SCHEMBL465583

SCHEMBL465583

C=C(C)Cc1ccc(O)cc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CA2 P00918 3/20 0.50
CAMK2A Q9UQM7 1/20 0.50
ESR1 P03372 6/20 0.48
ESR2 Q92731 2/20 0.48
ALDH1A1 P00352 2/20 0.45
ADRA2A P08913 2/20 0.45
ADORA3 P0DMS8 2/20 0.45
TACR2 P21452 2/20 0.45
SLC6A2 P23975 2/20 0.45
SLC6A4 P31645 2/20 0.45
SLC6A3 Q01959 2/20 0.45
KDM4E B2RXH2 1/20 0.45
LMNA P02545 1/20 0.45
SHBG P04278 1/20 0.45
TP53 P04637 1/20 0.45
CYP3A4 P08684 1/20 0.45
HSPD1 P10809 1/20 0.45
ADRB3 P13945 1/20 0.45
HTR2C P28335 1/20 0.45
HSPE1 P61604 1/20 0.45

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
Bicarbonate SCHEMBL3128473 0.91 CA2 (0.59) CA2CAMK2AESR1ESR2ALDH1A1
SCHEMBL6015468 0.89 ALDH1A1 (0.38) CA2CAMK2AALDH1A1HSD17B10
SCHEMBL23230257 0.82 LMNA (0.43) ALDH1A1LMNAHSD17B10PTGS1
SCHEMBL14397192 0.81 CA2 (0.46) CA2CAMK2AESR1ESR2ALDH1A1
SCHEMBL10984806 0.80 NOS3 (0.43) CA2ALDH1A1HSD17B10
SCHEMBL1511861 0.80 LPL (0.44) CA2ALDH1A1LMNATP53HSD17B10
SCHEMBL3899314 0.80 IDO1 (0.44) ALDH1A1LMNAACHETAAR1
SCHEMBL6522029 0.79 CA2 (0.54) CA2CAMK2AESR1ESR2ALDH1A1
Anolignan B SCHEMBL23268876 0.79 CA2 (0.54) CA2CAMK2AESR1ESR2ALDH1A1
SCHEMBL14495580 0.78 POLB (0.52) CA2CAMK2AALDH1A1LMNAHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114276530-A Intermittent phosgene interface method preparation process of polycarbonate and application thereof 深圳市德力塑化工科技有限公司 2022-04-05 CN claimed
CN-1273515-C Melt polycarbonate catalyst system GEN ELECTRIC (US) 2006-09-06 CN claimed
CN-1541239-A Melt Polycarbonate Catalyst System ͨ�õ�����˾ 2004-10-27 CN claimed
CN-1492897-A Melt polycarbonate catalyst system ͨ�õ�����˾ 2004-04-28 CN claimed
US-12577391-B2 Chemically-resistant flame retardant compositions SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2026-03-17 US disclosed
US-20260071046-A1 METHODS OF MAKING POLYVINYL CYCLOHEXANE VIA HYDROGENATION OF WASTE POLYSTYRENE SOURCES SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2026-03-12 US disclosed
US-12570848-B2 Scratch-resistant high impact strength PMMA compositions SHPP GLOBAL TECHNOLOGIES B.V. (NL) 2026-03-10 US disclosed
EP-4110849-B1 HIGH HEAT POLYCARBONATE COPOLYMER FORMULATIONS SHPP GLOBAL TECH BV (NL) 2025-12-24 EP disclosed
EP-4590727-A1 METHODS OF MAKING POLYVINYL CYCLOHEXANE VIA HYDROGENATION OF WASTE POLYSTYRENE SOURCES SABIC Global Technologies B.V. (NL) 2025-07-30 EP disclosed
EP-4172269-B1 THERMOPLASTIC COMPOSITIONS WITH IMPROVED HYDROLYTIC AND HEAT STABILITY SHPP GLOBAL TECH BV (NL) 2025-05-28 EP disclosed
CN-119894944-A Process for preparing polyvinylcyclohexane by hydrogenation of waste polystyrene sources SABIC环球技术有限责任公司 2025-04-25 CN disclosed
US-20250034364-A1 FUNCTIONALIZED SILICA FOR ODOR REDUCTION OF POLYOLEFIN AND ENGINEERING THERMOPLASTIC POLYMERS SABIC GLOBAL TECHNOLOGIES B.V. (NL) 2025-01-30 US disclosed
US-4748230-A Preparation of resin from phenolic and oxazoline using phosphine catalyst ASHLAND OIL, INC. (US) 1988-05-31 US disclosed
EP-0243318-A2 Phenol ether containing epoxy groups CIBA-GEIGY AG (CH) 1987-10-28 EP disclosed
US-4629764-A EPOXIDES COMPRISING GLYCIDOL, POLYPHENOL AND COPOLYMERIZED ALKENYL PHENO ADDITION POLYMER; HIGH STRENGTH THE DOW CHEMICAL COMPANY (US) 1986-12-16 US disclosed
US-4629762-A ADVANCED EPOXIDES; MECHANICAL PROPERTIES THE DOW CHEMICAL COMPANY (US) 1986-12-16 US disclosed
US-4629763-A REACTING A MIXTURE OF A COPOLYMERIZED ALKENYLPHENOL ADDITION POLYMER AND A POLYPHENOL WITH A CYANOGEN HALIDE THE DOW CHEMICAL COMPANY (US) 1986-12-16 US disclosed
US-4611022-A A MIXTURE OF A POLYPHENOL COMPOUND AND A POLYMER OF AN ALKENYL PHENOL AND UNSATURATED MONOMER; POLYEPOXIDES AND-CYANURATES THE DOW CHEMICAL COMPANY (US) 1986-09-09 US disclosed
US-4388451-A EPOXY CURATIVES, ION EXCHANGE MEMBRANES, LAMINATES, DETERGENT ADDITIVES ASHLAND OIL, INC. (US) 1983-06-14 US disclosed
US-4140769-A ANALGESICS MILES LABORATORIES, INC. (US) 1979-02-20 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-12577391-B2 Chemically-resistant flame retardant compositions RPL3, RPL4, UFM1 CA2 3190/4885CAMK2A 4658/4885ESR1 1778/4885
US-20260071046-A1 METHODS OF MAKING POLYVINYL CYCLOHEXANE VIA HYDROGENATION OF WASTE POLYSTYRENE SOURCES HTT, VHL, PARG CA2 2114/4885CAMK2A 4322/4885ESR1 867/4885
US-12570848-B2 Scratch-resistant high impact strength PMMA compositions PCNA, COL2A1, COL1A1 CA2 3537/4885CAMK2A 4216/4885ESR1 1717/4885

“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.