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Molecule
ID:3070
Structure
Similarity
Functional Group
Text
General Information
Structure
Molecular Formula
C₅H₁₀O₅
Molecular Mass
150.1299
Exact Mass
150.05282342
Charge
0
InChI
InChI=1S/C5H10O5/c6-2-1-10-5(9)4(8)3(2)7/h2-9H,1H2/t2-,3+,4-,5+/m1/s1
InChIKey
SRBFZHDQGSBBOR-LECHCGJUSA-N
Canonic Smiles
O[C@@H]1CO[C@@H]([C@@H]([C@H]1O)O)O
Isomeric Smiles
C1[C@H]([C@@H]([C@H]([C@H](O1)O)O)O)O
Calculated Properties
JChem
LogD (pH = 7.4)
-2.30
LogD (pH = 5.5)
-2.30
Log P
-2.30
Rotatable Bonds
0
H Donor
4
H Acceptors
5
Lipinski's Rule of Five
true
Acid pKa
11.31
Polar Surface Area
90.15
Polarizability
13.23
Molar Refractivity
29.96
LOG S
0.24
Data Source
Loading...
Names and Identifiers
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Registration numbers
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Properties
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Related Proteins
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Molecular Spectra
No Data Available
Click here to submit data
Molecule Details
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References
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Bioactivity
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Quote
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General Information
Calculated Properties
•
RDKit
•
JChem
Data Source
•
Academic Data
•
Commercial Catalog
Names and Identifiers
•
IUPAC name
•
IUPAC Traditional name
•
Synonyms
Registration numbers
Properties
•
Physical Property
•
Product Information
•
Safety Information
Related Proteins
•
PDB Bank
Molecular Spectra
Molecule Details
•
DrugBank
•
ChEBI
References
•
PubChem Literature
•
From Data Sources
Bioactivity
•
PubChem BioAssay
Data Source
Academic Data
DrugBank
DB03389
PubChem
6027
ChEBI
CHEBI:28518
Commercial Catalog
Enamine
EN300-95483
Alfa Aesar
A10643
Names and Identifiers
IUPAC name
(2S,3R,4S,5R)-oxane-2,3,4,5-tetrol
IUPAC Traditional name
α-D-xylose
α-D-xylopyranose
Synonyms
Xylopyranose
(2S,3R,4S,5R)-oxane-2,3,4,5-tetrol
D-(+)-木糖
D-(+)-Xylose
alpha-D-xylose
alpha-D-xylose
WURCS=2.0/1,1,0/[a212h-1a_1-5]/1/
alpha-D-Xylose
Registration numbers
PubChem SID
162103337
8144330
PubChem CID
6027
Beilstein Number
1562108
EC Number
200-400-7
MDL Number
MFCD00151475
MFCD20731172
CAS Number
58-86-6
25990-60-7
6763-34-4
Merck Index
1410087
BRENDA Database
5.1.3.3
3.1.3.23
3.2.1.156
2.4.1.49
3.2.1.177
3.2.1.22
3.2.1.40
3.2.1.37
2.4.1.64
Protein Data Bank
4fe7
4wnh
2cnc
2cdc
5nh7
1h4h
1umz
4bj0
3vl9
6t8f
2d23
6p2l
7eap
4wm0
5a6m
6b6o
3w29
1uqz
6p2o
1b3z
5vyg
5kor
1v6u
2g3j
5koe
2ypj
6dzf
1apv
2yfz
5dpn
5oye
6avl
7plb
2hcz
5dzg
2vh9
6dru
3xis
4wma
5ik8
5oyd
7knc
2d20
6p2m
1cpo
2exj
5a03
4w88
5yqs
4wmb
3e80
5l6g
1b3y
2bs6
4ylq
1ppl
2d44
7pvi
2jeq
1h12
6haa
2bfg
6d6f
5e76
6n4w
5fks
2yih
4w8b
3rdk
4wmi
1ur2
5uk5
2c8n
2fuq
1f8q
3zmr
7kn8
3w27
3w28
5gqd
7plc
1b3v
1qk0
5e7g
5nhe
6b6p
