SCHEMBL4234473

SCHEMBL4234473

CNCCCNC(=O)C1CCCO1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
POLB P06746 2/20 0.51
ALPG P10696 1/20 0.50
HPGD P15428 5/20 0.49
PKM P14618 2/20 0.47
MEN1 O00255 5/20 0.47
KMT2A Q03164 5/20 0.47
ALDH1A1 P00352 3/20 0.47
KDM4E B2RXH2 2/20 0.47
GLA P06280 1/20 0.47
GAA P10253 1/20 0.47
TSHR P16473 1/20 0.47
HSD17B10 Q99714 1/20 0.47
SMN1; SMN2 Q16637 2/20 0.43
NPC1 O15118 1/20 0.43
TP53 P04637 1/20 0.43
RAB9A P51151 1/20 0.43
HTR1A P08908 1/20 0.43
DRD2 P14416 1/20 0.43
DRD4 P21917 1/20 0.43
KCNH2 Q12809 1/20 0.42

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
SCHEMBL24177180 0.85 HPGD (0.62) POLBALPGHPGDPKMMEN1
SCHEMBL21941760 0.85 HPGD (0.62) POLBALPGHPGDPKMMEN1
SCHEMBL21880364 0.84 HPGD (0.57) POLBALPGHPGDALDH1A1HSD17B10
SCHEMBL29306572 0.84 HPGD (0.57) POLBALPGHPGDALDH1A1HSD17B10
SCHEMBL26127583 0.82 POLB (0.52) POLBALPGHPGDPKMMEN1
SCHEMBL26120640 0.82 POLB (0.52) POLBALPGHPGDPKMMEN1
SCHEMBL27806423 0.82 POLB (0.52) POLBALPGHPGDPKMMEN1
SCHEMBL6360835 0.81 POLB (0.55) POLBALPGHPGDPKMMEN1
SCHEMBL24177181 0.81 POLB (0.55) POLBALPGHPGDPKMMEN1
SCHEMBL29306396 0.81 POLB (0.49) POLBALPGHPGDPKMMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250197380-A1 PHARMACEUTICAL INTERMEDIATE AND SYNTHESIS METHOD, AND ISOQUINOLINE DERIVATIVE AND SYNTHESIS METHOD THEREFOR BANGENTAI(SHANDONG) BIOSCIENCES GROUP SHARE CO., LTD. (CN) 2025-06-19 US claimed
CN-114573506-B Drug intermediate and synthetic method thereof, isoquinoline derivative and synthetic method thereof 邦恩泰(山东)生物医药科技集团股份有限公司 2022-09-30 CN claimed
US-20250197380-A1 PHARMACEUTICAL INTERMEDIATE AND SYNTHESIS METHOD, AND ISOQUINOLINE DERIVATIVE AND SYNTHESIS METHOD THEREFOR BANGENTAI(SHANDONG) BIOSCIENCES GROUP SHARE CO., LTD. (CN) 2025-06-19 US disclosed
CN-113801069-B Alfuzosin hydrochloride intermediate compound 鲁南制药集团股份有限公司 2024-03-15 CN disclosed
WO-2023185027-A1 PREPARATION METHOD FOR ISOQUINOLINE COMPOUND 邦恩泰(山东)生物医药科技集团股份有限公司 2023-10-05 WO disclosed
WO-2023179068-A1 DRUG INTERMEDIATE AND SYNTHETIC METHOD, AND ISOQUINOLINE DERIVATIVE AND SYNTHETIC METHOD THEREFOR 邦恩泰(山东)生物医药科技集团股份有限公司 2023-09-28 WO disclosed
WO-2023179068-A1 DRUG INTERMEDIATE AND SYNTHETIC METHOD, AND ISOQUINOLINE DERIVATIVE AND SYNTHETIC METHOD THEREFOR 邦恩泰(山东)生物医药科技集团股份有限公司 2023-09-28 WO disclosed
CN-114573506-B Drug intermediate and synthetic method thereof, isoquinoline derivative and synthetic method thereof 邦恩泰(山东)生物医药科技集团股份有限公司 2022-09-30 CN disclosed
