOR 正大天晴药业集团股份有限公司 2020-03-26 WO disclosed
EP-3231797-B1 QUINOLINE DERIVATIVE AGAINST NON-SMALL CELL LUNG CANCER CHIA TAI TIANQING PHARMACEUTICAL GROUP CO LTD (CN) 2020-02-26 EP disclosed
WO-2019174590-A1 QUINOLINE DERIVATIVE FOR TREATMENT OF TRIPLE-NEGATIVE BREAST CANCER 正大天晴药业集团股份有限公司 2019-09-19 WO disclosed
EP-2125776-B1 SPIRO SUBSTITUTED COMPOUNDS AS ANGIOGENESIS INHIBITORS ADVENCHEN LABORATORIES LLC (US) 2017-07-05 EP disclosed
EP-3153170-A1 METHODS AND USES OF QUINOLINE DERIVATIVES IN THE TREATMENT OF SOFT TISSUE SARCOMAS AND PHARMACEUTICAL COMPOSITIONS FOR TREATMENT OF SAME Chia Tai Tianqing Pharmaceutical Group Co.,Ltd (CN) 2017-04-12 EP disclosed
EP-3153169-A1 METHOD FOR TREATING TUMOUR, PHARMACEUTICAL COMPOSITION AND MEDICINE BOX KIT Chia Tai Tianqing Pharmaceutical Group Co.,Ltd (CN) 2017-04-12 EP disclosed
EP-2125776-A1 SPIRO SUBSTITUTED COMPOUNDS AS ANGIOGENESIS INHIBITORS Advenchen Laboratories, LLC (US) 2009-12-02 EP disclosed
WO-2008112407-A1 SPIRO SUBSTITUTED COMPOUNDS AS ANGIOGENESIS INHIBITORS ADVENCHEN LABORATORIES, LLC (US) 2008-09-18 WO disclosed
US-20080227811-A1 Spiro Substituted Compounds As Angiogenesis Inhibitors ADVENCHEN LABORATORIES, LLC 2008-09-18 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 (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-20080227811-A1 Spiro Substituted Compounds As Angiogenesis Inhibitors TEK, KDR, TIE1 KDR 2/4885PDGFRB 6/4885MET 176/4885

“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.