2ebs
4g68
6ha9
2hjp
5nhd
2dua
5sv8
6mgk
5ik5
1ur1
5unc
5z5i
2d24
1w9t
3ugh
6ycg
2fgl
5z5h
6r2w
3vsv
5d9m
6yce
7pvd
2exk
5d9n
2d22
4wn2
5nlq
4xis
5d9p
2jen
1gor
2cn3
4hkw
5gln
6t8e
1vbr
4wmk
5zn7
6ycf
5afe
7puy
6b6q
1uqy
4w87
4cuo
5nlp
5la2
1b3w
1j10
2vlc
2xsp
6mgl
1mn0
SABIO-RK Database
14993
2158
9634
793
6989
6561
14561
15757
9795
6549
6559
9847
14559
9849
UniProt Database
B2JFE9
Q7C637
B5R4P8
P12851
Q5GUF2
Q1MBL8
P56681
A4WVT8
F4J6T7
B0CKM9
Q57IG0
B4T952
Q3YVV0
Q022S9
P54273
P15587
B5RGL6
C0Q1C2
B2T929
C3K8E3
P14405
A6VLM8
Q8G3Q1
B5EX72
Q880Z4
Q8YFX5
A5UIN7
B7ULC6
Q8FCE3
A4IP67
Q1CDB8
Q8U7G6
A5UCZ3
B4ENA5
B3Q0R5
B8HA51
Q3KDW0
B6I3D6
A8LP53
Q92LW9
B0K1L3
Q9CFG7
Q5KYS6
B5YVL8
Q5GYQ7
P10654
P77832
A3PNM4
Q3BMF2
Q739D2
P50910
Q93RJ9
B5FLD6
Q0B1U7
A6VWH1
Q1C0D3
P26997
Q9KGU2
Q8PEW5
B3DR33
Q9L0B8
B1LJC7
A5ILR5
Q57EI4
A1JT10
Q15PG0
Q31V53
A7LXT0
B2U560
A6X4G3
P0CI80
B7MES1
B1Z405
P29441
Q7N4P7
A6L792
B4SWK9
B9JAF5
E0TVS5
C3M8Y0
B2SA37
A5VPA1
A0KE56
Q6T6K9
Q9S3Z4
Q89VC7
B0UT19
A0AF79
A4TS63
B9JSR6
P00944
B1LB08
Q9S7Y7
Q8P9T9
A3N3K2
A1A0H0
O82845
Q65PY0
Q9P999
Q9XBQ3
Q4UTU6
Q9FKK7
Q9K993
Q4ZSF5
Q2NXR2
B7NEL7
A5CPC1
Q5LCV9
A7Z522
Q8G204
P21938
B7NP65
P30435
Q9S306
B9MPG8
B7L6Y0
Q162B6
Q93HF3
C4ZXF6
Q48J73
B2K7D2
A7FP68
A0JXN9
P24300
Q8P3H1
B0BTI9
A9M9H3
Q03HN1
P19149
A8FE33
Q7C3R3
A7ZTB2
Q8A9M2
Q11EH9
Q40082
A9R5Q1
Q03TX3
Q2K433
Q7A9X4
Q4QLI2
Q13RB8
Q64U20
P37031
Q3IYM4
P31434
A4W566
Q2YMQ2
Q7UVG2
B9K7G3
P29442
B4TZ55
Q663Y3
B7M3I8
P54272
A8G7W8
Q2GAB9
O08325
A8A623
Q8PLL9
P29443
C6DIH5
B1KB47
Q5PLM6
B7N1L9
Q98CR8
B5ZQV6
A7MNI5
Q9RFM4
P45687
P27157
C0RHQ0
A9ARG7
Q5WKJ3
Q9X1Z5
Q5LV46
A9MUV0
B0RIF1
Q6LUY7
B1X8I1
A4JSU5
Q1BG90
A6UD89
Q02Y75
P24299
Q8ZL90
Q8ELU7
Q0TBN7
P44398
Q4UNZ4
Q2SW40
P09033
B3H2X9
B1JH40
P12070
P22857
B1IZM7
Q8Z9Z1
P22842
Q1GKQ4
B9KPP8
Q9L558
P19148
Q6DB05
B7LTH9
Golm Database
d46e1acf-7696-4b9a-9c03-5eecd8384bbf
43714407-37a7-40aa-983b-8386969d5340
45150704-3419-4f48-98c4-bde7496a9920
6b3e6f60-4e04-41e3-97b7-b775fb48e271
184329ee-dcc7-4bf7-a7e6-2982823d8035
29612a28-d2ac-4a3d-9401-77f6ca30007f
7d9f5de1-8437-4938-a721-fd6a6ea53ba8
74bd5172-0640-43e9-b154-502f442be61b
54f8e5bb-6791-4d3e-995a-6ddd46b12c1d
905e752c-9c5d-4722-a80f-ff5515526481
db73c1e8-d094-4395-bc9a-09a6f1706fe3
8861c8b9-42cb-40b5-99ad-f81e930576af
4230d8f3-9376-4012-b50a-1cf3536ff220
b8553418-bd01-495c-8e05-3a967d4501fb
08329bda-4127-4f0f-a6f7-a4576438e927
5374d0dc-505c-47b6-9aa4-0b8053544b82
87813bfd-ab70-4931-9381-95768d19065b
a6f45e94-12a0-44f2-b782-7306ac48e9f4
8a18cdd1-e352-4724-8cb0-5be3f75e5230
e45acd47-2ccf-44a7-96bf-341bc4ff3492
6cff072b-2a3a-46ca-9fdd-ddb1244dd31f
ca19a764-3709-45d7-9d73-8507aae0e19a
b115c092-6239-4ab9-aca3-ed65a1bea8ef
f31aa003-ad2d-4ffa-886d-61a409787b70
0a114939-7b22-41d3-981f-2f25ed5c7bd6
aabf5d46-38f6-4df4-9d25-a7203d263a08
084f2692-58cd-436c-80fc-7772173f475e
3b6d98b5-4cd9-49c1-a7fe-1b80e0cace88
d05ee57f-a3b2-47f7-b714-7dd50e5a7df8
a83d5a09-d886-43a3-8532-7447668ef388