CN-114591273-A Synthesis method and application of N-methyl-N' -tetrahydrofuran formyl propane diamine oxalate 邦恩泰(山东)生物医药科技集团股份有限公司 2022-06-07 CN disclosed
CN-114573569-A Preparation method of isoquinoline compounds 邦恩泰(山东)生物医药科技集团股份有限公司 2022-06-03 CN disclosed
CN-114573506-A Drug intermediate and synthetic method thereof, isoquinoline derivative and synthetic method thereof 邦恩泰(山东)生物医药科技集团股份有限公司 2022-06-03 CN disclosed
WO-2008021891-A2 PREPARATION AND UTILITY OF SUBSTITUTED QUINAZOLINE COMPOUNDS WITH ALPHA-ADRENERGIC BLOCKING EFFECTS AUSPEX PHARMACEUTICALS, INC. (US) 2008-02-21 WO disclosed
WO-2008021891-A2 PREPARATION AND UTILITY OF SUBSTITUTED QUINAZOLINE COMPOUNDS WITH ALPHA-ADRENERGIC BLOCKING EFFECTS AUSPEX PHARMACEUTICALS, INC. (US) 2008-02-21 WO disclosed
US-20080039473-A1 PREPARATION AND UTILITY OF SUBSTITUTED QUINAZOLINE COMPOUNDS WITH ALPHA-ADRENERGIC BLOCKING EFFECTS AUSPEX PHARMACEUTICALS, INC. (US) 2008-02-14 US disclosed
US-20080039473-A1 PREPARATION AND UTILITY OF SUBSTITUTED QUINAZOLINE COMPOUNDS WITH ALPHA-ADRENERGIC BLOCKING EFFECTS AUSPEX PHARMACEUTICALS, INC. (US) 2008-02-14 US disclosed
US-20080039473-A1 PREPARATION AND UTILITY OF SUBSTITUTED QUINAZOLINE COMPOUNDS WITH ALPHA-ADRENERGIC BLOCKING EFFECTS AUSPEX PHARMACEUTICALS, INC. (US) 2008-02-14 US disclosed
WO-2008015525-A2 AN IMPROVED PROCESS FOR THE PREPARATION OF ALFUZOSIN HYDROCHLORIDE ORCHID CHEMICALS & PHARMACEUTICALS LIMITED (IN) 2008-02-07 WO disclosed
WO-2007063556-A2 AN IMPROVED AND INDUSTRIAL PROCESS FOR THE PREPARATION OF ALFUZOSIN HYDROCHLORIDE AND ITS NOVEL POLYMORPHS MSN LABORATORIES LIMITED (IN) 2007-06-07 WO disclosed
US-20070066824-A1 PREPARATION OF ALFUZOSIN DR. REDDY'S LABORATORIES, INC. 2007-03-22 US disclosed
US-20070066824-A1 PREPARATION OF ALFUZOSIN DR. REDDY'S LABORATORIES, INC. 2007-03-22 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 (3 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-20080039473-A1 PREPARATION AND UTILITY OF SUBSTITUTED QUINAZOLINE COMPOUNDS WITH ALPHA-ADRENERGIC BLOCKING EFFECTS ADRB1, ADRB2, ADRB3 POLB 2328/4885ALPG 2088/4885HPGD 148/4885
US-20250197380-A1 PHARMACEUTICAL INTERMEDIATE AND SYNTHESIS METHOD, AND ISOQUINOLINE DERIVATIVE AND SYNTHESIS METHOD THEREFOR PARK7, SQLE, CYP4F11 POLB 961/4885ALPG 4804/4885HPGD 133/4885
US-20070066824-A1 PREPARATION OF ALFUZOSIN MAP7, LPXN, QDPR POLB 4616/4885ALPG 4024/4885HPGD 1777/4885

“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.