SCHEMBL7464312

SCHEMBL7464312

CC(C)NC(C)C.CS(=O)(=O)O

nearest known ligand 0.57

Known targets — ChEMBL curated mechanism

ABL1ADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB2AGTR1BCL2BCL2A1BCL2L1BCL2L10BCL2L2BCRBRAFCHRM1CHRNA10CHRNA9DRD1DRD2DRD3DRD4DRD5EGFRF2FLT1FLT4GCKGHSRGNRHRGRIN1GRIN2AGRIN2BGRIN2CGRIN2DGRIN3AGRIN3BHTR1AHTR1BHTR1DHTR2AHTR2CHTR3AIDH2KDRKITMAOBMCL1MTTPPP4HBPDGFRBPIK3CAPIK3CBPIK3CDPIK3CGPIK3R1PIK3R2PIK3R3PIK3R5PIKFYVEROCK1ROCK2SLC18A2SLC6A2SLC6A3SLC6A4TACR1TUBA1ATUBA1BTUBA1CTUBA3CTUBA3ETUBA4ATUBBTUBB1TUBB2ATUBB2BTUBB3TUBB4ATUBB4BTUBB6TUBB8gyrAgyrBparCparEpol

The experimentally established mechanism targets of None. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ADRB2 known ✓ P07550 1/20 0.35
TDP1 Q9NUW8 1/20 0.57
CA2 P00918 1/20 0.39
KDM4E B2RXH2 3/20 0.35
HIF1A Q16665 2/20 0.35
CYP3A4 P08684 2/20 0.35
LMNA P02545 1/20 0.35
GAA P10253 1/20 0.35
MAPT P10636 1/20 0.35
HTT P42858 1/20 0.35
BLM P54132 1/20 0.35
RXFP1 Q9HBX9 1/20 0.35
TP53 P04637 1/20 0.35
CYP1A2 P05177 1/20 0.35
CYP2D6 P10635 1/20 0.35
TSHR P16473 1/20 0.35
NFKB1 P19838 1/20 0.35
MAPK1 P28482 1/20 0.35
CYP2C19 P33261 1/20 0.35
THPO P40225 1/20 0.35

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
Sulfuric Acid SCHEMBL10528253 0.93 TDP1 (0.57) TDP1CA2KDM4EHIF1ACYP3A4
Sulfuric Acid SCHEMBL16470839 0.90 TDP1 (0.53) TDP1CA2KDM4EHIF1ACYP3A4
Sulfuric Acid SCHEMBL9550776 0.90 TDP1 (0.53) TDP1CA2KDM4EHIF1ACYP3A4
Sulfuric Acid SCHEMBL16344486 0.90 TDP1 (0.53) TDP1CA2KDM4EHIF1ACYP3A4
SCHEMBL28360936 0.79 TDP1 (0.57) TDP1
SCHEMBL23451648 0.78 TDP1 (0.39) TDP1
SCHEMBL575531 0.77 CA2 (0.44) TDP1CA2KDM4ECYP3A4LMNA
Isopropyl Alcohol SCHEMBL9431191 0.77
Hydrogen Peroxide SCHEMBL135017 0.76 TDP1 (0.80) TDP1LMNAGAATP53ALDH1A1
Methyl Alcohol SCHEMBL2170375 0.76

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3684749-A1 CATALYTIC CYCLE FOR PRODUCTION OF 1,1-DISUBSTITUTED ALKENES Sirrus, Inc. (US) 2020-07-29 EP claimed
US-20200223779-A1 CATALYTIC CYCLE FOR PRODUCTION OF 1,1-DISUBSTITUTED ALKENES SIRRUS, INC. 2020-07-16 US claimed
CN-111108087-A Catalytic recycle for production of 1, 1-disubstituted olefins 赛鲁斯股份有限公司 2020-05-05 CN claimed
WO-2019060188-A1 CATALYTIC CYCLE FOR PRODUCTION OF 1,1-DISUBSTITUTED ALKENES SIRRUS, INC. (US) 2019-03-28 WO claimed
EP-3684749-A1 CATALYTIC CYCLE FOR PRODUCTION OF 1,1-DISUBSTITUTED ALKENES Sirrus, Inc. (US) 2020-07-29 EP disclosed
US-20200223779-A1 CATALYTIC CYCLE FOR PRODUCTION OF 1,1-DISUBSTITUTED ALKENES SIRRUS, INC. 2020-07-16 US disclosed
CN-111108087-A Catalytic recycle for production of 1, 1-disubstituted olefins 赛鲁斯股份有限公司 2020-05-05 CN disclosed
WO-2019060188-A1 CATALYTIC CYCLE FOR PRODUCTION OF 1,1-DISUBSTITUTED ALKENES SIRRUS, INC. (US) 2019-03-28 WO disclosed
EP-0703221-B1 5 alpha-reductase Inhibitors LILLY CO ELI (US) 2002-03-27 EP disclosed
US-6150375-A INHIBITORS OF BOTH OF THE HUMAN 5AR ISOZYMES; BENIGN PROSTATE HYPERPLASIA, MALE PATTERN BALDNESS, ACNE VULGARIS, SEBORRHEA, ANDROGENIC ALOPECIA, HIRSUTISM AND PROSTATE CANCER; BLOCKS THE CONVERSION OF TESTOSTERONE TO 5-ALPHA-DIHYDROTESTOSTERONE ELI LILLY AND COMPANY (US) 2000-11-21 US disclosed
EP-0684234-B1 Synthesis of benzoquinolinones LILLY CO ELI (US) 2000-07-26 EP disclosed
CN-1163565-A 5 alpha-reductase inhibitors LILLY CO ELI (US) 1997-10-29 CN disclosed
WO-1996036610-A1 SYNTHESIS OF BENZOQUINOLINONES ELI LILLY AND COMPANY (US) 1996-11-21 WO disclosed
EP-0743303-A1 Synthesis of bezoquinolinones ELI LILLY AND COMPANY (US) 1996-11-20 EP disclosed
WO-1996035422-A1 METHODS FOR INHIBITING BONE LOSS ELI LILLY AND COMPANY (US) 1996-11-14 WO disclosed
EP-0742010-A2 Benzoquinolin-3-ones to inhibit bone loss ELI LILLY AND COMPANY (US) 1996-11-13 EP disclosed
US-5574160-A Syntheis of benzoquinolinones ELI LILLY AND COMPANY (US) 1996-11-12 US disclosed
EP-0733365-A2 Use of benzoquinolin-3-ones for the treatment and prevention of prostatic cancer ELI LILLY AND COMPANY (US) 1996-09-25 EP disclosed
US-5550134-A ADMINISTERING TO A MAMMAL FROM A SERIES OF BENZOQUINOLIN-3-ONE COMPOUNDS ELI LILLY AND COMPANY (US) 1996-08-27 US disclosed
EP-0703221-A1 5 alpha-reductase Inhibitors ELI LILLY AND COMPANY (US) 1996-03-27 EP 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-20200223779-A1 CATALYTIC CYCLE FOR PRODUCTION OF 1,1-DISUBSTITUTED ALKENES ME1, ME3, ME2 ADRB2 3858/4885TDP1 1568/4885CA2 198/4885

“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.