fc808966-b576-4ad4-bdf8-101bfb1c5e29
c4afb7b0-babf-43fe-b899-5c762306687e
661e68b7-2e43-4657-be5b-d9f375977e58
5768280f-bf37-403c-ad9f-cd3df4be46b5
655af224-f5a5-4cb7-a77a-9ab49ffed04f
f2071c6f-bfe6-4ff8-8a5d-9f11815a148f
c28c8af1-e75f-4633-8248-27d5a6863c7a
bd86310a-bea0-41b4-b4a9-ad6885642b4e
f7cd6fb7-7ee1-4f31-8993-7f8ad64ddd85
d54cf220-5ff1-400f-a564-8f040acbc10a
b0749042-faa4-4145-8769-a0658d1c1002
c4ee563a-1163-4fb6-a3d3-e3e549f1cb19
510889d3-f8bb-4685-ac87-8ca999d4c1f5
0ddb498e-1e8d-4f6d-a72e-934bed06009c
6bd3cfee-9cfe-4251-94d3-0be03b7580ed
CHEBI ID
CHEBI:10272
CHEBI:28518
CHEBI:46595
CHEBI:22415
GlyTouKan Database
G03144EF
Rhea Database
RHEA:63336
ACToR Database
25990-60-7
133-56-2
6763-34-4
SureChEMBL Database
SCHEMBL345574
BKMS React Database
55027
2945
KEGG ID
C01394
C02205
MetaboLights Database
MTBLS208
MTBLS1622
MTBLS187
KNApSAcK Database
C00007290
BRENDA Ligand Database
2945
55027
DrugBank ID
DB03389
GlyGen Database
G03144EF
Properties
Physical Property
Hydrophobicity(logP)
-2.181
Source
Density
1.525
Source
Melting Point
147-151°C
Source
Flash Point
> 100°C(212°F)
Source
Optical Rotation
+19 (c=10 in water + NH4OH)
Source
Product Information
Purity
95%
Source
98+%
Source
Safety Information
TSCA Listed
是
Source
RTECS
ZF2285000
Source
Storage Warning
Hygroscopic
Source
Related Proteins
PDB Bank
Loading...
4FE7
Loading...
4WNH
Loading...
2CNC
Loading...
2CDC
Loading...
5NH7
Loading...
1H4H
1UMZ
4BJ0
3VL9
6T8F
2D23
6P2L
7EAP
4WM0
5A6M
6B6O
3W29
1UQZ
6P2O
1B3Z
5VYG
5KOR
1V6U
2G3J
5KOE
2YPJ
6DZF
1APV
2YFZ
5DPN
5OYE
6AVL
7PLB
2HCZ
5DZG
2VH9
6DRU
3XIS
4WMA
5IK8
5OYD
7KNC
2D20
6P2M
1CPO
2EXJ
5A03
4W88
5YQS
4WMB
3E80
5L6G
1B3Y
2BS6
4YLQ
1PPL
2D44
7PVI
2JEQ
1H12
6HAA
2BFG
6D6F
5E76
6N4W
5FKS
2YIH
4W8B
3RDK
4WMI
1UR2
5UK5
2C8N
2FUQ
1F8Q
3ZMR
7KN8
3W27
3W28
5GQD
7PLC
1B3V
1QK0
5E7G
5NHE
6B6P
2EBS
4G68
6HA9
2HJP
5NHD
2DUA
5SV8
6MGK
5IK5
1UR1
5UNC
5Z5I
2D24
1W9T
3UGH
6YCG
2FGL
5Z5H
6R2W
3VSV
5D9M
6YCE
7PVD
2EXK
5D9N
2D22
4WN2
5NLQ
4XIS
5D9P
2JEN
1GOR
2CN3
4HKW
5GLN
6T8E
1VBR
4WMK
5ZN7
6YCF
5AFE
7PUY
6B6Q
1UQY
4W87
4CUO
5NLP
5LA2
1B3W
1J10
2VLC
2XSP
6MGL
1MN0
Molecule Details
DrugBank
DB03389
Drug information: experimental
ChEBI
CHEBI:28518
A D-xylopyranose in with an alpha-configuration at the anomeric position.
References
PubChem Literature
From Data Sources
•
For conversion to the useful chiral synthon (2S,4S)-2,4,5-trihydroxypentanoic acid 4,5-acetonide methyl ester, see:
Org. Synth. Coll.
,
9
, 717 (1998).
Bioactivity
PubChem BioAssay
Registration numbers
•
PubChem SID
•
PubChem CID
•
Beilstein Number
•
EC Number
•
MDL Number
•
CAS Number
•
Merck Index
•
BRENDA Database
•
Protein Data Bank
•
SABIO-RK Database
•
UniProt Database
•
Golm Database
•
CHEBI ID
•
GlyTouKan Database
•
Rhea Database
•
ACToR Database
•
SureChEMBL Database
•
BKMS React Database
•
KEGG ID
•
MetaboLights Database
•
KNApSAcK Database
•
BRENDA Ligand Database
•
DrugBank ID
•
GlyGen Database